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19 results for Couvert,+Philippe

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ArticlesPeer ReviewedFull Text
Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity
Author / Creator:Small, Lewin ; Ingerslev, Lars R. ; Manitta, Eleonora ; Laker, Rhianna C. ; Hansen, Ann N. ; Deeney, Brendan ; Carrié, Alain ; Couvert, Philippe ; Barrès, Romain
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2021-01, Vol.17 (1), p.e1009325-e1009325
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ArticlesPeer ReviewedFull Text
Rotor Syndrome Presenting as Dubin-Johnson Syndrome
Author / Creator:Morais, Mariana ; Couvert, Philippe ; Jéru, Isabelle ; Machado, Mariana Verdelho
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Case reports in gastroenterology, 2022-08, Vol.16 (2), p.452-455
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ArticlesPeer ReviewedFull Text
Association between a frequent allele of the gene encoding OATP1B1 and enhanced LDL-lowering response to fluvastatin therapy
Author / Creator:Couvert, Philippe ; Giral, Philippe ; Dejager, Sylvie ; Gu, Jessie ; Huby, Thierry ; Chapman, M John ; Bruckert, Eric ; Carriéé, Alain
Publisher:England: Future Medicine Ltd
Journal title:Pharmacogenomics, 2008-09, Vol.9 (9), p.1217-1227
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ArticlesPeer ReviewedFull Text
In vitro follicular growth affects oocyte imprinting establishment in mice
Author / Creator:Kerjean, Antoine ; Couvert, Philippe ; Heams, Thomas ; Chalas, Céline ; Poirier, Karine ; Chelly, Jamel ; Jouannet, Pierre ; Paldi, Andras ; Poirot, Catherine
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2003-07, Vol.11 (7), p.493-496
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ArticlesPeer ReviewedFull Text
Parental origin of de novo MECP2 mutations in Rett syndrome
Author / Creator:Girard, Muriel ; Couvert, Philippe ; Carrié, Alain ; Tardieu, Marc ; Chelly, Jamel ; Beldjord, Cherif ; Bienvenu, Thierry
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2001-03, Vol.9 (3), p.231-236
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ArticlesPeer ReviewedFull Text
Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity
Author / Creator:Small, Lewin ; Ingerslev, Lars ; Manitta, Eleonora ; Laker, Rhianna ; Hansen, Ann ; Deeney, Brendan ; Carrié, Alain ; Couvert, Philippe ; Barrès, Romain
Publisher:Public Library of Science
Journal title:PLoS genetics, 2021-01, Vol.17 (1)
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ArticlesPeer ReviewedFull Text
Natural history of cerebrotendinous xanthomatosis: a paediatric disease diagnosed in adulthood
Author / Creator:Degos, Bertrand ; Nadjar, Yann ; Amador, Maria del Mar ; Lamari, Foudil ; Sedel, Frédéric ; Roze, Emmanuel ; Couvert, Philippe ; Mochel, Fanny
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2016-04, Vol.11 (1), p.41-41, Article 41
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ArticlesPeer ReviewedFull Text
Rotor syndrome presenting as Dubin-Johnson syndrome
Author / Creator:Morais, Mariana ; Couvert, Philippe ; Jéru, Isabelle ; Machado, Mariana
Publisher:Karger
Journal title:Case reports in gastroenterology, 2022, Vol.16 (2), p.452-455
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ArticlesPeer ReviewedFull Text
Identification of the specific molecular and functional signatures of pre-beta-HDL: relevance to cardiovascular disease
Author / Creator:Guillas, Isabelle ; Lhomme, Marie ; Pionneau, Cédric ; Matheron, Lucrèce ; Ponnaiah, Maharajah ; Galier, Sophie ; Lebreton, Sandrine ; Delbos, Marie ; Ma, Feng ; Darabi, Maryam ; Khoury, Petra El ; Abifadel, Marianne ; Couvert, Philippe ; Giral, Philippe ; Lesnik, Philippe ; Guerin, Maryse ; Le Goff, Wilfried ; Kontush, Anatol
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Basic research in cardiology, 2023-08, Vol.118 (1), p.33-33, Article 33
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ArticlesPeer ReviewedFull Text
Impact of genetic variation in the
Author / Creator:Couvert, Philippe ; Chapman, M John ; Carriéé, Alain
Publisher:Future Medicine Ltd
Journal title:Pharmacogenomics, 2011-02, Vol.12 (2), p.137-139
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ArticlesPeer ReviewedFull Text
Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease
Author / Creator:Zyss, Julie ; Béhin, Anthony ; Couvert, Philippe ; Bouhour, Françoise ; Sassolas, Agnès ; Kolev, Ivan ; Denys, Violaine ; Vial, Christophe ; Lacour, A. ; Carrié, Alain ; Stojkovic, Tanya
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Journal of neurology, 2012-06, Vol.259 (6), p.1222-1226
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ArticlesPeer ReviewedFull Text
Leukodystrophy with a cerebellar cystic aspect and intracranial atherosclerosis: an atypical presentation of cerebrotendinous xanthomatosis
Author / Creator:Androdias, Géraldine ; Vukusic, Sandra ; Gignoux, Laurence ; Boespflug-Tanguy, Odile ; Acquaviva, Cécile ; Zabot, Marie-Thérèse ; Couvert, Philippe ; Carrie, Alain ; Confavreux, Christian ; Labauge, Pierre
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Journal of neurology, 2012-02, Vol.259 (2), p.364-366
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ArticlesPeer ReviewedFull Text
Impact of Genetic Variation in the SLCO1B1 Gene on Statin Efficacy in Low-Density Lipoprotein Cholesterol-Lowering Therapy
Author / Creator:Couvert, Philippe ; Chapman, M John ; Carrié, Alain
Publisher:England: Future Medicine Ltd
Journal title:Pharmacogenomics, 2011-02, Vol.12 (2), p.137-139
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ArticlesPeer ReviewedFull Text
A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation
Author / Creator:Zemni, Ramzi ; Bienvenu, Thierry ; Vinet, Marie C. ; Sefiani, Aziz ; Carrié, Alain ; Billuart, Pierre ; McDonell, Nathalie ; Couvert, Philippe ; Francis, Fiona ; Chafey, Philippe ; Fauchereau, Fabien ; Friocourt, Gaelle ; Portes, Vincent des ; Cardona, Anna ; Frints, Suzanna ; Meindl, Alfonse ; Brandau, Oliver ; Ronce, Nathalie ; Moraine, Claude ; Bokhoven, Han van ; Ropers, Hans H. ; Sudbrak, Ralf ; Kahn, Axel ; Fryns, Jean P ; Beldjord, Cherif ; Chelly, Jamel
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2000-02, Vol.24 (2), p.167-170
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ReportsFull Text
Rotor Syndrome Presenting as Dubin-Johnson Syndrome
Author / Creator:Morais, Mariana ; Couvert, Philippe ; Jéru, Isabelle ; Machado, Mariana Verdelho
Journal title:Case reports in gastroenterology, 2022, Vol.16 (2), p.452-455
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ArticlesPeer ReviewedFull Text
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy: Mutations in Brief
Author / Creator:Bienvenu, Thierry ; Souville, Isabelle ; Poirier, Karine ; Aquaviva, Cécile ; Burglen, Lydie ; Amiel, Jeanne ; Héron, Bénédicte ; Kaminska, Anna ; Couvert, Philippe ; Beldjord, Cherif ; Chelly, Jamel
Journal title:Human mutation, 2001-09, Vol.18 (3), p.251-252
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ArticlesPeer ReviewedFull Text
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy
Author / Creator:Bienvenu, Thierry ; Souville, Isabelle ; Poirier, Karine ; Aquaviva, Cécile ; Burglen, Lydie ; Amiel, Jeanne ; Héron, Bénédicte ; Kaminska, Anna ; Couvert, Philippe ; Beldjord, Cherif ; Chelly, Jamel
Publisher:New York: John Wiley & Sons, Inc
Journal title:Human mutation, 2001-09, Vol.18 (3), p.251-252
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ReportsFull Text
Leukodystrophy with a cerebellar cystic aspect and intracranial atherosclerosis: an atypical presentation of cerebrotendinous xanthomatosis
Author / Creator:Androdias, Géraldine ; Vukusic, Sandra ; Gignoux, Laurence ; Boespflug-Tanguy, Odile ; Acquaviva, Cécile ; Zabot, Marie-Thérèse ; Couvert, Philippe ; Carrie, Alain ; Confavreux, Christian ; Labauge, Pierre
Journal title:Journal of neurology, 2012, Vol.259 (2), p.364-366
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ReviewsPeer ReviewedFull Text
Apolipoprotein AV: gene expression, physiological role in lipid metabolism and clinical relevance
Author / Creator:Prieur, Xavier ; Huby, Thierry ; Rodrííguez, Joan C ; Couvert, Philippe ; Chapman, M John
Publisher:London: Future Medicine Ltd
Journal title:Clinical lipidology and metabolic disorders, 2008, Vol.3 (4), p.371-384
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Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity

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Rotor Syndrome Presenting as Dubin-Johnson Syndrome

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Association between a frequent allele of the gene encoding OATP1B1 and enhanced LDL-lowering response to fluvastatin therapy

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In vitro follicular growth affects oocyte imprinting establishment in mice

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Parental origin of de novo MECP2 mutations in Rett syndrome

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Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity

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Natural history of cerebrotendinous xanthomatosis: a paediatric disease diagnosed in adulthood

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Rotor syndrome presenting as Dubin-Johnson syndrome

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Identification of the specific molecular and functional signatures of pre-beta-HDL: relevance to cardiovascular disease

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Impact of genetic variation in the

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Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease

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Leukodystrophy with a cerebellar cystic aspect and intracranial atherosclerosis: an atypical presentation of cerebrotendinous xanthomatosis

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Impact of Genetic Variation in the SLCO1B1 Gene on Statin Efficacy in Low-Density Lipoprotein Cholesterol-Lowering Therapy

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A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation

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Rotor Syndrome Presenting as Dubin-Johnson Syndrome

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Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy: Mutations in Brief

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Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy

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Leukodystrophy with a cerebellar cystic aspect and intracranial atherosclerosis: an atypical presentation of cerebrotendinous xanthomatosis

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Apolipoprotein AV: gene expression, physiological role in lipid metabolism and clinical relevance

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