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N Cooper

Showing results (861-870 of 1,220) with videos related to

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Journal of Surgical Oncology|June 27, 2019
Prevention of postsurgical lymphedema via immediate delivery of sustained-release 9-cis retinoic acid to the lymphedenectomy siteGiulia Daneshgaran, Connie B Paik, Michael N Cooper, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|January 13, 2015
A Comprehensive Evaluation of a Two-Channel Portable Monitor to "Rule in" Obstructive Sleep ApneaKim L Ward, Nigel McArdle, Alan James, et al.
Bioinformatics (Oxford, England)|September 9, 2017
When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variantsKymberleigh A Pagel, Vikas Pejaver, Guan Ning Lin, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|June 3, 2023
Identification of protease-sensitive but not misfolding PNLIP variants in familial and hereditary pancreatitisEmmanuelle Masson, Stéphanie Berthet, Gerald Le Gac, et al.
Health Technology Assessment (Winchester, England)|June 27, 2006
The clinical effectiveness and cost-effectiveness of enzyme replacement therapy for Gaucher's disease: a systematic reviewM Connock, A Burls, E Frew, et al.
Journal of Pediatric Surgery|March 20, 2019
Ultrasound Elastography as a Non-Invasive Method to Monitor Liver Disease in Children with Short Bowel Syndrome: Updated ResultsAmy E Lawrence, Molly Dienhart, Jennifer N Cooper, et al.
Molecular Cancer|July 3, 2009
The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemiasLuke B Hesson, Thomas L Dunwell, Wendy N Cooper, et al.
American Journal of Human Genetics|November 14, 2007
Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombinationKatharina Steinmann, David N Cooper, Lan Kluwe, et al.
Human Genomics|August 16, 2022
Expanding ACMG variant classification guidelines into a general frameworkEmmanuelle Masson, Wen-Bin Zou, Emmanuelle Génin, et al.
Stroke|January 4, 2011
Soluble glycoprotein VI is raised in the plasma of patients with acute ischemic strokeMohammad Al-Tamimi, Elizabeth E Gardiner, Jim Y Thom, et al.
Pageof 122

Showing results (861-870 of 1,220) with videos related to

Sort By:
Pageof 122
Journal of Surgical Oncology|June 27, 2019
Prevention of postsurgical lymphedema via immediate delivery of sustained-release 9-cis retinoic acid to the lymphedenectomy siteGiulia Daneshgaran, Connie B Paik, Michael N Cooper, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|January 13, 2015
A Comprehensive Evaluation of a Two-Channel Portable Monitor to "Rule in" Obstructive Sleep ApneaKim L Ward, Nigel McArdle, Alan James, et al.
Bioinformatics (Oxford, England)|September 9, 2017
When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variantsKymberleigh A Pagel, Vikas Pejaver, Guan Ning Lin, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|June 3, 2023
Identification of protease-sensitive but not misfolding PNLIP variants in familial and hereditary pancreatitisEmmanuelle Masson, Stéphanie Berthet, Gerald Le Gac, et al.
Health Technology Assessment (Winchester, England)|June 27, 2006
The clinical effectiveness and cost-effectiveness of enzyme replacement therapy for Gaucher's disease: a systematic reviewM Connock, A Burls, E Frew, et al.
Journal of Pediatric Surgery|March 20, 2019
Ultrasound Elastography as a Non-Invasive Method to Monitor Liver Disease in Children with Short Bowel Syndrome: Updated ResultsAmy E Lawrence, Molly Dienhart, Jennifer N Cooper, et al.
Molecular Cancer|July 3, 2009
The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemiasLuke B Hesson, Thomas L Dunwell, Wendy N Cooper, et al.
American Journal of Human Genetics|November 14, 2007
Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombinationKatharina Steinmann, David N Cooper, Lan Kluwe, et al.
Human Genomics|August 16, 2022
Expanding ACMG variant classification guidelines into a general frameworkEmmanuelle Masson, Wen-Bin Zou, Emmanuelle Génin, et al.
Stroke|January 4, 2011
Soluble glycoprotein VI is raised in the plasma of patients with acute ischemic strokeMohammad Al-Tamimi, Elizabeth E Gardiner, Jim Y Thom, et al.
Pageof 122