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Search life-sciences literature (45,105,671 articles, preprints and more)

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Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol.
Dubar V, Pascreau T, Dupont A, Dubucquoi S, Dautigny AL, Ghozlan B, Zuber B, Mellot F, Vasse M, Susen S, Poissy J, Gaudet A
Biomedicines, 11(6):1504, 23 May 2023
Cited by: 1 article | PMID: 37371599 | PMCID: PMC10295063
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease.
Mignot C, Delarasse C, Escaich S, Della Gaspera B, Noé E, Colucci-Guyon E, Babinet C, Pekny M, Vicart P, Boespflug-Tanguy O, Dautigny A, Rodriguez D, Pham-Dinh D
Exp Cell Res, 313(13):2766-2779, 24 May 2007
Cited by: 26 articles | PMID: 17604020
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Complex alternative splicing of the myelin oligodendrocyte glycoprotein gene is unique to human and non-human primates.
Delarasse C, Della Gaspera B, Lu CW, Lachapelle F, Gelot A, Rodriguez D, Dautigny A, Genain C, Pham-Dinh D
J Neurochem, 98(6):1707-1717, 11 Aug 2006
Cited by: 24 articles | PMID: 16903876
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Alexander disease: putative mechanisms of an astrocytic encephalopathy.
Mignot C, Boespflug-Tanguy O, Gelot A, Dautigny A, Pham-Dinh D, Rodriguez D
Cell Mol Life Sci, 61(3):369-385, 01 Feb 2004
Cited by: 58 articles | PMID: 14770299 | PMCID: PMC11146026
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Myelin/oligodendrocyte glycoprotein-deficient (MOG-deficient) mice reveal lack of immune tolerance to MOG in wild-type mice.
Delarasse C, Daubas P, Mars LT, Vizler C, Litzenburger T, Iglesias A, Bauer J, Della Gaspera B, Schubart A, Decker L, Dimitri D, Roussel G, Dierich A, Amor S, Dautigny A, Liblau R, Pham-Dinh D
J Clin Invest, 112(4):544-553, 01 Aug 2003
Cited by: 84 articles | PMID: 12925695 | PMCID: PMC171383
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Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation.
Rodriguez D, Gauthier F, Bertini E, Bugiani M, Brenner M, N'guyen S, Goizet C, Gelot A, Surtees R, Pedespan JM, Hernandorena X, Troncoso M, Uziel G, Messing A, Ponsot G, Pham-Dinh D, Dautigny A, Boespflug-Tanguy O
Am J Hum Genet, 69(5):1134-1140, 20 Sep 2001
Cited by: 74 articles | PMID: 11567214 | PMCID: PMC1274357
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Development of myelin oligodendrocyte glycoprotein autoreactive transgenic B lymphocytes: receptor editing in vivo after encounter of a self-antigen distinct from myelin oligodendrocyte glycoprotein.
Litzenburger T, Blüthmann H, Morales P, Pham-Dinh D, Dautigny A, Wekerle H, Iglesias A
J Immunol, 165(9):5360-5366, 01 Nov 2000
Cited by: 23 articles | PMID: 11046072
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Linkage analysis of candidate myelin genes in familial multiple sclerosis.
Seboun E, Oksenberg JR, Rombos A, Usuku K, Goodkin DE, Lincoln RR, Wong M, Pham-Dinh D, Boesplug-Tanguy O, Carsique R, Fitoussi R, Gartioux C, Reyes C, Ribierre F, Faure S, Fizames C, Gyapay G, Weissenbach J, Dautigny A, [...] Hauser SL
Neurogenetics, 2(3):155-162, 01 Sep 1999
Cited by: 12 articles | PMID: 10541588
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Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two cases.
Rodriguez D, Gelot A, della Gaspera B, Robain O, Ponsot G, Sarliève LL, Ghandour S, Pompidou A, Dautigny A, Aubourg P, Pham-Dinh D
Acta Neuropathol, 97(5):469-480, 01 May 1999
Cited by: 49 articles | PMID: 10334484
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Membrane topology of the myelin/oligodendrocyte glycoprotein.
della Gaspera B, Pham-Dinh D, Roussel G, Nussbaum JL, Dautigny A
Eur J Biochem, 258(2):478-484, 01 Dec 1998
Cited by: 21 articles | PMID: 9874214
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Connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease show two distinct behaviors: loss of function and altered gating properties.
Ressot C, Gomès D, Dautigny A, Pham-Dinh D, Bruzzone R
J Neurosci, 18(11):4063-4075, 01 Jun 1998
Cited by: 62 articles | PMID: 9592087 | PMCID: PMC6792797
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Identification of a Val 145 Ile substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis. The Réseau de Recherche Clinique INSERM sur la Susceptibilité Génétique à la Sclérose en Plaques.
Rodriguez D, Della Gaspera B, Zalc B, Hauw JJ, Fontaine B, Edan G, Clanet M, Dautigny A, Pham-Dinh D
Mult Scler, 3(6):377-381, 01 Dec 1997
Cited by: 14 articles | PMID: 9493637
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X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene.
Ressot C, Latour P, Blanquet-Grossard F, Sturtz F, Duthel S, Battin J, Corbillon E, Ollagnon E, Serville F, Vandenberghe A, Dautigny A, Pham-Dinh D
Hum Genet, 98(2):172-175, 01 Aug 1996
Cited by: 14 articles | PMID: 8698335
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Functional analysis of the mouse myelin/oligodendrocyte glycoprotein gene promoter in the oligodendroglial CG4 cell line.
Solly SK, Daubas P, Monge M, Dautigny A, Zalc B
J Neurochem, 68(4):1705-1711, 01 Apr 1997
Cited by: 7 articles | PMID: 9084444
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New mutations in the X-linked form of Charcot-Marie-Tooth disease.
Latour P, Fabreguette A, Ressot C, Blanquet-Grossard F, Antoine JC, Calvas P, Chapon F, Corbillon E, Ollagnon E, Sturtz F, Boucherat M, Chazot G, Dautigny A, Pham-Dinh D, Vandenberghe A
Eur Neurol, 37(1):38-42, 01 Jan 1997
Cited by: 5 articles | PMID: 9018031
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Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po.
Blanquet-Grossard F, Pham-Dinh D, Dautigny A, Latour P, Bonnebouche C, Diraison P, Chapon F, Chazot G, Vandenberghe A
Hum Mutat, 8(2):185-186, 01 Jan 1996
Cited by: 15 articles | PMID: 8844219
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Structure and polymorphism of the mouse myelin/oligodendrocyte glycoprotein gene.
Daubas P, Pham-Dinh D, Dautigny A
Genomics, 23(1):36-41, 01 Sep 1994
Cited by: 17 articles | PMID: 7829100
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Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO gene.
Blanquet-Grossard F, Pham-Dinh D, Dautigny A, Latour P, Bonnebouche C, Corbillon E, Chazot G, Vandenberghe A
Clin Genet, 48(6):281-283, 01 Dec 1995
Cited by: 10 articles | PMID: 8835320
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Structure of the human myelin/oligodendrocyte glycoprotein gene and multiple alternative spliced isoforms.
Pham-Dinh D, Della Gaspera B, Kerlero de Rosbo N, Dautigny A
Genomics, 29(2):345-352, 01 Sep 1995
Cited by: 21 articles | PMID: 8666381
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Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B.
Latour P, Blanquet F, Nelis E, Bonnebouche C, Chapon F, Diraison P, Ollagnon E, Dautigny A, Pham-Dinh D, Chazot G
Hum Mutat, 6(1):50-54, 01 Jan 1995
Cited by: 21 articles | PMID: 7550231
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Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene.
Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, Martin JJ, Van Broeckhoven C
Hum Genet, 94(6):653-657, 01 Dec 1994
Cited by: 61 articles | PMID: 7527371
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Characterization and expression of the cDNA coding for the human myelin/oligodendrocyte glycoprotein.
Pham-Dinh D, Allinquant B, Ruberg M, Della Gaspera B, Nussbaum JL, Dautigny A
J Neurochem, 63(6):2353-2356, 01 Dec 1994
Cited by: 25 articles | PMID: 7964757
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Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical Group.
Boespflug-Tanguy O, Mimault C, Melki J, Cavagna A, Giraud G, Pham Dinh D, Dastugue B, Dautigny A
Am J Hum Genet, 55(3):461-467, 01 Sep 1994
Cited by: 38 articles | PMID: 7915877 | PMCID: PMC1918422
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Physical mapping of the human and mouse MOG gene at the distal end of the MHC class Ib region.
Pham-Dinh D, Jones EP, Pitiot G, Della Gaspera B, Daubas P, Mallet J, Le Paslier D, Fischer Lindahl K, Dautigny A
Immunogenetics, 42(5):386-391, 01 Jan 1995
Cited by: 25 articles | PMID: 7590972
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Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex.
Pham-Dinh D, Mattei MG, Nussbaum JL, Roussel G, Pontarotti P, Roeckel N, Mather IH, Artzt K, Lindahl KF, Dautigny A
Proc Natl Acad Sci U S A, 90(17):7990-7994, 01 Sep 1993
Cited by: 113 articles | PMID: 8367453 | PMCID: PMC47273
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