Test-SequenceVariant  

Documents (100) JSON TSV

source DB source ID text size updated at # proj. # Ann. updated_at
PubMed 16330669 Array-based comparative genomic hybridization analysis reveals recurrent chromosomal alterations and prognostic parameters in primary cutaneous large B-cell lymphoma. PURPOSE: To evaluate the clinical 2 KB 2015-11-19 11 1 2021-12-23
PubMed 16001362 An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repe 2.06 KB 2015-11-19 11 1 2021-12-23
PubMed 19696792 Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression. Irinotecan is an anti-neoplastic agent that is widely used for treating colorectal and lung cance 1.3 KB 2025-10-02 11 1 2021-12-23
PubMed 21810259 HIV-1 Tat activates indoleamine 2,3 dioxygenase in murine organotypic hippocampal slice cultures in a p38 mitogen-activated protein kinase-dependent manner. BACKGROUND: We have established that activa 2.06 KB 2015-11-26 11 0 2021-12-23
PubMed 16970763 Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity. BACKGROUND: To examine the contribution of mutations within the Norrie d 1.89 KB 2015-11-20 11 4 2021-12-23
PubMed 17327131 Molecular analysis of the CYP2F1 gene: identification of a frequent non-functional allelic variant. The CYP2F1 is a human cytochrome P450 that is selectively expressed in lung tissue and involved in t 1.71 KB 2015-12-28 11 4 2021-12-23
PubMed 17391797 The phosphatidylethanolamine N-methyltransferase gene V175M single nucleotide polymorphism confers the susceptibility to NASH in Japanese population. BACKGROUND/AIMS: The genetic predisposition on the 1.48 KB 2015-11-23 12 8 2021-12-23
PubMed 22180037 Genetic polymorphism of the glutathione-S-transferase P1 gene (GSTP1) and susceptibility to prostate cancer in the Kashmiri population. Glutathione-S-transferase P1 (GSTP1) is a critical enzyme of the 1.33 KB 2015-11-26 12 4 2021-12-23
PubMed 19353688 Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1). Insert 1.81 KB 2015-11-25 12 0 2021-12-23
PubMed 21699520 PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas. BACKGROUND: Basal cell carcinomas (BCCs) are the most frequen 1.54 KB 2016-01-03 12 5 2021-12-23