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Plos Genetics
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February 24, 2012
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations
Ayşe Demirkan, Cornelia M van Duijn, Peter Ugocsai, et al.
American Journal of Human Genetics
|
November 19, 2019
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities
Laura V Vandervore, Rachel Schot, Chiara Milanese, et al.
American Journal of Human Genetics
|
September 10, 2019
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
Pamela Magini, Daphne J Smits, Laura Vandervore, et al.
Nature Genetics
|
September 10, 2013
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra, Marjolein J Peters, Tõnu Esko, et al.
Nucleic Acids Research
|
November 27, 2018
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, et al.
Science (New York, N.Y.)
|
October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC
Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.
Brain : a Journal of Neurology
|
September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia
Darius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
Nature Reviews. Genetics
|
November 25, 2003
The nature and identification of quantitative trait loci: a community's view
Oduola Abiola, Joe M Angel, Philip Avner, et al.
Nature Genetics
|
October 30, 2004
The Collaborative Cross, a community resource for the genetic analysis of complex traits
Gary A Churchill, David C Airey, Hooman Allayee, et al.
Plos One
|
February 8, 2011
Expanding the diversity of mycobacteriophages: insights into genome architecture and evolution
Welkin H Pope, Deborah Jacobs-Sera, Daniel A Russell, et al.
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Search research articles
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Showing results (1221-1230 of 1,230) with videos related to
Sort By:
Page
of 123
You have reached the last page of results.
This site can display upto 1,230 results.
Plos Genetics
|
February 24, 2012
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations
Ayşe Demirkan, Cornelia M van Duijn, Peter Ugocsai, et al.
American Journal of Human Genetics
|
November 19, 2019
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities
Laura V Vandervore, Rachel Schot, Chiara Milanese, et al.
American Journal of Human Genetics
|
September 10, 2019
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
Pamela Magini, Daphne J Smits, Laura Vandervore, et al.
Nature Genetics
|
September 10, 2013
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra, Marjolein J Peters, Tõnu Esko, et al.
Nucleic Acids Research
|
November 27, 2018
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, et al.
Science (New York, N.Y.)
|
October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC
Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.
Brain : a Journal of Neurology
|
September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia
Darius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
Nature Reviews. Genetics
|
November 25, 2003
The nature and identification of quantitative trait loci: a community's view
Oduola Abiola, Joe M Angel, Philip Avner, et al.
Nature Genetics
|
October 30, 2004
The Collaborative Cross, a community resource for the genetic analysis of complex traits
Gary A Churchill, David C Airey, Hooman Allayee, et al.
Plos One
|
February 8, 2011
Expanding the diversity of mycobacteriophages: insights into genome architecture and evolution
Welkin H Pope, Deborah Jacobs-Sera, Daniel A Russell, et al.
Page
of 123