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Journal of Medical Genetics
|
August 22, 2020
De novo missense variants in <i>LMBRD2</i> are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features
Alka Malhotra, Alban Ziegler, Li Shu, et al.
Cell Reports
|
November 3, 2021
Structural basis of glycan276-dependent recognition by HIV-1 broadly neutralizing antibodies
Christopher A Cottrell, Kartik Manne, Rui Kong, et al.
Neurogenetics
|
August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1
Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Nature Communications
|
November 16, 2024
An allosteric inhibitor of RhoGAP class-IX myosins suppresses the metastatic features of cancer cells
Despoina Kyriazi, Lea Voth, Almke Bader, et al.
Cell
|
August 7, 2021
Human TBK1 deficiency leads to autoinflammation driven by TNF-induced cell death
Justin Taft, Michael Markson, Diana Legarda, et al.
Annals of Neurology
|
May 10, 2016
Whole exome sequencing in patients with white matter abnormalities
Adeline Vanderver, Cas Simons, Guy Helman, et al.
Annals of Neurology
|
April 29, 2020
Randomized Clinical Trial of First-Line Genome Sequencing in Pediatric White Matter Disorders
Adeline Vanderver, Geneviève Bernard, Guy Helman, et al.
European Journal of Medical Genetics
|
July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services
C A Stutterd, A Vanderver, P J Lockhart, et al.
Antimicrobial Agents and Chemotherapy
|
June 21, 2021
Identification of Quinolinones as Antivirals against Venezuelan Equine Encephalitis Virus
Nicole N Haese, Nicholas A May, Sharon Taft-Benz, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 4, 2007
Identification of the IL-17 receptor related molecule IL-17RC as the receptor for IL-17F
Rolf E Kuestner, David W Taft, Aaron Haran, et al.
Page
of 136
Search research articles
Search
Showing results (1291-1300 of 1,360) with videos related to
Sort By:
Page
of 136
Journal of Medical Genetics
|
August 22, 2020
De novo missense variants in <i>LMBRD2</i> are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features
Alka Malhotra, Alban Ziegler, Li Shu, et al.
Cell Reports
|
November 3, 2021
Structural basis of glycan276-dependent recognition by HIV-1 broadly neutralizing antibodies
Christopher A Cottrell, Kartik Manne, Rui Kong, et al.
Neurogenetics
|
August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1
Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Nature Communications
|
November 16, 2024
An allosteric inhibitor of RhoGAP class-IX myosins suppresses the metastatic features of cancer cells
Despoina Kyriazi, Lea Voth, Almke Bader, et al.
Cell
|
August 7, 2021
Human TBK1 deficiency leads to autoinflammation driven by TNF-induced cell death
Justin Taft, Michael Markson, Diana Legarda, et al.
Annals of Neurology
|
May 10, 2016
Whole exome sequencing in patients with white matter abnormalities
Adeline Vanderver, Cas Simons, Guy Helman, et al.
Annals of Neurology
|
April 29, 2020
Randomized Clinical Trial of First-Line Genome Sequencing in Pediatric White Matter Disorders
Adeline Vanderver, Geneviève Bernard, Guy Helman, et al.
European Journal of Medical Genetics
|
July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services
C A Stutterd, A Vanderver, P J Lockhart, et al.
Antimicrobial Agents and Chemotherapy
|
June 21, 2021
Identification of Quinolinones as Antivirals against Venezuelan Equine Encephalitis Virus
Nicole N Haese, Nicholas A May, Sharon Taft-Benz, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 4, 2007
Identification of the IL-17 receptor related molecule IL-17RC as the receptor for IL-17F
Rolf E Kuestner, David W Taft, Aaron Haran, et al.
Page
of 136