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TranscriptomicsNeurofibromin (Nf1) is required for skeletal muscle development
Neurofibromatosis type 1 (NF1) is a multi-system disease caused by mutations in the NF1 gene encoding a Ras-GAP protein, neurofibromin, which negatively regulates Ras signalling. Besides neuroectodermal malformations and tumours, the skeletal system is often affected (e.g. scoliosis and long bone dy...
ORGANISM(S): Mus musculus 
2011-05-18 | E-GEOD-29343 | biostudies-arrayexpress
UnknownAn analysis of a multiple biomarker panel to better predict prostate cancer metastasis after radical prostatectomy.
Not available
S-EPMC6661891 | biostudies-literature
UnknownComparison of Characteristics, Follow-up and Outcomes of Active Surveillance for Prostate Cancer According to Ethnicity in the GAP3 Global Consortium Database.
Not available
S-EPMC8655390 | biostudies-literature
GenomicsATAC-seq of BMP response in glioblastoma-derived neural stem cells
Chromatin accessibility was profiled by ATAC-seq in normal and glioblastoma-derived neural stem (GNS) cells, in self-renewing conditions and in response to differentiation stimulus with bone morphogenic protein (BMP).
ORGANISM(S): Homo sapiens 
2015-10-01 | E-MTAB-3868 | biostudies-arrayexpress
TranscriptomicsRNA-seq of BMP response in glioblastoma-derived neural stem cells
The transcriptional response of normal and glioblastoma-derived neural (GNS) cells was profiled in self-renewing conditions and over a time course of differentiation in the presence of bone morphogenic protein (BMP).
ORGANISM(S): Homo sapiens 
2015-10-02 | E-MTAB-3867 | biostudies-arrayexpress
TranscriptomicsMicroRNA expression profiling of normal and glioblastoma-derived neural stem cells
MicroRNA analysis of glioblastoma-derived neural stem (GNS) cells performed in parallel with normal neural stem (NS) cell lines
ORGANISM(S): Homo sapiens 
2016-11-01 | E-MTAB-3865 | biostudies-arrayexpress
TranscriptomicsCopy number analysis in de novo and therapy-related myeloproliferative neoplasms
Loss of chromosome 7 and del(7q) [-7/del(7q)] are recurring cytogenetic abnormalities in hematologic malignancies, including acute myeloid leukemia and therapy-related myeloid neoplasms, and associated with an adverse prognosis. We performed SNP array analysis on de novo and therapy-related myeloi...
ORGANISM(S): Homo sapiens 
2012-11-24 | E-GEOD-42482 | biostudies-arrayexpress
UnknownTransatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders-A successful strategy for clinical research of rare diseases.
Not available
S-EPMC7329920 | biostudies-literature
UnknownLimited contribution of common genetic variants to risk for liver injury due to a variety of drugs.
Not available
S-EPMC3636716 | biostudies-literature
UnknownCommon variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
Not available
S-EPMC3338195 | biostudies-literature
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