Loss of heterozygosity in squamous cell carcinomas of the head and neck defines a tumor suppressor gene region on 11q13. (Q40851153)

24 September 2017

Loss of heterozygosity in squamous cell carcinomas of the head and neck defines a tumor suppressor gene region on 11q13. (English)

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24 September 2017

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Venugopalan M

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24 September 2017

Wood TF

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24 September 2017

Wilczynski SP

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24 September 2017

Sen S

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24 September 2017

Peters J

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24 September 2017

Ma GC

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24 September 2017

Evans GA

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24 September 2017

Srivatsan ES

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24 September 2017

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1 July 1998

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Cancer Genetics and Cytogenetics

24 September 2017

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24 September 2017

104

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24 September 2017

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24 September 2017

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24 September 2017

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Estimates of the worldwide frequency of sixteen major cancers in 1980

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Dietary Factors in Oral and Pharyngeal Cancer

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Analysis of lymphoepithelioma and lymphoepithelioma-like carcinomas for Epstein-Barr viral genomes by in situ hybridization

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7 January 2021

Multiple clonal chromosome aberrations in squamous cell carcinomas of the larynx

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7 January 2021

Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neck

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7 January 2021

Recurrent cytogenetic abnormalities in squamous cell carcinomas of the head and neck region

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7 January 2021

Consistent chromosomal losses in head and neck squamous cell carcinoma cell lines

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7 January 2021

Oncogene amplification in squamous cell carcinoma of the oral cavity.

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900461-5

7 January 2021

Chromosome 11Q13 amplification in head and neck squamous cell carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900461-5

7 January 2021

Frequent amplification of 11q13 DNA markers is associated with lymph node involvement in human head and neck squamous cell carcinomas

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7 January 2021

Amplification of the Int-2 gene in head and neck squamous cell carcinoma

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7 January 2021

Chromosome 11q13 amplification in head and neck squamous cell carcinoma. Association with poor prognosis

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7 January 2021

Deletion of chromosome 11 and of 14q sequences in neuroblastoma

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7 January 2021

Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24

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7 January 2021

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

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7 January 2021

Loss of heterozygosity on chromosome 11 in sporadic gastrinomas

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Positional cloning of the gene for multiple endocrine neoplasia-type 1

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Human tumor suppressor genes

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7 January 2021

Loss of constitutional heterozygosity in human cancer.

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7 January 2021

DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1

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7 January 2021

Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers

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7 January 2021

Loss of heterozygosity involving the APC gene in oral squamous cell carcinomas.

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7 January 2021

RFLP for MboI in the human tyrosinase (TYR) gene detected by PCR.

1 reference

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7 January 2021

PCR-based detection of two MspI polymorphic sites at D18S8.

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7 January 2021

Ordering three DNA polymorphisms on human chromosome 3 by sperm typing

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7 January 2021

Haellpolymorphism within 3′ untranslated region of PRAD1

1 reference

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7 January 2021

Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13

1 reference

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7 January 2021

Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3

1 reference

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7 January 2021

Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint

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7 January 2021

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

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7 January 2021

Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B.

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7 January 2021

Identification of the von Hippel-Lindau disease tumor suppressor gene

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7 January 2021

Assignment of the human beta-catenin gene (CTNNB1) to 3p22-->p21.3 by fluorescence in situ hybridization.

1 reference

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7 January 2021

Definition of a tumor suppressor locus within human chromosome 3p21-p22

1 reference

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7 January 2021

Description of a 700-kb yeast artificial chromosome contig containing the BCL1 translocation breakpoint region at 11q13.

1 reference

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7 January 2021

10.1016/S0165-4608(97)00461-5

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DOI

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24 September 2017

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