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Journal of Psychiatric Research
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December 26, 2007
Sexually dimorphic changes in the amygdala in relation to delusional beliefs in first episode psychosis
Ayana A Gibbs, Paola Dazzan, Kevin D Morgan, et al.
Biotechniques
|
April 20, 2004
Large-scale RT-PCR recovery of full-length cDNA clones
Jia Qian Wu, Angela M Garcia, Steven Hulyk, et al.
Biorxiv : the Preprint Server for Biology
|
January 23, 2026
Expanding the Genome in a Bottle Truth Set: Detection and Validation of Novel Low-frequency Variants Using High-accuracy NanoSeq
Yang Zhang, Hsu Chao, Muchun Niu, et al.
Journal of Clinical Pharmacology
|
November 19, 2016
Impact of Target-Mediated Elimination on the Dose and Regimen of Evolocumab, a Human Monoclonal Antibody Against Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9)
John P Gibbs, Sameer Doshi, Mita Kuchimanchi, et al.
American Journal of Human Genetics
|
March 21, 2003
Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series
Eiji Hattori, Chunyu Liu, Judith A Badner, et al.
BMC Genomics
|
May 24, 2017
Extremely low-coverage whole genome sequencing in South Asians captures population genomics information
Navin Rustagi, Anbo Zhou, W Scott Watkins, et al.
Bioorganic & Medicinal Chemistry
|
December 7, 2011
Amide-modified prenylcysteine based Icmt inhibitors: Structure-activity relationships, kinetic analysis and cellular characterization
Jaimeen D Majmudar, Heather B Hodges-Loaiza, Kalub Hahne, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 7, 2011
Demographic history and rare allele sharing among human populations
Simon Gravel, Brenna M Henn, Ryan N Gutenkunst, et al.
The Journal of Trauma and Acute Care Surgery
|
October 27, 2015
Impact of common crystalloid solutions on resuscitation markers following Class I hemorrhage: A randomized control trial
Samuel W Ross, A Britton Christmas, Peter E Fischer, et al.
Human Molecular Genetics
|
January 17, 2020
Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder
Chun-An Chen, Rituraj Pal, Jiani Yin, et al.
Page
of 117
Search research articles
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Showing results (581-590 of 1,165) with videos related to
Sort By:
Page
of 117
Journal of Psychiatric Research
|
December 26, 2007
Sexually dimorphic changes in the amygdala in relation to delusional beliefs in first episode psychosis
Ayana A Gibbs, Paola Dazzan, Kevin D Morgan, et al.
Biotechniques
|
April 20, 2004
Large-scale RT-PCR recovery of full-length cDNA clones
Jia Qian Wu, Angela M Garcia, Steven Hulyk, et al.
Biorxiv : the Preprint Server for Biology
|
January 23, 2026
Expanding the Genome in a Bottle Truth Set: Detection and Validation of Novel Low-frequency Variants Using High-accuracy NanoSeq
Yang Zhang, Hsu Chao, Muchun Niu, et al.
Journal of Clinical Pharmacology
|
November 19, 2016
Impact of Target-Mediated Elimination on the Dose and Regimen of Evolocumab, a Human Monoclonal Antibody Against Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9)
John P Gibbs, Sameer Doshi, Mita Kuchimanchi, et al.
American Journal of Human Genetics
|
March 21, 2003
Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series
Eiji Hattori, Chunyu Liu, Judith A Badner, et al.
BMC Genomics
|
May 24, 2017
Extremely low-coverage whole genome sequencing in South Asians captures population genomics information
Navin Rustagi, Anbo Zhou, W Scott Watkins, et al.
Bioorganic & Medicinal Chemistry
|
December 7, 2011
Amide-modified prenylcysteine based Icmt inhibitors: Structure-activity relationships, kinetic analysis and cellular characterization
Jaimeen D Majmudar, Heather B Hodges-Loaiza, Kalub Hahne, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 7, 2011
Demographic history and rare allele sharing among human populations
Simon Gravel, Brenna M Henn, Ryan N Gutenkunst, et al.
The Journal of Trauma and Acute Care Surgery
|
October 27, 2015
Impact of common crystalloid solutions on resuscitation markers following Class I hemorrhage: A randomized control trial
Samuel W Ross, A Britton Christmas, Peter E Fischer, et al.
Human Molecular Genetics
|
January 17, 2020
Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder
Chun-An Chen, Rituraj Pal, Jiani Yin, et al.
Page
of 117