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Literature DB >> 10508506

Familial endometrial cancer in female carriers of MSH6 germline mutations.

J Wijnen, W de Leeuw, H Vasen, H van der Klift, P Møller, A Stormorken, H Meijers-Heijboer, D Lindhout, F Menko, S Vossen, G Möslein, C Tops, A Bröcker-Vriends, Y Wu, R Hofstra, R Sijmons, C Cornelisse, H Morreau, R Fodde.

Abstract

Entities: Disease Gene Mutation

Mesh：

Substances：

Year: 1999 PMID： 10508506 DOI： 10.1038/13773

Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330

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96 in total

Review 1. [Carcinogenesis and hereditart colon cancers].

Authors: F Kullmann
Journal: Internist (Berl) Date: 2003-03 Impact factor: 0.743

2. Regulation of the human MSH6 gene by the Sp1 transcription factor and alteration of promoter activity and expression by polymorphisms.

Authors: Isabella Gazzoli; Richard D Kolodner
Journal: Mol Cell Biol Date: 2003-11 Impact factor: 4.272

Review 3. Mouse models of inherited cancer syndromes.

Authors: Sohail Jahid; Steven Lipkin
Journal: Hematol Oncol Clin North Am Date: 2010-12 Impact factor: 3.722

4. The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.

Authors: Fay Kastrinos; Ewout W Steyerberg; Rowena Mercado; Judith Balmaña; Spring Holter; Steven Gallinger; Kimberly D Siegmund; James M Church; Mark A Jenkins; Noralane M Lindor; Stephen N Thibodeau; Lynn Anne Burbidge; Richard J Wenstrup; Sapna Syngal
Journal: Gastroenterology Date: 2010-08-19 Impact factor: 22.682

5. Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

Authors: Gabriella Livide; Maria Carmela Epistolato; Mariangela Amenduni; Vittoria Disciglio; Annabella Marozza; Maria Antonietta Mencarelli; Paolo Toti; Stefano Lazzi; Theodora Hadjistilianou; Sonia De Francesco; Alfonso D'Ambrosio; Alessandra Renieri; Francesca Ariani
Journal: Pathol Oncol Res Date: 2012-01-26 Impact factor: 3.201

Familial endometrial cancer in female carriers of MSH6 germline mutations.

Review 1. [Carcinogenesis and hereditart colon cancers].

2. Regulation of the human MSH6 gene by the Sp1 transcription factor and alteration of promoter activity and expression by polymorphisms.

Review 3. Mouse models of inherited cancer syndromes.

4. The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.

5. Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

6. Detection of germline mutations of hMLH1 and hMSH2 based on cDNA sequencing in China.

7. Muir-Torre Syndrome: expanding the genotype and phenotype--a further family with a MSH6 mutation.

Review 8. History, genetics, and strategies for cancer prevention in Lynch syndrome.

9. Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers.

10. Extracolonic manifestations of hereditary colorectal cancer syndromes.