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Gastroenterology
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November 20, 2019
Drug Screen Identifies Leflunomide for Treatment of Inflammatory Bowel Disease Caused by TTC7A Deficiency
Sasha Jardine, Sierra Anderson, Stephen Babcock, et al.
ACS Chemical Biology
|
August 26, 2022
Shaping Neonatal Immunization by Tuning the Delivery of Synergistic Adjuvants via Nanocarriers
Soumik Barman, Francesco Borriello, Byron Brook, et al.
Vaccine
|
November 28, 2018
Increasing FIM2/3 antigen-content improves efficacy of Bordetella pertussis vaccines in mice in vivo without altering vaccine-induced human reactogenicity biomarkers in vitro
Anne Marie Queenan, David J Dowling, Wing Ki Cheng, et al.
Developmental Cognitive Neuroscience
|
February 13, 2022
Measuring retention within the adolescent brain cognitive development (ABCD)<sup>SM</sup> study
Sarah W Feldstein Ewing, Genevieve F Dash, Wesley K Thompson, et al.
Nature Medicine
|
June 28, 2024
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient
James J Dowling, Terry Pirovolakis, Keshini Devakandan, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
May 16, 2023
Pandemic-Related Changes in the Prevalence of Early Adolescent Alcohol and Drug Use, 2020-2021: Data From a Multisite Cohort Study
William E Pelham, Susan F Tapert, María Luisa Zúñiga, et al.
Neuromuscular Disorders : NMD
|
December 7, 2023
The myotubular and centronuclear myopathy patient registry: a multifunctional tool for translational research
Joanne Bullivant, Anando Sen, Jess Page, et al.
Neurobiology of Disease
|
January 26, 2016
Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder
Julie M Jones, Louise Dionne, James Dell'Orco, et al.
HGG Advances
|
April 25, 2024
A systematic assessment of the impact of rare canonical splice site variants on splicing using functional and in silico methods
Rachel Y Oh, Ali AlMail, David Cheerie, et al.
Human Molecular Genetics
|
November 10, 2011
Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype
Christopher R Pierson, Ashley N Dulin-Smith, Ashley N Durban, et al.
Page
of 50
Search research articles
Search
Showing results (391-400 of 493) with videos related to
Sort By:
Page
of 50
Gastroenterology
|
November 20, 2019
Drug Screen Identifies Leflunomide for Treatment of Inflammatory Bowel Disease Caused by TTC7A Deficiency
Sasha Jardine, Sierra Anderson, Stephen Babcock, et al.
ACS Chemical Biology
|
August 26, 2022
Shaping Neonatal Immunization by Tuning the Delivery of Synergistic Adjuvants via Nanocarriers
Soumik Barman, Francesco Borriello, Byron Brook, et al.
Vaccine
|
November 28, 2018
Increasing FIM2/3 antigen-content improves efficacy of Bordetella pertussis vaccines in mice in vivo without altering vaccine-induced human reactogenicity biomarkers in vitro
Anne Marie Queenan, David J Dowling, Wing Ki Cheng, et al.
Developmental Cognitive Neuroscience
|
February 13, 2022
Measuring retention within the adolescent brain cognitive development (ABCD)<sup>SM</sup> study
Sarah W Feldstein Ewing, Genevieve F Dash, Wesley K Thompson, et al.
Nature Medicine
|
June 28, 2024
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient
James J Dowling, Terry Pirovolakis, Keshini Devakandan, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
May 16, 2023
Pandemic-Related Changes in the Prevalence of Early Adolescent Alcohol and Drug Use, 2020-2021: Data From a Multisite Cohort Study
William E Pelham, Susan F Tapert, María Luisa Zúñiga, et al.
Neuromuscular Disorders : NMD
|
December 7, 2023
The myotubular and centronuclear myopathy patient registry: a multifunctional tool for translational research
Joanne Bullivant, Anando Sen, Jess Page, et al.
Neurobiology of Disease
|
January 26, 2016
Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder
Julie M Jones, Louise Dionne, James Dell'Orco, et al.
HGG Advances
|
April 25, 2024
A systematic assessment of the impact of rare canonical splice site variants on splicing using functional and in silico methods
Rachel Y Oh, Ali AlMail, David Cheerie, et al.
Human Molecular Genetics
|
November 10, 2011
Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype
Christopher R Pierson, Ashley N Dulin-Smith, Ashley N Durban, et al.
Page
of 50