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Niels de Wind

Showing results (71-80 of 78) with videos related to

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Nucleic Acids Research|January 30, 2023
Unexpected moves: a conformational change in MutSα enables high-affinity DNA mismatch bindingSusanne R Bruekner, Wietske Pieters, Alexander Fish, et al.
Experimental and Molecular Pathology|October 22, 2024
Assessing pathogenicity of mismatch repair variants of uncertain significance by molecular tumor analysisAnne-Sophie van der Werf't Lam, Noah C Helderman, Arnoud Boot, et al.
Blood|August 23, 2017
Genomic and functional integrity of the hematopoietic system requires tolerance of oxidative DNA lesionsAna Martín-Pardillos, Anastasia Tsaalbi-Shtylik, Si Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndromeMark Drost, Yvonne Tiersma, Bryony A Thompson, et al.
Nature Communications|June 13, 2015
De novo mutations in PLXND1 and REV3L cause Möbius syndromeLaura Tomas-Roca, Anastasia Tsaalbi-Shtylik, Jacob G Jansen, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 12, 2023
Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant CarriersAnne-Sophie van der Werf-'t Lam, Diantha Terlouw, Carli M Tops, et al.
Human Mutation|March 10, 2011
Deciphering the colon cancer genes--report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010Maija R J Kohonen-Corish, Finlay Macrae, Maurizio Genuardi, et al.
Human Mutation|July 21, 2016
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency SyndromeHeleen M van der Klift, Arjen R Mensenkamp, Mark Drost, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Nucleic Acids Research|January 30, 2023
Unexpected moves: a conformational change in MutSα enables high-affinity DNA mismatch bindingSusanne R Bruekner, Wietske Pieters, Alexander Fish, et al.
Experimental and Molecular Pathology|October 22, 2024
Assessing pathogenicity of mismatch repair variants of uncertain significance by molecular tumor analysisAnne-Sophie van der Werf't Lam, Noah C Helderman, Arnoud Boot, et al.
Blood|August 23, 2017
Genomic and functional integrity of the hematopoietic system requires tolerance of oxidative DNA lesionsAna Martín-Pardillos, Anastasia Tsaalbi-Shtylik, Si Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndromeMark Drost, Yvonne Tiersma, Bryony A Thompson, et al.
Nature Communications|June 13, 2015
De novo mutations in PLXND1 and REV3L cause Möbius syndromeLaura Tomas-Roca, Anastasia Tsaalbi-Shtylik, Jacob G Jansen, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 12, 2023
Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant CarriersAnne-Sophie van der Werf-'t Lam, Diantha Terlouw, Carli M Tops, et al.
Human Mutation|March 10, 2011
Deciphering the colon cancer genes--report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010Maija R J Kohonen-Corish, Finlay Macrae, Maurizio Genuardi, et al.
Human Mutation|July 21, 2016
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency SyndromeHeleen M van der Klift, Arjen R Mensenkamp, Mark Drost, et al.
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