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P Campbell

Showing results (951-960 of 1,288) with videos related to

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Human Molecular Genetics|July 1, 1995
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyM R Bueno, E S Moreira, M Vainzof, et al.
Neuromuscular Disorders : NMD|September 1, 1993
The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophiesK Matsumura, K Ohlendieck, V V Ionasescu, et al.
Science (New York, N.Y.)|January 2, 2010
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin bindingTakako Yoshida-Moriguchi, Liping Yu, Stephanie H Stalnaker, et al.
BMC Physiology|August 10, 2001
Modulation of L-type Ca2+ current but not activation of Ca2+ release by the gamma1 subunit of the dihydropyridine receptor of skeletal muscleC A Ahern, P A Powers, G H Biddlecome, et al.
Diabetes|December 1, 1984
Demonstration of a dawn phenomenon in normal human volunteersG B Bolli, P De Feo, S De Cosmo, et al.
European Cells & Materials|September 22, 2021
IgG4-specific responses in patients with Staphylococcus aureus bone infections are not predictive of postoperative complicationsJ R Owen, M P Campbell, M D Mott, et al.
Neuromuscular Disorders : NMD|May 16, 2018
Uniparental disomy unveils a novel recessive mutation in POMT2Brianna N Brun, Tobias Willer, Benjamin W Darbro, et al.
JAMA Network Open|January 28, 2025
Phenotypic Classification of Multisystem Inflammatory Syndrome in Children Using Latent Class AnalysisKevin C Ma, Anna R Yousaf, Allison Miller, et al.
Neurotoxicology|July 11, 2024
Impaired memory in Sprague-Dawley rats exposed to complex groundwater mixtures of contaminants is associated with reduced cranial blood flow and hippocampal neurotoxicityB Boamah, C Morse, S Siciliano, et al.
Cureus|November 29, 2023
Outcomes of Osteochondral Allograft Transplantation: A Comparative Study of BioUni and Snowman Techniques for Ovoid LesionsCarlo Coladonato, Andres R Perez, Adeeb J Hanna, et al.
Pageof 129

Showing results (951-960 of 1,288) with videos related to

Sort By:
Pageof 129
Human Molecular Genetics|July 1, 1995
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyM R Bueno, E S Moreira, M Vainzof, et al.
Neuromuscular Disorders : NMD|September 1, 1993
The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophiesK Matsumura, K Ohlendieck, V V Ionasescu, et al.
Science (New York, N.Y.)|January 2, 2010
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin bindingTakako Yoshida-Moriguchi, Liping Yu, Stephanie H Stalnaker, et al.
BMC Physiology|August 10, 2001
Modulation of L-type Ca2+ current but not activation of Ca2+ release by the gamma1 subunit of the dihydropyridine receptor of skeletal muscleC A Ahern, P A Powers, G H Biddlecome, et al.
Diabetes|December 1, 1984
Demonstration of a dawn phenomenon in normal human volunteersG B Bolli, P De Feo, S De Cosmo, et al.
European Cells & Materials|September 22, 2021
IgG4-specific responses in patients with Staphylococcus aureus bone infections are not predictive of postoperative complicationsJ R Owen, M P Campbell, M D Mott, et al.
Neuromuscular Disorders : NMD|May 16, 2018
Uniparental disomy unveils a novel recessive mutation in POMT2Brianna N Brun, Tobias Willer, Benjamin W Darbro, et al.
JAMA Network Open|January 28, 2025
Phenotypic Classification of Multisystem Inflammatory Syndrome in Children Using Latent Class AnalysisKevin C Ma, Anna R Yousaf, Allison Miller, et al.
Neurotoxicology|July 11, 2024
Impaired memory in Sprague-Dawley rats exposed to complex groundwater mixtures of contaminants is associated with reduced cranial blood flow and hippocampal neurotoxicityB Boamah, C Morse, S Siciliano, et al.
Cureus|November 29, 2023
Outcomes of Osteochondral Allograft Transplantation: A Comparative Study of BioUni and Snowman Techniques for Ovoid LesionsCarlo Coladonato, Andres R Perez, Adeeb J Hanna, et al.
Pageof 129