Results 191 to 200 of about 32,048 (238)

Reticulated acanthoma with sebaceous differentiation: A case report. [PDF]

Medicine (Baltimore)
Yu WT, Zhang Q, Shen H, Liu ZH.
europepmc   +1 more source

Mismatch repair deficiency reshapes glioblastoma through immune suppression rather than hypermutation. [PDF]

J Clin Invest
Li A, Sears TK, Horbinski CM.
europepmc   +1 more source

Germline Variants in Bladder and Upper Tract Urothelial Cancers: Prevalence and Clinical Context in a Large Testing Registry. [PDF]

Eur Urol Open Sci
Monda SM, Oh E, Lewicki PJ, Kaffenberger SD, Else T, Reichert ZR, Tsung I, Ghani KR, Nguyen CB, Humble R, Schiewer MJ, Finch R, Salami S, Stoffel EM, Morgan TM, Chandrasekar T, Singhal U.   +16 more
europepmc   +1 more source

Pancreatic cancer risk and survival in patients with Lynch syndrome: a nationwide Dutch cohort study. [PDF]

EClinicalMedicine
Bogdanski AM, Klatte DCF, Bonsing BA, Brosens LAA, Dekker E, van der Geest LG, Ijspeert JEG, Koornstra JJ, van Kouwen MCA, Langers AMJ, Nielsen M, Ramsoekh D, Spaander MC, de Vos Tot Nederveen Cappel WH, Van Hooft JE, van Leerdam ME, Dutch Pancreatic Cancer Group, Collaborative investigators from the Dutch Foundation for Detection of Hereditary Tumors.   +17 more
europepmc   +1 more source

Immune checkpoint inhibitors in children with replication-repair-deficient high-grade gliomas. The South London Paediatric & TYA Neuro-Oncology Network experience

Perez-Somarriba M, Campello A, Benjamin P, Reisz Z, Bodi I, Al-Sarraj S, Bridges LR, Kumar A, Jacques TS, Zebian B, Bleil C, Aquilina K, Hettige S, Mastronuzzi A, Srivatsa K, Cockle J, Mandeville H, Marshall LV, Vaidya S, Stengs L, Bianchi V, Jones C, Lassaletta A, Das A, Tabori U, Carceller F.   +25 more
europepmc   +1 more source

Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers [PDF]

Journal of the National Cancer Institute, 2010
Germline mutations in MSH6 account for 10%-20% of Lynch syndrome colorectal cancers caused by hereditary DNA mismatch repair gene mutations. Because there have been only a few studies of mutation carriers, their cancer risks are uncertain.We identified 113 families of MSH6 mutation carriers from five countries that we ascertained through family cancer ...
Laura Baglietto, James G Dowty, Rebecca A Barnetson   +2 more
exaly   +6 more sources

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Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6

Familial Cancer, 2017
Lynch Syndrome (LS) is the most common dominantly inherited colorectal cancer (CRC) predisposition and is caused by a heterozygous germline defect in one of the DNA mismatch repair (MMR) genes MLH1, MSH2, MSH6, or PMS2. High microsatellite instability (MSI-H) and loss of MMR protein expression in tumours reflecting a defective MMR are indicators for LS,
Monika Morak, Sarah Käsbauer, Martina Kerscher, Andreas Laner, Anke M. Nissen, Anna Benet-Pagès, Hans K. Schackert, Gisela Keller, Trisari Massdorf, Elke Holinski-Feder   +9 more
openaire   +2 more sources

NordiQC Assessments of MSH6 Immunoassays

Applied Immunohistochemistry & Molecular Morphology, 2018
This paper is number 4 in a series developed through a partnership between ISIMM and Nordic immunohistochemical Quality Control for the purpose of reporting research assessing the performance characteristics of immunoassays in an external proficiency testing program.
Vyberg, Mogens, Røge, Rasmus, Bzorek, Michael, Nielsen, Ole   +3 more
openaire   +4 more sources

A novel infram deletion in MSH6 gene in glioma: Conversation on MSH6 mutations in brain tumors

Journal of Cellular Physiology, 2018
AbstractObjective and backgroundHistological and molecular information and biopsy help in the diagnosis of the type and grade of tumors and increase the value of estimation of the biological behavior of tumors. In this study, we focused on a consanguineous Iranian Family with high prevalence of brain tumors in their pedigree and reviewed the literature
Zeinab Deris Zayeri, Maryam Tahmasebi Birgani, Javad Mohammadi Asl, Davood Kashipazha, Mohammadreza Hajjari   +4 more
openaire   +2 more sources