ABTEILUNG MIKROGRAVITATION UND TRANSLATIONALE REGENERATIVE MEDIZIN

Dr. rer. medic. Herbert Schulz

Arbeitsgruppenleiter, IT-Beauftragter

Dr. rer. medic. Herbert Schulz

Abteilung Mikrogravitation und Translationale Regenerative Medizin (MTRM)
AG Bioinformatik in der Weltraummedizin
Universitätsplatz 2, 39106 Magdeburg, G28-010
Publikationen

2022

Begutachteter Zeitschriftenartikel

Adesoji, Oluyomi M.;  Schulz, Herbert;  May, Patrick;  Krause, Roland;  Lerche, Holger;  Nothnagel, Michael 

Benchmarking of univariate pleiotropy detection methods applied to epilepsy
In: Human mutation - New York, NY [u.a.]: Wiley-Liss, 1992, Bd. 43 (2022), insges. 19 S.

Baran, Ronni;  Wehland, Markus;  Schulz, Herbert;  Heer, Martina;  Infanger, Manfred;  Grimm, Daniela 

Microgravity-related changes in bone density and treatment options - a systematic review
In: International journal of molecular sciences - Basel: Molecular Diversity Preservation International, 2000, Bd. 23 (2022), 15, insges. 23 S.

Dietrichs, Dorothea;  Grimm, Daniela Gabriele;  Sahana, Jayashree;  Melnik, Daniela;  Corydon, Thomas J.;  Wehland, Markus;  Krüger, Marcus;  Vermeesen, Randy;  Baselet, Bjorn;  Baatout, Sarah;  Hybel, Trine Engelbrecht;  Kahlert, Stefan;  Schulz, Herbert;  Infanger, Manfred;  Kopp, Sascha 

Three-dimensional growth of prostate cancer cells exposed to simulated microgravity
In: Frontiers in cell and developmental biology - Lausanne: Frontiers Media, 2013, Bd. 10 (2022), insges. 21 S.

Grimm, Daniela Gabriele;  Schulz, Herbert;  Krüger, Marcus;  Cortés-Sánchez, José Luis;  Egli, Marcel;  Kraus, Armin;  Sahana, Jayashree;  Corydon, Thomas J.;  Hemmersbach, Ruth;  Wise, Petra;  Infanger, Manfred;  Wehland, Markus 

The fight against cancer by microgravity - the multicellular spheroid as a metastasis model
In: International journal of molecular sciences - Basel: Molecular Diversity Preservation International, 2000, Bd. 23 (2022), 6, insges. 45 S.

Schulz, Herbert;  Dietrichs, Dorothea;  Wehland, Markus;  Corydon, Thomas J.;  Hemmersbach, Ruth;  Liemersdorf, Christian;  Melnik, Daniela;  Hübner, Norbert;  Saar, Kathrin;  Infanger, Manfred;  Grimm, Daniela 

In prostate cancer cells cytokines are early responders to gravitational changes occurring in parabolic flights
In: International journal of molecular sciences - Basel: Molecular Diversity Preservation International, 2000, Bd. 23 (2022), 14, insges. 18 S.

Schulz, Herbert;  Strauch, Sebastian M.;  Richter, Peter;  Wehland, Markus;  Krüger, Marcus;  Sahana, Jayashree;  Corydon, Thomas J.;  Wise, Petra;  Baran, Ronni;  Lebert, Michael;  Grimm, Daniela Gabriele 

Latest knowledge about changes in the proteome in microgravity
In: Expert review of proteomics - Abingdon: Taylor & Francis Group, Bd. 19 (2022), 1, S. 43-59

Tsortouktzidis, Despina;  Tröscher, Anna R.;  Schulz, Herbert;  Opitz, Thoralf;  Schoch, Susanne;  Becker, Albert;  Loo, Karen M. J. 

A versatile clustered regularly interspaced palindromic repeats toolbox to study neurological CaV3.2 channelopathies by promoter-mediated transcription control
In: Frontiers in molecular neuroscience - Lausanne: Frontiers Research Foundation, 2008, Bd. 14 (2022), insges. 9 S.

2021

Begutachteter Zeitschriftenartikel

Bauer, Johann;  Gombocz, Erich;  Schulz, Herbert;  Hauslage, Jens;  Grimm, Daniela Gabriele 

Interaction network provides clues on the role of BCAR1 in cellular response to changes in gravity
In: Computation - Basel: MDPI, 2013, Bd. 9 (2021), 8, insges. 25 S.

Melnik, Daniela;  Krüger, Marcus;  Schulz, Herbert;  Kopp, Sascha;  Wehland, Markus;  Bauer, Johann;  Baselet, Bjorn;  Vermeesen, Randy;  Baatout, Sarah;  Corydon, Thomas J.;  Infanger, Manfred;  Grimm, Daniela Gabriele 

The CellBox-2 Mission to the International Space Station - thyroid cancer cells in space
In: International journal of molecular sciences - Basel: Molecular Diversity Preservation International, 2000, Bd. 22 (2021), 16, insges. 21 S.

Tsortouktzidis, D.;  Schulz, H.;  Hamed, M.;  Vatter, H.;  Surges, R.;  Schoch, S.;  Sander, T.;  Becker, A.J.;  van Loo, K.M.J. 

Gene expression analysis in epileptic hippocampi reveals a promoter haplotype conferring reduced aldehyde dehydrogenase 5a1 expression and responsiveness
In: In: Epilepsia, Blackwell Publishing Inc., Bd. 62, 1, S. e29-e34, 2021, 00139580

2020

Begutachteter Zeitschriftenartikel

Wolking, Stefan;  Schulz, Herbert;  Nies, Anne T;  McCormack, Mark;  Schaeffeler, Elke;  Auce, Pauls;  Avbersek, Andreja;  Becker, Felicitas;  Klein, Karl M;  Krenn, Martin;  Møller, Rikke S;  Nikanorova, Marina;  Weckhuysen, Sarah;  Consortium, EpiPGx;  Cavalleri, Gianpiero L;  Delanty, Norman;  Depondt, Chantal;  Johnson, Michael R;  Koeleman, Bobby Pc;  Kunz, Wolfram S;  Marson, Anthony G;  Sander, Josemir W;  Sills, Graeme J;  Striano, Pasquale;  Zara, Federico;  Zimprich, Fritz;  Weber, Yvonne G;  Krause, Roland;  Sisodiya, Sanjay;  Schwab, Matthias;  Sander, Thomas;  Lerche, Holger 

Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.
In: Pharmacogenomics, 2020, Bd. 21, Heft 5, S. 325-335

2019

Begutachteter Zeitschriftenartikel

Lützenberg, Ronald;  Wehland, Markus;  Solano, Kendrick;  Nassef, Mohamed Z.;  Buken, Christoph;  Melnik, Daniela;  Bauer, Johann;  Kopp, Sascha;  Krüger, Marcus;  Riwaldt, Stefan;  Hemmersbach, Ruth;  Schulz, Herbert;  Infanger, Manfred;  Grimm, Daniela Gabriele 

Beneficial effects of low frequency vibration on human chondrocytes in vitro
In: Cellular physiology and biochemistry - Düsseldorf: Cell Physiol Biochem Press GmbH & Co KG, 1991, Bd. 53 (2019), 4, S. 623-637

Prüss, Harald;  Gessner, Guido;  Heinemann, Stefan H;  Rüschendorf, Franz;  Ruppert, Ann-Kathrin;  Schulz, Herbert;  Sander, Thomas;  Rimpau, Wilhelm 

Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel KCNQ1 Loss-of-Function Mutation.
In: Frontiers in neurology, 2019, Bd. 10, S. 648

Schulz, Herbert;  Ruppert, Ann-Kathrin;  Zara, Federico;  Madia, Francesca;  Iacomino, Michele;  S Vari, Maria;  Balagura, Ganna;  Minetti, Carlo;  Striano, Pasquale;  Bianchi, Amedeo;  Marini, Carla;  Guerrini, Renzo;  Weber, Yvonne G;  Becker, Felicitas;  Lerche, Holger;  Kapser, Claudia;  Schankin, Christoph J;  Kunz, Wolfram S;  Møller, Rikke S;  Oliver, Karen L;  Bellows, Susannah T;  Mullen, Saul A;  Berkovic, Samuel F;  Scheffer, Ingrid E;  Caglayan, Hande;  Ozbek, Ugur;  Hoffmann, Per;  Schramm, Sara;  Tsortouktzidis, Despina;  Becker, Albert J;  Sander, Thomas 

No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.
In: Epilepsia, 2019, Bd. 60, Heft 5, S. e31-e36

2018

Begutachteter Zeitschriftenartikel

Gorvin, Caroline M;  Ahmad, Bushra N;  Stechman, Michael J;  Loh, Nellie Y;  Hough, Tertius A;  Leo, Paul;  Marshall, Mhairi;  Sethi, Siddharth;  Bentley, Liz;  Piret, Sian E;  Reed, Anita;  Jeyabalan, Jeshmi;  Christie, Paul T;  Wells, Sara;  Simon, Michelle M;  Mallon, Ann-Marie;  Schulz, Herbert;  Huebner, Norbert;  Brown, Matthew A;  Cox, Roger D;  Brown, Steve D;  Thakker, Rajesh V 

An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2018, Bd. 34, Heft 3, S. 497-507

Kopp, Sascha;  Krüger, Marcus;  Bauer, Johann;  Wehland, Markus;  Corydon, Thomas J.;  Sahana, Jayashree;  Nassef, Mohamed Zakaria;  Melnik, Daniela;  Bauer, Thomas J.;  Schulz, Herbert;  Schütte, Andreas;  Schmitz, Burkhard;  Oltmann, Hergen;  Feldmann, Stefan;  Infanger, Manfred;  Grimm, Daniela Gabriele 

Microgravity affects thyroid cancer cells during the TEXUS-53 mission stronger than hypergravity
In: International journal of molecular sciences - Basel: Molecular Diversity Preservation International, 2000, Bd. 19.2018, 12, Art.-Nr. 4001, insges. 20 S.

Kopp, Sascha;  Sahana, Jayashree;  Islam, Tawhidul;  Petersen, Asbjørn Graver;  Bauer, Johann;  Corydon, Thomas J.;  Schulz, Herbert;  Saar, Kathrin;  Hübner, Norbert;  Slumstrup, Lasse;  Riwaldt, Stefan;  Wehland, Markus;  Infanger, Manfred;  Luetzenberg, Ronald;  Grimm, Daniela Gabriele 

The role of NF[kappa]B in spheroid formation of human breast cancer cells cultured on the Random Positioning Machine
In: Scientific reports - [London]: Macmillan Publishers Limited, part of Springer Nature, 2011, Bd. 8.2018, Art.-Nr. 921, insges. 17 S.

Kopp, Sascha;  Krüger, Marcus;  Feldmann, Stefan;  Oltmann, Hergen;  Schütte, Andreas;  Schmitz, Burkhard;  Bauer, Johann;  Schulz, Herbert;  Saar, Kathrin;  Hübner, Norbert;  Wehland, Markus;  Nassef, Mohamed Zakaria;  Melnik, Daniela;  Meltendorf, Stefan;  Infanger, Manfred;  Grimm, Daniela Gabriele 

Thyroid cancer cells in space during the TEXUS-53 sounding rocket mission - the THYROID project
In: Scientific reports - [London]: Macmillan Publishers Limited, part of Springer Nature, 2011, Bd. 8.2018, Art.-Nr. 10355, insges. 13 S.

Lützenberg, Ronald;  Solano, Kendrick;  Buken, Christoph;  Sahana, Jayashree;  Riwaldt, Stefan;  Kopp, Sascha;  Krüger, Marcus;  Schulz, Herbert;  Saar, Kathrin;  Hübner, Norbert;  Hemmersbach, Ruth;  Bauer, Johann;  Infanger, Manfred;  Grimm, Daniela Gabriele;  Wehland, Markus 

Pathway analysis hints towards beneficial effects of long-term vibration on human chondrocytes
In: Cellular physiology and biochemistry - Düsseldorf: Cell Physiol Biochem Press GmbH & Co KG, 1991, Bd. 47 (2018), 4, S. 1729-1741

Neirijnck, Yasmine;  Reginensi, Antoine;  Renkema, Kirsten Y;  Massa, Filippo;  Kozlov, Vladimir M;  Dhib, Haroun;  Bongers, Ernie M H F;  Feitz, Wout F;  van Eerde, Albertien M;  Lefebvre, Veronique;  Knoers, Nine V A M;  Tabatabaei, Mansoureh;  Schulz, Herbert;  McNeill, Helen;  Schaefer, Franz;  Wegner, Michael;  Sock, Elisabeth;  Schedl, Andreas 

Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).
In: Kidney international, 2018, Bd. 93, Heft 5, S. 1142-1153

2017

Begutachteter Zeitschriftenartikel

Aggarwal, Abhishek;  Schulz, Herbert;  Manhardt, Teresa;  Bilban, Martin;  Thakker, Rajesh V;  Kallay, Enikö 

Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium.
In: Biochimica et biophysica acta. Molecular cell research, 2017, Bd. 1864, Heft 6, S. 987-996

Akcakaya, Nihan Hande;  Capan, Özlem Yalcin;  Schulz, Herbert;  Sander, Thomas;  Caglayan, Server Hande;  Yapc, Zuhal 

De novo 8p23.1 deletion in a patient with absence epilepsy.
In: Epileptic disorders : international epilepsy journal with videotape, 2017, Bd. 19, Heft 2, S. 217-221

Kudin, Alexei P;  Baron, Gregor;  Zsurka, Gábor;  Hampel, Kevin G;  Elger, Christian E;  Grote, Alexander;  Weber, Yvonne;  Lerche, Holger;  Thiele, Holger;  Nürnberg, Peter;  Schulz, Herbert;  Ruppert, Ann-Kathrin;  Sander, Thomas;  Cheng, Qing;  Arnér, Elias Sj;  Schomburg, Lutz;  Seeher, Sandra;  Fradejas-Villar, Noelia;  Schweizer, Ulrich;  Kunz, Wolfram S 

Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.
In: Free radical biology & medicine, 2017, Bd. 106, S. 270-277

Schulz, Herbert;  Ruppert, Ann-Kathrin;  Herms, Stefan;  Wolf, Christiane;  Mirza-Schreiber, Nazanin;  Stegle, Oliver;  Czamara, Darina;  Forstner, Andreas J;  Sivalingam, Sugirthan;  Schoch, Susanne;  Moebus, Susanne;  Pütz, Benno;  Hillmer, Axel;  Fricker, Nadine;  Vatter, Hartmut;  Müller-Myhsok, Bertram;  Nöthen, Markus M;  Becker, Albert J;  Hoffmann, Per;  Sander, Thomas;  Cichon, Sven 

Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus.
In: Nature communications, 2017, Bd. 8, Heft 1, S. 1511

Zadora, Julianna;  Singh, Manvendra;  Herse, Florian;  Przybyl, Lukasz;  Haase, Nadine;  Golic, Michaela;  Yung, Hong Wa;  Huppertz, Berthold;  Cartwright, Judith E;  Whitley, Guy;  Johnsen, Guro M;  Levi, Giovanni;  Isbruch, Annette;  Schulz, Herbert;  Luft, Friedrich C;  Müller, Dominik N;  Staff, Anne Cathrine;  Hurst, Laurence D;  Dechend, Ralf;  Izsvák, Zsuzsanna 

Disturbed Placental Imprinting in Preeclampsia Leads to Altered Expression of DLX5, a Human-Specific Early Trophoblast Marker.
In: Circulation, 2017, Bd. 136, Heft 19, S. 1824-1839

2016

Begutachteter Zeitschriftenartikel

Järve, Anne;  Mühlstedt, Silke;  Qadri, Fatimunnisa;  Nickl, Bernadette;  Schulz, Herbert;  Hübner, Norbert;  Özcelik, Cemil;  Bader, Michael 

Adverse left ventricular remodeling by glycoprotein nonmetastatic melanoma protein B in myocardial infarction.
In: FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2016, Bd. 31, Heft 2, S. 556-568

2015

Begutachteter Zeitschriftenartikel

Herlan, L.;  Schulz, A.;  Schulte, L.;  Schulz, H.;  Hübner, N.;  Kreutz, R. 

Novel candidate genes for impaired nephron development in a rat model with inherited nephron deficit and albuminuria
In: In: Clin Exp Pharmacol Physiol, Bd. 42, 10, S. 1051-1058, 2015

Jost, K. L.;  Bertulat, B.;  Rapp, A.;  Brero, A.;  Hardt, T.;  Domaing, P.;  Gösele, C.;  Schulz, H.;  Hübner, N.;  Cardoso, M. C. 

Gene repositioning within the cell nucleus is not random and is determined by its genomic neighborhood
In: In: Epigenetics Chromatin, Bd. 8, S. 36, 2015

Lal, D.;  Ruppert, A. K.;  Trucks, H.;  Schulz, H.;  de Kovel, C. G.;  Kasteleijn-Nolst Trenité, D.;  Sonsma, A. C.;  Koeleman, B. P.;  Lindhout, D.;  Weber, Y. G.;  Lerche, H.;  Kapser, C.;  Schankin, C. J.;  Kunz, W. S.;  Surges, R.;  Elger, C. E.;  Gaus, V.;  Schmitz, B.;  Helbig, I.;  Muhle, H.;  Stephani, U.;  Klein, K. M.;  Rosenow, F.;  Neubauer, B. A.;  Reinthaler, E. M.;  Zimprich, F.;  Feucht, M.;  Møller, R. S.;  Hjalgrim, H.;  De Jonghe, P.;  Suls, A.;  Lieb, W.;  Franke, A.;  Strauch, K.;  Gieger, C.;  Schurmann, C.;  Schminke, U.;  Nürnberg, P.;  Sander, T.;  Mörzinger, M.;  Weckhuysen, S.;  Claes, L.;  Deprez, L.;  Smets, K.;  Van Dyck, T.;  Deconinck, T.;  Campus, K.;  Klitten, L. L.;  Johannsen, W.;  Ostertag, P.;  von Spiczak, S.;  Strasse, S. F.;  Kleefuß-Lie, A.;  Janz, D.;  Marburg, P. U.;  Reif, P. S.;  Oertel, W. H.;  Hamer, H. M.;  Becker, F.;  Weber, Y.;  de Kovel, C. 

Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies
In: In: PLoS Genet, Bd. 11, 5, S. e1005226, 2015

Lefebvre, J.;  Clarkson, M.;  Massa, F.;  Bradford, S. T.;  Charlet, A.;  Buske, F.;  Lacas-Gervais, S.;  Schulz, H.;  Gimpel, C.;  Hata, Y.;  Schaefer, F.;  Schedl, A. 

Alternatively spliced isoforms of WT1 control podocyte-specific gene expression
In: In: Kidney Int, Bd. 88, 2, S. 321-331, 2015

Maass, P. G.;  Aydin, A.;  Luft, F. C.;  Schächterle, C.;  Weise, A.;  Stricker, S.;  Lindschau, C.;  Vaegler, M.;  Qadri, F.;  Toka, H. R.;  Schulz, H.;  Krawitz, P. M.;  Parkhomchuk, D.;  Hecht, J.;  Hollfinger, I.;  Wefeld-Neuenfeld, Y.;  Bartels-Klein, E.;  Mühl, A.;  Kann, M.;  Schuster, H.;  Chitayat, D.;  Bialer, M. G.;  Wienker, T. F.;  Ott, J.;  Rittscher, K.;  Liehr, T.;  Jordan, J.;  Plessis, G.;  Tank, J.;  Mai, K.;  Naraghi, R.;  Hodge, R.;  Hopp, M.;  Hattenbach, L. O.;  Busjahn, A.;  Rauch, A.;  Vandeput, F.;  Gong, M.;  Rüschendorf, F.;  Hübner, N.;  Haller, H.;  Mundlos, S.;  Bilginturan, N.;  Movsesian, M. A.;  Klussmann, E.;  Toka, O.;  Bähring, S. 

PDE3A mutations cause autosomal dominant hypertension with brachydactyly
In: In: Nat Genet, Bd. 47, 6, S. 647-653, 2015

Wehland, Markus;  Aleshcheva, Ganna;  Schulz, Herbert;  Saar, Katrin;  Hübner, Norbert;  Hemmersbach, Ruth;  Braun, Markus;  Ma, Xiao;  Frett, Timo;  Warnke, Elisabeth;  Riwaldt, Stefan;  Pietsch, Jessica;  Corydon, Thomas J.;  Infanger, Manfred;  Grimm, Daniela 

Differential gene expression of human chondrocytes cultured under short-term altered gravity conditions during parabolic flight maneuvers
In: Cell communication and signaling - London: Biomed Central, Bd. 13.2015, Art.-Nr. 18, insges. 13 S.

2014

Begutachteter Zeitschriftenartikel

Aksoy, I.;  Giudice, V.;  Delahaye, E.;  Wianny, F.;  Aubry, M.;  Mure, M.;  Chen, J.;  Jauch, R.;  Bogu, G. K.;  Nolden, T.;  Himmelbauer, H.;  Xavier Doss, M.;  Sachinidis, A.;  Schulz, H.;  Hummel, O.;  Martinelli, P.;  Hübner, N.;  Stanton, L. W.;  Real, F. X.;  Bourillot, P. Y.;  Savatier, P. 

Klf4 and Klf5 differentially inhibit mesoderm and endoderm differentiation in embryonic stem cells
In: In: Nat Commun, Bd. 5, S. 3719, 2014

Baud, A.;  Guryev, V.;  Hummel, O.;  Johannesson, M.;  Flint, J.;  Hermsen, R.;  Stridh, P.;  Graham, D.;  McBride, M.;  Foroud, T.;  Calderari, S.;  Diez, M.;  Ockinger, J.;  Beyeen, A.;  Gillett, A.;  Abdelmagid, N.;  Guerreiro-Cacais, A.;  Jagodic, M.;  Tuncel, J.;  Norin, U.;  Beattie, E.;  Huynh, N.;  Miller, W.;  Koller, D.;  Alam, I.;  Falak, S.;  Osborne-Pellegrin, M.;  Martinez-Membrives, E.;  Canete, T.;  Blazquez, G.;  Vicens-Costa, E.;  Mont-Cardona, C.;  Diaz-Moran, S.;  Tobena, A.;  Zelenika, D.;  Saar, K.;  Patone, G.;  Bauerfeind, A.;  Bihoreau, M. T.;  Heinig, M.;  Lee, Y. A.;  Rintisch, C.;  Schulz, H.;  Wheeler, D.;  Worley, K.;  Muzny, D.;  Gibbs, R.;  Lathrop, M.;  Lansu, N.;  Toonen, P.;  Ruzius, F.;  de Bruijn, E.;  Hauser, H.;  Adams, D.;  Keane, T.;  Atanur, S.;  Aitman, T.;  Flicek, P.;  Malinauskas, T.;  Jones, E.;  Ekman, D.;  Lopez-Aumatell, R.;  Dominiczak, A.;  Holmdahl, R.;  Olsson, T.;  Gauguier, D.;  Hubner, N.;  Fernandez-Teruel, A.;  Cuppen, E.;  Mott, R. 

Erratum: Genomes and phenomes of a population of outbred rats and its progenitors
In: In: Sci Data, Bd. 1, S. 140016, 2014

Baud, A.;  Guryev, V.;  Hummel, O.;  Johannesson, M.;  Flint, J.;  Hermsen, R.;  Stridh, P.;  Graham, D.;  McBride, M.;  Foroud, T.;  Calderari, S.;  Diez, M.;  Ockinger, J.;  Beyeen, A.;  Gillett, A.;  Abdelmagid, N.;  Guerreiro-Cacais, A.;  Jagodic, M.;  Tuncel, J.;  Norin, U.;  Beattie, E.;  Huynh, N.;  Miller, W.;  Koller, D.;  Alam, I.;  Falak, S.;  Osborne-Pellegrin, M.;  Martinez-Membrives, E.;  Canete, T.;  Blazquez, G.;  Vicens-Costa, E.;  Mont-Cardona, C.;  Diaz-Moran, S.;  Tobena, A.;  Zelenika, D.;  Saar, K.;  Patone, G.;  Bauerfeind, A.;  Bihoreau, M. T.;  Heinig, M.;  Lee, Y. A.;  Rintisch, C.;  Schulz, H.;  Wheeler, D.;  Worley, K.;  Muzny, D.;  Gibbs, R.;  Lathrop, M.;  Lansu, N.;  Toonen, P.;  Ruzius, F.;  de Bruijn, E.;  Hauser, H.;  Adams, D.;  Keane, T.;  Atanur, S.;  Aitman, T.;  Flicek, P.;  Malinauskas, T.;  Jones, E.;  Ekman, D.;  Lopez-Aumatell, R.;  Dominiczak, A.;  Holmdahl, R.;  Olsson, T.;  Gauguier, D.;  Hubner, N.;  Fernandez-Teruel, A.;  Cuppen, E.;  Mott, R. 

Genomes and phenomes of a population of outbred rats and its progenitors
In: In: Sci Data, Bd. 1, S. 140011, 2014

Falak, S.;  Schafer, S.;  Baud, A.;  Hummel, O.;  Schulz, H.;  Gauguier, D.;  Hubner, N.;  Osborne-Pellegrin, M. 

Protease inhibitor 15, a candidate gene for abdominal aortic internal elastic lamina ruptures in the rat
In: In: Physiol Genomics, Bd. 46, 12, S. 418-428, 2014

Hirt, M. N.;  Boeddinghaus, J.;  Mitchell, A.;  Schaaf, S.;  Börnchen, C.;  Müller, C.;  Schulz, H.;  Hubner, N.;  Stenzig, J.;  Stoehr, A.;  Neuber, C.;  Eder, A.;  Luther, P. K.;  Hansen, A.;  Eschenhagen, T. 

Functional improvement and maturation of rat and human engineered heart tissue by chronic electrical stimulation
In: In: J Mol Cell Cardiol, Bd. 74, S. 151-161, 2014

Langhans, C.;  Weber-Carstens, S.;  Schmidt, F.;  Hamati, J.;  Kny, M.;  Zhu, X.;  Wollersheim, T.;  Koch, S.;  Krebs, M.;  Schulz, H.;  Lodka, D.;  Saar, K.;  Labeit, S.;  Spies, C.;  Hubner, N.;  Spranger, J.;  Spuler, S.;  Boschmann, M.;  Dittmar, G.;  Butler-Browne, G.;  Mouly, V.;  Fielitz, J. 

Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy
In: In: PLoS One, Bd. 9, 3, S. e92048, 2014

Ragancokova, D.;  Rocca, E.;  Oonk, A. M.;  Schulz, H.;  Rohde, E.;  Bednarsch, J.;  Feenstra, I.;  Pennings, R. J.;  Wende, H.;  Garratt, A. N. 

TSHZ1-dependent gene regulation is essential for olfactory bulb development and olfaction
In: In: J Clin Invest, Bd. 124, 3, S. 1214-1227, 2014

Schlossarek, S.;  Singh, S. R.;  Geertz, B.;  Schulz, H.;  Reischmann, S.;  Hübner, N.;  Carrier, L. 

Proteasome inhibition slightly improves cardiac function in mice with hypertrophic cardiomyopathy
In: In: Front Physiol, Bd. 5, S. 484, 2014

ilhavý, J.;  Zídek, V.;  Landa, V.;  imáková, M.;  Mlejnek, P.;  kop, V.;  Oliyarnyk, O.;  Kazdová, L.;  Mancini, M.;  Saar, K.;  Schulz, H.;  Hübner, N.;  Kurtz, T. W.;  Pravenec, M. 

Rosuvastatin can block pro-inflammatory actions of transgenic human C-reactive protein without reducing its circulating levels
In: In: Cardiovasc Ther, Bd. 32, 2, S. 59-65, 2014

2013

Begutachteter Zeitschriftenartikel

Baud, A.;  Hermsen, R.;  Guryev, V.;  Stridh, P.;  Graham, D.;  McBride, M. W.;  Foroud, T.;  Calderari, S.;  Diez, M.;  Ockinger, J.;  Beyeen, A. D.;  Gillett, A.;  Abdelmagid, N.;  Guerreiro-Cacais, A. O.;  Jagodic, M.;  Tuncel, J.;  Norin, U.;  Beattie, E.;  Huynh, N.;  Miller, W. H.;  Koller, D. L.;  Alam, I.;  Falak, S.;  Osborne-Pellegrin, M.;  Martinez-Membrives, E.;  Canete, T.;  Blazquez, G.;  Vicens-Costa, E.;  Mont-Cardona, C.;  Diaz-Moran, S.;  Tobena, A.;  Hummel, O.;  Zelenika, D.;  Saar, K.;  Patone, G.;  Bauerfeind, A.;  Bihoreau, M. T.;  Heinig, M.;  Lee, Y. A.;  Rintisch, C.;  Schulz, H.;  Wheeler, D. A.;  Worley, K. C.;  Muzny, D. M.;  Gibbs, R. A.;  Lathrop, M.;  Lansu, N.;  Toonen, P.;  Ruzius, F. P.;  de Bruijn, E.;  Hauser, H.;  Adams, D. J.;  Keane, T.;  Atanur, S. S.;  Aitman, T. J.;  Flicek, P.;  Malinauskas, T.;  Jones, E. Y.;  Ekman, D.;  Lopez-Aumatell, R.;  Dominiczak, A. F.;  Johannesson, M.;  Holmdahl, R.;  Olsson, T.;  Gauguier, D.;  Hubner, N.;  Fernandez-Teruel, A.;  Cuppen, E.;  Mott, R.;  Flint, J. 

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats
In: In: Nat Genet, Bd. 45, 7, S. 767-775, 2013

Chuykin, I.;  Schulz, H.;  Guan, K.;  Bader, M. 

Activation of the PTHRP/adenylate cyclase pathway promotes differentiation of rat XEN cells into parietal endoderm, whereas Wnt/ß-catenin signaling promotes differentiation into visceral endoderm
In: In: J Cell Sci, Bd. 126, Pt 1, S. 128-138, 2013

Freitag, N.;  Tirado-González, I.;  Barrientos, G.;  Herse, F.;  Thijssen, V. L.;  Weedon-Fekjær, S. M.;  Schulz, H.;  Wallukat, G.;  Klapp, B. F.;  Nevers, T.;  Sharma, S.;  Staff, A. C.;  Dechend, R.;  Blois, S. M. 

Interfering with Gal-1-mediated angiogenesis contributes to the pathogenesis of preeclampsia
In: In: Proc Natl Acad Sci U S A, Bd. 110, 28, S. 11451-11456, 2013

Knapp, D.;  Schulz, H.;  Rascon, C. A.;  Volkmer, M.;  Scholz, J.;  Nacu, E.;  Le, M.;  Novozhilov, S.;  Tazaki, A.;  Protze, S.;  Jacob, T.;  Hubner, N.;  Habermann, B.;  Tanaka, E. M. 

Comparative transcriptional profiling of the axolotl limb identifies a tripartite regeneration-specific gene program
In: In: PLoS One, Bd. 8, 5, S. e61352, 2013

Ma, X.;  Wehland, M.;  Schulz, H.;  Saar, K.;  Hübner, N.;  Infanger, M.;  Bauer, J.;  Grimm, D. 

Genomic approach to identify factors that drive the formation of three-dimensional structures by EA.hy926 endothelial cells
In: In: PLoS One, Bd. 8, 5, S. e64402, 2013

Pakula, A.;  Schneider, J.;  Janke, J.;  Zacharias, U.;  Schulz, H.;  Hübner, N.;  Mähler, A.;  Spuler, A.;  Spuler, S.;  Carlier, P.;  Boschmann, M. 

Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1)
In: In: PLoS One, Bd. 8, 9, S. e73573, 2013

Pernhorst, K.;  Herms, S.;  Hoffmann, P.;  Cichon, S.;  Schulz, H.;  Sander, T.;  Schoch, S.;  Becker, A. J.;  Grote, A. 

TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue
In: In: Seizure, Bd. 22, 8, S. 675-678, 2013

Wu, Y. J.;  Schulz, H.;  Lin, C. C.;  Saar, K.;  Patone, G.;  Fischer, H.;  Hübner, N.;  Heimrich, B.;  Schwemmle, M. 

Borna disease virus-induced neuronal degeneration dependent on host genetic background and prevented by soluble factors
In: In: Proc Natl Acad Sci U S A, Bd. 110, 5, S. 1899-1904, 2013

2012

Begutachteter Zeitschriftenartikel

Chakraborty, D.;  Kappei, D.;  Theis, M.;  Nitzsche, A.;  Ding, L.;  Paszkowski-Rogacz, M.;  Surendranath, V.;  Berger, N.;  Schulz, H.;  Saar, K.;  Hubner, N.;  Buchholz, F. 

Combined RNAi and localization for functionally dissecting long noncoding RNAs
In: In: Nat Methods, Bd. 9, 4, S. 360-362, 2012

Doss, M. X.;  Gaspar, J. A.;  Winkler, J.;  Hescheler, J.;  Schulz, H.;  Sachinidis, A. 

Specific gene signatures and pathways in mesodermal cells and their derivatives derived from embryonic stem cells
In: In: Stem Cell Rev Rep, Bd. 8, 1, S. 43-54, 2012

Gaspar, J. A.;  Doss, M. X.;  Winkler, J.;  Wagh, V.;  Hescheler, J.;  Kolde, R.;  Vilo, J.;  Schulz, H.;  Sachinidis, A. 

Gene expression signatures defining fundamental biological processes in pluripotent, early, and late differentiated embryonic stem cells
In: In: Stem Cells Dev, Bd. 21, 13, S. 2471-2484, 2012

Guo, W.;  Schafer, S.;  Greaser, M. L.;  Radke, M. H.;  Liss, M.;  Govindarajan, T.;  Maatz, H.;  Schulz, H.;  Li, S.;  Parrish, A. M.;  Dauksaite, V.;  Vakeel, P.;  Klaassen, S.;  Gerull, B.;  Thierfelder, L.;  Regitz-Zagrosek, V.;  Hacker, T. A.;  Saupe, K. W.;  Dec, G. W.;  Ellinor, P. T.;  MacRae, C. A.;  Spallek, B.;  Fischer, R.;  Perrot, A.;  Özcelik, C.;  Saar, K.;  Hubner, N.;  Gotthardt, M. 

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing
In: In: Nat Med, Bd. 18, 5, S. 766-773, 2012

Jackson, M.;  Axton, R. A.;  Taylor, A. H.;  Wilson, J. A.;  Gordon-Keylock, S. A.;  Kokkaliaris, K. D.;  Brickman, J. M.;  Schulz, H.;  Hummel, O.;  Hubner, N.;  Forrester, L. M. 

HOXB4 can enhance the differentiation of embryonic stem cells by modulating the hematopoietic niche
In: In: Stem Cells, Bd. 30, 2, S. 150-160, 2012

Klaus, A.;  Müller, M.;  Schulz, H.;  Saga, Y.;  Martin, J. F.;  Birchmeier, W. 

Wnt/ß-catenin and Bmp signals control distinct sets of transcription factors in cardiac progenitor cells
In: In: Proc Natl Acad Sci U S A, Bd. 109, 27, S. 10921-10926, 2012

Leu, C.;  de Kovel, C. G.;  Zara, F.;  Striano, P.;  Pezzella, M.;  Robbiano, A.;  Bianchi, A.;  Bisulli, F.;  Coppola, A.;  Giallonardo, A. T.;  Beccaria, F.;  Trenité, D. K.;  Lindhout, D.;  Gaus, V.;  Schmitz, B.;  Janz, D.;  Weber, Y. G.;  Becker, F.;  Lerche, H.;  Kleefuss-Lie, A. A.;  Hallman, K.;  Kunz, W. S.;  Elger, C. E.;  Muhle, H.;  Stephani, U.;  Møller, R. S.;  Hjalgrim, H.;  Mullen, S.;  Scheffer, I. E.;  Berkovic, S. F.;  Everett, K. V.;  Gardiner, M. R.;  Marini, C.;  Guerrini, R.;  Lehesjoki, A. E.;  Siren, A.;  Nabbout, R.;  Baulac, S.;  Leguern, E.;  Serratosa, J. M.;  Rosenow, F.;  Feucht, M.;  Unterberger, I.;  Covanis, A.;  Suls, A.;  Weckhuysen, S.;  Kaneva, R.;  Caglayan, H.;  Turkdogan, D.;  Baykan, B.;  Bebek, N.;  Ozbek, U.;  Hempelmann, A.;  Schulz, H.;  Rüschendorf, F.;  Trucks, H.;  Nürnberg, P.;  Avanzini, G.;  Koeleman, B. P.;  Sander, T.;  Zimprich, F.;  Mçrzinger, M.;  Claes, L.;  Deprez, L.;  Smets, K.;  Van Dyck, T.;  Deconinck, T.;  De Jonghe, P.;  Velizarova, R.;  Dimova, P.;  Radionova, M.;  Tournev, I.;  Kancheva, D.;  Jordanova, A.;  Baulac, M.;  Gourfinkel-An, I.;  Helbig, I.;  von Spiczak, S.;  Ostertag, P.;  Leber, M.;  Toliat, M. R.;  Hallmann, K.;  Klein, K. M.;  Reif, P. S.;  Oertel, W. H.;  Hamer, H. M.;  Weber, Y.;  Mei, D.;  Norci, V.;  Gambardella, A.;  Tinuper, P.;  La Neve, A.;  Capovilla, G.;  Vigliano, P.;  Crichiutti, G.;  Vanadia, F.;  Vignoli, A.;  Striano, S.;  Egeo, G.;  Franceschetti, S.;  Belcastro, V.;  Benna, P.;  Coppola, G.;  De Palo, A.;  Ferlazzo, E.;  Vecchi, M.;  Martinelli, V.;  Del Giudice, E.;  Mancardi, M.;  Stranci, G.;  Scabar, A.;  Gobbi, G.;  Giordano, I.;  Guerero, R.;  Giraldez, B. G.;  de Kovel, C.;  de Haan, G. J.;  Ozdemir, O.;  Ugur, S.;  Kocasoy-Orhan, E.;  Yücesan, E.;  Cine, N.;  Gokyigit, A.;  Gurses, C.;  Gul, G.;  Ayta, S.;  Yapici, Z.;  Ozkara, C.;  Yalcin, O.;  Yalcin, D.;  Arslan, K.;  Bozdemir, H.;  Dizdarer, G.;  Uluduz, D. 

Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
In: In: Epilepsia, Bd. 53, 2, S. 308-318, 2012

Maass, P. G.;  Rump, A.;  Schulz, H.;  Stricker, S.;  Schulze, L.;  Platzer, K.;  Aydin, A.;  Tinschert, S.;  Goldring, M. B.;  Luft, F. C.;  Bähring, S. 

A misplaced lncRNA causes brachydactyly in humans
In: In: J Clin Invest, Bd. 122, 11, S. 3990-4002, 2012

Schulte, L.;  Schulz, A.;  Unland, J.;  Schulz, H.;  Hubner, N.;  Schmidt-Ott, K. M.;  Kreutz, R. 

MWF rats with spontaneous albuminuria inherit a reduced efficiency of nephron induction during early nephrogenesis in comparison to SHR rats
In: In: J Hypertens, Bd. 30, 10, S. 2031-2038, 2012

Steffens, M.;  Leu, C.;  Ruppert, A. K.;  Zara, F.;  Striano, P.;  Robbiano, A.;  Capovilla, G.;  Tinuper, P.;  Gambardella, A.;  Bianchi, A.;  La Neve, A.;  Crichiutti, G.;  de Kovel, C. G.;  Kasteleijn-Nolst Trenité, D.;  de Haan, G. J.;  Lindhout, D.;  Gaus, V.;  Schmitz, B.;  Janz, D.;  Weber, Y. G.;  Becker, F.;  Lerche, H.;  Steinhoff, B. J.;  Kleefuß-Lie, A. A.;  Kunz, W. S.;  Surges, R.;  Elger, C. E.;  Muhle, H.;  von Spiczak, S.;  Ostertag, P.;  Helbig, I.;  Stephani, U.;  Møller, R. S.;  Hjalgrim, H.;  Dibbens, L. M.;  Bellows, S.;  Oliver, K.;  Mullen, S.;  Scheffer, I. E.;  Berkovic, S. F.;  Everett, K. V.;  Gardiner, M. R.;  Marini, C.;  Guerrini, R.;  Lehesjoki, A. E.;  Siren, A.;  Guipponi, M.;  Malafosse, A.;  Thomas, P.;  Nabbout, R.;  Baulac, S.;  Leguern, E.;  Guerrero, R.;  Serratosa, J. M.;  Reif, P. S.;  Rosenow, F.;  Mörzinger, M.;  Feucht, M.;  Zimprich, F.;  Kapser, C.;  Schankin, C. J.;  Suls, A.;  Smets, K.;  De Jonghe, P.;  Jordanova, A.;  Caglayan, H.;  Yapici, Z.;  Yalcin, D. A.;  Baykan, B.;  Bebek, N.;  Ozbek, U.;  Gieger, C.;  Wichmann, H. E.;  Balschun, T.;  Ellinghaus, D.;  Franke, A.;  Meesters, C.;  Becker, T.;  Wienker, T. F.;  Hempelmann, A.;  Schulz, H.;  Rüschendorf, F.;  Leber, M.;  Pauck, S. M.;  Trucks, H.;  Toliat, M. R.;  Nürnberg, P.;  Avanzini, G.;  Koeleman, B. P.;  Sander, T. 

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
In: In: Hum Mol Genet, Bd. 21, 24, S. 5359-5372, 2012

Originalartikel in begutachteter internationaler Zeitschrift

Grosse, Jirka;  Wehland, Markus;  Pietsch, Jessica;  Schulz, Herbert;  Saar, Katrin;  Hübner, Norbert;  Eilles, Christoph;  Bauer, Johann;  Abou-El-Ardat, Khalil;  Baatout, Sarah;  Ma, Xiao;  Infanger, Manfred;  Hemmersbach, Ruth;  Grimm, Daniela 

Gravity-sensitive signaling drives 3-dimensional formation of multicellular thyroid cancer spheroids
In: The FASEB journal/ Federation of American Societies for Experimental Biology - Bethesda, Md.: FASEB, Bd. 26 (2012), 12, S. 5124-5140

Grosse, Jirka;  Wehland, Markus;  Pietsch, Jessica;  Ma, Xiao;  Ulbrich, Claudia;  Schulz, Herbert;  Saar, Katrin;  Hübner, Norbert;  Hauslage, Jens;  Hemmersbach, Ruth;  Braun, Markus;  Loon, Jack;  Vagt, Nicole;  Infanger, Manfred;  Eilles, Christoph;  Egli, Marcel;  Richter, Peter;  Baltz, Theo;  Einspanier, Ralf;  Sharbati, Soroush;  Grimm, Daniela 

Short-term weightlessness produced by parabolic flight maneuvers altered gene expression patterns in human endothelial cells
In: The FASEB journal/ Federation of American Societies for Experimental Biology - Bethesda, Md.: FASEB, Bd. 26 (2012), 2, S. 639-655

2011

Begutachteter Zeitschriftenartikel

Nitzsche, A.;  Paszkowski-Rogacz, M.;  Matarese, F.;  Janssen-Megens, E. M.;  Hubner, N. C.;  Schulz, H.;  de Vries, I.;  Ding, L.;  Huebner, N.;  Mann, M.;  Stunnenberg, H. G.;  Buchholz, F. 

RAD21 cooperates with pluripotency transcription factors in the maintenance of embryonic stem cell identity
In: In: PLoS One, Bd. 6, 5, S. e19470, 2011

Wenzel, K.;  Rajakumar, A.;  Haase, H.;  Geusens, N.;  Hubner, N.;  Schulz, H.;  Brewer, J.;  Roberts, L.;  Hubel, C. A.;  Herse, F.;  Hering, L.;  Qadri, F.;  Lindschau, C.;  Wallukat, G.;  Pijnenborg, R.;  Heidecke, H.;  Riemekasten, G.;  Luft, F. C.;  Muller, D. N.;  Lamarca, B.;  Dechend, R. 

Angiotensin II type 1 receptor antibodies and increased angiotensin II sensitivity in pregnant rats
In: In: Hypertension, Bd. 58, 1, S. 77-84, 2011

Originalartikel in begutachteter internationaler Zeitschrift

Ulbrich, Claudia;  Pietsch, Jessica;  Grosse, Jirka;  Wehland, Markus;  Schulz, Herbert;  Saar, Katrin;  Hübner, Norbert;  Hauslage, Jens;  Hemmersbach, Ruth;  Braun, Markus;  Loon, Jack;  Vagt, Nicole;  Egli, Marcel;  Richter, Peter;  Einspanier, Ralf;  Sharbati, Soroush;  Baltz, Theo;  Infanger, Manfred;  Ma, Xiao;  Grimm, Daniela 

Differential gene regulation under altered gravity conditions in follicular thyroid cancer cells: relationship between the extracellular matrix and the cytoskeleton
In: Cellular physiology and biochemistry: international journal of experimental cellular physiology, biochemistry and pharmacology - Basel: Karger, Bd. 28 (2011), 2, S. 185-198

2010

Begutachteter Zeitschriftenartikel

Doss, M. X.;  Wagh, V.;  Schulz, H.;  Kull, M.;  Kolde, R.;  Pfannkuche, K.;  Nolden, T.;  Himmelbauer, H.;  Vilo, J.;  Hescheler, J.;  Sachinidis, A. 

Global transcriptomic analysis of murine embryonic stem cell-derived brachyury(+) (T) cells
In: In: Genes Cells, Bd. 15, 3, S. 209-228, 2010

Gong, M.;  Rueschendorf, F.;  Marx, P.;  Schulz, H.;  Kraft, H. G.;  Huebner, N.;  Koennecke, H. C. 

Clinical and genetic features in a family with CADASIL and high lipoprotein (a) values
In: In: J Neurol, Bd. 257, 8, S. 1240-1245, 2010

Heinig, M.;  Petretto, E.;  Wallace, C.;  Bottolo, L.;  Rotival, M.;  Lu, H.;  Li, Y.;  Sarwar, R.;  Langley, S. R.;  Bauerfeind, A.;  Hummel, O.;  Lee, Y. A.;  Paskas, S.;  Rintisch, C.;  Saar, K.;  Cooper, J.;  Buchan, R.;  Gray, E. E.;  Cyster, J. G.;  Erdmann, J.;  Hengstenberg, C.;  Maouche, S.;  Ouwehand, W. H.;  Rice, C. M.;  Samani, N. J.;  Schunkert, H.;  Goodall, A. H.;  Schulz, H.;  Roider, H. G.;  Vingron, M.;  Blankenberg, S.;  Münzel, T.;  Zeller, T.;  Szymczak, S.;  Ziegler, A.;  Tiret, L.;  Smyth, D. J.;  Pravenec, M.;  Aitman, T. J.;  Cambien, F.;  Clayton, D.;  Todd, J. A.;  Hubner, N.;  Cook, S. A.;  Braund, P.;  Gracey, J.;  Krishnan, U.;  Moore, J. S.;  Nelson, C. P.;  Pollard, H.;  Attwood, T.;  Crisp-Hihn, A.;  Foad, N.;  Jolley, J.;  Lloyd-Jones, H.;  Muir, D.;  Murray, E.;  O'Leary, K.;  Rankin, A.;  Sambrook, J.;  Godfroy, T.;  Brocheton, J.;  Proust, C.;  Schmitz, G.;  Heimerl, S.;  Lugauer, I.;  Belz, S.;  Gulde, S.;  Linsel-Nitschke, P.;  Sager, H.;  Schroeder, L.;  Lundmark, P.;  Syvannen, A. C.;  Neudert, J.;  Scholz, M.;  Deloukas, P.;  Gray, E.;  Gwilliams, R.;  Niblett, D. 

A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk
In: In: Nature, Bd. 467, 7314, S. 460-464, 2010

Ratelade, J.;  Arrondel, C.;  Hamard, G.;  Garbay, S.;  Harvey, S.;  Biebuyck, N.;  Schulz, H.;  Hastie, N.;  Pontoglio, M.;  Gubler, M. C.;  Antignac, C.;  Heidet, L. 

A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes
In: In: Hum Mol Genet, Bd. 19, 1, S. 1-15, 2010

Rolletschek, A.;  Schroeder, I. S.;  Schulz, H.;  Hummel, O.;  Huebner, N.;  Wobus, A. M. 

Characterization of mouse embryonic stem cell differentiation into the pancreatic lineage in vitro by transcriptional profiling, quantitative RT-PCR and immunocytochemistry
In: In: Int J Dev Biol, Bd. 54, 1, S. 41-54, 2010

Wenzel, K.;  Wallukat, G.;  Qadri, F.;  Hubner, N.;  Schulz, H.;  Hummel, O.;  Herse, F.;  Heuser, A.;  Fischer, R.;  Heidecke, H.;  Luft, F. C.;  Muller, D. N.;  Dietz, R.;  Dechend, R. 

Alpha1A-adrenergic receptor-directed autoimmunity induces left ventricular damage and diastolic dysfunction in rats
In: In: PLoS One, Bd. 5, 2, S. e9409, 2010

Yagil, Y.;  Hessner, M.;  Schulz, H.;  Gosele, C.;  Lebedev, L.;  Barkalifa, R.;  Sapojnikov, M.;  Hubner, N.;  Yagil, C. 

Geno-transcriptomic dissection of proteinuria in the uninephrectomized rat uncovers a molecular complexity with sexual dimorphism
In: In: Physiol Genomics, Bd. 42A, 4, S. 301-316, 2010

2009

Begutachteter Zeitschriftenartikel

Abranches, E.;  Silva, M.;  Pradier, L.;  Schulz, H.;  Hummel, O.;  Henrique, D.;  Bekman, E. 

Neural differentiation of embryonic stem cells in vitro: a road map to neurogenesis in the embryo
In: In: PLoS One, Bd. 4, 7, S. e6286, 2009

Bourillot, P. Y.;  Aksoy, I.;  Schreiber, V.;  Wianny, F.;  Schulz, H.;  Hummel, O.;  Hubner, N.;  Savatier, P. 

Novel STAT3 target genes exert distinct roles in the inhibition of mesoderm and endoderm differentiation in cooperation with Nanog
In: In: Stem Cells, Bd. 27, 8, S. 1760-1771, 2009

Ding, L.;  Paszkowski-Rogacz, M.;  Nitzsche, A.;  Slabicki, M. M.;  Heninger, A. K.;  de Vries, I.;  Kittler, R.;  Junqueira, M.;  Shevchenko, A.;  Schulz, H.;  Hubner, N.;  Doss, M. X.;  Sachinidis, A.;  Hescheler, J.;  Iacone, R.;  Anastassiadis, K.;  Stewart, A. F.;  Pisabarro, M. T.;  Caldarelli, A.;  Poser, I.;  Theis, M.;  Buchholz, F. 

A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity
In: In: Cell Stem Cell, Bd. 4, 5, S. 403-415, 2009

Grossmann, K. S.;  Wende, H.;  Paul, F. E.;  Cheret, C.;  Garratt, A. N.;  Zurborg, S.;  Feinberg, K.;  Besser, D.;  Schulz, H.;  Peles, E.;  Selbach, M.;  Birchmeier, W.;  Birchmeier, C. 

The tyrosine phosphatase Shp2 (PTPN11) directs Neuregulin-1/ErbB signaling throughout Schwann cell development
In: In: Proc Natl Acad Sci U S A, Bd. 106, 39, S. 16704-16709, 2009

Haug, K.;  Warnstedt, M.;  Alekov, A. K.;  Sander, T.;  Ramírez, A.;  Poser, B.;  Maljevic, S.;  Hebeisen, S.;  Kubisch, C.;  Rebstock, J.;  Horvath, S.;  Hallmann, K.;  Dullinger, J. S.;  Rau, B.;  Haverkamp, F.;  Beyenburg, S.;  Schulz, H.;  Janz, D.;  Giese, B.;  Müller-Newen, G.;  Propping, P.;  Elger, C. E.;  Fahlke, C.;  Lerche, H. 

Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
In: In: Nat Genet, Bd. 41, 9, S. 1043, 2009

Kleefuss-Lie, A.;  Friedl, W.;  Cichon, S.;  Haug, K.;  Warnstedt, M.;  Alekov, A.;  Sander, T.;  Ramirez, A.;  Poser, B.;  Maljevic, S.;  Hebeisen, S.;  Kubisch, C.;  Rebstock, J.;  Horvath, S.;  Hallmann, K.;  Dullinger, J. S.;  Rau, B.;  Haverkamp, F.;  Beyenburg, S.;  Schulz, H.;  Janz, D.;  Giese, B.;  Müller-Newen, G.;  Propping, P.;  Elger, C. E.;  Fahlke, C.;  Lerche, H. 

CLCN2 variants in idiopathic generalized epilepsy
In: In: Nat Genet, Bd. 41, 9, S. 954-955, 2009

Mariappan, D.;  Niemann, R.;  Gajewski, M.;  Winkler, J.;  Chen, S.;  Choorapoikayil, S.;  Bitzer, M.;  Schulz, H.;  Hescheler, J.;  Sachinidis, A. 

Somitovasculin, a novel endothelial-specific transcript involved in the vasculature development
In: In: Arterioscler Thromb Vasc Biol, Bd. 29, 11, S. 1823-1829, 2009

Mariappan, D.;  Winkler, J.;  Chen, S.;  Schulz, H.;  Hescheler, J.;  Sachinidis, A. 

Transcriptional profiling of CD31(+) cells isolated from murine embryonic stem cells
In: In: Genes Cells, Bd. 14, 2, S. 243-260, 2009

Potta, S. P.;  Liang, H.;  Pfannkuche, K.;  Winkler, J.;  Chen, S.;  Doss, M. X.;  Obernier, K.;  Kamisetti, N.;  Schulz, H.;  Hübner, N.;  Hescheler, J.;  Sachinidis, A. 

Functional characterization and transcriptome analysis of embryonic stem cell-derived contractile smooth muscle cells
In: In: Hypertension, Bd. 53, 2, S. 196-204, 2009

Schulz, H.;  Kolde, R.;  Adler, P.;  Aksoy, I.;  Anastassiadis, K.;  Bader, M.;  Billon, N.;  Boeuf, H.;  Bourillot, P. Y.;  Buchholz, F.;  Dani, C.;  Doss, M. X.;  Forrester, L.;  Gitton, M.;  Henrique, D.;  Hescheler, J.;  Himmelbauer, H.;  Hübner, N.;  Karantzali, E.;  Kretsovali, A.;  Lubitz, S.;  Pradier, L.;  Rai, M.;  Reimand, J.;  Rolletschek, A.;  Sachinidis, A.;  Savatier, P.;  Stewart, F.;  Storm, M. P.;  Trouillas, M.;  Vilo, J.;  Welham, M. J.;  Winkler, J.;  Wobus, A. M.;  Hatzopoulos, A. K. 

The FunGenES database: a genomics resource for mouse embryonic stem cell differentiation
In: In: PLoS One, Bd. 4, 9, S. e6804, 2009

Storm, M. P.;  Kumpfmueller, B.;  Thompson, B.;  Kolde, R.;  Vilo, J.;  Hummel, O.;  Schulz, H.;  Welham, M. J. 

Characterization of the phosphoinositide 3-kinase-dependent transcriptome in murine embryonic stem cells: identification of novel regulators of pluripotency
In: In: Stem Cells, Bd. 27, 4, S. 764-775, 2009

Trouillas, M.;  Saucourt, C.;  Guillotin, B.;  Gauthereau, X.;  Ding, L.;  Buchholz, F.;  Doss, M. X.;  Sachinidis, A.;  Hescheler, J.;  Hummel, O.;  Huebner, N.;  Kolde, R.;  Vilo, J.;  Schulz, H.;  Boeuf, H. 

Three LIF-dependent signatures and gene clusters with atypical expression profiles, identified by transcriptome studies in mouse ES cells and early derivatives
In: In: BMC Genomics, Bd. 10, S. 73, 2009

2008

Begutachteter Zeitschriftenartikel

Karantzali, E.;  Schulz, H.;  Hummel, O.;  Hubner, N.;  Hatzopoulos, A.;  Kretsovali, A. 

Histone deacetylase inhibition accelerates the early events of stem cell differentiation: transcriptomic and epigenetic analysis
In: In: Genome Biol, Bd. 9, 4, S. R65, 2008

Kota, L.;  Schulz, H.;  Falak, S.;  Hübner, N.;  Osborne-Pellegrin, M. 

Localization of genetic loci controlling hydronephrosis in the Brown Norway rat and its association with hematuria
In: In: Physiol Genomics, Bd. 34, 2, S. 215-224, 2008

Monti, J.;  Fischer, J.;  Paskas, S.;  Heinig, M.;  Schulz, H.;  Gösele, C.;  Heuser, A.;  Fischer, R.;  Schmidt, C.;  Schirdewan, A.;  Gross, V.;  Hummel, O.;  Maatz, H.;  Patone, G.;  Saar, K.;  Vingron, M.;  Weldon, S. M.;  Lindpaintner, K.;  Hammock, B. D.;  Rohde, K.;  Dietz, R.;  Cook, S. A.;  Schunck, W. H.;  Luft, F. C.;  Hubner, N. 

Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease
In: In: Nat Genet, Bd. 40, 5, S. 529-537, 2008

Saar, K.;  Beck, A.;  Bihoreau, M. T.;  Birney, E.;  Brocklebank, D.;  Chen, Y.;  Cuppen, E.;  Demonchy, S.;  Dopazo, J.;  Flicek, P.;  Foglio, M.;  Fujiyama, A.;  Gut, I. G.;  Gauguier, D.;  Guigo, R.;  Guryev, V.;  Heinig, M.;  Hummel, O.;  Jahn, N.;  Klages, S.;  Kren, V.;  Kube, M.;  Kuhl, H.;  Kuramoto, T.;  Kuroki, Y.;  Lechner, D.;  Lee, Y. A.;  Lopez-Bigas, N.;  Lathrop, G. M.;  Mashimo, T.;  Medina, I.;  Mott, R.;  Patone, G.;  Perrier-Cornet, J. A.;  Platzer, M.;  Pravenec, M.;  Reinhardt, R.;  Sakaki, Y.;  Schilhabel, M.;  Schulz, H.;  Serikawa, T.;  Shikhagaie, M.;  Tatsumoto, S.;  Taudien, S.;  Toyoda, A.;  Voigt, B.;  Zelenika, D.;  Zimdahl, H.;  Hubner, N. 

SNP and haplotype mapping for genetic analysis in the rat
In: In: Nat Genet, Bd. 40, 5, S. 560-566, 2008

Wenzel, K.;  Haase, H.;  Wallukat, G.;  Derer, W.;  Bartel, S.;  Homuth, V.;  Herse, F.;  Hubner, N.;  Schulz, H.;  Janczikowski, M.;  Lindschau, C.;  Schroeder, C.;  Verlohren, S.;  Morano, I.;  Muller, D. N.;  Luft, F. C.;  Dietz, R.;  Dechend, R.;  Karczewski, P. 

Potential relevance of alpha(1)-adrenergic receptor autoantibodies in refractory hypertension
In: In: PLoS One, Bd. 3, 11, S. e3742, 2008

2007

Begutachteter Zeitschriftenartikel

Doss, M. X.;  Winkler, J.;  Chen, S.;  Hippler-Altenburg, R.;  Sotiriadou, I.;  Halbach, M.;  Pfannkuche, K.;  Liang, H.;  Schulz, H.;  Hummel, O.;  Hübner, N.;  Rottscheidt, R.;  Hescheler, J.;  Sachinidis, A. 

Global transcriptome analysis of murine embryonic stem cell-derived cardiomyocytes
In: In: Genome Biol, Bd. 8, 4, S. R56, 2007

Doss, M. X.;  Chen, S.;  Winkler, J.;  Hippler-Altenburg, R.;  Odenthal, M.;  Wickenhauser, C.;  Balaraman, S.;  Schulz, H.;  Hummel, O.;  Hübner, N.;  Ghosh-Choudhury, N.;  Sotiriadou, I.;  Hescheler, J.;  Sachinidis, A. 

Transcriptomic and phenotypic analysis of murine embryonic stem cell derived BMP2+ lineage cells: an insight into mesodermal patterning
In: In: Genome Biol, Bd. 8, 9, S. R184, 2007

Kota, L.;  Osborne-Pellegrin, M.;  Schulz, H.;  Behmoaras, J.;  Coutard, M.;  Gong, M.;  Hübner, N. 

Quantitative genetic basis of arterial phenotypes in the Brown Norway rat
In: In: Physiol Genomics, Bd. 30, 1, S. 17-25, 2007

Söderhäll, C.;  Marenholz, I.;  Kerscher, T.;  Rüschendorf, F.;  Esparza-Gordillo, J.;  Worm, M.;  Gruber, C.;  Mayr, G.;  Albrecht, M.;  Rohde, K.;  Schulz, H.;  Wahn, U.;  Hubner, N.;  Lee, Y. A. 

Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis
In: In: PLoS Biol, Bd. 5, 9, S. e242, 2007

Wenzel, K.;  Geier, C.;  Qadri, F.;  Hubner, N.;  Schulz, H.;  Erdmann, B.;  Gross, V.;  Bauer, D.;  Dechend, R.;  Dietz, R.;  Osterziel, K. J.;  Spuler, S.;  Ozcelik, C. 

Dysfunction of dysferlin-deficient hearts
In: In: J Mol Med (Berl), Bd. 85, 11, S. 1203-1214, 2007

Wenzel, K.;  Daskalow, K.;  Herse, F.;  Seitz, S.;  Zacharias, U.;  Schenk, J. A.;  Schulz, H.;  Hubner, N.;  Micheel, B.;  Schlag, P. M.;  Osterziel, K. J.;  Ozcelik, C.;  Scherneck, S.;  Jandrig, B. 

Expression of the protein phosphatase 1 inhibitor KEPI is downregulated in breast cancer cell lines and tissues and involved in the regulation of the tumor suppressor EGR1 via the MEK-ERK pathway
In: In: Biol Chem, Bd. 388, 5, S. 489-495, 2007

2006

Begutachteter Zeitschriftenartikel

Lee-Kirsch, M. A.;  Gong, M.;  Schulz, H.;  Rüschendorf, F.;  Stein, A.;  Pfeiffer, C.;  Ballarini, A.;  Gahr, M.;  Hubner, N.;  Linné, M. 

Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p
In: In: Am J Hum Genet, Bd. 79, 4, S. 731-737, 2006

Petersen, H. H.;  Andreassen, T. K.;  Breiderhoff, T.;  Bräsen, J. H.;  Schulz, H.;  Gross, V.;  Gröne, H. J.;  Nykjaer, A.;  Willnow, T. E. 

Hyporesponsiveness to glucocorticoids in mice genetically deficient for the corticosteroid binding globulin
In: In: Mol Cell Biol, Bd. 26, 19, S. 7236-7245, 2006

2005

Begutachteter Zeitschriftenartikel

Hammes, A.;  Andreassen, T. K.;  Spoelgen, R.;  Raila, J.;  Hubner, N.;  Schulz, H.;  Metzger, J.;  Schweigert, F. J.;  Luppa, P. B.;  Nykjaer, A.;  Willnow, T. E. 

Role of endocytosis in cellular uptake of sex steroids
In: In: Cell, Bd. 122, 5, S. 751-762, 2005

Hubner, N.;  Wallace, C. A.;  Zimdahl, H.;  Petretto, E.;  Schulz, H.;  Maciver, F.;  Mueller, M.;  Hummel, O.;  Monti, J.;  Zidek, V.;  Musilova, A.;  Kren, V.;  Causton, H.;  Game, L.;  Born, G.;  Schmidt, S.;  Müller, A.;  Cook, S. A.;  Kurtz, T. W.;  Whittaker, J.;  Pravenec, M.;  Aitman, T. J. 

Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease
In: In: Nat Genet, Bd. 37, 3, S. 243-253, 2005

Wenzel, K.;  Zabojszcza, J.;  Carl, M.;  Taubert, S.;  Lass, A.;  Harris, C. L.;  Ho, M.;  Schulz, H.;  Hummel, O.;  Hubner, N.;  Osterziel, K. J.;  Spuler, S. 

Increased susceptibility to complement attack due to down-regulation of decay-accelerating factor/CD55 in dysferlin-deficient muscular dystrophy
In: In: J Immunol, Bd. 175, 9, S. 6219-6225, 2005

Yagil, C.;  Hubner, N.;  Monti, J.;  Schulz, H.;  Sapojnikov, M.;  Luft, F. C.;  Ganten, D.;  Yagil, Y. 

Identification of hypertension-related genes through an integrated genomic-transcriptomic approach
In: In: Circ Res, Bd. 96, 6, S. 617-625, 2005

2004

Begutachteter Zeitschriftenartikel

Zimdahl, H.;  Nyakatura, G.;  Brandt, P.;  Schulz, H.;  Hummel, O.;  Fartmann, B.;  Brett, D.;  Droege, M.;  Monti, J.;  Lee, Y. A.;  Sun, Y.;  Zhao, S.;  Winter, E. E.;  Ponting, C. P.;  Chen, Y.;  Kasprzyk, A.;  Birney, E.;  Ganten, D.;  Hubner, N. 

A SNP map of the rat genome generated from cDNA sequences
In: In: Science, Bd. 303, 5659, S. 807, 2004

2003

Begutachteter Zeitschriftenartikel

Gong, M.;  Zhang, H.;  Schulz, H.;  Lee, Y. A.;  Sun, K.;  Bähring, S.;  Luft, F. C.;  Nürnberg, P.;  Reis, A.;  Rohde, K.;  Ganten, D.;  Hui, R.;  Hübner, N. 

Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p
In: In: Hum Mol Genet, Bd. 12, 11, S. 1273-1277, 2003

Haug, K.;  Warnstedt, M.;  Alekov, A. K.;  Sander, T.;  Ramírez, A.;  Poser, B.;  Maljevic, S.;  Hebeisen, S.;  Kubisch, C.;  Rebstock, J.;  Horvath, S.;  Hallmann, K.;  Dullinger, J. S.;  Rau, B.;  Haverkamp, F.;  Beyenburg, S.;  Schulz, H.;  Janz, D.;  Giese, B.;  Müller-Newen, G.;  Propping, P.;  Elger, C. E.;  Fahlke, C.;  Lerche, H.;  Heils, A. 

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
In: In: Nat Genet, Bd. 33, 4, S. 527-532, 2003

Monti, J.;  Plehm, R.;  Schulz, H.;  Ganten, D.;  Kreutz, R.;  Hübner, N. 

Interaction between blood pressure quantitative trait loci in rats in which trait variation at chromosome 1 is conditional upon a specific allele at chromosome 10
In: In: Hum Mol Genet, Bd. 12, 4, S. 435-439, 2003

Monti, J.;  Zimdahl, H.;  Schulz, H.;  Plehm, R.;  Ganten, D.;  Hübner, N. 

The role of Wnk4 in polygenic hypertension: a candidate gene analysis on rat chromosome 10
In: In: Hypertension, Bd. 41, 4, S. 938-942, 2003

Sander, T.;  Windemuth, C.;  Schulz, H.;  Saar, K.;  Gennaro, E.;  Riggio, C.;  Bianchi, A.;  Zara, F.;  Rudolf, G.;  Picard, F.;  Bulteau, C.;  Kaminska, A.;  Cieuta, C.;  Prud'homme, J. F.;  Dulac, O.;  Bate, L.;  Robinson, R.;  Gardiner, R. M.;  Covanis, A.;  de Haan, G. J.;  Janssen, G. A.;  van Erp, M. G.;  Boezeman, E. H.;  Lindhout, D.;  Heils, A.;  Nürnberg, P.;  Janz, D. 

Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12
In: In: Epilepsia, Bd. 44, 1, S. 32-39, 2003

2002

Begutachteter Zeitschriftenartikel

Sander, T.;  Windemuth, C.;  Schulz, H.;  Saar, K.;  Gennaro, E.;  Bianchi, A.;  Zara, F.;  Bulteau, C.;  Kaminska, A.;  Ville, D.;  Cieuta, C.;  Prud'homme, J. F.;  Dulac, O.;  Bate, L.;  Gardiner, R. M.;  de Haan, G. J.;  Janssen, G. A.;  Witte, J.;  Halley, D. J.;  Lindhout, D.;  Wienker, T. F.;  Janz, D. 

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1
In: In: Am J Med Genet, Bd. 114, 6, S. 673-678, 2002

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