Back W - Search Results

1

Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients.

Friedl W, Kruse R, Uhlhaas S, Stolte M, Schartmann B, Keller KM, Jungck M, Stern M, Loff S, Back W, Propping P, Jenne DE. Friedl W, et al. Among authors: back w. Genes Chromosomes Cancer. 1999 Aug;25(4):403-6. Genes Chromosomes Cancer. 1999. PMID: 10398437

2

Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers.

Friedl W, Uhlhaas S, Schulmann K, Stolte M, Loff S, Back W, Mangold E, Stern M, Knaebel HP, Sutter C, Weber RG, Pistorius S, Burger B, Propping P. Friedl W, et al. Among authors: back w. Hum Genet. 2002 Jul;111(1):108-11. doi: 10.1007/s00439-002-0748-9. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136244

3

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

Aretz S, Stienen D, Uhlhaas S, Stolte M, Entius MM, Loff S, Back W, Kaufmann A, Keller KM, Blaas SH, Siebert R, Vogt S, Spranger S, Holinski-Feder E, Sunde L, Propping P, Friedl W. Aretz S, et al. Among authors: back w. J Med Genet. 2007 Nov;44(11):702-9. doi: 10.1136/jmg.2007.052506. Epub 2007 Sep 14. J Med Genet. 2007. PMID: 17873119 Free PMC article.

4

Novel de novo mutation of MADH4/SMAD4 in a patient with juvenile polyposis.

Burger B, Uhlhaas S, Mangold E, Propping P, Friedl W, Jenne D, Dockter G, Back W. Burger B, et al. Among authors: back w. Am J Med Genet. 2002 Jul 1;110(3):289-91. doi: 10.1002/ajmg.10411. Am J Med Genet. 2002. PMID: 12116240 No abstract available.

5

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.

Aretz S, Stienen D, Uhlhaas S, Loff S, Back W, Pagenstecher C, McLeod DR, Graham GE, Mangold E, Santer R, Propping P, Friedl W. Aretz S, et al. Among authors: back w. Hum Mutat. 2005 Dec;26(6):513-9. doi: 10.1002/humu.20253. Hum Mutat. 2005. PMID: 16287113

6

Immunolocalization of beta catenin in intestinal polyps of Peutz-Jeghers and juvenile polyposis syndromes.

Back W, Loff S, Jenne D, Bleyl U. Back W, et al. J Clin Pathol. 1999 May;52(5):345-9. doi: 10.1136/jcp.52.5.345. J Clin Pathol. 1999. PMID: 10560353 Free PMC article.

7

Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.

Kruse R, Uhlhaas S, Lamberti C, Keller KM, Jackisch C, Steinhard J, Knöpfle G, Loff S, Back W, Stolte M, Jungck M, Propping P, Friedl W, Jenne DE. Kruse R, et al. Among authors: back w. Hum Mutat. 1999;13(3):257-8. doi: 10.1002/(SICI)1098-1004(1999)13:3<257::AID-HUMU15>3.0.CO;2-A. Hum Mutat. 1999. PMID: 10090485

8

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.

Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, Müller O, Back W, Zimmer M. Jenne DE, et al. Among authors: back w. Nat Genet. 1998 Jan;18(1):38-43. doi: 10.1038/ng0198-38. Nat Genet. 1998. PMID: 9425897

9

Bronchioloalveolar carcinoma: a new cancer in Peutz-Jeghers syndrome.

von Herbay A, Arens N, Friedl W, Vogt-Moykopf I, Kayser K, Müller KM, Back W. von Herbay A, et al. Among authors: back w. Lung Cancer. 2005 Feb;47(2):283-8. doi: 10.1016/j.lungcan.2004.06.015. Lung Cancer. 2005. PMID: 15639728

10

Parenteral nutrition-induced hepatobiliary dysfunction in infants and prepubertal rabbits.

Loff S, Kränzlin B, Moghadam M, Dzakovic A, Wessel L, Back W, Hosie S, Wirth H, Waag KL. Loff S, et al. Among authors: back w. Pediatr Surg Int. 1999;15(7):479-82. doi: 10.1007/s003830050643. Pediatr Surg Int. 1999. PMID: 10525903

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