L MANDEL - JoVE Visualize

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Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|September 1, 1989

[The progeny of the two protan and deutan families described by Franceschetti and Klein (1949, 1956), one generation later. Genealogy, color vision and genomic DNA]A Roth, D Klein, F Paccolat, et al.

Human Molecular Genetics|August 7, 2001

SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell typesG Yvert, K S Lindenberg, D Devys, et al.

Human Genetics|September 1, 1987

Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27I Oberlé, G Camerino, K Wrogemann, et al.

Organic Letters|October 18, 2012

Structure of FD-895 revealed through total synthesisReymundo Villa, Alexander L Mandel, Brian D Jones, et al.

Human Molecular Genetics|October 13, 2000

Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic miceG Yvert, K S Lindenberg, S Picaud, et al.

Human Molecular Genetics|September 16, 1998

Characterization of the myotubularin dual specificity phosphatase gene family from yeast to humanJ Laporte, F Blondeau, A Buj-Bello, et al.

Plos One|October 23, 2010

Individual differences in AMY1 gene copy number, salivary α-amylase levels, and the perception of oral starchAbigail L Mandel, Catherine Peyrot des Gachons, Kimberly L Plank, et al.

Archives of Internal Medicine|April 14, 2004

Patients' interest in reading their medical record: relation with clinical and sociodemographic characteristics and patients' approach to health careJinnet B Fowles, Allan C Kind, Cheryl Craft, et al.

American Journal of Medical Genetics|April 1, 1992

Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic associationI Oberlé, J Boué, M F Croquette, et al.

Human Molecular Genetics|September 1, 1997

Characterization of mutations in the myotubularin gene in twenty six patients with X-linked myotubular myopathyB M de Gouyon, W Zhao, J Laporte, et al.

Pageof 31

Showing results (191-200 of 308) with videos related to

Sort By:

Pageof 31

Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|September 1, 1989

[The progeny of the two protan and deutan families described by Franceschetti and Klein (1949, 1956), one generation later. Genealogy, color vision and genomic DNA]A Roth, D Klein, F Paccolat, et al.

Human Molecular Genetics|August 7, 2001

SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell typesG Yvert, K S Lindenberg, D Devys, et al.

Human Genetics|September 1, 1987

Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27I Oberlé, G Camerino, K Wrogemann, et al.

Organic Letters|October 18, 2012

Structure of FD-895 revealed through total synthesisReymundo Villa, Alexander L Mandel, Brian D Jones, et al.

Human Molecular Genetics|October 13, 2000

Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic miceG Yvert, K S Lindenberg, S Picaud, et al.

Human Molecular Genetics|September 16, 1998

Characterization of the myotubularin dual specificity phosphatase gene family from yeast to humanJ Laporte, F Blondeau, A Buj-Bello, et al.

Plos One|October 23, 2010

Individual differences in AMY1 gene copy number, salivary α-amylase levels, and the perception of oral starchAbigail L Mandel, Catherine Peyrot des Gachons, Kimberly L Plank, et al.

Archives of Internal Medicine|April 14, 2004

Patients' interest in reading their medical record: relation with clinical and sociodemographic characteristics and patients' approach to health careJinnet B Fowles, Allan C Kind, Cheryl Craft, et al.

American Journal of Medical Genetics|April 1, 1992

Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic associationI Oberlé, J Boué, M F Croquette, et al.

Human Molecular Genetics|September 1, 1997

Characterization of mutations in the myotubularin gene in twenty six patients with X-linked myotubular myopathyB M de Gouyon, W Zhao, J Laporte, et al.

Pageof 31