Results 131 to 140 of about 27,093,662 (158)

Utilization of whole exome sequencing to identify hereditary mutations in Palestinian families with hereditary cancers. [PDF]

Front Genet
Qutob N, Hindiyeh M, Zahdeh F, Alian A, Thawabteh R, Sallam H, Natsheh A.   +6 more
europepmc   +1 more source

Concurrent Breast and Colon Cancer: Small Cohort Analysis. [PDF]

Cureus
Qavi Q, Islam KS, Hashmi Z, Ahmed R, Hamdani J, Rasheed N, Rani F, Chicken DW, Idaewor P, Saad Abdalla Al-Zawi A.   +9 more
europepmc   +1 more source

A rare case of colonic adenocarcinoma in a pediatric patient. [PDF]

JPGN Rep
Kaba C, Chatman K, Hames N, Velazquez Vega JE, Bashaw H.   +4 more
europepmc   +1 more source

Clinicopathologic, molecular and tumor immune microenvironment features of mismatch repair-deficient glioblastomas in Lynch syndrome: a multicenter study of 29 cases with therapeutic implications. [PDF]

Acta Neuropathol Commun
Yao ZG, Li XL, Wen WJ, Lin XY, Zhang GH, Sun YP, Nie YC, Zheng ZM, Xu YQ, Yang M, Yu TF, Dong Y, Hou YH, Dang LL, Chu SG, Li JM, Ma JW, Wang Z, Hua F, Wang XF, Wang DZ, Hu WM.   +21 more
europepmc   +1 more source

Mechanism of MutLβ-dependent DNA expansions. [PDF]

Proc Natl Acad Sci U S A
Kadyrova LY, Kadyrov FF, Hayward B, Usdin K, Kadyrov FA.   +4 more
europepmc   +1 more source

Muir-Torre Syndrome Associated With a Cryptic Intronic MSH2 Variant Identified via Whole-Genome Sequencing: A Case Report. [PDF]

Pathol Int
Noda K, Kurohama H, Matsuda K, Kinoshita A, Mishima H, Matsumoto M, Matsuda R, Ueki N, Kishikawa M, Miura K, Nonaka T, Yoshiura KI, Matsumoto K, Nakashima M.   +13 more
europepmc   +1 more source

Bacillus subtilis MutL samples multiple conformations during nucleotide binding and hydrolysis. [PDF]

Structure
Rodríguez González J, Davis CL, Wilkins H, Erie DA, Guarné A.   +4 more
europepmc   +1 more source

Low Yield of Genetic Testing in Serrated Polyposis Syndrome. [PDF]

Clin Transl Gastroenterol
Upadhye I, Al Maliki H, Cuthill V, Latchford A, Monahan K.   +4 more
europepmc   +1 more source

Promoter methylation of the hMLH1 gene and protein expression of human mutL homolog 1 and human mutS homolog 2 in resected esophageal squamous cell carcinoma [PDF]

Journal of Thoracic and Cardiovascular Surgery, 2005
ObjectiveAberrant expression of mismatch repair genes, such as human mutL homolog 1 (hMLH1) and human mutS homolog 2 (hMSH2), are common in some human cancers, and promoter methylation is believed to inactivate expression of hMLH1.
Ho-Jui Tung, Yi-Ching Wang, Shih-Chun Lee   +2 more
exaly   +2 more sources

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.

Cell, 1993
Recent studies have shown that a locus responsible for hereditary nonpolyposis colorectal cancer (HNPCC) is on chromosome 2p and that tumors developing in these patients contain alterations in microsatellite sequences (RER + phenotype).
Lauri Aaltonen, Päivi Peltomäki
exaly   +2 more sources