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Items: 1 to 50 of 68

1.

The Brown Norway opticospinal model of demyelination: does it mimic multiple sclerosis or neuromyelitis optica?

Collongues N, Chanson JB, Blanc F, Steibel J, Lam CD, Shabbir A, Trifilieff E, Honnorat J, Pham-Dinh D, Ghandour MS, de Seze J.

Int J Dev Neurosci. 2012 Oct;30(6):487-97. doi: 10.1016/j.ijdevneu.2012.05.004. Epub 2012 May 24.

PMID:
22634288
2.

Estradiol inhibits ongoing autoimmune neuroinflammation and NFkappaB-dependent CCL2 expression in reactive astrocytes.

Giraud SN, Caron CM, Pham-Dinh D, Kitabgi P, Nicot AB.

Proc Natl Acad Sci U S A. 2010 May 4;107(18):8416-21. doi: 10.1073/pnas.0910627107. Epub 2010 Apr 19.

3.

Tumor-like enlargement of the optic chiasm in an infant with Alexander disease.

Mignot C, Desguerre I, Burglen L, Hertz-Pannier L, Renaldo F, Gadisseux JF, Gallet S, Pham-Dinh D, Boespflug-Tanguy O, Rodriguez D.

Brain Dev. 2009 Mar;31(3):244-7. doi: 10.1016/j.braindev.2008.05.005. Epub 2008 Jun 26.

PMID:
18584981
4.

Autoimmunity against myelin oligodendrocyte glycoprotein is dispensable for the initiation although essential for the progression of chronic encephalomyelitis in common marmosets.

Jagessar SA, Smith PA, Blezer E, Delarasse C, Pham-Dinh D, Laman JD, Bauer J, Amor S, 't Hart B.

J Neuropathol Exp Neurol. 2008 Apr;67(4):326-40. doi: 10.1097/NEN.0b013e31816a6851.

PMID:
18379435
5.

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. 2007 Aug 1;313(13):2766-79. Epub 2007 May 24.

PMID:
17604020
6.

[Promoting myelin repair in disorders such as multiple sclerosis and some types of leukodystrophy: current studies].

Baron-Van Evercooren A, Lachapelle F, Nait-Oumesmar B, Pham-Dinh D.

Rev Neurol (Paris). 2007 May;163(5):523-31. Review. French.

PMID:
17571021
7.

T cell repertoire diversity is required for relapses in myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis.

Fazilleau N, Delarasse C, Motta I, Fillatreau S, Gougeon ML, Kourilsky P, Pham-Dinh D, Kanellopoulos JM.

J Immunol. 2007 Apr 15;178(8):4865-75.

8.

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. 2006 Sep;98(6):1707-17. Epub 2006 Aug 11.

9.

Persistence of autoreactive myelin oligodendrocyte glycoprotein (MOG)-specific T cell repertoires in MOG-expressing mice.

Fazilleau N, Delarasse C, Sweenie CH, Anderton SM, Fillatreau S, Lemonnier FA, Pham-Dinh D, Kanellopoulos JM.

Eur J Immunol. 2006 Mar;36(3):533-43.

10.

Upregulation of alpha-synuclein in neurons and glia in inflammatory demyelinating disease.

Papadopoulos D, Ewans L, Pham-Dinh D, Knott J, Reynolds R.

Mol Cell Neurosci. 2006 Apr;31(4):597-612. Epub 2006 Feb 28.

PMID:
16503161
11.

Antibodies to native myelin oligodendrocyte glycoprotein are serologic markers of early inflammation in multiple sclerosis.

Lalive PH, Menge T, Delarasse C, Della Gaspera B, Pham-Dinh D, Villoslada P, von Büdingen HC, Genain CP.

Proc Natl Acad Sci U S A. 2006 Feb 14;103(7):2280-5. Epub 2006 Feb 3.

12.

Axon loss is responsible for chronic neurological deficit following inflammatory demyelination in the rat.

Papadopoulos D, Pham-Dinh D, Reynolds R.

Exp Neurol. 2006 Feb;197(2):373-85. Epub 2005 Dec 9.

PMID:
16337942
13.

Native myelin oligodendrocyte glycoprotein promotes severe chronic neurological disease and demyelination in Biozzi ABH mice.

Smith PA, Heijmans N, Ouwerling B, Breij EC, Evans N, van Noort JM, Plomp AC, Delarasse C, 't Hart B, Pham-Dinh D, Amor S.

Eur J Immunol. 2005 Apr;35(4):1311-9.

14.

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. 2004 Feb;61(3):369-85. Review.

PMID:
14770299
15.

Myelin oligodendrocyte glycoprotein is expressed in the peripheral nervous system of rodents and primates.

Pagany M, Jagodic M, Schubart A, Pham-Dinh D, Bachelin C, Baron van Evercooren A, Lachapelle F, Olsson T, Linington C.

Neurosci Lett. 2003 Oct 30;350(3):165-8.

PMID:
14550920
16.

The response of NG2-expressing oligodendrocyte progenitors to demyelination in MOG-EAE and MS.

Reynolds R, Dawson M, Papadopoulos D, Polito A, Di Bello IC, Pham-Dinh D, Levine J.

J Neurocytol. 2002 Jul-Aug;31(6-7):523-36.

PMID:
14501221
17.

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. 2003 Aug;112(4):544-53.

19.

Experimental autoimmune encephalomyelitis mobilizes neural progenitors from the subventricular zone to undergo oligodendrogenesis in adult mice.

Picard-Riera N, Decker L, Delarasse C, Goude K, Nait-Oumesmar B, Liblau R, Pham-Dinh D, Baron-Van Evercooren A.

Proc Natl Acad Sci U S A. 2002 Oct 1;99(20):13211-6. Epub 2002 Sep 16.

20.

Pathological and regulatory effects of anti-myelin antibodies in experimental allergic encephalomyelitis in mice.

Morris-Downes MM, Smith PA, Rundle JL, Piddlesden SJ, Baker D, Pham-Dinh D, Heijmans N, Amor S.

J Neuroimmunol. 2002 Apr;125(1-2):114-24.

PMID:
11960647
21.

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. 2001 Nov;69(5):1134-40. Epub 2001 Sep 20. Erratum in: Am J Hum Genet 2001 Dec;69(6):1413.

22.

An immortalized jimpy oligodendrocyte cell line: defects in cell cycle and cAMP pathway.

Feutz AC, Pham-Dinh D, Allinquant B, Miehe M, Ghandour MS.

Glia. 2001 Jun;34(4):241-52.

PMID:
11360297
23.

Biology of oligodendrocyte and myelin in the mammalian central nervous system.

Baumann N, Pham-Dinh D.

Physiol Rev. 2001 Apr;81(2):871-927. Review.

24.
25.

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, Rimmler JB, Garcia ME, Pericak-Vance MA, Haines JL, Hauser SL.

Neurogenetics. 1999 Sep;2(3):155-62.

PMID:
10541588
26.

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. 1999 May;97(5):469-80.

PMID:
10334484
27.

Membrane topology of the myelin/oligodendrocyte glycoprotein.

della Gaspera B, Pham-Dinh D, Roussel G, Nussbaum JL, Dautigny A.

Eur J Biochem. 1998 Dec 1;258(2):478-84.

28.
30.

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. 1997;37(1):38-42. Review.

PMID:
9018031
31.

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. 1996 Aug;98(2):172-5.

PMID:
8698335
32.

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. 1996;8(2):185-6. No abstract available.

PMID:
8844219
33.

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. 1995 Dec;48(6):281-3.

PMID:
8835320
34.

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. 1995 Sep 20;29(2):345-52.

PMID:
8666381
35.

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. 1995;42(5):386-91.

PMID:
7590972
36.

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, et al.

Hum Mutat. 1995;6(1):50-4.

PMID:
7550231
37.

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. 1994 Dec;63(6):2353-6.

PMID:
7964757
38.

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. 1994 Dec;94(6):653-7.

PMID:
7527371
39.

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. 1994 Sep;55(3):461-7.

40.

Structure and polymorphism of the mouse myelin/oligodendrocyte glycoprotein gene.

Daubas P, Pham-Dinh D, Dautigny A.

Genomics. 1994 Sep 1;23(1):36-41.

PMID:
7829100
41.

The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23.

Pham-Dinh D, Fourbil Y, Blanquet F, Mattéi MG, Roeckel N, Latour P, Chazot G, Vandenberghe A, Dautigny A.

Hum Mol Genet. 1993 Dec;2(12):2051-4.

PMID:
7509228
42.

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. 1993 Sep 1;90(17):7990-4.

43.

The E. coli envY gene encodes a high affinity opioid binding site.

Cabon F, Morser J, Parmantier E, Solly SK, Pham-Dinh D, Zalc B.

Neurochem Res. 1993 Jul;18(7):795-800.

PMID:
8396214
44.

Infantile neuropathy with unstable myelin: study of the P0 protein.

Peudenier S, Deleuze JF, Pham-Dinh D, Lacroix C, Boulloche J, Landrieu P.

J Neurol. 1993 May;240(5):291-4.

PMID:
7686967
45.

Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid gene.

Pham-Dinh D, Boespflug-Tanguy O, Mimault C, Cavagna A, Giraud G, Leberre G, Lemarec B, Dautigny A.

Hum Mol Genet. 1993 Apr;2(4):465-7.

PMID:
7684945
46.

Developmental regulation of calmodulin gene expression in rat brain and skeletal muscle.

Weinman J, Della Gaspera B, Dautigny A, Pham Dinh D, Wang J, Nojima H, Weinman S.

Cell Regul. 1991 Oct;2(10):819-26.

47.

Major myelin proteolipid: the 4-alpha-helix topology.

Popot JL, Pham Dinh D, Dautigny A.

J Membr Biol. 1991 Sep;123(3):278. No abstract available.

PMID:
1744907
48.

Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.

Pham-Dinh D, Popot JL, Boespflug-Tanguy O, Landrieu P, Deleuze JF, Boué J, Jollès P, Dautigny A.

Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7562-6.

49.

Major Myelin proteolipid: the 4-alpha-helix topology.

Popot JL, Pham Dinh D, Dautigny A.

J Membr Biol. 1991 Mar;120(3):233-46. Erratum in: J Membr Biol. 1991 Sep;123(3):278.

PMID:
1711121
50.

cDNA and amino acid sequences of rainbow trout (Oncorhynchus mykiss) lysozymes and their implications for the evolution of lysozyme and lactalbumin.

Dautigny A, Prager EM, Pham-Dinh D, Jollès J, Pakdel F, Grinde B, Jollès P.

J Mol Evol. 1991 Feb;32(2):187-98.

PMID:
1901095

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