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Showing results (41-50 of 49) with videos related to

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Plos One|December 1, 2022
Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancerMarwa Mahdouani, Slim Ben Ahmed, Fahmi Hmila, et al.
International Journal of Molecular Sciences|June 19, 2024
Erk Inhibition as a Promising Therapeutic Strategy for High IL-8-Secreting and Low SPTAN1-Expressing Colorectal CancerClara Meier, Gianluca La Rocca, Virginia Nawrot, et al.
Journal of Medical Genetics|May 28, 2013
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variantsEster Borràs, Marta Pineda, Juan Cadiñanos, et al.
Gut|April 3, 2014
Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotypeNuria Seguí, Matilde Navarro, Marta Pineda, et al.
Plos One|June 6, 2024
Functional analysis of MMR gene VUS from potential Lynch syndrome patientsMarwa Mahdouani, Drenushe Zhuri, Hazal Sezginer Guler, et al.
Familial Cancer|April 3, 2017
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteriaMaribel González-Acosta, Jesús Del Valle, Matilde Navarro, et al.
International Journal of Cancer|December 23, 2014
Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomasIsabel Spier, Stefanie Holzapfel, Janine Altmüller, et al.
Genes, Chromosomes & Cancer|March 10, 2018
Evaluation of MLH1 variants of unclear significanceNicole Köger, Lea Paulsen, Francisco López-Kostner, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Analysis of structure and conservation for supporting functional evaluation of PMS2 missense variantsNicholas Zeuzem, Manon Quilan, Mev Dominguez-Valentin, et al.
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Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Plos One|December 1, 2022
Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancerMarwa Mahdouani, Slim Ben Ahmed, Fahmi Hmila, et al.
International Journal of Molecular Sciences|June 19, 2024
Erk Inhibition as a Promising Therapeutic Strategy for High IL-8-Secreting and Low SPTAN1-Expressing Colorectal CancerClara Meier, Gianluca La Rocca, Virginia Nawrot, et al.
Journal of Medical Genetics|May 28, 2013
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variantsEster Borràs, Marta Pineda, Juan Cadiñanos, et al.
Gut|April 3, 2014
Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotypeNuria Seguí, Matilde Navarro, Marta Pineda, et al.
Plos One|June 6, 2024
Functional analysis of MMR gene VUS from potential Lynch syndrome patientsMarwa Mahdouani, Drenushe Zhuri, Hazal Sezginer Guler, et al.
Familial Cancer|April 3, 2017
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteriaMaribel González-Acosta, Jesús Del Valle, Matilde Navarro, et al.
International Journal of Cancer|December 23, 2014
Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomasIsabel Spier, Stefanie Holzapfel, Janine Altmüller, et al.
Genes, Chromosomes & Cancer|March 10, 2018
Evaluation of MLH1 variants of unclear significanceNicole Köger, Lea Paulsen, Francisco López-Kostner, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Analysis of structure and conservation for supporting functional evaluation of PMS2 missense variantsNicholas Zeuzem, Manon Quilan, Mev Dominguez-Valentin, et al.
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