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

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

Association within a family of a balanced autosomal translocation with major mental illness

1990 • 730 citations

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

1989 • 624 citations

Ubiquitous, interspersed repeated sequences in mammalian genomes.

1980 • 568 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

Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma.

1989 • 367 citations

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

1985 • 313 citations

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

1990 • 296 citations

The fibroblast growth factor family.

1990 • 219 citations

Rearrangement and overexpression of D11S287E, a candidate oncogene on chromosome 11q13 in benign parathyroid tumors.

1991 • 203 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

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

1989 • 162 citations

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

1986 • 149 citations

Amplification of the int-2 gene in human head and neck squamous cell carcinomas.

1990 • 140 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

Human Gene Mapping 10

1990 • 129 citations

Amplification of human int-2 in breast cancers and squamous carcinomas.

1988 • 125 citations

Gene amplification on chromosome band 11q13 and oestrogen receptor status in breast cancer

1990 • 118 citations

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

1988 • 107 citations

Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23

1990 • 105 citations

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

1984 • 103 citations

Report of the committee on the genetic constitution of chromosome 11

1990 • 98 citations

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

1990 • 71 citations

Structure, chromosome mapping and expression of the murine Fgf-6 gene.

1990 • 67 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 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

Report of the comparative subcommittee for human and mouse homologies

1990 • 42 citations

Regional assignment of genes for human α-globin and phosphoglycollate phosphatase to the short arm of chromosome 16

1981 • 38 citations

Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence

1990 • 25 citations

Localization of 11q13 loci with respect to regional chromosomal breakpoints

1992 • 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

The 11q13 amplicon of a mammary carcinoma cell line

1990 • 21 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

Of charmed quarks and krankrans

1989 • 2 citations