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A Farrell

Showing results (661-670 of 714) with videos related to

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Annals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.
Nature Biotechnology|June 21, 2011
A pipeline that integrates the discovery and verification of plasma protein biomarkers reveals candidate markers for cardiovascular diseaseTerri A Addona, Xu Shi, Hasmik Keshishian, et al.
Canadian Family Physician Medecin De Famille Canadien|December 17, 2009
Genetic education for primary care providers: improving attitudes, knowledge, and confidenceJune C Carroll, Andrea L Rideout, Brenda J Wilson, et al.
Animals : an Open Access Journal From MDPI|November 27, 2021
Fibropapillomatosis and Chelonid Alphaherpesvirus 5 Infection in Kemp's Ridley Sea Turtles (<i>Lepidochelys kempii</i>)Annie Page-Karjian, Liam Whitmore, Brian A Stacy, et al.
Brain : a Journal of Neurology|January 31, 2013
CHOP regulates the p53-MDM2 axis and is required for neuronal survival after seizuresTobias Engel, Amaya Sanz-Rodgriguez, Eva M Jimenez-Mateos, et al.
Nature Genetics|October 20, 2009
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathyIngo Kurth, Torsten Pamminger, J Christopher Hennings, et al.
Diabetes|January 11, 2023
Protein Markers of Diabetes Discovered in an African American CohortZsu-Zsu Chen, Yan Gao, Michelle J Keyes, et al.
Circulation Research|July 18, 2023
Brown Adipose Tissue and BMP3b Decrease Injury in Cardiac Ischemia-ReperfusionÍngrid Martí-Pàmies, Robrecht Thoonen, Michael Morley, et al.
The New England Journal of Medicine|February 11, 2011
A randomized trial of prenatal versus postnatal repair of myelomeningoceleN Scott Adzick, Elizabeth A Thom, Catherine Y Spong, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Pageof 72

Showing results (661-670 of 714) with videos related to

Sort By:
Pageof 72
Annals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.
Nature Biotechnology|June 21, 2011
A pipeline that integrates the discovery and verification of plasma protein biomarkers reveals candidate markers for cardiovascular diseaseTerri A Addona, Xu Shi, Hasmik Keshishian, et al.
Canadian Family Physician Medecin De Famille Canadien|December 17, 2009
Genetic education for primary care providers: improving attitudes, knowledge, and confidenceJune C Carroll, Andrea L Rideout, Brenda J Wilson, et al.
Animals : an Open Access Journal From MDPI|November 27, 2021
Fibropapillomatosis and Chelonid Alphaherpesvirus 5 Infection in Kemp's Ridley Sea Turtles (<i>Lepidochelys kempii</i>)Annie Page-Karjian, Liam Whitmore, Brian A Stacy, et al.
Brain : a Journal of Neurology|January 31, 2013
CHOP regulates the p53-MDM2 axis and is required for neuronal survival after seizuresTobias Engel, Amaya Sanz-Rodgriguez, Eva M Jimenez-Mateos, et al.
Nature Genetics|October 20, 2009
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathyIngo Kurth, Torsten Pamminger, J Christopher Hennings, et al.
Diabetes|January 11, 2023
Protein Markers of Diabetes Discovered in an African American CohortZsu-Zsu Chen, Yan Gao, Michelle J Keyes, et al.
Circulation Research|July 18, 2023
Brown Adipose Tissue and BMP3b Decrease Injury in Cardiac Ischemia-ReperfusionÍngrid Martí-Pàmies, Robrecht Thoonen, Michael Morley, et al.
The New England Journal of Medicine|February 11, 2011
A randomized trial of prenatal versus postnatal repair of myelomeningoceleN Scott Adzick, Elizabeth A Thom, Catherine Y Spong, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Pageof 72