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Genomics
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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 Study
Ashwin 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 review
I 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 fish
Marie 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 pig
J 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 administrations
Lisa M McFadden, Madison M Hunt, Paula L Vieira-Brock, et al.
Pulmonary Circulation
|
July 10, 2014
Timed response to inhaled nitric oxide in pulmonary hypertension
James 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 emancipation
Amin 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-1
S 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 PRPF31
Evelyne C Deery, Eranga N Vithana, Richard J Newbold, et al.
Page
of 128
Search research articles
Search
Showing results (1111-1120 of 1,279) with videos related to
Sort By:
Page
of 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 Study
Ashwin 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 review
I 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 fish
Marie 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 pig
J 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 administrations
Lisa M McFadden, Madison M Hunt, Paula L Vieira-Brock, et al.
Pulmonary Circulation
|
July 10, 2014
Timed response to inhaled nitric oxide in pulmonary hypertension
James 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 emancipation
Amin 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-1
S 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 PRPF31
Evelyne C Deery, Eranga N Vithana, Richard J Newbold, et al.
Page
of 128