Deletion mapping on chromosome 1p in well-differentiated gastric cancer

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

A second-generation linkage map of the human genome

1992 • 1,721 citations

Estimates of the worldwide frequency of sixteen major cancers in 1980

1988 • 1,073 citations

Purification of DNA from formaldehyde fixed and paraffin embedded human tissue

1985 • 821 citations

Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer.

1990 • 511 citations

Genetic instability in pancreatic cancer and poorly differentiated type of gastric cancer.

1993 • 443 citations

Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.

1989 • 395 citations

Deletion of genes on chromosome 1 in endocrine neoplasia

1987 • 265 citations

K-sam, an amplified gene in stomach cancer, is a member of the heparin-binding growth factor receptor genes.

1990 • 260 citations

Genetic alterations of the c-erbB-2 oncogene occur frequently in tubular adenocarcinoma of the stomach and are often accompanied by amplification of the v-erbA homologue.

1988 • 251 citations

Frequent replication errors at microsatellite loci in tumors of patients with multiple primary cancers.

1994 • 246 citations

R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1)

1990 • 234 citations

Detection of frequent p53 gene mutations in primary gastric cancer by cell sorting and polymerase chain reaction single-strand conformation polymorphism analysis.

1991 • 230 citations

Somatic mutation of the APC gene in gastric cancer: frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma

1992 • 229 citations

The APC gene, responsible for familial adenomatous polyposis, is mutated in human gastric cancer.

1992 • 223 citations

Frequent loss of heterozygosity at the DCC locus in gastric cancer.

1992 • 204 citations

p53 mutations and microsatellite instability in sporadic gastric cancer: when guardians fail.

1994 • 183 citations

Neuroblastoma consensus deletion maps to 1p36.1–2

1989 • 172 citations

There may be two tumor suppressor genes on chromosome arm Ip closely associated with biologically distinct subtypes of neuroblastoma

1994 • 165 citations

Two distinct deleted regions on the short arm of chromosome I in neuroblastoma

1994 • 153 citations

Human colorectal cancer: high frequency of deletions at chromosome 1p35.

1990 • 140 citations

Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas.

1991 • 124 citations

c‐Ki‐rasPoint Mutations in Ductectatic‐type Mucinous Cystic Neoplasms of the Pancreas

1991 • 122 citations

Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas.

1994 • 122 citations

Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.

1992 • 118 citations

High-Resolution Cytogenetic Mapping of 342 New Cosmid Markers Including 43 RFLP Markers on Human Chromosome 17 by Fluorescence in Situ Hybridization

1993 • 107 citations

Deletion of 1p36 as a primary chromosomal aberration in intestinal tumorigenesis.

1993 • 101 citations

Two distinct regions involved in 1p deletion in human primary breast cancer.

1993 • 101 citations

Point Mutation of c‐Ki‐ras Oncogene in Gastric Adenoma and Adenocarcinoma with Tubular Differentiation

1991 • 81 citations

Frequent loss of heterozygosity of the long arm of chromosome 7 is closely associated with progression of human gastric carcinomas

1994 • 75 citations

Isolation of an Amplified DNA Sequence in Stomach Cancer

1990 • 72 citations

Physical Ordering of Three Polymorphic DNA Markers Spanning the Regions Containing a Tumor Suppressor Gene of Renal Cell Carcinoma by Three‐color Fluorescent in situ Hybridization

1992 • 50 citations

Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line.

1987 • 47 citations

Assignment of the human granulocyte colony-stimulating factor receptor gene (CSF3R) to chromosome 1 at region p35–p34.3

1991 • 44 citations

Allelic imbalance on chromosome I in human breast cancer. I. Minisatellite and rflp analysis

1995 • 37 citations

Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57]

1988 • 33 citations

Report of the First International Workshop on Human Chromosome 13 Mapping 1992

1993 • 10 citations

Isolation and mapping of a polymorphic DNA sequence (pMCT58) on chromosome 1p [D1S77]

1988 • 6 citations

Isolation and mapping of a polymorphic DNA sequence (pTHI54) on chromosome 1p [D1S62]

1988 • 4 citations