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J C Smith

Showing results (681-690 of 687) with videos related to

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Clinical Nutrition (Edinburgh, Scotland)|July 15, 2000
Prevalence of malnutrition on admission to four hospitals in England. The Malnutrition Prevalence GroupJ Edington, J Boorman, E R Durrant, et al.
Internal Medicine Journal|September 10, 2021
Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendationsCarolyn M Sue, Shanti Balasubramaniam, Drago Bratkovic, et al.
Human Molecular Genetics|December 16, 2014
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
The New England Journal of Medicine|October 5, 2017
Hematopoietic Stem-Cell Gene Therapy for Cerebral AdrenoleukodystrophyFlorian Eichler, Christine Duncan, Patricia L Musolino, et al.
The Journal of Physical Chemistry. B|June 4, 2014
All-atom empirical potential for molecular modeling and dynamics studies of proteinsA D MacKerell, D Bashford, M Bellott, et al.
Chemrxiv : the Preprint Server for Chemistry|November 17, 2020
Supercomputer-Based Ensemble Docking Drug Discovery Pipeline with Application to Covid-19A Acharya, R Agarwal, M Baker, et al.
Journal of Chemical Information and Modeling|December 16, 2020
Supercomputer-Based Ensemble Docking Drug Discovery Pipeline with Application to Covid-19A Acharya, R Agarwal, M B Baker, et al.
Pageof 69

Showing results (681-690 of 687) with videos related to

Sort By:
Pageof 69
You have reached the last page of results.This site can display upto 687 results.
Clinical Nutrition (Edinburgh, Scotland)|July 15, 2000
Prevalence of malnutrition on admission to four hospitals in England. The Malnutrition Prevalence GroupJ Edington, J Boorman, E R Durrant, et al.
Internal Medicine Journal|September 10, 2021
Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendationsCarolyn M Sue, Shanti Balasubramaniam, Drago Bratkovic, et al.
Human Molecular Genetics|December 16, 2014
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
The New England Journal of Medicine|October 5, 2017
Hematopoietic Stem-Cell Gene Therapy for Cerebral AdrenoleukodystrophyFlorian Eichler, Christine Duncan, Patricia L Musolino, et al.
The Journal of Physical Chemistry. B|June 4, 2014
All-atom empirical potential for molecular modeling and dynamics studies of proteinsA D MacKerell, D Bashford, M Bellott, et al.
Chemrxiv : the Preprint Server for Chemistry|November 17, 2020
Supercomputer-Based Ensemble Docking Drug Discovery Pipeline with Application to Covid-19A Acharya, R Agarwal, M Baker, et al.
Journal of Chemical Information and Modeling|December 16, 2020
Supercomputer-Based Ensemble Docking Drug Discovery Pipeline with Application to Covid-19A Acharya, R Agarwal, M B Baker, et al.
Pageof 69