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UnknownMultiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.
Not available
S-EPMC5901974 | biostudies-literature
UnknownA spatio-temporal atlas of the developing fetal brain with spina bifida aperta.
Not available
S-EPMC10445840 | biostudies-literature
UnknownALL-RIC trial protocol: a comparison of reduced dose total body irradiation (TBI) and cyclophosphamide with fludarabine and melphalan reduced intensity conditioning in adults with acute lymphoblastic leukaemia (ALL) in complete remission.
Not available
S-EPMC10255288 | biostudies-literature
UnknownPhase II Single-Arm Study of Preoperative Letrozole for Estrogen Receptor-Positive Postmenopausal Ductal Carcinoma In Situ: CALGB 40903 (Alliance).
Not available
S-EPMC7164489 | biostudies-literature
UnknownSurface guided radiation therapy: An international survey on current clinical practice.
Not available
S-EPMC8984757 | biostudies-literature
UnknownFoxp1 suppresses cortical angiogenesis and attenuates HIF-1alpha signaling to promote neural progenitor cell maintenance.
Not available
S-SCDT-10_1038-S44319-024-00131-8 | biostudies-other
UnknownPrimary graft failure, but not relapse, may be identified by early chimerism following double cord blood unit transplantation.
Not available
S-EPMC9006284 | biostudies-literature
TranscriptomicsChIP-chip from mouse 14.5 days fetal brain with P300 and H3K4Me1
Enhancers can regulate the transcription of genes over long genomic distances. This is thought to lead to selection against genomic rearrangements within such regions that may disrupt this functional linkage. We tested this concept experimentally using the human X chromosome. We describe a scoring m...
ORGANISM(S): Mus musculus 
2015-01-30 | E-GEOD-57357 | biostudies-arrayexpress
UnknownGenomic epidemiology of syphilis in England: a population-based study.
Not available
S-EPMC10547597 | biostudies-literature
GenomicsNational Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC)

Multi-center, prospective observational cohort study of individuals with congenital heart defects (CHD). Phenotypic data and source DNA of probands, parents, and families of interest are being collected to investigate relationships between genetic factors and phenotypic and clinical outcomes in p...

phs000571.v1.p1 | EGA
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