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G Laing

Showing results (161-170 of 494) with videos related to

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F1000Research|January 12, 2019
Recent advances in understanding congenital myopathiesGianina Ravenscroft, Robert J Bryson-Richardson, Kristen J Nowak, et al.
The American Journal of Physiology|February 1, 1995
Properties of gap junction channels formed of connexin 45 endogenously expressed in human hepatoma (SKHep1) cellsA P Moreno, J G Laing, E C Beyer, et al.
Physiology & Behavior|January 11, 2005
Perception of temporal order and the identification of components in taste mixturesKatrina Marshall, David G Laing, Anthony L Jinks, et al.
Neuromuscular Disorders : NMD|March 25, 2017
Lethal multiple pterygium syndrome: A severe phenotype associated with a novel mutation in the nebulin geneEbtesam Abdalla, Gianina Ravenscroft, Louay Zayed, et al.
Neuromuscular Disorders : NMD|July 1, 1997
Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?S D Wilton, D E Dye, L M Blechynden, et al.
Toxicon : Official Journal of the International Society on Toxinology|January 1, 1991
Isolation and comparison of myotoxins isolated from venoms of different species of Bothrops snakesA M Moura-da-Silva, H Desmond, G Laing, et al.
Seminars in Cell & Developmental Biology|August 14, 2016
New era in genetics of early-onset muscle disease: Breakthroughs and challengesGianina Ravenscroft, Mark R Davis, Phillipa Lamont, et al.
Circulation Research|September 19, 1998
Rapid turnover of connexin43 in the adult rat heartM A Beardslee, J G Laing, E C Beyer, et al.
Neurology|January 1, 1997
Prognosis in familial amyotrophic lateral sclerosis: progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutaseT Juneja, M A Pericak-Vance, N G Laing, et al.
The Clinical Biochemist. Reviews|September 14, 2011
Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapiesNigel G Laing, Mark R Davis, Klair Bayley, et al.
Pageof 50

Showing results (161-170 of 494) with videos related to

Sort By:
Pageof 50
F1000Research|January 12, 2019
Recent advances in understanding congenital myopathiesGianina Ravenscroft, Robert J Bryson-Richardson, Kristen J Nowak, et al.
The American Journal of Physiology|February 1, 1995
Properties of gap junction channels formed of connexin 45 endogenously expressed in human hepatoma (SKHep1) cellsA P Moreno, J G Laing, E C Beyer, et al.
Physiology & Behavior|January 11, 2005
Perception of temporal order and the identification of components in taste mixturesKatrina Marshall, David G Laing, Anthony L Jinks, et al.
Neuromuscular Disorders : NMD|March 25, 2017
Lethal multiple pterygium syndrome: A severe phenotype associated with a novel mutation in the nebulin geneEbtesam Abdalla, Gianina Ravenscroft, Louay Zayed, et al.
Neuromuscular Disorders : NMD|July 1, 1997
Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?S D Wilton, D E Dye, L M Blechynden, et al.
Toxicon : Official Journal of the International Society on Toxinology|January 1, 1991
Isolation and comparison of myotoxins isolated from venoms of different species of Bothrops snakesA M Moura-da-Silva, H Desmond, G Laing, et al.
Seminars in Cell & Developmental Biology|August 14, 2016
New era in genetics of early-onset muscle disease: Breakthroughs and challengesGianina Ravenscroft, Mark R Davis, Phillipa Lamont, et al.
Circulation Research|September 19, 1998
Rapid turnover of connexin43 in the adult rat heartM A Beardslee, J G Laing, E C Beyer, et al.
Neurology|January 1, 1997
Prognosis in familial amyotrophic lateral sclerosis: progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutaseT Juneja, M A Pericak-Vance, N G Laing, et al.
The Clinical Biochemist. Reviews|September 14, 2011
Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapiesNigel G Laing, Mark R Davis, Klair Bayley, et al.
Pageof 50