Zeitschriftenartikel (123)
Zeitschriftenartikel
34 (5), S. 838 - 844 (2013)
Familial aggregation of pure tone hearing thresholds in an aging European population. Otology & neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology
Zeitschriftenartikel
56 (7), S. 379 - 382 (2013)
HUWE1 mutation explains phenotypic severity in a case of familial idiopathic intellectual disability. European Journal of Medical Genetics
Zeitschriftenartikel
12 (7), S. 1965 - 1979 (2013)
Protein sets define disease states and predict in vivo effects of drug treatment. Molecular and Cellular Proteomics
Zeitschriftenartikel
30 (7), S. 1700 - 1712 (2013)
Twisted signatures of GC-biased gene conversion embedded in an evolutionary stable karyotype. Molecular Biology and Evolution
Zeitschriftenartikel
50 (6), S. 844 - 855 (2013)
Genome-wide Kinase-Chromatin Interactions Reveal the Regulatory Network of ERK Signaling in Human Embryonic Stem Cells. Molecular Cell
Zeitschriftenartikel
50 (6), S. 831 - 843 (2013)
Mutations in the intellectual disability gene Ube2a cause neuronal dysfunction and impair parkin-dependent mitophagy. Molecular Cell
Zeitschriftenartikel
8 (6), S. e65403 - e65403 (2013)
Synergism between Hedgehog-GLI and EGFR Signaling in Hedgehog-Responsive Human Medulloblastoma Cells Induces Downregulation of Canonical Hedgehog-Target Genes and Stabilized Expression of GLI1. PLoS One
Zeitschriftenartikel
4, S. 4:124 - 4:124 (2013)
Integrative analysis of cancer-related signaling pathways. Frontiers in Physiology
Zeitschriftenartikel
10 (6), S. e1001462 - e1001462 (2013)
Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study. PLoS Medicine
Zeitschriftenartikel
52 (22), S. 3899 - 3912 (2013)
Ubiquilin-1 Modulates gamma-Secretase-Mediated epsilon-Site Cleavage in Neuronal Cells. Biochemistry
Zeitschriftenartikel
161A (6), S. 1207 - 1213 (2013)
A newly recognized autosomal recessive syndrome affecting neurologic function and vision. American Journal of Medical Genetics Part A
Zeitschriftenartikel
25 (20), S. 2765 - 71 (2013)
Current methods for inducing pluripotency in somatic cells. Advanced Materials
Zeitschriftenartikel
30 (4), S. 362 - 365 (2013)
IT Future of Medicine: from molecular analysis to clinical diagnosis and improved treatment. New Biotechnology
Zeitschriftenartikel
52 (19), S. 5171 - 5174 (2013)
Discovery and Characterization of Protein-Modifying Natural Products by MALDI Mass Spectrometry Reveal Potent SIRT1 and p300 Inhibitors. Angewandte Chemie International Edition
Zeitschriftenartikel
92 (5), S. 681 - 695 (2013)
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity. The American Journal of Human Genetics
Zeitschriftenartikel
23 (5), S. 749 - 761 (2013)
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes. Genome Research
Zeitschriftenartikel
52 (5), S. 512 - 522 (2013)
Breakpoint characterization of the der(19)t(11;19)(q13;p13) in the ovarian cancer cell line SKOV-3. Genes, Chromosomes and Cancer
Zeitschriftenartikel
83 (5), S. 488 - 490 (2013)
Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations. Clinical Genetics: an international journal of genetics in medicine
Zeitschriftenartikel
123 (5), S. 2244 - 2256 (2013)
CCDC22 deficiency in humans blunts activation of proinflammatory NF-kappaB signaling. The Journal of Clinical Investigation
Zeitschriftenartikel
4, S. 4:54 - 4:54 (2013)
Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders. Frontiers in Genetics