Journal Article (1120)
701.
Journal Article
469 (3), pp. 409 - 420 (2015)
Cyclin Y phosphorylation- and 14-3-3-binding-dependent activation of PCTAIRE-1/CDK16. Biochemical Journal 702.
Journal Article
60 (8), pp. 419 - 425 (2015)
Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations? JOURNAL OF HUMAN GENETICS 703.
Journal Article
52 (7), pp. 476 - 483 (2015)
Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type. Journal of Medical Genetics 704.
Journal Article
47 (7), pp. 822 - 826 (2015)
Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics 705.
Journal Article
29 (7), pp. 1037 - 1054 (2015)
miR-22 and miR-29a are members of the androgen receptor cistrome modulating LAMC1 and Mcl-1 in prostate cancer. Molecular Endocrinology 706.
Journal Article
24 (12), pp. 3335 - 3347 (2015)
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain. Human Molecular Genetics 707.
Journal Article
112 (22), pp. 7009 - 7014 (2015)
Structural rearrangements in the phage head-to-tail interface during assembly and infection. Proceedings of the National Academy of Sciences of the United States of America 708.
Journal Article
7 (6), pp. 2771 - 2793 (2015)
The Molecular Switch of Telomere Phages: High Binding Specificity of the PY54 Cro Lytic Repressor to a Single Operator Site. Viruses 709.
Journal Article
23 (3), pp. 367 - 377 (2015)
Effects of different oocyte retrieval and in vitro maturation systems on bovine embryo development and quality. Zygote 710.
Journal Article
31 (6), pp. 329 - 335 (2015)
Long noncoding RNAs in organogenesis: Making the difference. Trends in Genetics 711.
Journal Article
16, p. 84 (2015)
Erratum: Induced pluripotent stem cell-derived neuronal cells from a sporadic Alzheimer's disease donor as a model for investigating AD-associated gene regulatory networks. BMC Genomics 712.
Journal Article
47 (6), pp. 647 - 653 (2015)
PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nature Genetics 713.
Journal Article
58 (6-7), pp. 364 - 368 (2015)
Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndrome. European Journal of Medical Genetics 714.
Journal Article
25 (6), pp. 825 - 835 (2015)
ChIP-exo signal associated with DNA-binding motifs provides insight into the genomic binding of the glucocorticoid receptor and cooperating transcription factors. Genome Res 715.
Journal Article
36 (6), pp. 593 - 598 (2015)
DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies. Human Mutations 716.
Journal Article
6, 6:7200 (2015)
Translational regulation shapes the molecular landscape of complex disease phenotypes. Nat Commun 717.
Journal Article
78 (5), pp. 1160 - 1164 (2015)
Amorfrutins Are Natural PPARgamma Agonists with Potent Anti-inflammatory Properties. Journal of Natural Products 718.
Journal Article
161 (5), pp. 1012 - 1025 (2015)
Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions. Cell 719.
Journal Article
112 (20), pp. E2630 - E2639 (2015)
Bestrophin 1 is indispensable for volume regulation in human retinal pigment epithelium cells. Proceedings of the National Academy of Sciences of the United States of America 720.
Journal Article
334 (1), pp. 114 - 125 (2015)
PRMT1-mediated arginine methylation controls ATXN2L localization. Experimental Cell Research