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Luciano Merlini

Showing results (61-70 of 117) with videos related to

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Matrix Biology : Journal of the International Society for Matrix Biology|March 6, 2016
Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury responseFrancesca Sardone, Spartaco Santi, Francesca Tagliavini, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 12, 2011
Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenitaAnna Modoni, Adele D'Amico, Bruno Dallapiccola, et al.
Frontiers in Aging Neuroscience|September 6, 2014
Aggresome-Autophagy Involvement in a Sarcopenic Patient with Rigid Spine Syndrome and a p.C150R Mutation in FHL1 GenePatrizia Sabatelli, Silvia Castagnaro, Francesca Tagliavini, et al.
Biochimica Et Biophysica Acta|May 22, 2003
Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutationPatrizia Sabatelli, Marta Columbaro, Isabella Mura, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Refined mapping of the HMSNR critical gene region--construction of a high-density integrated genetic and physical mapJanina Hantke, Tamara Rogers, Lisa French, et al.
International Journal of Molecular Sciences|July 13, 2024
Characterization of Proteome Changes in Aged and Collagen VI-Deficient Human Pericyte CulturesManuela Moriggi, Enrica Torretta, Matilde Cescon, et al.
Nature Genetics|November 20, 2003
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiencyWilliam A Irwin, Natascha Bergamin, Patrizia Sabatelli, et al.
Journal of Cellular Physiology|November 22, 2012
Melanocytes--a novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophyCamilla Pellegrini, Alessandra Zulian, Francesca Gualandi, et al.
BMC Medical Genetics|March 23, 2010
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathiesMatteo Bovolenta, Marcella Neri, Elena Martoni, et al.
The Journal of Investigative Dermatology|October 1, 2010
Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathiesPatrizia Sabatelli, Sudheer K Gara, Paolo Grumati, et al.
Pageof 12

Showing results (61-70 of 117) with videos related to

Sort By:
Pageof 12
Matrix Biology : Journal of the International Society for Matrix Biology|March 6, 2016
Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury responseFrancesca Sardone, Spartaco Santi, Francesca Tagliavini, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 12, 2011
Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenitaAnna Modoni, Adele D'Amico, Bruno Dallapiccola, et al.
Frontiers in Aging Neuroscience|September 6, 2014
Aggresome-Autophagy Involvement in a Sarcopenic Patient with Rigid Spine Syndrome and a p.C150R Mutation in FHL1 GenePatrizia Sabatelli, Silvia Castagnaro, Francesca Tagliavini, et al.
Biochimica Et Biophysica Acta|May 22, 2003
Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutationPatrizia Sabatelli, Marta Columbaro, Isabella Mura, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Refined mapping of the HMSNR critical gene region--construction of a high-density integrated genetic and physical mapJanina Hantke, Tamara Rogers, Lisa French, et al.
International Journal of Molecular Sciences|July 13, 2024
Characterization of Proteome Changes in Aged and Collagen VI-Deficient Human Pericyte CulturesManuela Moriggi, Enrica Torretta, Matilde Cescon, et al.
Nature Genetics|November 20, 2003
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiencyWilliam A Irwin, Natascha Bergamin, Patrizia Sabatelli, et al.
Journal of Cellular Physiology|November 22, 2012
Melanocytes--a novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophyCamilla Pellegrini, Alessandra Zulian, Francesca Gualandi, et al.
BMC Medical Genetics|March 23, 2010
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathiesMatteo Bovolenta, Marcella Neri, Elena Martoni, et al.
The Journal of Investigative Dermatology|October 1, 2010
Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathiesPatrizia Sabatelli, Sudheer K Gara, Paolo Grumati, et al.
Pageof 12