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Showing results (451-460 of 551) with videos related to

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Molecular Genetics and Genomics : MGG|October 18, 2006
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndromeErwin Petek, Thomas Schwarzbraun, Abdul Noor, et al.
Blood|September 13, 2011
Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patientsMonia Ouederni, Quentin B Vincent, Pierre Frange, et al.
American Journal of Human Genetics|May 21, 2004
Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxiaYoshio Ikeda, Joline C Dalton, Melinda L Moseley, et al.
Mbio|March 20, 2023
Listeria monocytogenes GlmR Is an Accessory Uridyltransferase Essential for Cytosolic Survival and VirulenceDaniel A Pensinger, Kimberly V Gutierrez, Hans B Smith, et al.
Frontiers in Immunology|April 23, 2021
GILZ Regulates the Expression of Pro-Inflammatory Cytokines and Protects Against End-Organ Damage in a Model of LupusChampa Nataraja, Wendy Dankers, Jacqueline Flynn, et al.
Human Molecular Genetics|August 13, 2024
Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoformsLadan Kalani, Bo-Hyun Kim, Alberto Ruiz de Chavez, et al.
European Journal of Human Genetics : EJHG|June 24, 2021
Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric featuresMaha S Zaki, Andrea Accogli, Ghayda Mirzaa, et al.
Evolution; International Journal of Organic Evolution|April 24, 2012
Do trade-offs have explanatory power for the evolution of organismal interactions?Mark K Asplen, Emily Bruns, Aaron S David, et al.
Journal of Molecular Biology|July 27, 2001
Large-scale analysis of the Alu Ya5 and Yb8 subfamilies and their contribution to human genomic diversityM L Carroll, A M Roy-Engel, S V Nguyen, et al.
Circulation. Cardiovascular Genetics|August 28, 2012
Spongious hypertrophic cardiomyopathy in patients with mutations in the four-and-a-half LIM domain 1 geneJosepha S Binder, Frank Weidemann, Benedikt Schoser, et al.
Pageof 56

Showing results (451-460 of 551) with videos related to

Sort By:
Pageof 56
Molecular Genetics and Genomics : MGG|October 18, 2006
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndromeErwin Petek, Thomas Schwarzbraun, Abdul Noor, et al.
Blood|September 13, 2011
Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patientsMonia Ouederni, Quentin B Vincent, Pierre Frange, et al.
American Journal of Human Genetics|May 21, 2004
Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxiaYoshio Ikeda, Joline C Dalton, Melinda L Moseley, et al.
Mbio|March 20, 2023
Listeria monocytogenes GlmR Is an Accessory Uridyltransferase Essential for Cytosolic Survival and VirulenceDaniel A Pensinger, Kimberly V Gutierrez, Hans B Smith, et al.
Frontiers in Immunology|April 23, 2021
GILZ Regulates the Expression of Pro-Inflammatory Cytokines and Protects Against End-Organ Damage in a Model of LupusChampa Nataraja, Wendy Dankers, Jacqueline Flynn, et al.
Human Molecular Genetics|August 13, 2024
Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoformsLadan Kalani, Bo-Hyun Kim, Alberto Ruiz de Chavez, et al.
European Journal of Human Genetics : EJHG|June 24, 2021
Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric featuresMaha S Zaki, Andrea Accogli, Ghayda Mirzaa, et al.
Evolution; International Journal of Organic Evolution|April 24, 2012
Do trade-offs have explanatory power for the evolution of organismal interactions?Mark K Asplen, Emily Bruns, Aaron S David, et al.
Journal of Molecular Biology|July 27, 2001
Large-scale analysis of the Alu Ya5 and Yb8 subfamilies and their contribution to human genomic diversityM L Carroll, A M Roy-Engel, S V Nguyen, et al.
Circulation. Cardiovascular Genetics|August 28, 2012
Spongious hypertrophic cardiomyopathy in patients with mutations in the four-and-a-half LIM domain 1 geneJosepha S Binder, Frank Weidemann, Benedikt Schoser, et al.
Pageof 56