Deletion mapping of gliomas suggest the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q.

The 1993–94 Généthon human genetic linkage map

1994 • 1,870 citations

A second-generation linkage map of the human genome

1992 • 1,721 citations

Mxi1, a protein that specifically interacts with Max to bind Myc-Max recognition sites

1993 • 786 citations

Mammalian O6-alkylguanine-DNA alkyltransferase: regulation and importance in response to alkylating carcinogenic and therapeutic agents.

1990 • 736 citations

Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map

1994 • 405 citations

A YAC contig map of the human genome.

1995 • 333 citations

Pathways leading to glioblastoma multiforme: a molecular analysis of genetic alterations in 65 astrocytic tumors

1994 • 304 citations

A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?

1993 • 261 citations

Loss of the chromosomal region 10q23-25 in prostate cancer.

1995 • 238 citations

Mutation of the MXI1 gene in prostate cancer

1995 • 207 citations

Chromosome 10 deletion mapping in human gliomas: a common deletion region in 10q25.

1995 • 184 citations

Allelic loss of sequences from the long arm of chromosome 10 and replication errors in endometrial cancers.

1995 • 181 citations

Common regions of deletion on chromosomes 5q, 6q, and 10q in renal cell carcinoma.

1991 • 154 citations

Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10

1993 • 138 citations

Loss of heterozygosity for loci on chromosome 10 is associated with morphologically malignant meningioma progression.

1993 • 129 citations

Methylation-related chromatin structure is associated with exclusion of transcription factors from and suppressed expression of the O-6-methylguanine DNA methyltransferase gene in human glioma cell lines.

1994 • 116 citations

Loss of heterozygosity for 10q loci in human gliomas

1992 • 115 citations

Deletion mapping of the long arm of chromosome 10 in glioblastoma multiforme

1993 • 110 citations

Loss of heterozygosity for 10q22-10qter in malignant melanoma progression.

1994 • 101 citations

Mapping of two genes encoding members of a distinct subfamily of MAX interacting proteins: MAD to human chromosome 2 and mouse chromosome 6, and MXI1 to human chromosome 10 and mouse chromosome 19.

1994 • 92 citations

Analysis of the functional role of chromosome 10 loss in human glioblastomas.

1993 • 76 citations

Recurrent abnormalities of chromosome bands 10q23–25 in non‐Hodgkin's lymphoma

1992 • 59 citations

Increasing complexity of the karyotype in 50 human gliomas

1994 • 58 citations

Stabilization of c-myc protein in human glioma cells

1993 • 37 citations

Methylation-Related Chromatin Structure Is Associated with Exclusion of Transcription Factors from and Suppressed Expression of the O-6-Methylguanine DNA Methyltransferase Gene in Human Glioma Cell Lines

1994 • 29 citations

Linkage mapping of human chromosome 10 microsatellite polymorphisms

1992 • 27 citations

Redefinition of the coding sequence of the MXI1 gene and identification of a polymorphic repeat in the 3? non-coding region that allows the detection of loss of heterozygosity of chromosome 10q25 in glioblastomas

1995 • 24 citations

O⁶-Methylgaunine-DNA Methyltransferase Activity in Cerebral Gliomas: A guidance for nitrosourea treatment?

1994 • 14 citations

P53 mutations and microsatellite analysis of loss of heterozygosity in malignant gliomas

1994 • 13 citations

Localization of the human O6-methylguanine-DNA methyltransferase gene to chromosome 10q24.33-qter

1991 • 11 citations