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RNA (New York, N.Y.)
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February 18, 2006
The RNA Ontology Consortium: an open invitation to the RNA community
Neocles B Leontis, Russ B Altman, Helen M Berman, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 15, 2022
Newborn screening for neurodevelopmental diseases: Are we there yet?
Wendy K Chung, Jonathan S Berg, Jeffrey R Botkin, et al.
Journal of Proteome Research
|
October 27, 2012
High-throughput isolation and characterization of untagged membrane protein complexes: outer membrane complexes of Desulfovibrio vulgaris
Peter J Walian, Simon Allen, Maxim Shatsky, et al.
Human Mutation
|
May 30, 2019
Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges
Gregory McInnes, Roxana Daneshjou, Panagiostis Katsonis, et al.
NPJ Genomic Medicine
|
October 13, 2021
Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders
Joseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.
NPJ Genomic Medicine
|
September 24, 2021
Application of full-genome analysis to diagnose rare monogenic disorders
Joseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.
Genome Research
|
October 9, 2002
The Bioperl toolkit: Perl modules for the life sciences
Jason E Stajich, David Block, Kris Boulez, et al.
Human Genetics
|
February 11, 2025
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers
Yile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Research Square
|
July 16, 2024
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers
Yile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Human Mutation
|
July 2, 2019
Performance of computational methods for the evaluation of pericentriolar material 1 missense variants in CAGI-5
Alexander Miguel Monzon, Marco Carraro, Luigi Chiricosta, et al.
Page
of 17
Search research articles
Search
Showing results (121-130 of 166) with videos related to
Sort By:
Page
of 17
RNA (New York, N.Y.)
|
February 18, 2006
The RNA Ontology Consortium: an open invitation to the RNA community
Neocles B Leontis, Russ B Altman, Helen M Berman, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 15, 2022
Newborn screening for neurodevelopmental diseases: Are we there yet?
Wendy K Chung, Jonathan S Berg, Jeffrey R Botkin, et al.
Journal of Proteome Research
|
October 27, 2012
High-throughput isolation and characterization of untagged membrane protein complexes: outer membrane complexes of Desulfovibrio vulgaris
Peter J Walian, Simon Allen, Maxim Shatsky, et al.
Human Mutation
|
May 30, 2019
Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges
Gregory McInnes, Roxana Daneshjou, Panagiostis Katsonis, et al.
NPJ Genomic Medicine
|
October 13, 2021
Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders
Joseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.
NPJ Genomic Medicine
|
September 24, 2021
Application of full-genome analysis to diagnose rare monogenic disorders
Joseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.
Genome Research
|
October 9, 2002
The Bioperl toolkit: Perl modules for the life sciences
Jason E Stajich, David Block, Kris Boulez, et al.
Human Genetics
|
February 11, 2025
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers
Yile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Research Square
|
July 16, 2024
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers
Yile Chen, Kyoungyeul Lee, Junwoo Woo, et al.
Human Mutation
|
July 2, 2019
Performance of computational methods for the evaluation of pericentriolar material 1 missense variants in CAGI-5
Alexander Miguel Monzon, Marco Carraro, Luigi Chiricosta, et al.
Page
of 17