These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
412 related items for PubMed ID: 27705013
41. Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations? Gómez-Fernández N, Castellví-Bel S, Fernández-Rozadilla C, Balaguer F, Muñoz J, Madrigal I, Milà M, Graña B, Vega A, Castells A, Carracedo A, Ruiz-Ponte C. BMC Med Genet; 2009 Jun 16; 10():57. PubMed ID: 19531215 [Abstract] [Full Text] [Related]
42. Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects. Stekrova J, Sulova M, Kebrdlova V, Zidkova K, Kotlas J, Ilencikova D, Vesela K, Kohoutova M. BMC Med Genet; 2007 Apr 05; 8():16. PubMed ID: 17411426 [Abstract] [Full Text] [Related]
43. Colon cancer prevention by detection of APC gene mutation in a family with attenuated familial adenomatous polyposis. Poovorawan K, Suksawatamnuay S, Sahakitrungruang C, Treeprasertsuk S, Wisedopas N, Komolmit P, Poovorawan Y. Asian Pac J Cancer Prev; 2012 Apr 05; 13(10):5101-4. PubMed ID: 23244118 [Abstract] [Full Text] [Related]
44. Increased MUTYH mutation frequency among Dutch families with breast cancer and colorectal cancer. Wasielewski M, Out AA, Vermeulen J, Nielsen M, van den Ouweland A, Tops CM, Wijnen JT, Vasen HF, Weiss MM, Klijn JG, Devilee P, Hes FJ, Schutte M. Breast Cancer Res Treat; 2010 Dec 05; 124(3):635-41. PubMed ID: 20191381 [Abstract] [Full Text] [Related]
45. Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study. Ricci MT, Miccoli S, Turchetti D, Bondavalli D, Viel A, Quaia M, Giacomini E, Gismondi V, Sanchez-Mete L, Stigliano V, Martayan A, Mazzei F, Bignami M, Bonelli L, Varesco L. J Hum Genet; 2017 Feb 05; 62(2):309-315. PubMed ID: 27829682 [Abstract] [Full Text] [Related]
46. Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation. Giarola M, Stagi L, Presciuttini S, Mondini P, Radice MT, Sala P, Pierotti MA, Bertario L, Radice P. Hum Mutat; 1999 Feb 05; 13(2):116-23. PubMed ID: 10094547 [Abstract] [Full Text] [Related]
47. Mutation analysis of the APC gene in Taiwanese FAP families: low incidence of APC germline mutation in a distinct subgroup of FAP families. Chiang JM, Chen HW, Tang RP, Chen JS, Changchien CR, Hsieh PS, Wang JY. Fam Cancer; 2010 Jun 05; 9(2):117-24. PubMed ID: 19768578 [Abstract] [Full Text] [Related]
48. [Advance in research on the correlation between genotypes of susceptible mutations and clinical phenotype of familial adenomatous polyposis]. He S, Du J, Liu F. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec 10; 34(6):919-923. PubMed ID: 29188631 [Abstract] [Full Text] [Related]
49. Burden and Profile of Somatic Mutation in Duodenal Adenomas from Patients with Familial Adenomatous- and MUTYH-associated Polyposis. Thomas LE, Hurley JJ, Meuser E, Jose S, Ashelford KE, Mort M, Idziaszczyk S, Maynard J, Brito HL, Harry M, Walters A, Raja M, Walton SJ, Dolwani S, Williams GT, Morgan M, Moorghen M, Clark SK, Sampson JR. Clin Cancer Res; 2017 Nov 01; 23(21):6721-6732. PubMed ID: 28790112 [Abstract] [Full Text] [Related]
50. MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype. Aretz S, Uhlhaas S, Goergens H, Siberg K, Vogel M, Pagenstecher C, Mangold E, Caspari R, Propping P, Friedl W. Int J Cancer; 2006 Aug 15; 119(4):807-14. PubMed ID: 16557584 [Abstract] [Full Text] [Related]
52. Gene variants associated to malignant thyroid disease in familial adenomatous polyposis: a novel APC germline mutation. Martayan A, Sanchez-Mete L, Baldelli R, Falvo E, Barnabei A, Conti L, Giacomini P, Appetecchia M, Stigliano V. J Endocrinol Invest; 2010 Oct 15; 33(9):603-6. PubMed ID: 20935450 [Abstract] [Full Text] [Related]
53. Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. Spier I, Drichel D, Kerick M, Kirfel J, Horpaopan S, Laner A, Holzapfel S, Peters S, Adam R, Zhao B, Becker T, Lifton RP, Perner S, Hoffmann P, Kristiansen G, Timmermann B, Nöthen MM, Holinski-Feder E, Schweiger MR, Aretz S. J Med Genet; 2016 Mar 15; 53(3):172-9. PubMed ID: 26613750 [Abstract] [Full Text] [Related]
54. Transcript dosage effect in familial adenomatous polyposis: model offered by two kindreds with exon 9 APC gene mutations. Curia MC, Esposito DL, Aceto G, Palmirotta R, Crognale S, Valanzano R, Ficari F, Tonelli F, Battista P, Mariani-Costantini R, Cama A. Hum Mutat; 1998 Mar 15; 11(3):197-201. PubMed ID: 9521420 [Abstract] [Full Text] [Related]
59. Inactivation of germline mutant APC alleles by attenuated somatic mutations: a molecular genetic mechanism for attenuated familial adenomatous polyposis. Su LK, Barnes CJ, Yao W, Qi Y, Lynch PM, Steinbach G. Am J Hum Genet; 2000 Sep 15; 67(3):582-90. PubMed ID: 10924409 [Abstract] [Full Text] [Related]
60. Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition. Wallis YL, Morton DG, McKeown CM, Macdonald F. J Med Genet; 1999 Jan 15; 36(1):14-20. PubMed ID: 9950360 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]