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P Hamel

Showing results (91-100 of 233) with videos related to

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European Journal of Human Genetics : EJHG|November 5, 1998
Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 geneF Marlhens, J M Griffoin, C Bareil, et al.
Biochemistry|March 22, 2000
Effect of an alternative disulfide bond on the structure, stability, and folding of human lysozymeM Arai, P Hamel, E Kanaya, et al.
Ophthalmic Research|November 6, 2010
Simple and efficient: validation of a cotton wick electrode for animal electroretinographyKarim Chekroud, Carl Arndt, Danièle Basset, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1994
[The estimation of fetal weight by measurement of the adipose tissue of the extremities. Use in the diagnosis of hypotrophy]P Balouet, P Hamel, D Domessent, et al.
Ophthalmology|August 4, 2004
Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65Birgit Lorenz, Bettina Wabbels, Erika Wegscheider, et al.
Genetics|April 7, 2011
A forward genetic screen identifies mutants deficient for mitochondrial complex I assembly in Chlamydomonas reinhardtiiM Rosario Barbieri, Véronique Larosa, Cécile Nouet, et al.
International Journal of Sports Medicine|December 1, 1985
Specificity of aerobic and anaerobic work capacities and powersM R Boulay, G Lortie, J A Simoneau, et al.
Frontiers in Genetics|November 6, 2015
A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disabilityMajida Charif, Agathe Roubertie, Sara Salime, et al.
FEBS Letters|March 25, 1998
Rat messenger RNA for the retinal pigment epithelium-specific protein RPE65 gradually accumulates in two weeks from late embryonic daysG Manès, R Leducq, J Kucharczak, et al.
JAMA Ophthalmology|August 10, 2013
Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1Elodie Dessalces, Béatrice Bocquet, Jérôme Bourien, et al.
Pageof 24

Showing results (91-100 of 233) with videos related to

Sort By:
Pageof 24
European Journal of Human Genetics : EJHG|November 5, 1998
Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 geneF Marlhens, J M Griffoin, C Bareil, et al.
Biochemistry|March 22, 2000
Effect of an alternative disulfide bond on the structure, stability, and folding of human lysozymeM Arai, P Hamel, E Kanaya, et al.
Ophthalmic Research|November 6, 2010
Simple and efficient: validation of a cotton wick electrode for animal electroretinographyKarim Chekroud, Carl Arndt, Danièle Basset, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1994
[The estimation of fetal weight by measurement of the adipose tissue of the extremities. Use in the diagnosis of hypotrophy]P Balouet, P Hamel, D Domessent, et al.
Ophthalmology|August 4, 2004
Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65Birgit Lorenz, Bettina Wabbels, Erika Wegscheider, et al.
Genetics|April 7, 2011
A forward genetic screen identifies mutants deficient for mitochondrial complex I assembly in Chlamydomonas reinhardtiiM Rosario Barbieri, Véronique Larosa, Cécile Nouet, et al.
International Journal of Sports Medicine|December 1, 1985
Specificity of aerobic and anaerobic work capacities and powersM R Boulay, G Lortie, J A Simoneau, et al.
Frontiers in Genetics|November 6, 2015
A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disabilityMajida Charif, Agathe Roubertie, Sara Salime, et al.
FEBS Letters|March 25, 1998
Rat messenger RNA for the retinal pigment epithelium-specific protein RPE65 gradually accumulates in two weeks from late embryonic daysG Manès, R Leducq, J Kucharczak, et al.
JAMA Ophthalmology|August 10, 2013
Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1Elodie Dessalces, Béatrice Bocquet, Jérôme Bourien, et al.
Pageof 24