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P Amati

Showing results (51-60 of 79) with videos related to

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Journal Francais D'Ophtalmologie|February 24, 2007
[A novel mutation of the OPA1 gene responsible for isolated autosomal dominant optic atrophy in two brothers]R Macarez, P Amati-Bonneau, X Burelle, et al.
Nature Genetics|February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNAA Suomalainen, J Kaukonen, P Amati, et al.
Revue Neurologique|November 9, 2010
[Hereditary optic atrophies]C Scherer, V Procaccio, M Ferre, et al.
American Journal of Medical Genetics|September 24, 1999
Splenogonadal fusion limb defect syndrome: report of five new cases and reviewD Bonneau, J Roume, M Gonzalez, et al.
Molecular and Cellular Probes|September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome geneL Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Oncogene|May 18, 1999
Medullary thyroid carcinomas in transgenic mice expressing a Polyoma carboxyl-terminal truncated middle-T and wild type small-T antigensA Felici, M Giorgio, N Krauzewicz, et al.
Rivista Di Neurologia|July 1, 1991
[Expression of a defect in the respiratory chain in cultured human cells]G Meola, G Rotondo, M Velicogna, et al.
American Journal of Human Genetics|December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.
American Journal of Human Genetics|December 5, 1998
A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2F Canzian, P Amati, H R Harach, et al.
Revue Neurologique|May 6, 2014
Perspectives of drug-based neuroprotection targeting mitochondriaV Procaccio, C Bris, J M Chao de la Barca, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
Journal Francais D'Ophtalmologie|February 24, 2007
[A novel mutation of the OPA1 gene responsible for isolated autosomal dominant optic atrophy in two brothers]R Macarez, P Amati-Bonneau, X Burelle, et al.
Nature Genetics|February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNAA Suomalainen, J Kaukonen, P Amati, et al.
Revue Neurologique|November 9, 2010
[Hereditary optic atrophies]C Scherer, V Procaccio, M Ferre, et al.
American Journal of Medical Genetics|September 24, 1999
Splenogonadal fusion limb defect syndrome: report of five new cases and reviewD Bonneau, J Roume, M Gonzalez, et al.
Molecular and Cellular Probes|September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome geneL Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Oncogene|May 18, 1999
Medullary thyroid carcinomas in transgenic mice expressing a Polyoma carboxyl-terminal truncated middle-T and wild type small-T antigensA Felici, M Giorgio, N Krauzewicz, et al.
Rivista Di Neurologia|July 1, 1991
[Expression of a defect in the respiratory chain in cultured human cells]G Meola, G Rotondo, M Velicogna, et al.
American Journal of Human Genetics|December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.
American Journal of Human Genetics|December 5, 1998
A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2F Canzian, P Amati, H R Harach, et al.
Revue Neurologique|May 6, 2014
Perspectives of drug-based neuroprotection targeting mitochondriaV Procaccio, C Bris, J M Chao de la Barca, et al.
Pageof 8