Literature DB >> 9545417

Molecular classification of the inherited hamartoma polyposis syndromes: clearing the muddied waters.

C Eng1, H Ji.   

Abstract

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Year:  1998        PMID： 9545417      PMCID： PMC1377104          DOI： 10.1086/301847

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  17 in total

1.  The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases.

Authors:  H C Tsou; D H Teng; X L Ping; V Brancolini; T Davis; R Hu; X X Xie; A C Gruener; C A Schrager; A M Christiano; C Eng; P Steck; J Ott; S V Tavtigian; M Peacocke
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

2.  Germline mutations in PTEN are present in Bannayan-Zonana syndrome.

Authors:  D J Marsh; P L Dahia; Z Zheng; D Liaw; R Parsons; R J Gorlin; C Eng
Journal:  Nat Genet       Date:  1997-08       Impact factor: 38.330

3.  TEP1, encoded by a candidate tumor suppressor locus, is a novel protein tyrosine phosphatase regulated by transforming growth factor beta.

Authors:  D M Li; H Sun
Journal:  Cancer Res       Date:  1997-06-01       Impact factor: 12.701

4.  Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.

Authors:  D Liaw; D J Marsh; J Li; P L Dahia; S I Wang; Z Zheng; S Bose; K M Call; H C Tsou; M Peacocke; C Eng; R Parsons
Journal:  Nat Genet       Date:  1997-05       Impact factor: 38.330

5.  Localization of the gene for Cowden disease to chromosome 10q22-23.

Authors:  M R Nelen; G W Padberg; E A Peeters; A Y Lin; B van den Helm; R R Frants; V Coulon; A M Goldstein; M M van Reen; D F Easton; R A Eeles; S Hodgsen; J J Mulvihill; V A Murday; M A Tucker; E C Mariman; T M Starink; B A Ponder; H H Ropers; H Kremer; M Longy; C Eng
Journal:  Nat Genet       Date:  1996-05       Impact factor: 38.330

6.  A juvenile polyposis tumor suppressor locus at 10q22 is deleted from nonepithelial cells in the lamina propria.

Authors:  R F Jacoby; S Schlack; C E Cole; M Skarbek; C Harris; L F Meisner
Journal:  Gastroenterology       Date:  1997-04       Impact factor: 22.682

7.  Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers.

Authors:  P A Steck; M A Pershouse; S A Jasser; W K Yung; H Lin; A H Ligon; L A Langford; M L Baumgard; T Hattier; T Davis; C Frye; R Hu; B Swedlund; D H Teng; S V Tavtigian
Journal:  Nat Genet       Date:  1997-04       Impact factor: 38.330

8.  Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease.

Authors:  E M Arch; B K Goodman; R A Van Wesep; D Liaw; K Clarke; R Parsons; V A McKusick; M T Geraghty
Journal:  Am J Med Genet       Date:  1997-09-05

9.  PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer.

Authors:  J Li; C Yen; D Liaw; K Podsypanina; S Bose; S I Wang; J Puc; C Miliaresis; L Rodgers; R McCombie; S H Bigner; B C Giovanella; M Ittmann; B Tycko; H Hibshoosh; M H Wigler; R Parsons
Journal:  Science       Date:  1997-03-28       Impact factor: 47.728

10.  Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.

Authors:  H J Thomas; S C Whitelaw; S E Cottrell; V A Murday; I P Tomlinson; D Markie; T Jones; D T Bishop; S V Hodgson; D Sheer; J M Northover; I C Talbot; E Solomon; W F Bodmer
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025
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  16 in total

Review 1.  Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23.

Authors:  F S Dahdaleh; J C Carr; D Calva; J R Howe
Journal:  Clin Genet       Date:  2011-09-06       Impact factor: 4.438

Review 2.  Colorectal cancer risk in hamartomatous polyposis syndromes.

Authors:  Fábio Guilherme Campos; Marleny Novaes Figueiredo; Carlos Augusto Real Martinez
Journal:  World J Gastrointest Surg       Date:  2015-03-27

Review 3.  Genetic predisposition to colorectal cancer: where we stand and future perspectives.

Authors:  Laura Valle
Journal:  World J Gastroenterol       Date:  2014-08-07       Impact factor: 5.742

4.  Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndrome.

Authors:  S Bevan; K Woodford-Richens; P Rozen; C Eng; J Young; M Dunlop; K Neale; R Phillips; D Markie; M Rodriguez-Bigas; B Leggett; E Sheridan; S Hodgson; T Iwama; D Eccles; W Bodmer; R Houlston; I Tomlinson
Journal:  Gut       Date:  1999-09       Impact factor: 23.059

5.  Frequent loss of PTEN expression is linked to elevated phosphorylated Akt levels, but not associated with p27 and cyclin D1 expression, in primary epithelial ovarian carcinomas.

Authors:  K Kurose; X P Zhou; T Araki; S A Cannistra; E R Maher; C Eng
Journal:  Am J Pathol       Date:  2001-06       Impact factor: 4.307

6.  Hereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood.

Authors:  Michael Manfredi
Journal:  Gastroenterol Hepatol (N Y)       Date:  2010-03

7.  A gene for familial juvenile polyposis maps to chromosome 18q21.1.

Authors:  J R Howe; J C Ringold; R W Summers; F A Mitros; D Y Nishimura; E M Stone
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

8.  High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome.

Authors:  S Aretz; D Stienen; S Uhlhaas; M Stolte; M M Entius; S Loff; W Back; A Kaufmann; K-M Keller; S H Blaas; R Siebert; S Vogt; S Spranger; E Holinski-Feder; L Sunde; P Propping; W Friedl
Journal:  J Med Genet       Date:  2007-09-14       Impact factor: 6.318

9.  No TGFBRII germline mutations in juvenile polyposis patients without SMAD4 or BMPR1A mutation.

Authors:  L A A Brosens; W A van Hattem; M C E Kools; C Ezendam; F H Morsink; W W J de Leng; F M Giardiello; G J A Offerhaus
Journal:  Gut       Date:  2009-01       Impact factor: 23.059

10.  The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations.

Authors:  J R Howe; M G Sayed; A F Ahmed; J Ringold; J Larsen-Haidle; A Merg; F A Mitros; C A Vaccaro; G M Petersen; F M Giardiello; S T Tinley; L A Aaltonen; H T Lynch
Journal:  J Med Genet       Date:  2004-07       Impact factor: 6.318
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