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A Munnich

Showing results (211-220 of 426) with videos related to

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Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|May 1, 1990
[Prenatal diagnosis of various hereditary blinding diseases]A Michel-Awad, J Kaplan, M L Briard, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
ABCR gene analysis in familial exudative age-related macular degenerationE H Souied, D Ducroq, J M Rozet, et al.
Biochemical and Biophysical Research Communications|November 30, 1984
Cyclic AMP as a transcriptional inhibitor of upper eukaryotic gene transcriptionS Vaulont, A Munnich, J Marie, et al.
Human Genetics|January 1, 1990
Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiencyA Pelet, A Rotig, C Bonaïti-Pellié, et al.
American Journal of Ophthalmology|March 25, 1998
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degenerationE H Souied, P Benlian, P Amouyel, et al.
Journal of Medical Genetics|January 20, 2004
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndromeP Bénit, A Slama, F Cartault, et al.
American Journal of Human Genetics|February 1, 1992
Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxiaA Rötig, J L Bessis, N Romero, et al.
Journal of Medical Genetics|January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux typeL Faivre, M Le Merrer, A Megarbane, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
The Biochemical Journal|March 15, 1985
Characterization and metabolic regulation of a liver-specific 5.4-kilobase mRNA whose synthesis is transcriptionally induced by carbohydrates and repressed by glucagon and cyclic AMPA L Pichard, A Munnich, M C Meienhofer, et al.
Pageof 43

Showing results (211-220 of 426) with videos related to

Sort By:
Pageof 43
Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|May 1, 1990
[Prenatal diagnosis of various hereditary blinding diseases]A Michel-Awad, J Kaplan, M L Briard, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
ABCR gene analysis in familial exudative age-related macular degenerationE H Souied, D Ducroq, J M Rozet, et al.
Biochemical and Biophysical Research Communications|November 30, 1984
Cyclic AMP as a transcriptional inhibitor of upper eukaryotic gene transcriptionS Vaulont, A Munnich, J Marie, et al.
Human Genetics|January 1, 1990
Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiencyA Pelet, A Rotig, C Bonaïti-Pellié, et al.
American Journal of Ophthalmology|March 25, 1998
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degenerationE H Souied, P Benlian, P Amouyel, et al.
Journal of Medical Genetics|January 20, 2004
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndromeP Bénit, A Slama, F Cartault, et al.
American Journal of Human Genetics|February 1, 1992
Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxiaA Rötig, J L Bessis, N Romero, et al.
Journal of Medical Genetics|January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux typeL Faivre, M Le Merrer, A Megarbane, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
The Biochemical Journal|March 15, 1985
Characterization and metabolic regulation of a liver-specific 5.4-kilobase mRNA whose synthesis is transcriptionally induced by carbohydrates and repressed by glucagon and cyclic AMPA L Pichard, A Munnich, M C Meienhofer, et al.
Pageof 43