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TranscriptomicsCopy number analysis of human glioblastoma multiforme
Copy number analysis of human GBM samples were performed, and a high frequency of deletions of the PTPRD gene on chromosome 9p23-24.1 were identified. Keywords: SNP microarray, glioblastoma multiforme, copy number, amplification, deletion Genomic DNA from 58 GBM tumor samples were hybridized to Aff...
ORGANISM(S): Homo sapiens 
2009-01-04 | E-GEOD-13021 | biostudies-arrayexpress
ProteomicsA Proteomic Approach to Understanding the Pathogenesis of Idiopathic Macular Hole Formation
Idiopathic macular holes (IMH) are full-thickness defects of retinal tissue that cause severe vision loss due to disruption of the anatomic fovea. Abnormal vitreous traction is involved in the formation of macular holes. Both glial cells and hyalocytes contribute to epiretinal membrane formation in ...
ORGANISM(S): Homo sapiens (Human) 
2018-04-11 | PXD006687 | Pride
Eye Proteomics Vitreous Idiopathic macular hole Retina 
UnknownHippocampal thinning linked to longer TOMM40 poly-T variant lengths in the absence of the APOE ε4 variant.
Not available
S-EPMC5496778 | biostudies-literature
UnknownOlder adults with newly diagnosed high-risk/secondary AML who achieved remission with CPX-351: phase 3 post hoc analyses.
Not available
S-EPMC7993093 | biostudies-literature
UnknownReanalysis of RNA sequencing data ends diagnostic odyssey and expands the phenotypic spectrum of congenital titinopathy.
Not available
S-EPMC11934095 | biostudies-literature
UnknownA recurrent kinase domain mutation in PRKCA defines chordoid glioma of the third ventricle.
Not available
S-EPMC5824822 | biostudies-literature
UnknownResults of a randomized phase 3 study of oral sapacitabine in elderly patients with newly diagnosed acute myeloid leukemia (SEAMLESS).
Not available
S-EPMC9523989 | biostudies-literature
UnknownLoss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly.
Not available
S-EPMC11648989 | biostudies-literature
UnknownMutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
Not available
S-EPMC3208626 | biostudies-literature
UnknownELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy.
Not available
S-EPMC12260708 | biostudies-literature
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