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F Robinson

Showing results (741-750 of 896) with videos related to

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Birth Defects Research|March 1, 2023
Society for Birth Defects Research and Prevention 2022-2027 strategic planSusan L Makris, Bruce K Beyer, Anthony DeLise, et al.
Injury Epidemiology|May 22, 2024
An updated analysis of safety climate and downstream outcomes in two convenience samples of U.S. fire departments (FOCUS 1.0 and 2.0 survey waves)Ashley M Geczik, Jin Lee, Joseph A Allen, et al.
Journal of Radiological Protection : Official Journal of the Society for Radiological Protection|March 1, 2008
HSE's Safety Assessment Principles for radiation protectionD N Simister, A Bunker, M D Finnerty, et al.
Journal of Human Genetics|October 13, 2006
Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profilesJian Wang, John F Robinson, Caroline H O'Neil, et al.
BMC Medical Imaging|March 14, 2007
Quantitative and qualitative differences in subcutaneous adipose tissue stores across lipodystrophy types shown by magnetic resonance imagingSalam A Al-Attar, Rebecca L Pollex, John F Robinson, et al.
American Indian and Alaska Native Mental Health Research (Online)|September 30, 2022
Retention in a 6-Month Smoking Cessation Study Among Alaska Native and American Indian PeopleDawson E Mills, Krista R Schaefer, Julie A Beans, et al.
Journal of Nematology|March 5, 2009
Suppression of Rotylenchulus reniformis 122-cm Deep Endorses Resistance Introgression in GossypiumA F Robinson, J R Akridge, J M Bradford, et al.
Epilepsia|July 26, 2014
Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxiaSali M K Farhan, Lisa M Murphy, John F Robinson, et al.
Orphanet Journal of Rare Diseases|August 21, 2013
A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorderPiya Lahiry, Lemuel Racacho, Jian Wang, et al.
European Journal of Endocrinology|December 3, 2005
Variability of isolated autosomal dominant GH deficiency (IGHD II): impact of the P89L GH mutation on clinical follow-up and GH secretionSouzan Salemi, Shida Yousefi, Kurt Baltensperger, et al.
Pageof 90

Showing results (741-750 of 896) with videos related to

Sort By:
Pageof 90
Birth Defects Research|March 1, 2023
Society for Birth Defects Research and Prevention 2022-2027 strategic planSusan L Makris, Bruce K Beyer, Anthony DeLise, et al.
Injury Epidemiology|May 22, 2024
An updated analysis of safety climate and downstream outcomes in two convenience samples of U.S. fire departments (FOCUS 1.0 and 2.0 survey waves)Ashley M Geczik, Jin Lee, Joseph A Allen, et al.
Journal of Radiological Protection : Official Journal of the Society for Radiological Protection|March 1, 2008
HSE's Safety Assessment Principles for radiation protectionD N Simister, A Bunker, M D Finnerty, et al.
Journal of Human Genetics|October 13, 2006
Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profilesJian Wang, John F Robinson, Caroline H O'Neil, et al.
BMC Medical Imaging|March 14, 2007
Quantitative and qualitative differences in subcutaneous adipose tissue stores across lipodystrophy types shown by magnetic resonance imagingSalam A Al-Attar, Rebecca L Pollex, John F Robinson, et al.
American Indian and Alaska Native Mental Health Research (Online)|September 30, 2022
Retention in a 6-Month Smoking Cessation Study Among Alaska Native and American Indian PeopleDawson E Mills, Krista R Schaefer, Julie A Beans, et al.
Journal of Nematology|March 5, 2009
Suppression of Rotylenchulus reniformis 122-cm Deep Endorses Resistance Introgression in GossypiumA F Robinson, J R Akridge, J M Bradford, et al.
Epilepsia|July 26, 2014
Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxiaSali M K Farhan, Lisa M Murphy, John F Robinson, et al.
Orphanet Journal of Rare Diseases|August 21, 2013
A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorderPiya Lahiry, Lemuel Racacho, Jian Wang, et al.
European Journal of Endocrinology|December 3, 2005
Variability of isolated autosomal dominant GH deficiency (IGHD II): impact of the P89L GH mutation on clinical follow-up and GH secretionSouzan Salemi, Shida Yousefi, Kurt Baltensperger, et al.
Pageof 90