Germline mutation prevalence in the base excision repair gene, MYH, in patients with endometrial cancer

No abstract is available for this paper.

• Publication year

  2007

• Venue

  Clinical Genetics

• Publication date

  2007-12-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1111/j.1399-0004.2007.00900.xPMID 17956577
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Association of MUTYH and colorectal cancer

  2006cited by this paper
• Correlation of polyp number and family history of colon cancer with germline MYH mutations.

  2005cited by this paper
• Germline susceptibility to colorectal cancer due to base-excision repair gene defects.

  2005cited by this paper
• Re: Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk.

  2005cited by this paper
• MutYH (MYH) and colorectal cancer.

  2005cited by this paper
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  2005cited by this paper
• A kindred with MYH‐associated polyposis and pilomatricomas

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• Molecular analysis of familial endometrial carcinoma: a manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome?

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• Genetic alterations of the KLF6 gene in gastric cancer

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• Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk.

  2004cited by this paper
• Germline MUTYH (MYH) mutations in Portuguese individuals with multiple colorectal adenomas

  2004cited by this paper
• Genetic alterations of the MYH gene in gastric cancer

  2004cited by this paper
• Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers.

  2003cited by this paper
• Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH.

  2003cited by this paper
• Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH.

  2003cited by this paper
• Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations.

  2002cited by this paper
• Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors

  2002cited by this paper
• Duodenal cancer in patients with familial adenomatous polyposis (FAP): results of a 10 year prospective study

  2002cited by this paper
• A single nucleotide polymorphism at the splice donor site of the human MYH base excision repair gene results in reduced translation efficiency of its transcripts

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• Multiple Familial Pilomatricomas: A Cutaneous Marker for Gardner Syndrome?

  1995cited by this paper
• Life‐time risk of different cancers in hereditary non‐polyposis colorectal cancer (hnpcc) syndrome

  1995cited by this paper
• Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis.

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• Synchronous Endometrial and Ovarian Endometrioid Carcinoma With MUTYH Germline Mutation: A Case Report With Genetic Analysis.

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• Inherited Cancer Susceptibility Gene Sequence Variations Among Patients With Appendix Cancer.

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• Endometrial cancer may be part of the MUTYH-associated polyposis cancer spectrum.

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• MUTYH-associated polyposis: review and update of the French recommendations established in 2012 under the auspices of the National Cancer Institute (INCa).

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• [MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer Institute (INCa)].

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• Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis

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• Oxidative stress and mule-driven X-linked intellectual disability

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• Update on Hereditary Colorectal Cancer: Improving the Clinical Utility of Multigene Panel Testing.

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• PREVALENCE OF GERMLINE MUTATIONS IN CANCER GENES AMONG PANCREATIC CANCER PATIENTS WITH POSITIVE FAMILY HISTORY

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• Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH

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• Cutaneous Sebaceous Lesions in a Patient With MUTYH-Associated Polyposis Mimicking Muir-Torre Syndrome

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  2015cites this paper
• Next-generation sequencing for genetic testing of familial colorectal cancer syndromes

  2015cites this paper
• Colorectal carcinomas, a consideration on MUTYH-associated polyposis.

  2014cites this paper
• Caracterización fenotípica y genotípica de las poliposis colónicas atenuadas. Biomarcadores diagnósticos y pronósticos

  2014cites this paper
• Prevalence and Characteristics of MUTYH-Associated Polyposis in Patients with Multiple Adenomatous and Serrated Polyps

  2014cites this paper
• MutY-glycosylase: an overview on mutagenesis and activities beyond the GO system.

  2014cites this paper
• Two Chinese pedigrees for adenomatous polyposis coli: new mutations at codon 1309 and predisposition to phenotypic variations

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• Molecular Pathology and Diagnostics of Colorectal Cancer

  2014cites this paper
• MUTYH the base excision repair gene family member associated with polyposis colorectal cancer

  2013cites this paper
• MUTYH the base excision repair gene family member associated with colorectal cancer polyposis

  2013cites this paper
• Novel insertion mutation p.Asp610GlyfsX23 in APC gene causes familial adenomatous polyposis in Chinese families.

  2013cites this paper
• Role of MUTYH in human cancer.

  2013cites this paper
• MUTYH-associated polyposis (MAP), the syndrome implicating base excision repair in inherited predisposition to colorectal tumors

  2012cites this paper
• MUTYH gene expression and alternative splicing in controls and polyposis patients

  2012cites this paper
• MUTYH-associated polyposis (MAP).

  2011cites this paper
• Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer

  2011cites this paper
• When is a desmoid not a desmoid? Endometrial cancer as an extracolonic manifestation of MYH Associated Polyposis (MAP)

  2011cites this paper
• Sebaceous neoplasia and the Muir–Torre syndrome: important connections with clinical implications

  2010cites this paper
• MUTYH Exon 7 and 13 Mutations Associated with Colorectal Cancer (MAP Syndrome) Are Not Commonly Associated with Sporadic Pancreatic Cancer

  2010cites this paper
• Hereditary Colorectal Cancer

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• Rodzinna polipowatość gruczolakowata jelita grubego

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• Leiden open variation database of the MUTYH gene

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• The MYH gene status in patients with sporadic colorectal polyps

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• Biallelic MYH germline mutations as cause of Muir-Torre syndrome

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• Personalized genomic medicine

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• Diagnosis and management of hereditary colorectal cancer syndromes: Lynch syndrome as a model

  2009cites this paper
• Endometrial cancer and somatic G>T KRAS transversion in patients with constitutional MUTYH biallelic mutations.

  2009cites this paper
• Genetic variation and risk of endometrial cancer

  2009cites this paper
• Expanded extracolonic tumor spectrum in MUTYH-associated polyposis.

  2009cites this paper
• MYH-associated disease: attenuated adenomatous polyposis of the colon is only part of the story.

  2009cites this paper
• Genetic variants in MUTYH are not associated with endometrial cancer risk

  2009influential citation
• MUTYH-associated polyposis.

  2009cites this paper
• MUTYH Associated Polyposis (MAP)

  2008influential citation
• Molecular genetic and phenotypic characteristics of patients with adenomatous colorectal polyposis

  2008cites this paper