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Localization of 11q13 loci with respect to regional chromosomal breakpoints

Data up to Jan 2025

Published1992
Citations22
References52

Total Citations Per Year

Abstract

References (52)

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

1986 • 3,231 citations

High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones

1990 • 1,357 citations

A novel cyclin encoded by a bcl1-linked candidate oncogene

1991 • 1,286 citations

Colony-stimulating factor 1 regulates novel cyclins during the G1 phase of the cell cycle

1991 • 1,190 citations

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

1988 • 1,022 citations

Human D-type cyclin

1991 • 712 citations

LINKAGE BETWEEN IMMUNOGLOBULIN E RESPONSES UNDERLYING ASTHMA AND RHINITIS AND CHROMOSOME 11q

1989 • 624 citations

Clustering of breakpoints on chromosome 11 in human B-cell neoplasms with the t(11 ; 14) chromosome translocation

1985 • 446 citations

D11S287, a putative oncogene on chromosome 11q13, is amplified and expressed in squamous cell and mammary carcinomas and linked to BCL-1.

1991 • 376 citations

Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.

1990 • 296 citations

DOES T4 TOXICOSIS EXIST ?

1975 • 252 citations

Maps of linkage and synteny homologies between mouse and man

1989 • 212 citations

Isolation of complementary DNA clones encoding the human lymphocyte glycoprotein T1/Leu-1

1986 • 205 citations

Frequent amplification of the bcl-1 locus in head and neck squamous cell carcinomas.

1989 • 195 citations

Characterization and Chromosome Assignment of the Human Homolog of int-2, a Potential Proto-Oncogene

1986 • 178 citations

Amplification of the int-2 gene in primary human breast tumors.

1988 • 172 citations

Human tyrosinase gene, mapped to chromosome 11 (q14 → q21), defines second region of homology with mouse chromosome 7

1988 • 171 citations

High incidence of coamplification of hst-1 and int-2 genes in human esophageal carcinomas.

1989 • 162 citations

The mouse homolog of the hst/k-FGF gene is adjacent to int-2 and is activated by proviral insertion in some virally induced mammary tumors.

1989 • 160 citations

Molecular cloning of Ly-1, a membrane glycoprotein of mouse T lymphocytes and a subset of B cells: molecular homology to its human counterpart Leu-1/T1 (CD5).

1987 • 155 citations

Characterization and chromosome assignment of the human homolog of int-2, a potential proto-oncogene.

1986 • 149 citations

Amplification at chromosome 11q13 in transitional cell tumours of the bladder.

1991 • 135 citations

Amplification of FGF-related genes in human tumors: possible involvement of HST in breast carcinomas.

1989 • 134 citations

A fine-structure deletion map of human chromosome 11p: Analysis of J1 series hybrids

1989 • 126 citations

Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11.

1989 • 112 citations

Sequences flanking the repeat arrays of human minlsatellites: association with tandem and dispersed repeat elements

1989 • 108 citations

Chromosomal localization of the hst oncogene and its co-amplification with the int.2 oncogene in a human melanoma.

1988 • 107 citations

The chromosome 14 breakpoint in neoplastic B cells with the t(11;14) translocation involves the immunoglobulin heavy chain locus.

1984 • 103 citations

A detailed genetic map of the long arm of chromosome 11

1990 • 102 citations

Report of the committee on the genetic constitution of chromosome 11

1990 • 98 citations

Cloning of a complementary DNA encoding a new mouse B lymphocyte differentiation antigen, homologous to the human B1 (CD20) antigen, and localization of the gene to chromosome 19.

1988 • 85 citations

Cloning, characterization, expression, and chromosomal localization of a human ferritin heavy-chain gene.

1986 • 83 citations

cDNA cloning of human oxysterol-binding protein and localization of the gene to human chromosome 11 and mouse chromosome 19

1990 • 81 citations

BCL-1 participates in the 11q13 amplification found in breast cancer.

1990 • 78 citations

Mouse mammary tumor virus integration regions int-1 and int-2 map on different mouse chromosomes.

1984 • 74 citations

Functional analysis of the cDNA encoding human tyrosinase precursor

1989 • 74 citations

Localization of the gene encoding a type I protein phosphatase catalytic subunit to human chromosome band 11q13

1990 • 65 citations

Frequent amplification of the bcl-1 locus in poorly differentiated squamous cell carcinoma of the lung. The Lung Cancer Study Group.

1990 • 55 citations

The gene that encodes the human CD20 (B1) differentiation antigen is located on chromosome 11 near the t(11;14)(q13;q32) translocation site.

1989 • 52 citations

The FGF-related oncogenes hst and int.2, and the bcl.1 locus are contained within one megabase in band q13 of chromosome 11, while the fgf.5 oncogene maps to 4q21.

1988 • 49 citations

Report of the committee on the genetic constitution of chromosome 11

1989 • 45 citations

Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively

1989 • 45 citations

New gene in the homologous human 11q13?q14 and mouse 7F chromosomal regions

1992 • 31 citations

Amplification of 11q13 DNA sequences in human breast cancer: D11S97 identifies a region tightly linked to BCL1 which can be amplified separately.

1992 • 28 citations

A human sequence homologous to v-sea maps to chromosome 11, band q13.

1988 • 22 citations

A proximal mouse chromosome 9 linkage map that further defines linkage groups homologous with segments of human chromosomes 11, 15, and 19

1991 • 21 citations

Frequent amplification of the bcl-1 locus in poorly differentiated squamous cell carcinoma of the lung

1991 • 20 citations

D11S146 and BCL1 are physically linked but can be discriminated by their amplification status in human breast cancer

1991 • 16 citations

Localization of the HST/FGFK gene with regard to 11 q 13 chromosomal breakpoint and fragile site

1991 • 15 citations

Isolation and mapping of a polymorphic DNA sequence (pHBI59) on chromosome 11 [D11S146]

1988 • 12 citations

Mouse ferritin H sequences map to chromosomes 3, 6, and 19

1991 • 9 citations

Isolation and mapping of a polymorphic DNA sequence pHB159 on chromosome 11 [D11S146]

1988 • 8 citations

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Localization of 11q13 loci with respect to regional chromosomal breakpoints (1992) – Genomics | Metascience Observatory Explorer