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UnknownEndogenous histidine peptides are physiological antioxidants that prevent oligodendrocyte cell death and myelin loss in vivo.
Not available
S-EPMC11661932 | biostudies-literature
UnknownA new type of blood-brain barrier aminoacidopathy underlies metabolic microcephaly associated with SLC1A4 mutations.
Not available
S-EPMC11531853 | biostudies-literature
GenomicsStudy of Addiction: Genetics and Environment (SAGE)

This study is part of the Gene Environment Association Studies initiative (GENEVA) funded by the National Human Genome Research Institute. The overarching goal is to identify novel genetic factors that contribute to addiction through a large-scale genome-wide association study of DSM-IV alcoh...

phs000092.v1.p1 | EGA
GenomicsCIDR: Collaborative Study on the Genetics of Alcoholism Case Control Study

This is a case-control study of alcoholism, in which the subjects have been drawn from the Collaborative Study on the Genetics of Alcoholism (COGA), a large, ongoing family-based study that includes subjects from seven sites around the US. COGA has gathered detailed, standardized data on ...

phs000125.v1.p1 | EGA
UnknownD-serine availability modulates prefrontal cortex inhibitory interneuron development and circuit maturation.
Not available
S-EPMC10264435 | biostudies-literature
Genomicsena-DATASET-MSKCC-27-01-2017-19:20:42:018-272 - samples
Sequencing of untreated pancreatic cancer metastases and primary tumor sections.
EGAD00001003153 | EGA
GenomicsSequencing of pancreatic cancer primary tumors and metastases
The extent of heterogeneity of driver gene mutations present in naturally occurring metastases is largely unknown, i.e. treatment-naïve metastatic disease. To address this issue, 60x whole genome sequencing of 26 metastases from 4 patients was carried out. We found that the identical driver gene m...
EGAS00001002186 | EGA
TranscriptomicsTranscription profiling of human children with mental retardation and immediate family members
The cause of mental retardation in one-third to one-half of all affected individuals is unknown. Microscopically-detectable chromosomal abnormalities are the most frequent recognized cause, but gain or loss of chromosomal segments that are too small to be seen by conventional cytogenetic analysis ha...
ORGANISM(S): Homo sapiens 
2008-06-21 | E-GEOD-7226 | biostudies-arrayexpress
TranscriptomicsImmune cells direct epithelial maturation during early human lung development
The adult human lung harbours a significant proportion of immune cells, which are known to play a crucial role in both normal lung homeostasis and pathogenesis. In this work, we collected CD45-enriched human lung cells from 6 to 22 week post conception (pcw) and built a single-cell transcriptome and...
ORGANISM(S): Homo sapiens 
2022-12-09 | E-MTAB-11528 | biostudies-arrayexpress
GenomicsMSKCC Medical Donation Program Data Access Committee
Data Access Committee EGAC00001000588
EGAC00001000588 | EGA
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