Results 121 to 130 of about 29,501 (185)

Lynch syndrome-associated urothelial carcinoma: clinical and molecular findings from a single-institution cohort. [PDF]

Fam Cancer
Rametta A, Barella M, Scardino A, Barbetta F, Tamborini E, Perrone F, Busico A, Agnelli L, Rota S, Gusmaroli E, Stellato M, Nuzzo A, Guadalupi V, Claps M, Ricci MT, Procopio G, Pruneri G, Milione M, Giannatempo P, Vitellaro M.   +19 more
europepmc   +1 more source

Lynch syndrome caused by a pathogenic SINE-VNTR-Alu (SVA) insertion in MSH2 gene identified by long-read DNA sequencing. [PDF]

Fam Cancer
Joo JE, Mahmood K, Clendenning M, Georgeson P, Walker R, Como J, Phillips F, Pope BJ, Batinovic S, Diepenhorst N, McDonald J, Rice T, Rosty C, Jenkins MA, Macrae FA, Winship IM, High H, Buchanan DD.   +17 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

Molecular characterization of mismatch repair deficient tumors in young Jordanian patients. [PDF]

Discov Oncol
Ahmad O, Sultan I, Hussaini M, Alsmadi O, Sutter C, Hirsch S, Autry RJ, Previti C, Försti A, Schwalm B, AbuJamous L, Amayiri N, Shanap MA, Amareen R, Aljawabrah S, Fryjat L, Al-Naimat A, Qaisi A, Alnaimat H, Reuss DE, Fernandez NR, Das A, Tabori U, Pfister SM, Schaaf CP.   +24 more
europepmc   +1 more source

Polymorphism can extensively reshape the genome-wide crossover landscape in Arabidopsis thaliana. [PDF]

Nat Commun
Madec B, Sémery M, Lian Q, Yassine M, Léonard-Moniot L, Espagne É, Piquerez S, Girard C.   +7 more
europepmc   +1 more source

Pathological features and prognosis based on microsatellite stability status in colorectal cancer patients: a retrospective analysis. [PDF]

Int J Clin Exp Pathol
Liu X, Yang Y, Zheng H, Zhang Y.
europepmc   +1 more source

Phenotypic heterogeneity in carriers of a pathogenic MSH2 variant: implications for the diagnosis of Lynch syndrome. [PDF]

J Cancer Res Clin Oncol
Apuhan T, Demir O, Sagnak Yilmaz Z, Karaman E, Turkyilmaz A, Cebi AH.   +5 more
europepmc   +1 more source

Nuclear PI3P produced by the Beclin-1/Vps34 complex regulates DNA mismatch repair. [PDF]

Nucleic Acids Res
Li X, Vicinanza M, Lopez A, Festa BP, Schlotawa L, Barbosa AD, Takla M, Balmus G, Fleming A, Rubinsztein DC.   +9 more
europepmc   +1 more source

Bayesian Integration of Tumor Mutational Signatures and Somatic Features Refines Pathogenicity Assessment of Germline Mismatch Repair Variants. [PDF]

Hum Mutat
Amzaleg Y, McDonnell KJ, Idos GE, Mathai C, Gray SW, Hampel H, Craig DW.   +6 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