193 related articles for article (PubMed ID: 34817745)
41. Update on genetic predisposition to colorectal cancer and polyposis.
Valle L; de Voer RM; Goldberg Y; Sjursen W; Försti A; Ruiz-Ponte C; Caldés T; Garré P; Olsen MF; Nordling M; Castellvi-Bel S; Hemminki K
Mol Aspects Med; 2019 Oct; 69():10-26. PubMed ID: 30862463
[TBL] [Abstract][Full Text] [Related]
42. Genotype-phenotype correlation in 99 familial adenomatous polyposis patients: A prospective prevention protocol.
de Oliveira JC; Viana DV; Zanardo C; Santos EMM; de Paula AE; Palmero EI; Rossi BM
Cancer Med; 2019 May; 8(5):2114-2122. PubMed ID: 30897307
[TBL] [Abstract][Full Text] [Related]
43. Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
Spier I; Kerick M; Drichel D; Horpaopan S; Altmüller J; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Holinski-Feder E; Perner S; Thiele H; Nöthen MM; Hoffmann P; Timmermann B; Schweiger MR; Aretz S
Fam Cancer; 2016 Apr; 15(2):281-8. PubMed ID: 26780541
[TBL] [Abstract][Full Text] [Related]
44. A novel pathogenic frameshift variant in AXIN2 in a man with polyposis and hypodontia.
Broekema MF; Redeker EJW; Uiterwaal MT; van Hest LP
Hered Cancer Clin Pract; 2023 Aug; 21(1):16. PubMed ID: 37626374
[TBL] [Abstract][Full Text] [Related]
45. [Hyperplastic polyposis syndrome: phenotypic diversity and association to colorectal cancer].
Navarro M; González S; Iglesias S; Capellá G; Rodríguez-Moranta F; Blanco I
Med Clin (Barc); 2013 Jul; 141(2):62-6. PubMed ID: 22809968
[TBL] [Abstract][Full Text] [Related]
46. Low frequency of POLD1 and POLE exonuclease domain variants in patients with multiple colorectal polyps.
Elsayed FA; Tops CMJ; Nielsen M; Ruano D; Vasen HFA; Morreau H; J Hes F; van Wezel T
Mol Genet Genomic Med; 2019 Apr; 7(4):e00603. PubMed ID: 30827058
[TBL] [Abstract][Full Text] [Related]
47. Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH.
Sieber OM; Lipton L; Crabtree M; Heinimann K; Fidalgo P; Phillips RK; Bisgaard ML; Orntoft TF; Aaltonen LA; Hodgson SV; Thomas HJ; Tomlinson IP
N Engl J Med; 2003 Feb; 348(9):791-9. PubMed ID: 12606733
[TBL] [Abstract][Full Text] [Related]
48. A truncated protein product of the germline variant of the
Yang M; Zhao Y; Ding Y; Wang J; Tan Y; Xu D; Yuan Y
Cancer Biol Med; 2021 Feb; 18(1):215-226. PubMed ID: 33628596
[TBL] [Abstract][Full Text] [Related]
49. Novel Pathogenic Germline Variant of the Adenomatous Polyposis Coli (APC) Gene, p.S2627Gfs*12 Identified in a Mild Phenotype of APC-Associated Polyposis: A Case Report.
Koeller DR; Schwartz A; Manning DK; Dong F; Lindeman NI; Garber JE; Ghazani AA
Am J Case Rep; 2020 Dec; 21():e927293. PubMed ID: 33303731
[TBL] [Abstract][Full Text] [Related]
50. An AXIN2 Mutant Allele Associated With Predisposition to Colorectal Neoplasia Has Context-Dependent Effects on AXIN2 Protein Function.
Mazzoni SM; Petty EM; Stoffel EM; Fearon ER
Neoplasia; 2015 May; 17(5):463-72. PubMed ID: 26025668
[TBL] [Abstract][Full Text] [Related]
51. Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition.
Olkinuora A; Nieminen TT; Mårtensson E; Rohlin A; Ristimäki A; Koskenvuo L; Lepistö A; ; Gebre-Medhin S; Nordling M; Peltomäki P
Genet Med; 2019 Aug; 21(8):1868-1873. PubMed ID: 30573798
[TBL] [Abstract][Full Text] [Related]
52. Germline mutations in
Soares de Lima Y; Arnau-Collell C; Muñoz J; Herrera-Pariente C; Moreira L; Ocaña T; Díaz-Gay M; Franch-Expósito S; Cuatrecasas M; Carballal S; Lopez-Novo A; Moreno L; Fernàndez G; Díaz de Bustamante A; Peters S; Sommer AK; Spier I; Te Paske IBAW; van Herwaarden YJ; Castells A; Bujanda L; Capellà G; Steinke-Lange V; Mahmood K; Joo JE; Arnold J; Parry S; Macrae FA; Winship IM; Rosty C; Cubiella J; Rodríguez-Alcalde D; Holinski-Feder E; de Voer R; Buchanan DD; Aretz S; Ruiz-Ponte C; Valle L; Balaguer F; Bonjoch L; Castellvi-Bel S
J Med Genet; 2023 Jun; 60(6):557-567. PubMed ID: 36270769
[TBL] [Abstract][Full Text] [Related]
53. A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.
Weren RD; Ligtenberg MJ; Kets CM; de Voer RM; Verwiel ET; Spruijt L; van Zelst-Stams WA; Jongmans MC; Gilissen C; Hehir-Kwa JY; Hoischen A; Shendure J; Boyle EA; Kamping EJ; Nagtegaal ID; Tops BB; Nagengast FM; Geurts van Kessel A; van Krieken JH; Kuiper RP; Hoogerbrugge N
Nat Genet; 2015 Jun; 47(6):668-71. PubMed ID: 25938944
[TBL] [Abstract][Full Text] [Related]
54. Singapore familial adenomatous polyposis (FAP) patients with classical adenomatous polyposis but undetectable APC mutations have accelerated cancer progression.
Cao X; Hong Y; Eu KW; Loi C; Cheah PY
Am J Gastroenterol; 2006 Dec; 101(12):2810-7. PubMed ID: 17026565
[TBL] [Abstract][Full Text] [Related]
55. NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
Belhadj S; Quintana I; Mur P; Munoz-Torres PM; Alonso MH; Navarro M; Terradas M; Piñol V; Brunet J; Moreno V; Lázaro C; Capellá G; Valle L
Sci Rep; 2019 Jun; 9(1):9020. PubMed ID: 31227763
[TBL] [Abstract][Full Text] [Related]
56. Adenomatous Polyposis Phenotype in BMPR1A and SMAD4 Variant Carriers.
Rosner G; Petel-Galil Y; Laish I; Levi Z; Kariv R; Strul H; Gilad O; Gluck N
Clin Transl Gastroenterol; 2022 Oct; 13(10):e00527. PubMed ID: 36049049
[TBL] [Abstract][Full Text] [Related]
57. MUTYH hotspot mutations in unselected colonoscopy patients.
Casper M; Plotz G; Juengling B; Zeuzem S; Lammert F; Raedle J
Colorectal Dis; 2012 May; 14(5):e238-44. PubMed ID: 22469480
[TBL] [Abstract][Full Text] [Related]
58. Detection of a heterozygous germline APC mutation in a three-generation family with familial adenomatous polyposis using targeted massive parallel sequencing in Vietnam.
Giang H; Nguyen VT; Nguyen SD; Nguyen HP; Vo BT; Nguyen TM; Nguyen NH; Truong KD; Do TT; Phan MD; Nguyen HN
BMC Med Genet; 2018 Oct; 19(1):188. PubMed ID: 30340471
[TBL] [Abstract][Full Text] [Related]
59. Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing.
Lorca V; Rueda D; Martín-Morales L; Fernández-Aceñero MJ; Grolleman J; Poves C; Llovet P; Tapial S; García-Barberán V; Sanz J; Pérez-Segura P; de Voer RM; Díaz-Rubio E; de la Hoya M; Caldés T; Garre P
Sci Rep; 2019 Jul; 9(1):9814. PubMed ID: 31285513
[TBL] [Abstract][Full Text] [Related]
60.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]