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Michael R Stratton

Showing results (201-210 of 262) with videos related to

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American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.
Nature Genetics|December 3, 2021
Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitroLuz Garcia-Alonso, Louis-François Handfield, Kenny Roberts, et al.
Nature|March 23, 2017
Somatic mutations reveal asymmetric cellular dynamics in the early human embryoYoung Seok Ju, Inigo Martincorena, Moritz Gerstung, et al.
Nature|January 21, 2011
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinomaIgnacio Varela, Patrick Tarpey, Keiran Raine, et al.
American Journal of Human Genetics|December 7, 2010
Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndromeKeith W McLarren, Tesa M Severson, Christèle du Souich, et al.
Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
Science Translational Medicine|August 9, 2013
Genome-wide mutational signatures of aristolochic acid and its application as a screening toolSong Ling Poon, See-Tong Pang, John R McPherson, et al.
Nature Communications|April 10, 2014
Processed pseudogenes acquired somatically during cancer developmentSusanna L Cooke, Adam Shlien, John Marshall, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2025
Horizontal transfer of nuclear DNA in transmissible cancerKevin Gori, Adrian Baez-Ortega, Andrea Strakova, et al.
Pageof 27

Showing results (201-210 of 262) with videos related to

Sort By:
Pageof 27
American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.
Nature Genetics|December 3, 2021
Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitroLuz Garcia-Alonso, Louis-François Handfield, Kenny Roberts, et al.
Nature|March 23, 2017
Somatic mutations reveal asymmetric cellular dynamics in the early human embryoYoung Seok Ju, Inigo Martincorena, Moritz Gerstung, et al.
Nature|January 21, 2011
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinomaIgnacio Varela, Patrick Tarpey, Keiran Raine, et al.
American Journal of Human Genetics|December 7, 2010
Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndromeKeith W McLarren, Tesa M Severson, Christèle du Souich, et al.
Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
Science Translational Medicine|August 9, 2013
Genome-wide mutational signatures of aristolochic acid and its application as a screening toolSong Ling Poon, See-Tong Pang, John R McPherson, et al.
Nature Communications|April 10, 2014
Processed pseudogenes acquired somatically during cancer developmentSusanna L Cooke, Adam Shlien, John Marshall, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2025
Horizontal transfer of nuclear DNA in transmissible cancerKevin Gori, Adrian Baez-Ortega, Andrea Strakova, et al.
Pageof 27