Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Risk of breast cancer not increased in translocation 11;22 carriers: analysis of 80 pedigrees.

Literature DB >> 20034094

Risk of breast cancer not increased in translocation 11;22 carriers: analysis of 80 pedigrees.

Melissa T Carter¹, Nicholas J Barrowman, Stephanie A St Pierre, Beverly S Emanuel, Kym M Boycott.

Abstract

Entities: Disease Gene Species

Mesh：

Year: 2010 PMID： 20034094 PMCID： PMC2802109 DOI： 10.1002/ajmg.a.33166

Source DB: PubMed Journal: Am J Med Genet A ISSN： 1552-4825 Impact factor: 2.802

× No keyword cloud information.

18 in total

1. Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

Authors: H Kurahashi; T H Shaikh; E H Zackai; L Celle; D A Driscoll; M L Budarf; B S Emanuel
Journal: Am J Hum Genet Date: 2000-07-20 Impact factor: 11.025

2. Assignment of the human melanoma cell adhesion molecule gene (MCAM) to chromosome 11 band q23.3 by radiation hybrid mapping.

Authors: M D Kuske; J P Johnson
Journal: Cytogenet Cell Genet Date: 1999

3. Candidate tumour suppressor genes at 11q23-q24 in breast cancer: evidence of alterations in PIG8, a gene involved in p53-induced apoptosis.

Authors: M Gentile; M Ahnström; F Schön; S Wingren
Journal: Oncogene Date: 2001-11-22 Impact factor: 9.867

4. A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma.

Authors: R A Herbst; A Larson; J Weiss; W K Cavenee; G M Hampton; K C Arden
Journal: Cancer Res Date: 1995-06-15 Impact factor: 12.701

5. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.

Authors: E H Zackai; B S Emanuel
Journal: Am J Med Genet Date: 1980

6. The 11q;22q translocation: a European collaborative analysis of 43 cases.

Authors: M Fraccaro; J Lindsten; C E Ford; L Iselius
Journal: Hum Genet Date: 1980 Impact factor: 4.132

Review 7. Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history.

Authors: Harvey J Murff; David R Spigel; Sapna Syngal
Journal: JAMA Date: 2004-09-22 Impact factor: 56.272

8. Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals.

Authors: Melissa T Carter; Stephanie A St Pierre; Elaine H Zackai; Beverly S Emanuel; Kym M Boycott
Journal: Am J Med Genet A Date: 2009-08 Impact factor: 2.802

Risk of breast cancer not increased in translocation 11;22 carriers: analysis of 80 pedigrees.

1. Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

2. Assignment of the human melanoma cell adhesion molecule gene (MCAM) to chromosome 11 band q23.3 by radiation hybrid mapping.

3. Candidate tumour suppressor genes at 11q23-q24 in breast cancer: evidence of alterations in PIG8, a gene involved in p53-induced apoptosis.

4. A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma.

5. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.

6. The 11q;22q translocation: a European collaborative analysis of 43 cases.

Review 7. Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history.

8. Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals.

9. Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.

10. Loss of heterozygosity on the long arm of chromosome 11 in colorectal tumours.

1. The effect of translocation-induced nuclear reorganization on gene expression.

2. Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study.