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I Takata

Showing results (61-70 of 74) with videos related to

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Clinical Genetics|October 3, 2009
Mutational screening of ACVR1 gene in Brazilian fibrodysplasia ossificans progressiva patientsD R Carvalho, M M M Navarro, B J A F Martins, et al.
American Journal of Medical Genetics|April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Clinical Dysmorphology|March 2, 2010
Mandibular hypoplasia in fibrodysplasia ossificans progressiva causing obstructive sleep apnoea with pulmonary hypertensionDaniel R Carvalho, Giulio C Pinnola, Danielle R A Ferreira, et al.
Disease Models & Mechanisms|January 24, 2020
Modelling the pathogenesis of X-linked distal hereditary motor neuropathy using patient-derived iPSCsGonzalo Perez-Siles, Anthony Cutrupi, Melina Ellis, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridizationC Rosenberg, L Navajas, D F Vagenas, et al.
Journal of Medical Genetics|February 27, 2004
A new locus for recessive distal spinal muscular atrophy at Xq13.1-q21R I Takata, C E Speck Martins, M R Passosbueno, et al.
British Journal of Cancer|July 5, 2001
Fractionated administration of irinotecan and cisplatin for treatment of non-small-cell lung cancer: a phase II study of Okayama Lung Cancer Study GroupH Ueoka, M Tanimoto, K Kiura, et al.
Journal of Molecular Neuroscience : MN|August 15, 2019
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial VariabilityAna Cotta, Julia F Paim, Elmano Carvalho, et al.
Journal of Molecular Neuroscience : MN|March 13, 2013
Muscle phenotypic variability in limb girdle muscular dystrophy 2 GJulia F Paim, Ana Cotta, Antonio P Vargas, et al.
Muscle & Nerve|February 7, 2017
Central core myopathy with autophagyAna Cotta, Julia F Paim, Rita De C M Pavanello, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Clinical Genetics|October 3, 2009
Mutational screening of ACVR1 gene in Brazilian fibrodysplasia ossificans progressiva patientsD R Carvalho, M M M Navarro, B J A F Martins, et al.
American Journal of Medical Genetics|April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Clinical Dysmorphology|March 2, 2010
Mandibular hypoplasia in fibrodysplasia ossificans progressiva causing obstructive sleep apnoea with pulmonary hypertensionDaniel R Carvalho, Giulio C Pinnola, Danielle R A Ferreira, et al.
Disease Models & Mechanisms|January 24, 2020
Modelling the pathogenesis of X-linked distal hereditary motor neuropathy using patient-derived iPSCsGonzalo Perez-Siles, Anthony Cutrupi, Melina Ellis, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridizationC Rosenberg, L Navajas, D F Vagenas, et al.
Journal of Medical Genetics|February 27, 2004
A new locus for recessive distal spinal muscular atrophy at Xq13.1-q21R I Takata, C E Speck Martins, M R Passosbueno, et al.
British Journal of Cancer|July 5, 2001
Fractionated administration of irinotecan and cisplatin for treatment of non-small-cell lung cancer: a phase II study of Okayama Lung Cancer Study GroupH Ueoka, M Tanimoto, K Kiura, et al.
Journal of Molecular Neuroscience : MN|August 15, 2019
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial VariabilityAna Cotta, Julia F Paim, Elmano Carvalho, et al.
Journal of Molecular Neuroscience : MN|March 13, 2013
Muscle phenotypic variability in limb girdle muscular dystrophy 2 GJulia F Paim, Ana Cotta, Antonio P Vargas, et al.
Muscle & Nerve|February 7, 2017
Central core myopathy with autophagyAna Cotta, Julia F Paim, Rita De C M Pavanello, et al.
Pageof 8