Zeitschriftenartikel (3055)
521.
Zeitschriftenartikel
14 (3), e1007242 (2018)
Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplastica. PLoS Genetics 522.
Zeitschriftenartikel
22 (6), e5, S. 851 - 864 (2018)
An Intermediate Pluripotent State Controlled by MicroRNAs Is Required for the Naive-to-Primed Stem Cell Transition. Cell Stem Cell 523.
Zeitschriftenartikel
13 (6), e0198510 (2018)
Loss of murine Gfi1 causes neutropenia and induces osteoporosis depending on the pathogen load and systemic inflammation. PLoS One 524.
Zeitschriftenartikel
A mouse model for intellectual disability caused by mutations in the X-linked 2'Omethyltransferase Ftsj1 gene. Biochim Biophys Acta Mol Basis Dis, S0925-4439(18)30497-6 (2018)
525.
Zeitschriftenartikel
92 (1), S. 553 - 555 (2018)
A model-based assay design to reproduce in vivo patterns of acute drug-induced toxicity. Archives of Toxicology 526.
Zeitschriftenartikel
77 (Suppl.1), S. S12 - S15 (2018)
Osteoimmunologie – IMMUNOBONE: Regulation des Knochens durch Entzündung. Zeitschrift für Rheumatologie 527.
Zeitschriftenartikel
29 (1), S. 243 - 246 (2018)
A novel COL1A2 C-propeptide cleavage site mutation causing high bone mass osteogenesis imperfecta with a regional distribution pattern. Osteoporosis International 528.
Zeitschriftenartikel
18 (1), 1:240 (2017)
PureCLIP: Capturing target-specific protein-RNA interaction footprints from single-nucleotide CLIP-seq data. Genome Biology 529.
Zeitschriftenartikel
33 (24), S. 3929 - 3937 (2017)
An improved compound Poisson model for the number of motif hits in DNA sequences. Bioinformatics 530.
Zeitschriftenartikel
21 (10), S. 2813 - 2828 (2017)
Non-Canonical Hedgehog Signaling Is a Positive Regulator of the WNT Pathway and Is Required for the Survival of Colon Cancer Stem Cells. Cell Reports 531.
Zeitschriftenartikel
3 (6), e200 (2017)
CDKL5 variants: Improving our understanding of a rare neurologic disorder. Neurology Genetics 532.
Zeitschriftenartikel
2017, 8:105882-105904 (2017)
Renal oncocytoma characterized by the defective complex I of the respiratory chain boosts the synthesis of the ROS scavenger glutathione. Oncotarget 533.
Zeitschriftenartikel
261, S. 157 - 168 (2017)
The SeqAn C++ template library for efficient sequence analysis: A resource for programmers. Journal of Biotechnology 534.
Zeitschriftenartikel
372 (1733), pii: 20160366 (2017)
X-chromosome dosage as a modulator of pluripotency, signalling and differentiation? Philosophical Transactions of the Royal Society of London, Series B: Biological Sciences 535.
Zeitschriftenartikel
101 (5), S. 833 - 843 (2017)
De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. The American Journal of Human Genetics 536.
Zeitschriftenartikel
45 (19), S. 11004 - 11018 (2017)
ssHMM: extracting intuitive sequence-structure motifs from high-throughput RNA-binding protein data. Nucleic Acids Research (London) 537.
Zeitschriftenartikel
27 (11), S. 1916 - 1929 (2017)
The Mobile Element Locator Tool (MELT): Population-scale mobile element discovery and biology. Genome Research 538.
Zeitschriftenartikel
140 (11), S. 2879 - 2894 (2017)
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features. Brain 539.
Zeitschriftenartikel
54 (11), S. 754 - 761 (2017)
Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction. Journal of Medical Genetics 540.
Zeitschriftenartikel
8 (1), 1218 (2017)
Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development. Nature Communications