(Q34746514)

4 August 2017

Molecular anatomy of chromosome 7q deletions in myeloid neoplasms: evidence for multiple critical loci (English)

1 reference

4 August 2017

H Liang

1

1 reference

4 August 2017

J Fairman

2

1 reference

4 August 2017

D F Claxton

3

1 reference

4 August 2017

P C Nowell

4

1 reference

4 August 2017

E D Green

5

1 reference

4 August 2017

L Nagarajan

6

1 reference

4 August 2017

language of work or name

English

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publication date

1 March 1998

1 reference

4 August 2017

5

1 reference

Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

1 reference

4 August 2017

95

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4 August 2017

3781-3785

1 reference

4 August 2017

7

1 reference

Decrease in amplified telomeric sequences and induction of senescence markers by introduction of human chromosome 7 or its segments in SUSM-1.

4 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Frequent loss of heterozygosity in the region of the D7S523 locus in advanced ovarian cancer

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Rarity of microsatellite alterations in acute myeloid leukaemia.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Cytogenetic, molecular and functional evidence for novel tumor suppressor genes on the long arm of human chromosome 7.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Comparison between interphase and metaphase cytogenetics in detecting chromosome 7 defects in hematological neoplasias

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Chromosome 7 suppresses indefinite division of nontumorigenic immortalized human fibroblast cell lines KMST-6 and SUSM-1

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Inhibition of tumorigenicity of a murine squamous cell carcinoma (SCC) cell line by a putative tumor suppressor gene on human chromosome 7.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

(C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Loss of heterozygosity in human primary prostate carcinomas: a possible tumor suppressor gene at 7q31.1

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Childhood monosomy 7: epidemiology, biology, and mechanistic implications.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Allelic loss at 7q31.1 in human primary ovarian carcinomas suggests the existence of a tumor suppressor gene

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Frequency of carriers of cystic fibrosis gene among patients with myeloid malignancy and melanoma

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Quantitative acute leukemia cytogenetics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Loss of heterozygosity at 7q31 in breast cancer: results from an International Collaborative Study Group. The Breast Cancer Somatic Genetics Consortium

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Karyotype is prognostically more important than the FAB system's distinction between myelodysplastic syndrome and acute myelogenous leukemia.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19914

Toward a clinically relevant cytogenetic classification of acute myelogenous leukemia

26 October 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3781

Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3781

Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3781

A factor encoded by 7q31 suppresses expansion of the 7q- clone and delays cytogenetic progression

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3781

5q- chromosome. Evidence for complex interstitial breaks in a case of refractory anemia with excess blasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3781

Fragile sites induced by FUdR, caffeine, and aphidicolin. Their frequency, distribution, and analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3781

Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 7q31.1: evidence for a broad range tumor suppressor gene

21 January 2018

1 reference

12 December 2020

Frequent loss of heterozygosity at 7q31.1 in primary prostate cancer is associated with tumor aggressiveness and progression

1 reference

12 December 2020

Frequent clonal loss of heterozygosity but scarcity of microsatellite instability at chromosomal breakpoint cluster regions in adult leukemias

1 reference

12 December 2020

Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET

1 reference

12 December 2020

Development of a sensitive PCR to detect allele loss in a model hematopoietic neoplasm

1 reference

12 December 2020

Molecular delineation of the commonly deleted segment in mature B-cell lymphoid neoplasias with deletion of 7q

1 reference

12 December 2020

Loss of heterozygosity at chromosome 7q in human breast cancer: association with clinical variables

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.95.7.3781

1 reference

4 August 2017

0 references

1 reference

4 August 2017

1 reference