Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Infrequent mutations of the WT1 gene in primary cancers of the adult urinary tract.

Japanese journal of clinical oncology - 1 Oct 1995

Kageyama Y, Yamamura Y, Oshima H, Ikawa Y

Abstract excerpt

Polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) analysis of all of the ten exons of the WT1 gene and restriction fragment length polymorphism (RFLP) analysis of the WT1 locus were performed on primary urinary tract cancers: seven renal pelvic cancers, one ureteral cancer, 11 bladder cancers, and 22 renal cell cancers. Four human bladder cancer cell lines (T24, JTC30, JTC32, and HUB41)...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Aged, 80 and over
Share to Base Sequence

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Molecular Sequence Data

Share to Mutation

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Source

Identifiers

PMID: 7474403

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Infrequent mutations of the WT1 gene in primary cancers of the adult urinary tract.PMID 7474403Read ↗

Infrequent somatic mutation of the MTS1 gene in primary bladder carcinomas.Semantic proximity Read ↗

Low frequency of mutations in the WT1 coding region in Wilms' tumor.Semantic proximity Read ↗

Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome.Semantic proximity Read ↗

Infrequent mutation of the hBUB1 and hBUBR1 genes in human lung cancer.Semantic proximity Read ↗

Exclusion of the Wilms tumour gene (WT1) promoter as a site of frequent mutation in Wilms tumour.Semantic proximity Read ↗

Mutation of H-ras is infrequent in bladder cancer: confirmation by single-strand conformation polymorphism analysis, designed restriction fragment length polymorphisms, and direct sequencing.Semantic proximity Read ↗

Infrequent genetic alterations of the PTEN/MMAC1 gene in Japanese patients with primary cancers of the breast, lung, pancreas, kidney, and ovary.Semantic proximity Read ↗

Infrequent somatic mutations of the p16 and p15 genes in human bladder cancer: p16 mutations occur only in low-grade and superficial bladder cancers.Semantic proximity Read ↗

Mutations of the p16 gene product are rare in prostate cancer.Semantic proximity Read ↗

Fine structure analysis of the WT1 gene in sporadic Wilms tumors.Semantic proximity Read ↗

Loss of heterozygosity on chromosome 11p13 in primary bladder carcinoma.Semantic proximity Read ↗

p53 oncogene mutations in human prostate cancer specimens.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.