Omics studies of tumor cells under microgravity conditions
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Structural and molecular changes of human chondrocytes exposed to the rotating wall vessel bioreactor
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Omics studies of specialized cells and stem cells under microgravity conditions
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The formation of stable lung tumor spheroids during random positioning involves increased estrogen sensitivity
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Current knowledge about the impact of microgravity on gene regulation
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Effects of high glucose on human endothelial cells exposed to simulated microgravity
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Long-term simulation of microgravity induces changes in gene expression in breast cancer cells
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A systematic review of the effect of vericiguat on patients with heart failure
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Three-dimensional growth of prostate cancer cells exposed to simulated microgravity
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The fight against cancer by microgravity - the multicellular spheroid as a metastasis model
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Benchmarking of univariate pleiotropy detection methods applied to epilepsy
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Latest knowledge about changes in the proteome in microgravity
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A versatile clustered regularly interspaced palindromic repeats toolbox to study neurological CaV3.2 channelopathies by promoter-mediated transcription control
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In prostate cancer cells cytokines are early responders to gravitational changes occurring in parabolic flights
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Microgravity-related changes in bone density and treatment options - a systematic review
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Prolonged exposure to simulated microgravity changes release of small extracellular vesicle in breast cancer cells
In: International journal of molecular sciences - Basel: Molecular Diversity Preservation International, 2000, Bd. 23 (2022), 24, insges. 20 S.

The CellBox-2 Mission to the International Space Station - thyroid cancer cells in space
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Interaction network provides clues on the role of BCAR1 in cellular response to changes in gravity
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Gene expression analysis in epileptic hippocampi reveals a promoter haplotype conferring reduced aldehyde dehydrogenase 5a1 expression and responsiveness
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Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.
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Beneficial effects of low frequency vibration on human chondrocytes in vitro
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No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.
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Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel KCNQ1 Loss-of-Function Mutation.
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Microgravity affects thyroid cancer cells during the TEXUS-53 mission stronger than hypergravity
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The role of NF[kappa]B in spheroid formation of human breast cancer cells cultured on the Random Positioning Machine
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Thyroid cancer cells in space during the TEXUS-53 sounding rocket mission - the THYROID project
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Pathway analysis hints towards beneficial effects of long-term vibration on human chondrocytes
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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.
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Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).
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The effects of long-term vibration on human chondrocytes
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Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium.
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Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.
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De novo 8p23.1 deletion in a patient with absence epilepsy.
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Disturbed Placental Imprinting in Preeclampsia Leads to Altered Expression of DLX5, a Human-Specific Early Trophoblast Marker.
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Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus.
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Adverse left ventricular remodeling by glycoprotein nonmetastatic melanoma protein B in myocardial infarction.
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PDE3A mutations cause autosomal dominant hypertension with brachydactyly
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Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies
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Alternatively spliced isoforms of WT1 control podocyte-specific gene expression
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Novel candidate genes for impaired nephron development in a rat model with inherited nephron deficit and albuminuria
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Differential gene expression of human chondrocytes cultured under short-term altered gravity conditions during parabolic flight maneuvers
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Gene repositioning within the cell nucleus is not random and is determined by its genomic neighborhood
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Differential gene expression profile and altered cytokine secretion of thyroid cancer cells in space
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Genomes and phenomes of a population of outbred rats and its progenitors
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Erratum: Genomes and phenomes of a population of outbred rats and its progenitors
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Rosuvastatin can block pro-inflammatory actions of transgenic human C-reactive protein without reducing its circulating levels
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TSHZ1-dependent gene regulation is essential for olfactory bulb development and olfaction
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Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy
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Klf4 and Klf5 differentially inhibit mesoderm and endoderm differentiation in embryonic stem cells
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Protease inhibitor 15, a candidate gene for abdominal aortic internal elastic lamina ruptures in the rat
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Functional improvement and maturation of rat and human engineered heart tissue by chronic electrical stimulation
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Proteasome inhibition slightly improves cardiac function in mice with hypertrophic cardiomyopathy
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Combined sequence-based and genetic mapping analysis of complex traits in outbred rats
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Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1)
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Interfering with Gal-1-mediated angiogenesis contributes to the pathogenesis of preeclampsia
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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
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Borna disease virus-induced neuronal degeneration dependent on host genetic background and prevented by soluble factors
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Comparative transcriptional profiling of the axolotl limb identifies a tripartite regeneration-specific gene program
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Genomic approach to identify factors that drive the formation of three-dimensional structures by EA.hy926 endothelial cells
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TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue
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Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
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RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing
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Gene expression signatures defining fundamental biological processes in pluripotent, early, and late differentiated embryonic stem cells
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Combined RNAi and localization for functionally dissecting long noncoding RNAs
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HOXB4 can enhance the differentiation of embryonic stem cells by modulating the hematopoietic niche
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Specific gene signatures and pathways in mesodermal cells and their derivatives derived from embryonic stem cells
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A misplaced lncRNA causes brachydactyly in humans
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Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
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MWF rats with spontaneous albuminuria inherit a reduced efficiency of nephron induction during early nephrogenesis in comparison to SHR rats
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Wnt/ß-catenin and Bmp signals control distinct sets of transcription factors in cardiac progenitor cells
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Short-term weightlessness produced by parabolic flight maneuvers altered gene expression patterns in human endothelial cells
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Gravity-sensitive signaling drives 3-dimensional formation of multicellular thyroid cancer spheroids
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Angiotensin II type 1 receptor antibodies and increased angiotensin II sensitivity in pregnant rats
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RAD21 cooperates with pluripotency transcription factors in the maintenance of embryonic stem cell identity
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Differential gene regulation under altered gravity conditions in follicular thyroid cancer cells: relationship between the extracellular matrix and the cytoskeleton
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Characterization of mouse embryonic stem cell differentiation into the pancreatic lineage in vitro by transcriptional profiling, quantitative RT-PCR and immunocytochemistry
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A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk
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A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes
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Alpha1A-adrenergic receptor-directed autoimmunity induces left ventricular damage and diastolic dysfunction in rats
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Global transcriptomic analysis of murine embryonic stem cell-derived brachyury(+) (T) cells
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Clinical and genetic features in a family with CADASIL and high lipoprotein (a) values
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Geno-transcriptomic dissection of proteinuria in the uninephrectomized rat uncovers a molecular complexity with sexual dimorphism
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Novel STAT3 target genes exert distinct roles in the inhibition of mesoderm and endoderm differentiation in cooperation with Nanog
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Somitovasculin, a novel endothelial-specific transcript involved in the vasculature development
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Characterization of the phosphoinositide 3-kinase-dependent transcriptome in murine embryonic stem cells: identification of novel regulators of pluripotency
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A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity
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Three LIF-dependent signatures and gene clusters with atypical expression profiles, identified by transcriptome studies in mouse ES cells and early derivatives
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Transcriptional profiling of CD31(+) cells isolated from murine embryonic stem cells
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Functional characterization and transcriptome analysis of embryonic stem cell-derived contractile smooth muscle cells
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The tyrosine phosphatase Shp2 (PTPN11) directs Neuregulin-1/ErbB signaling throughout Schwann cell development
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The FunGenES database: a genomics resource for mouse embryonic stem cell differentiation
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Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
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CLCN2 variants in idiopathic generalized epilepsy
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Neural differentiation of embryonic stem cells in vitro: a road map to neurogenesis in the embryo
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SNP and haplotype mapping for genetic analysis in the rat
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Histone deacetylase inhibition accelerates the early events of stem cell differentiation: transcriptomic and epigenetic analysis
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Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease
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Localization of genetic loci controlling hydronephrosis in the Brown Norway rat and its association with hematuria
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Potential relevance of alpha(1)-adrenergic receptor autoantibodies in refractory hypertension
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Quantitative genetic basis of arterial phenotypes in the Brown Norway rat
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Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis
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Dysfunction of dysferlin-deficient hearts
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Transcriptomic and phenotypic analysis of murine embryonic stem cell derived BMP2+ lineage cells: an insight into mesodermal patterning
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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
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Global transcriptome analysis of murine embryonic stem cell-derived cardiomyocytes
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Hyporesponsiveness to glucocorticoids in mice genetically deficient for the corticosteroid binding globulin
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Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p
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Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease
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Increased susceptibility to complement attack due to down-regulation of decay-accelerating factor/CD55 in dysferlin-deficient muscular dystrophy
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Role of endocytosis in cellular uptake of sex steroids
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Identification of hypertension-related genes through an integrated genomic-transcriptomic approach
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A SNP map of the rat genome generated from cDNA sequences
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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
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Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p
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The role of Wnk4 in polygenic hypertension: a candidate gene analysis on rat chromosome 10
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Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
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Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12
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No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1
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