(Q36801269)

English

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

scientific article published on June 1996

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scholarly article

1 reference

Europe PubMed Central

16 August 2017

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

1 reference

Europe PubMed Central

16 August 2017

author name string

Albarosa R

1

1 reference

Europe PubMed Central

16 August 2017

Colombo BM

2

1 reference

Europe PubMed Central

16 August 2017

Roz L

3

1 reference

Europe PubMed Central

16 August 2017

Magnani I

4

1 reference

Europe PubMed Central

16 August 2017

Pollo B

5

1 reference

Europe PubMed Central

16 August 2017

Cirenei N

6

1 reference

Europe PubMed Central

16 August 2017

Giani C

7

1 reference

Europe PubMed Central

16 August 2017

Conti AM

8

1 reference

Europe PubMed Central

16 August 2017

DiDonato S

9

1 reference

Europe PubMed Central

16 August 2017

Finocchiaro G

10

1 reference

Europe PubMed Central

16 August 2017

language of work or name

0 references

publication date

1 June 1996

1 reference

Europe PubMed Central

16 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

16 August 2017

58

1 reference

Europe PubMed Central

16 August 2017

1260-1267

1 reference

Europe PubMed Central

16 August 2017

6

1 reference

Europe PubMed Central

16 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

Increasing complexity of the karyotype in 50 human gliomas. Progressive evolution and de novo occurrence of cytogenetic alterations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

Mutation of the MXI1 gene in prostate cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

A YAC contig map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

The 1993-94 Généthon human genetic linkage map

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

A second-generation linkage map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

27 June 2018

Loss of heterozygosity for 10q loci in human gliomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

5 September 2018

Stabilization of c-myc protein in human glioma cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

5 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

5 September 2018

O6-methylguanine-DNA methyltransferase activity in cerebral gliomas. A guidance for nitrosourea treatment?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

5 September 2018

p53 mutations and microsatellite analysis of loss of heterozygosity in malignant gliomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915052

5 September 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage mapping of human chromosome 10 microsatellite polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

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