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Biallelic missense variants in ZBTB11 can cause intellectual disability in humans. Hum Mol Genet 462.
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34 (17), S. i766 - 1772 (2018)
DREAM-Yara: an exact read mapper for very large databases with short update time. Bioinformatics 463.
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24 (10), S. 2784 - 2794 (2018)
Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils. Cell Reports 464.
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176 (9), S. 2028 - 2033 (2018)
A novel mutation in CDH11, encoding cadherin-11, cause Branchioskeletogenital (Elsahy-Waters) syndrome. American Journal of Medical Genetics Part A 465.
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15 (9), S. 732 - 740 (2018)
Reduced MEK inhibition preserves genomic stability in naive human embryonic stem cells. Nature methods 466.
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14 (8), e1006372 (2018)
coTRaCTE predicts co-occurring transcription factors within cell-type specific enhancers. PLoS Computational Biology 467.
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218 (7), S. 1066 - 1074 (2018)
Serum HBV RNA as a Predictor of Peginterferon Alfa-2a Response in Patients With HBeAg-Positive Chronic Hepatitis B. The Journal of Infectious Diseases 468.
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23 (2), S. 266 - 275 (2018)
Esrrb Unlocks Silenced Enhancers for Reprogramming to Naive Pluripotency. Cell Stem Cell 469.
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23 (2), e5, S. 289 - 305 (2018)
Prospective Isolation of Poised iPSC Intermediates Reveals Principles of Cellular Reprogramming. Cell Stem Cell 470.
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113, S. 29 - 40 (2018)
Transcriptional profiling of murine osteoblast differentiation based on RNA-seq expression analyses. Bone 471.
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8 (8), 180075 (2018)
It takes two transducins to activate the cGMP-phosphodiesterase 6 in retinal rods. Open Biology 472.
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Coactivator condensation at super-enhancers links phase separation and gene control. Science (6400), eaar3958 (2018)
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10 (1), 10:55 (2018)
Epigenomic profiling of non-small cell lung cancer xenografts uncover LRP12 DNA methylation as predictive biomarker for carboplatin resistance. Genome Medicine 474.
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The power of the Mediator complex—Expanding the genetic architecture and phenotypic spectrum of MED12‐related disorders. Clinical Genetics: an international journal of genetics in medicine 475.
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9, 9:1533 (2018)
Structure and function of the Campylobacter jejuni chromosome replication origin. Frontiers in Microbiology 476.
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174 (2), S. 391 - 405 (2018)
A LINE1-Nucleolin Partnership Regulates Early Development and ESC Identity. Cell 477.
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293 (27), S. 10810 - 10824 (2018)
O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling. Journal of Biological Chemistry 478.
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29 (7), S. 1643 - 1651 (2018)
Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2. Osteoporosis International 479.
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19 (7), S. 453 - 467 (2018)
Structural variation in the 3D genome. Nature Reviews Genetics 480.
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Designing miRNA-Based Synthetic Cell Classifier Circuits Using Answer Set Programming. Frontiers in Bioengineering and Biotechnology