about
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairmentEpigenetics and life-long consequences of an adverse nutritional and diabetic intrauterine environmentWidespread differences in cortex DNA methylation of the "language gene" CNTNAP2 between humans and chimpanzeesExtreme methylation values of imprinted genes in human abortions and stillbirths.Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression.De novo mutations in HCN1 cause early infantile epileptic encephalopathy.Epigenetic heterogeneity of developmentally important genes in human sperm: implications for assisted reproduction outcome.Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitus.Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.Epigenetic Dysregulation in the Prefrontal Cortex of Suicide Completers.Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate cortices.Epigenetic information from ancient DNA provides new insights into human evolution. Commentary on Gokhman D et al. (2014): Reconstructing the DNA methylation maps of the Neanderthal and the Denisovan. Science 344:523-527.Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception.Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices.A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices.Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing loss.Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile males.Fulminant hepatic failure requiring liver transplantation in 22q13.3 deletion syndrome.Humans and chimpanzees differ in their cellular response to DNA damage and non-coding sequence elements of DNA repair-associated genes.
P50
Q24317151-692AD3DC-60AD-4A43-90DE-5620590249E3Q27022688-14C7A61B-F546-4882-BF69-C77698E44109Q28654973-71A78A1F-A4D1-404B-A816-837A5B8D274AQ33703623-8028D941-773C-48C8-9E4A-A4510B14DE9DQ33959408-3181CF43-718E-48DA-B166-EFB2306D5B15Q34057753-9B9256E0-A4CD-4497-B8E9-178C1A0998AEQ34416011-31F491F4-4E82-41D9-BF7D-DDA94F2C5B17Q36213712-3EFDAD94-2E6D-46A8-8E76-25ABE844517EQ36720609-AC444483-9943-4A1F-B64A-6CBB9970E8E7Q37573604-1DF5AC8A-CC33-42C3-96AC-3C973D54FD45Q40752648-DED7275D-118D-495C-A14D-19A5F27F9211Q44739462-8753DDFD-7272-4BBF-9255-1D298CAEFE35Q47598751-C284C5FE-F3DF-44AA-9047-3C08E528144FQ47844861-CD41D744-641C-4504-8675-0CA3C98DFDEBQ48594052-0165A417-33C6-4478-9B70-FBC09DAB45EAQ48702112-EB6B4768-50F5-4382-8C19-804C7D4421ADQ50442752-9C01FC87-F328-45E5-84B5-C2C5E32599CDQ51508916-1C592F40-6478-4FB0-A18A-177688388B64Q51904045-37E7E115-7E37-4FCE-88D7-C16735AEEC30Q52839562-8345A0DE-AD0C-48B4-A757-9B63A9918863
P50
description
Forscher
@de
chercheur
@fr
investigador
@es
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
研究者
@zh
name
Eberhard Schneider
@ast
Eberhard Schneider
@en
Eberhard Schneider
@es
Eberhard Schneider
@nl
type
label
Eberhard Schneider
@ast
Eberhard Schneider
@en
Eberhard Schneider
@es
Eberhard Schneider
@nl
prefLabel
Eberhard Schneider
@ast
Eberhard Schneider
@en
Eberhard Schneider
@es
Eberhard Schneider
@nl
P106
P31
P496
0000-0003-4320-3652