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Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation.
Not available
S-EPMC5223032
|
biostudies-literature
Cite
Biological heterogeneity in idiopathic pulmonary arterial hypertension identified through unsupervised transcriptomic profiling of whole blood.
Not available
S-EPMC8651638
|
biostudies-literature
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Prognostic gene expression signature for high-grade serous ovarian cancer.
Not available
S-EPMC7484370
|
biostudies-literature
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Methylation of all BRCA1 copies predicts response to the PARP inhibitor rucaparib in ovarian carcinoma.
Not available
S-EPMC6162272
|
biostudies-literature
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Deregulation of MYCN, LIN28B and LET7 in a molecular subtype of aggressive high-grade serous ovarian cancers.
Not available
S-EPMC3076323
|
biostudies-literature
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BRCA1 secondary splice-site mutations drive exon-skipping and PARP inhibitor resistance.
Not available
S-EPMC11299415
|
biostudies-literature
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MyD88 and TLR4 Expression in Epithelial Ovarian Cancer.
Not available
S-EPMC5870793
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biostudies-literature
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Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2.
Not available
S-EPMC3387216
|
biostudies-literature
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Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Not available
S-EPMC6507039
|
biostudies-literature
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Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.
Not available
S-EPMC6634302
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biostudies-literature
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