Associated Papers
Achieving high-sensitivity for clinical applications using augmented exome sequencing.
Patwardhan A et al.
Genome Medicine, 2015
26269718 (PubMed )
Supplement: 13073_2015_197_MOESM8_ESM.xlsx › Sheet1
Crystal structures of the armadillo repeat domain of adenomatous polyposis coli and its complex with the tyrosine-rich domain of Sam68.
Morishita EC et al.
Structure (london, England : 1993), 2011
Messing up disorder: how do missense mutations in the tumor suppressor protein APC lead to cancer?
Minde DP et al.
Molecular Cancer, 2011
21859464 (PubMed )
Supplement: 1476-4598-10-101-S1.DOC
Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients.
Sulová M et al.
European Journal of Cancer (oxford, England : 1990), 2007
Increased frequency of disease-causing MYH mutations in colon cancer families.
Peterlongo P et al.
Carcinogenesis, 2006
Microsatellite stable colorectal cancers in clinically suspected hereditary nonpolyposis colorectal cancer patients without vertical transmission of disease are unlikely to be caused by biallelic germline mutations in MYH.
Görgens H et al.
The Journal of Molecular Diagnostics : Jmd, 2006
Inherited variants in MYH are unlikely to contribute to the risk of lung carcinoma.
Al-Tassan N et al.
Human Genetics, 2004
Detection of sequence variations in the adenomatous polyposis coli (APC) gene using denaturing high-performance liquid chromatography.
Wu G et al.
Genetic Testing, 2001
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