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A Peat

Showing results (61-70 of 70) with videos related to

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The Journal of Biological Chemistry|July 3, 2010
Reduced plasma membrane expression of dysferlin mutants is attributed to accelerated endocytosis via a syntaxin-4-associated pathwayFrances J Evesson, Rachel A Peat, Angela Lek, et al.
Arthritis Research & Therapy|January 26, 2026
Effects of pentosan polysulfate sodium on synovial fluid biomarkers in moderate to severe knee osteoarthritis: an exploratory, phase 2, randomized, double-blind, placebo-controlled trialDonna L Skerrett, Catherine J M Stapledon, Mukesh Ahuja, et al.
Neuromuscular Disorders : NMD|July 8, 2008
Exclusion of biglycan mutations in a cohort of patients with neuromuscular disordersRachel A Peat, Jozef Gécz, Justin R Fallon, et al.
Neurology|December 28, 2007
Diagnosis and etiology of congenital muscular dystrophyR A Peat, J M Smith, A G Compton, et al.
The Journal of Biological Chemistry|August 24, 2010
Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophyLeona D Tooley, Laura K Zamurs, Nicola Beecher, et al.
The American Journal of Tropical Medicine and Hygiene|January 17, 2002
Mechanisms of hemorrhage in dengue without circulatory collapseC Krishnamurti, S Kalayanarooj, M A Cutting, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE geneNigel F Clarke, Svetlana Maugenre, Aurélie Vandebrouck, et al.
Annals of Neurology|October 1, 2008
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severityRishika A Pace, Rachel A Peat, Naomi L Baker, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Circulation. Cardiovascular Genetics|July 17, 2013
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeSabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
The Journal of Biological Chemistry|July 3, 2010
Reduced plasma membrane expression of dysferlin mutants is attributed to accelerated endocytosis via a syntaxin-4-associated pathwayFrances J Evesson, Rachel A Peat, Angela Lek, et al.
Arthritis Research & Therapy|January 26, 2026
Effects of pentosan polysulfate sodium on synovial fluid biomarkers in moderate to severe knee osteoarthritis: an exploratory, phase 2, randomized, double-blind, placebo-controlled trialDonna L Skerrett, Catherine J M Stapledon, Mukesh Ahuja, et al.
Neuromuscular Disorders : NMD|July 8, 2008
Exclusion of biglycan mutations in a cohort of patients with neuromuscular disordersRachel A Peat, Jozef Gécz, Justin R Fallon, et al.
Neurology|December 28, 2007
Diagnosis and etiology of congenital muscular dystrophyR A Peat, J M Smith, A G Compton, et al.
The Journal of Biological Chemistry|August 24, 2010
Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophyLeona D Tooley, Laura K Zamurs, Nicola Beecher, et al.
The American Journal of Tropical Medicine and Hygiene|January 17, 2002
Mechanisms of hemorrhage in dengue without circulatory collapseC Krishnamurti, S Kalayanarooj, M A Cutting, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE geneNigel F Clarke, Svetlana Maugenre, Aurélie Vandebrouck, et al.
Annals of Neurology|October 1, 2008
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severityRishika A Pace, Rachel A Peat, Naomi L Baker, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Circulation. Cardiovascular Genetics|July 17, 2013
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeSabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Pageof 7