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Halley

Showing results (971-980 of 1,394) with videos related to

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European Journal of Human Genetics : EJHG|January 10, 2002
Analysis of TSC2 stop codon variants found in tuberous sclerosis patientsM A Goedbloed, M Nellist, B Verhaaf, et al.
Gut|July 16, 2008
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic settingD Ramsoekh, A Wagner, M E van Leerdam, et al.
Clinical Transplantation|May 21, 2009
Severe vitamin D deficiency among heart and liver transplant recipientsEmily M Stein, Adi Cohen, Matthew Freeby, et al.
Pharmaceutics|December 5, 2013
Encapsulation of hydrocortisone and mesalazine in zein microparticlesEsther T L Lau, Steven J Giddings, Salmaan G Mohammed, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|May 29, 2007
Body mass index and the prevalence of metabolic syndrome among children and adolescents in two Mexican populationsElizabeth Halley Castillo, Guilherme Borges, Juan O Talavera, et al.
Carbohydrate Polymers|March 31, 2015
Characteristics of starch-based films with different amylose contents plasticised by 1-ethyl-3-methylimidazolium acetateFengwei Xie, Bernadine M Flanagan, Ming Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 8, 2015
Fishing amplifies forage fish population collapsesTimothy E Essington, Pamela E Moriarty, Halley E Froehlich, et al.
The Journal of Clinical Endocrinology and Metabolism|April 14, 2015
Abnormal Skeletal Strength and Microarchitecture in Women With Celiac DiseaseEmily M Stein, Halley Rogers, Alexa Leib, et al.
Archives of Pathology & Laboratory Medicine|January 13, 2026
Phenotype-Driven In Silico Proficiency Testing Represents a Viable Approach for Undiagnosed Disorders by Exome SequencingRyan J Schmidt, Birgit Funke, Ann King, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2026
"It didn't feel like anything unusual because we had already been through so much": Disability-Related Research Experiences of Families with Children Enrolled in the Undiagnosed Diseases NetworkKevin T Mintz, Elisa N Altamirano, Meghan C Halley, et al.
Pageof 140

Showing results (971-980 of 1,394) with videos related to

Sort By:
Pageof 140
European Journal of Human Genetics : EJHG|January 10, 2002
Analysis of TSC2 stop codon variants found in tuberous sclerosis patientsM A Goedbloed, M Nellist, B Verhaaf, et al.
Gut|July 16, 2008
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic settingD Ramsoekh, A Wagner, M E van Leerdam, et al.
Clinical Transplantation|May 21, 2009
Severe vitamin D deficiency among heart and liver transplant recipientsEmily M Stein, Adi Cohen, Matthew Freeby, et al.
Pharmaceutics|December 5, 2013
Encapsulation of hydrocortisone and mesalazine in zein microparticlesEsther T L Lau, Steven J Giddings, Salmaan G Mohammed, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|May 29, 2007
Body mass index and the prevalence of metabolic syndrome among children and adolescents in two Mexican populationsElizabeth Halley Castillo, Guilherme Borges, Juan O Talavera, et al.
Carbohydrate Polymers|March 31, 2015
Characteristics of starch-based films with different amylose contents plasticised by 1-ethyl-3-methylimidazolium acetateFengwei Xie, Bernadine M Flanagan, Ming Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 8, 2015
Fishing amplifies forage fish population collapsesTimothy E Essington, Pamela E Moriarty, Halley E Froehlich, et al.
The Journal of Clinical Endocrinology and Metabolism|April 14, 2015
Abnormal Skeletal Strength and Microarchitecture in Women With Celiac DiseaseEmily M Stein, Halley Rogers, Alexa Leib, et al.
Archives of Pathology & Laboratory Medicine|January 13, 2026
Phenotype-Driven In Silico Proficiency Testing Represents a Viable Approach for Undiagnosed Disorders by Exome SequencingRyan J Schmidt, Birgit Funke, Ann King, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2026
"It didn't feel like anything unusual because we had already been through so much": Disability-Related Research Experiences of Families with Children Enrolled in the Undiagnosed Diseases NetworkKevin T Mintz, Elisa N Altamirano, Meghan C Halley, et al.
Pageof 140