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Journal of Inherited Metabolic Disease
|
March 29, 2026
Heritability of Long-Term Complications in Classic Galactosemia
Olivia S Garrett, Nicole H Smith, David J Cutler, et al.
The Journal of Clinical Psychiatry
|
June 25, 2024
Efficacy and Safety of Esmethadone (REL-1017) in Patients With Major Depressive Disorder and Inadequate Response to Standard Antidepressants: A Phase 3 Randomized Controlled Trial
Maurizio Fava, Stephen M Stahl, Luca Pani, et al.
Nature Genetics
|
September 6, 2005
Genomic alterations in cultured human embryonic stem cells
Anirban Maitra, Dan E Arking, Narayan Shivapurkar, et al.
Diabetes
|
February 25, 2014
A type I interferon transcriptional signature precedes autoimmunity in children genetically at risk for type 1 diabetes
Ricardo C Ferreira, Hui Guo, Richard M R Coulson, et al.
Nature Microbiology
|
June 1, 2022
Genome-wide protein-DNA interaction site mapping in bacteria using a double-stranded DNA-specific cytosine deaminase
Larry A Gallagher, Elena Velazquez, S Brook Peterson, et al.
American Journal of Human Genetics
|
October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios
Kelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome
Ha Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Arthritis and Rheumatism
|
March 2, 2013
Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci
Sampath Prahalad, Karen N Conneely, Yunxuan Jiang, et al.
HGG Advances
|
September 18, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate
Kelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Genome Research
|
October 19, 2004
Generation of the Brucella melitensis ORFeome version 1.1
Amélie Dricot, Jean-François Rual, Philippe Lamesch, et al.
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of 81
Search research articles
Search
Showing results (741-750 of 803) with videos related to
Sort By:
Page
of 81
Journal of Inherited Metabolic Disease
|
March 29, 2026
Heritability of Long-Term Complications in Classic Galactosemia
Olivia S Garrett, Nicole H Smith, David J Cutler, et al.
The Journal of Clinical Psychiatry
|
June 25, 2024
Efficacy and Safety of Esmethadone (REL-1017) in Patients With Major Depressive Disorder and Inadequate Response to Standard Antidepressants: A Phase 3 Randomized Controlled Trial
Maurizio Fava, Stephen M Stahl, Luca Pani, et al.
Nature Genetics
|
September 6, 2005
Genomic alterations in cultured human embryonic stem cells
Anirban Maitra, Dan E Arking, Narayan Shivapurkar, et al.
Diabetes
|
February 25, 2014
A type I interferon transcriptional signature precedes autoimmunity in children genetically at risk for type 1 diabetes
Ricardo C Ferreira, Hui Guo, Richard M R Coulson, et al.
Nature Microbiology
|
June 1, 2022
Genome-wide protein-DNA interaction site mapping in bacteria using a double-stranded DNA-specific cytosine deaminase
Larry A Gallagher, Elena Velazquez, S Brook Peterson, et al.
American Journal of Human Genetics
|
October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios
Kelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome
Ha Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Arthritis and Rheumatism
|
March 2, 2013
Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci
Sampath Prahalad, Karen N Conneely, Yunxuan Jiang, et al.
HGG Advances
|
September 18, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate
Kelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Genome Research
|
October 19, 2004
Generation of the Brucella melitensis ORFeome version 1.1
Amélie Dricot, Jean-François Rual, Philippe Lamesch, et al.
Page
of 81