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Genome Medicine
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October 27, 2017
Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosis
Hayk Barseghyan, Wilson Tang, Richard T Wang, et al.
The New England Journal of Medicine
|
June 11, 2020
Disseminated Coccidioidomycosis Treated with Interferon-γ and Dupilumab
Monica Tsai, Timothy J Thauland, Alden Y Huang, et al.
Psychiatric Genetics
|
April 26, 2012
Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort
Emma S Nyman, Anu Loukola, Teppo Varilo, et al.
Plos One
|
February 1, 2013
Corneal wound healing is compromised by immunoproteasome deficiency
Deborah A Ferrington, Heidi Roehrich, Angela A Chang, et al.
Frontiers in Genetics
|
August 14, 2023
Transcriptomic analysis of paired healthy human skeletal muscles to identify modulators of disease severity in DMD
Shirley Nieves-Rodriguez, Florian Barthélémy, Jeremy D Woods, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 15, 2007
Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit
Rick F Nelson, Kevin A Glenn, Yuzhou Zhang, et al.
Scientific Reports
|
January 14, 2021
Quantitative immuno-mass spectrometry imaging of skeletal muscle dystrophin
David P Bishop, Mika T Westerhausen, Florian Barthelemy, et al.
American Journal of Human Genetics
|
December 7, 2010
Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signaling
Jing Tian, Ling Ling, Mohammad Shboul, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
November 28, 2013
Exome sequencing finds a novel PCSK1 mutation in a child with generalized malabsorptive diarrhea and diabetes insipidus
Michael Yourshaw, R Sergio Solorzano-Vargas, Lindsay A Pickett, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
March 28, 2012
Genome-wide association study of intelligence: additive effects of novel brain expressed genes
Sandra K Loo, Corina Shtir, Alysa E Doyle, et al.
Page
of 84
Search research articles
Search
Showing results (641-650 of 835) with videos related to
Sort By:
Page
of 84
Genome Medicine
|
October 27, 2017
Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosis
Hayk Barseghyan, Wilson Tang, Richard T Wang, et al.
The New England Journal of Medicine
|
June 11, 2020
Disseminated Coccidioidomycosis Treated with Interferon-γ and Dupilumab
Monica Tsai, Timothy J Thauland, Alden Y Huang, et al.
Psychiatric Genetics
|
April 26, 2012
Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort
Emma S Nyman, Anu Loukola, Teppo Varilo, et al.
Plos One
|
February 1, 2013
Corneal wound healing is compromised by immunoproteasome deficiency
Deborah A Ferrington, Heidi Roehrich, Angela A Chang, et al.
Frontiers in Genetics
|
August 14, 2023
Transcriptomic analysis of paired healthy human skeletal muscles to identify modulators of disease severity in DMD
Shirley Nieves-Rodriguez, Florian Barthélémy, Jeremy D Woods, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 15, 2007
Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit
Rick F Nelson, Kevin A Glenn, Yuzhou Zhang, et al.
Scientific Reports
|
January 14, 2021
Quantitative immuno-mass spectrometry imaging of skeletal muscle dystrophin
David P Bishop, Mika T Westerhausen, Florian Barthelemy, et al.
American Journal of Human Genetics
|
December 7, 2010
Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signaling
Jing Tian, Ling Ling, Mohammad Shboul, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
November 28, 2013
Exome sequencing finds a novel PCSK1 mutation in a child with generalized malabsorptive diarrhea and diabetes insipidus
Michael Yourshaw, R Sergio Solorzano-Vargas, Lindsay A Pickett, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
March 28, 2012
Genome-wide association study of intelligence: additive effects of novel brain expressed genes
Sandra K Loo, Corina Shtir, Alysa E Doyle, et al.
Page
of 84