Results 151 to 160 of about 33,127 (201)

Fluorescent reporter assay reveals ribonucleotides promote mismatch correction in vivo. [PDF]

Nucleic Acids Res
Erlich S, Mazzucato P, Laverty DJ, Samson LD, Nagel ZD.   +4 more
europepmc   +1 more source

Constitutional methylation of the MLH1 promoter: a case series including tumors not typically caused by Lynch Syndrome. [PDF]

Eur J Hum Genet
Graversen L, Assenholt J, Pedersen IS, Stoico MP, Hager H, Lautrup C, Geilswijk M, Buchanan DD, Macrae FA, Winship IM, Christiansen M, Petersen AH, Højland A, Sunde L.   +13 more
europepmc   +1 more source

Histopathologic clues to mismatch repair deficiency in colon adenocarcinoma: the role of mucinous component and intratumoral/Crohn-like immune response. [PDF]

BMC Gastroenterol
Atmış Ö, Ocak S, Pehli̇van FS, Mavi̇li̇ HS, Tan A, Ayhan S.   +5 more
europepmc   +1 more source

The germline MLH1 c.2054 C>T mutation disrupts DNA mismatch repair and is detectable by digital PCR. [PDF]

Cancer Lett
Moldenhauer MR, Mahadevan A, Hom C, Nguyen ATM, Rangel V, Hasson S, Hsu NH, Ubbaonu C, Nathan D, Chandan VS, Shen KV, Damozonio EM, Zhou GG, Chichili T, Le A, Masri S, Dayyani F, Qiao F, Valerin JB, Pannunzio NR.   +19 more
europepmc   +1 more source

Adenomas and Beyond: Colonoscopy Surveillance, Racial and Socioeconomic Disparities in Lynch Syndrome. [PDF]

Gastro Hep Adv
Atarere J, Bilalaga MM, Vasireddy R, Mensah B, Gaddipati GN, Singh S, Akhiwu TO, Woo S, Dash C, Kanth P.   +9 more
europepmc   +1 more source

Prevalence of Mismatch Repair Deficiency and Its Association with Histopathological Parameters in Endometrial Cancer: A Prospective Cohort Study. [PDF]

Int J Mol Sci
Almperi EA, Margioula-Siarkou C, Almperis A, Zwimpfer TA, Daponte A, Daponte N, Vrekoussis T, Papamitsou T, Dinas K, Petousis S.   +9 more
europepmc   +1 more source

<i>NTRK</i>-positive collision tumor of the gastrointestinal tract: a rare entity case report. [PDF]

Ann Med Surg (Lond)
Sirek A, Amann VC, Uzun S, Bubendorf L, Rosenberg R, Burri E, Häuptle P, Roma L, Mertz KD.   +8 more
europepmc   +1 more source

Molecular assessment of recombination processing across genetically diverse mouse strains reveals sexually dimorphic determinants of crossover distribution beyond chromosome length. [PDF]

Mol Biol Evol
Horan TS, Wood A, Tanis S, Peirau-Gabarrell C, Cohen PE.   +4 more
europepmc   +1 more source

<i>MLH1</i> Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level. [PDF]

Hum Mutat
Facon C, Vermaut C, Delattre L, Flament C, Dardenne A, Brahimi A, Lejeune S, Cattan S, Bonnet F, Basset N, Bensen A, Dupré A, Berthet P, Dhooge M, Colas C, Mouret-Fourme E, Delhomelle H, Nambot S, Baurand A, Planes M, Menjard J, Benusiglio PR, Pigny P, Buisine MP, Leclerc J.   +24 more
europepmc   +1 more source

Genetic Variation of <i>MLH1</i> (rs63749820) in Patients With Oral Squamous Cell Carcinoma. [PDF]

Int J Dent
Zare R, Mokhtari MJ, Rahimi H, Fattahi MJ, Khademi B.   +4 more
europepmc   +1 more source