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Susan Walker

Showing results (151-160 of 260) with videos related to

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JAMA|June 9, 2025
Intrapartum Sildenafil to Improve Perinatal Outcomes: A Randomized Clinical TrialSailesh Kumar, William Tarnow-Mordi, Ben W Mol, et al.
Clinical Drug Investigation|June 28, 2018
Effect of Renal Impairment on the Pharmacokinetics and Pharmacodynamics of Verinurad, a Selective Uric Acid Reabsorption InhibitorWilliam B Smith, Jesse Hall, Jolene K Berg, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 22, 2019
Relative contributions of diabetes and chronic kidney disease to neuropathy development in diabetic nephropathy patientsTushar Issar, Ria Arnold, Natalie C G Kwai, et al.
Cancer Drug Resistance (Alhambra, Calif.)|September 30, 2022
A nano-enhanced vaccine for metastatic melanoma immunotherapyKatelyn E Salotto, Walter C Olson, Karlyn E Pollack, et al.
NPJ Genomic Medicine|December 22, 2017
Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosageBreanne Dale, Bonnie MacKinnon Modi, Sanne Jilderda, et al.
NPJ Genomic Medicine|June 27, 2017
Variable phenotype expression in a family segregating microdeletions of the <i>NRXN1</i> and <i>MBD5</i> autism spectrum disorder susceptibility genesMarc Woodbury-Smith, Rob Nicolson, Mehdi Zarrei, et al.
European Journal of Immunology|March 16, 2007
The impact of HLA-B micropolymorphism outside primary peptide anchor pockets on the CTL response to CMVJacqueline M Burrows, Katherine K Wynn, Fleur E Tynan, et al.
NPJ Genomic Medicine|May 3, 2019
Expanding the neurodevelopmental phenotypes of individuals with de novo <i>KMT2A</i> variantsAda J S Chan, Cheryl Cytrynbaum, Ny Hoang, et al.
Nature Communications|November 3, 2025
Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
American Journal of Medical Genetics. Part A|August 18, 2016
Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencingMuhammad Imran Naseer, Sameera Sogaty, Mahmood Rasool, et al.
Pageof 26

Showing results (151-160 of 260) with videos related to

Sort By:
Pageof 26
JAMA|June 9, 2025
Intrapartum Sildenafil to Improve Perinatal Outcomes: A Randomized Clinical TrialSailesh Kumar, William Tarnow-Mordi, Ben W Mol, et al.
Clinical Drug Investigation|June 28, 2018
Effect of Renal Impairment on the Pharmacokinetics and Pharmacodynamics of Verinurad, a Selective Uric Acid Reabsorption InhibitorWilliam B Smith, Jesse Hall, Jolene K Berg, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 22, 2019
Relative contributions of diabetes and chronic kidney disease to neuropathy development in diabetic nephropathy patientsTushar Issar, Ria Arnold, Natalie C G Kwai, et al.
Cancer Drug Resistance (Alhambra, Calif.)|September 30, 2022
A nano-enhanced vaccine for metastatic melanoma immunotherapyKatelyn E Salotto, Walter C Olson, Karlyn E Pollack, et al.
NPJ Genomic Medicine|December 22, 2017
Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosageBreanne Dale, Bonnie MacKinnon Modi, Sanne Jilderda, et al.
NPJ Genomic Medicine|June 27, 2017
Variable phenotype expression in a family segregating microdeletions of the <i>NRXN1</i> and <i>MBD5</i> autism spectrum disorder susceptibility genesMarc Woodbury-Smith, Rob Nicolson, Mehdi Zarrei, et al.
European Journal of Immunology|March 16, 2007
The impact of HLA-B micropolymorphism outside primary peptide anchor pockets on the CTL response to CMVJacqueline M Burrows, Katherine K Wynn, Fleur E Tynan, et al.
NPJ Genomic Medicine|May 3, 2019
Expanding the neurodevelopmental phenotypes of individuals with de novo <i>KMT2A</i> variantsAda J S Chan, Cheryl Cytrynbaum, Ny Hoang, et al.
Nature Communications|November 3, 2025
Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
American Journal of Medical Genetics. Part A|August 18, 2016
Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencingMuhammad Imran Naseer, Sameera Sogaty, Mahmood Rasool, et al.
Pageof 26