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B Agrawal

Showing results (301-310 of 360) with videos related to

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Cellular and Molecular Gastroenterology and Hepatology|May 2, 2024
WNT2B Deficiency Causes Enhanced Susceptibility to Colitis Due to Increased Inflammatory Cytokine ProductionAmy E O'Connell, Sathuwarman Raveenthiraraj, Luiz Fernando Silva Oliveira, et al.
Genes|June 26, 2026
Multimodal Sequencing and Reanalysis Approaches to End the Diagnostic Odyssey of Individuals with Suspected Rare Monogenic DiseasesCatherine A Brownstein, Jill A Madden, Wanqing Shao, et al.
HGG Advances|September 13, 2021
A data-driven architecture using natural language processing to improve phenotyping efficiency and accelerate genetic diagnoses of rare disordersJignesh R Parikh, Casie A Genetti, Asli Aykanat, et al.
The European Respiratory Journal|June 2, 2019
Phenotype characterisation of <i>TBX4</i> mutation and deletion carriers with neonatal and paediatric pulmonary hypertensionCsaba Galambos, Mary P Mullen, Joseph T Shieh, et al.
Journal of Psychopharmacology (Oxford, England)|November 10, 2006
Pharmacodynamic and pharmacokinetic effects of TPA023, a GABA(A) alpha(2,3) subtype-selective agonist, compared to lorazepam and placebo in healthy volunteersS L de Haas, S J de Visser, J P van der Post, et al.
European Journal of Human Genetics : EJHG|May 15, 2025
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndromeShiyu Luo, Valérie Gailus-Durner, Bobbi McGivern, et al.
Immunity|October 3, 2025
Notch3 destabilizes regulatory T cells to drive autoimmune neuroinflammation in multiple sclerosisMehdi Benamar, Paola Contini, Klaus Schmitz-Abe, et al.
Plos Genetics|July 7, 2021
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findingsQifei Li, Michal Dibus, Alicia Casey, et al.
Journal of Clinical Pharmacology|December 19, 2003
Pharmacokinetics of etoricoxib in patients with renal impairmentNancy G B Agrawal, Catherine Z Matthews, Ralph S Mazenko, et al.
Journal of Medical Internet Research|March 16, 2021
Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort StudyJianqiao Li, Margaret A Hojlo, Sampath Chennuri, et al.
Pageof 36

Showing results (301-310 of 360) with videos related to

Sort By:
Pageof 36
Cellular and Molecular Gastroenterology and Hepatology|May 2, 2024
WNT2B Deficiency Causes Enhanced Susceptibility to Colitis Due to Increased Inflammatory Cytokine ProductionAmy E O'Connell, Sathuwarman Raveenthiraraj, Luiz Fernando Silva Oliveira, et al.
Genes|June 26, 2026
Multimodal Sequencing and Reanalysis Approaches to End the Diagnostic Odyssey of Individuals with Suspected Rare Monogenic DiseasesCatherine A Brownstein, Jill A Madden, Wanqing Shao, et al.
HGG Advances|September 13, 2021
A data-driven architecture using natural language processing to improve phenotyping efficiency and accelerate genetic diagnoses of rare disordersJignesh R Parikh, Casie A Genetti, Asli Aykanat, et al.
The European Respiratory Journal|June 2, 2019
Phenotype characterisation of <i>TBX4</i> mutation and deletion carriers with neonatal and paediatric pulmonary hypertensionCsaba Galambos, Mary P Mullen, Joseph T Shieh, et al.
Journal of Psychopharmacology (Oxford, England)|November 10, 2006
Pharmacodynamic and pharmacokinetic effects of TPA023, a GABA(A) alpha(2,3) subtype-selective agonist, compared to lorazepam and placebo in healthy volunteersS L de Haas, S J de Visser, J P van der Post, et al.
European Journal of Human Genetics : EJHG|May 15, 2025
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndromeShiyu Luo, Valérie Gailus-Durner, Bobbi McGivern, et al.
Immunity|October 3, 2025
Notch3 destabilizes regulatory T cells to drive autoimmune neuroinflammation in multiple sclerosisMehdi Benamar, Paola Contini, Klaus Schmitz-Abe, et al.
Plos Genetics|July 7, 2021
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findingsQifei Li, Michal Dibus, Alicia Casey, et al.
Journal of Clinical Pharmacology|December 19, 2003
Pharmacokinetics of etoricoxib in patients with renal impairmentNancy G B Agrawal, Catherine Z Matthews, Ralph S Mazenko, et al.
Journal of Medical Internet Research|March 16, 2021
Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort StudyJianqiao Li, Margaret A Hojlo, Sampath Chennuri, et al.
Pageof 36