Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
2004 2
2005 4
2006 7
2007 12
2008 14
2009 21
2010 30
2011 18
2012 25
2013 31
2014 28
2015 25
2016 21
2017 28
2018 17
2019 26
2020 24
2021 26
2022 22
2023 17
2024 20
2025 1

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

361 results

Results by year

Filters applied: . Clear all
Page 1
Did you mean mutyhassociated polyposis (231 results)?
MutYH-associated polyposis.
Toboeva MK, Shelygin YA, Frolov SA, Kuzminov MA, Tsukanov AS. Toboeva MK, et al. Ter Arkh. 2019 Mar 18;91(2):97-100. doi: 10.26442/00403660.2019.02.000124. Ter Arkh. 2019. PMID: 31094179 Review.
MutYH-associated polyposis is the only polyposis syndrome with an autosomal recessive type of inheritance, often phenotypically similar to a weakened form of familial adenomatous polyposis. For the development of the disease mutations in both al
MutYH-associated polyposis is the only polyposis syndrome with an autosomal recessive type of inheritance, often
Management of familial adenomatous polyposis and MUTYH-associated polyposis; new insights.
Aelvoet AS, Buttitta F, Ricciardiello L, Dekker E. Aelvoet AS, et al. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101793. doi: 10.1016/j.bpg.2022.101793. Epub 2022 Mar 16. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988966 Free article. Review.
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis syndromes with a high colorectal cancer (CRC) risk. ...Whereas up until recently upper gastrointestinal surveillance was mostly diagnostic and …
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis sy …
MUTYH-associated polyposis (MAP).
Nielsen M, Morreau H, Vasen HF, Hes FJ. Nielsen M, et al. Crit Rev Oncol Hematol. 2011 Jul;79(1):1-16. doi: 10.1016/j.critrevonc.2010.05.011. Epub 2010 Jul 21. Crit Rev Oncol Hematol. 2011. PMID: 20663686 Review.
The human mutY homologue (MUTYH) gene is responsible for inheritable polyposis and colorectal cancer. This review discusses the molecular genetic aspects of the MUTYH gene and protein, the clinical impact of mono- and biallelic MUTYH mutations and hist …
The human mutY homologue (MUTYH) gene is responsible for inheritable polyposis and colorectal cancer. This review discusses th …
Expanded extracolonic tumor spectrum in MUTYH-associated polyposis.
Vogt S, Jones N, Christian D, Engel C, Nielsen M, Kaufmann A, Steinke V, Vasen HF, Propping P, Sampson JR, Hes FJ, Aretz S. Vogt S, et al. Gastroenterology. 2009 Dec;137(6):1976-85.e1-10. doi: 10.1053/j.gastro.2009.08.052. Epub 2009 Sep 2. Gastroenterology. 2009. PMID: 19732775
BACKGROUND & AIMS: MUTYH-associated polyposis (MAP) is characterized by a lifetime risk of colorectal cancer of up to 100%. ...The median ages of onset of these 4 malignancies ranged from 51 to 61 years. In contrast to familial adenomatous polyposis
BACKGROUND & AIMS: MUTYH-associated polyposis (MAP) is characterized by a lifetime risk of colorectal cancer of up …
MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer institute (INCa).
Colas C, Bonadona V, Baert-Desurmont S, Bonnet D, Coulet F, Dhooge M, Saurin JC, Remenieras A, Bignon YJ, Caron O, De Pauw A, Buisine MP, Buecher B. Colas C, et al. Eur J Med Genet. 2020 Dec;63(12):104078. doi: 10.1016/j.ejmg.2020.104078. Epub 2020 Oct 12. Eur J Med Genet. 2020. PMID: 33059073 Review.
MUTYH-associated polyposis (MAP) was first described in 2002. It is an autosomal recessive condition associated with germline pathogenic variants of both MUTYH alleles. ...We also discuss the phenotype and tumor risks associated with mono
MUTYH-associated polyposis (MAP) was first described in 2002. It is an autosomal recessive condition associated
MUTYH Polyposis.
Nielsen M, Infante E, Brand R. Nielsen M, et al. 2012 Oct 4 [updated 2021 May 27]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2012 Oct 4 [updated 2021 May 27]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 23035301 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: MUTYH polyposis (also referred to as MUTYH-associated polyposis, or MAP) is characterized by a greatly increased lifetime risk of colorectal cancer (CRC). Although typically associated with ten to a few hundred c …
CLINICAL CHARACTERISTICS: MUTYH polyposis (also referred to as MUTYH-associated polyposis, or MAP) is cha …
MUTYH-associated polyposis.
Sampson JR, Jones N. Sampson JR, et al. Best Pract Res Clin Gastroenterol. 2009;23(2):209-18. doi: 10.1016/j.bpg.2009.03.006. Best Pract Res Clin Gastroenterol. 2009. PMID: 19414147 Review.
MUTYH-associated polyposis (MAP) is an autosomal recessive disorder characterised by adenomatous polyps of the colorectum and a very high risk of colorectal cancer. It appears to be at least as prevalent as autosomal dominant familial adenomatous polyposis
MUTYH-associated polyposis (MAP) is an autosomal recessive disorder characterised by adenomatous polyps of the colorect
Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision.
Zaffaroni G, Mannucci A, Koskenvuo L, de Lacy B, Maffioli A, Bisseling T, Half E, Cavestro GM, Valle L, Ryan N, Aretz S, Brown K, Buttitta F, Carneiro F, Claber O, Blanco-Colino R, Collard M, Crosbie E, Cunha M, Doulias T, Fleming C, Heinrich H, Hüneburg R, Metras J, Nagtegaal I, Negoi I, Nielsen M, Pellino G, Ricciardiello L, Sagir A, Sánchez-Guillén L, Seppälä TT, Siersema P, Striebeck B, Sampson JR, Latchford A, Parc Y, Burn J, Möslein G. Zaffaroni G, et al. Br J Surg. 2024 May 3;111(5):znae070. doi: 10.1093/bjs/znae070. Br J Surg. 2024. PMID: 38722804 Free PMC article.
BACKGROUND: Hereditary adenomatous polyposis syndromes, including familial adenomatous polyposis and other rare adenomatous polyposis syndromes, increase the lifetime risk of colorectal and other cancers. ...RESULTS: One hundred and forty statements reached a …
BACKGROUND: Hereditary adenomatous polyposis syndromes, including familial adenomatous polyposis and other rare adenomatous …
MUTYH-associated colorectal cancer and adenomatous polyposis.
Yamaguchi S, Ogata H, Katsumata D, Nakajima M, Fujii T, Tsutsumi S, Asao T, Sasaki K, Kuwano H, Kato H. Yamaguchi S, et al. Surg Today. 2014 Apr;44(4):593-600. doi: 10.1007/s00595-013-0592-7. Epub 2013 Apr 19. Surg Today. 2014. PMID: 23605219 Review.
MUTYH-associated polyposis (MAP) was first described in 2002. MUTYH is a component of a base excision repair system that protects the genomic information from oxidative damage. ...In the Asian population, Y179C and G396D are uncommon, whereas other var
MUTYH-associated polyposis (MAP) was first described in 2002. MUTYH is a component of a base excision repair sys
[MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer Institute (INCa)].
Buisine MP, Bonadona V, Baert-Desurmont S, Bonnet D, Coulet F, Dhooge M, Saurin JC, Remenieras A, Bignon YJ, Caron O, De Pauw A, Colas C, Buecher B. Buisine MP, et al. Bull Cancer. 2020 May;107(5):586-600. doi: 10.1016/j.bulcan.2020.02.004. Epub 2020 May 1. Bull Cancer. 2020. PMID: 32362383 Review. French.
MUTYH-associated polyposis (MUTYH-associated polyposis, MAP) is an autosomal recessive inheritance disorder related to bi-allelic constitutional pathogenic variants of the MUTYH gene which was first described in 2002. ...We also di
MUTYH-associated polyposis (MUTYH-associated polyposis, MAP) is an autosomal recessive inheritance
361 results