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M Hunt

Showing results (1111-1120 of 1,279) with videos related to

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Genomics|March 28, 2003
Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)Samantha Johnson, Stephanie Halford, Alex G Morris, et al.
JMIR Formative Research|January 18, 2022
A Digital Mental Health Intervention in an Orthopedic Setting for Patients With Symptoms of Depression and/or Anxiety: Feasibility Prospective Cohort StudyAshwin J Leo, Matthew J Schuelke, Devyani M Hunt, et al.
Disability and Rehabilitation|February 21, 2022
Knowledge translation in rehabilitation settings in low, lower-middle and upper-middle-income countries: a scoping reviewI C R Regalado, A R Lindquist, R Cardoso, et al.
The Journal of Experimental Biology|June 9, 2005
Adaptations to an extreme environment: retinal organisation and spectral properties of photoreceptors in Antarctic notothenioid fishMarie A Pointer, Chi-Hing Christina Cheng, James K Bowmaker, et al.
The American Journal of Physiology|July 1, 1990
Renal responses to graded hemorrhage in conscious pigJ L Sondeen, G A Gonzaludo, J A Loveday, et al.
Drug and Alcohol Dependence|June 1, 2012
Prior methamphetamine self-administration attenuates serotonergic deficits induced by subsequent high-dose methamphetamine administrationsLisa M McFadden, Madison M Hunt, Paula L Vieira-Brock, et al.
Pulmonary Circulation|July 10, 2014
Timed response to inhaled nitric oxide in pulmonary hypertensionJames M Hunt, Michael G Risbano, John C Messenger, et al.
Biotechnology Progress|June 9, 2017
Efficient tRNA degradation and quantification in Escherichia coli cell extract using RNase-coated magnetic beads: A key step toward codon emancipationAmin S M Salehi, Mark T Smith, Song-Min Schinn, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
Human Molecular Genetics|November 22, 2002
Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31Evelyne C Deery, Eranga N Vithana, Richard J Newbold, et al.
Pageof 128

Showing results (1111-1120 of 1,279) with videos related to

Sort By:
Pageof 128
Genomics|March 28, 2003
Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)Samantha Johnson, Stephanie Halford, Alex G Morris, et al.
JMIR Formative Research|January 18, 2022
A Digital Mental Health Intervention in an Orthopedic Setting for Patients With Symptoms of Depression and/or Anxiety: Feasibility Prospective Cohort StudyAshwin J Leo, Matthew J Schuelke, Devyani M Hunt, et al.
Disability and Rehabilitation|February 21, 2022
Knowledge translation in rehabilitation settings in low, lower-middle and upper-middle-income countries: a scoping reviewI C R Regalado, A R Lindquist, R Cardoso, et al.
The Journal of Experimental Biology|June 9, 2005
Adaptations to an extreme environment: retinal organisation and spectral properties of photoreceptors in Antarctic notothenioid fishMarie A Pointer, Chi-Hing Christina Cheng, James K Bowmaker, et al.
The American Journal of Physiology|July 1, 1990
Renal responses to graded hemorrhage in conscious pigJ L Sondeen, G A Gonzaludo, J A Loveday, et al.
Drug and Alcohol Dependence|June 1, 2012
Prior methamphetamine self-administration attenuates serotonergic deficits induced by subsequent high-dose methamphetamine administrationsLisa M McFadden, Madison M Hunt, Paula L Vieira-Brock, et al.
Pulmonary Circulation|July 10, 2014
Timed response to inhaled nitric oxide in pulmonary hypertensionJames M Hunt, Michael G Risbano, John C Messenger, et al.
Biotechnology Progress|June 9, 2017
Efficient tRNA degradation and quantification in Escherichia coli cell extract using RNase-coated magnetic beads: A key step toward codon emancipationAmin S M Salehi, Mark T Smith, Song-Min Schinn, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
Human Molecular Genetics|November 22, 2002
Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31Evelyne C Deery, Eranga N Vithana, Richard J Newbold, et al.
Pageof 128