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Journal of Clinical Laboratory Analysis
|
May 3, 2016
Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients
Eun-Hyung Yoo, Kyung-Jin Park, Hong-Hee Won, et al.
Nature Genetics
|
January 17, 2012
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium
Ji Eun Lee, Jennifer L Silhavy, Maha S Zaki, et al.
Science (New York, N.Y.)
|
March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
Tom Walsh, Jon M McClellan, Shane E McCarthy, et al.
The New England Journal of Medicine
|
April 3, 2009
Effect of early versus deferred antiretroviral therapy for HIV on survival
Mari M Kitahata, Stephen J Gange, Alison G Abraham, et al.
Nature Genetics
|
January 22, 2022
Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features
Bruno Reversade, Nathalie Escande-Beillard, Aikaterini Dimopoulou, et al.
Nature Genetics
|
August 4, 2009
Mutations in PYCR1 cause cutis laxa with progeroid features
Bruno Reversade, Nathalie Escande-Beillard, Aikaterini Dimopoulou, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2022
Molecular electronics sensors on a scalable semiconductor chip: A platform for single-molecule measurement of binding kinetics and enzyme activity
Carl W Fuller, Pius S Padayatti, Hadi Abderrahim, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
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of 6
Search research articles
Search
Showing results (51-60 of 58) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 58 results.
Journal of Clinical Laboratory Analysis
|
May 3, 2016
Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients
Eun-Hyung Yoo, Kyung-Jin Park, Hong-Hee Won, et al.
Nature Genetics
|
January 17, 2012
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium
Ji Eun Lee, Jennifer L Silhavy, Maha S Zaki, et al.
Science (New York, N.Y.)
|
March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
Tom Walsh, Jon M McClellan, Shane E McCarthy, et al.
The New England Journal of Medicine
|
April 3, 2009
Effect of early versus deferred antiretroviral therapy for HIV on survival
Mari M Kitahata, Stephen J Gange, Alison G Abraham, et al.
Nature Genetics
|
January 22, 2022
Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features
Bruno Reversade, Nathalie Escande-Beillard, Aikaterini Dimopoulou, et al.
Nature Genetics
|
August 4, 2009
Mutations in PYCR1 cause cutis laxa with progeroid features
Bruno Reversade, Nathalie Escande-Beillard, Aikaterini Dimopoulou, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2022
Molecular electronics sensors on a scalable semiconductor chip: A platform for single-molecule measurement of binding kinetics and enzyme activity
Carl W Fuller, Pius S Padayatti, Hadi Abderrahim, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Page
of 6