D. Pham‐Dinh

发表

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

N. Baumann, D. Pham‐Dinh, N. Baumann, 2001, Physiological reviews.

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

Anne Baron-Van Evercooren, D. Pham‐Dinh, R. Liblau, 2002, Proceedings of the National Academy of Sciences of the United States of America.

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

D. Pham‐Dinh, P. Kitabgi, A. Nicot, 2010, Proceedings of the National Academy of Sciences.

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

D. Pham‐Dinh, M. Ghandour, M. Miehe, 2001, Glia.

Connexin32 Mutations Associated with X-Linked Charcot–Marie–Tooth Disease Show Two Distinct Behaviors: Loss of Function and Altered Gating Properties

D. Pham‐Dinh, R. Bruzzone, C. Ressot, 1998, The Journal of Neuroscience.

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

D. Pham‐Dinh, R. Reynolds, J. Levine, 2002, Journal of neurocytology.

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

D. Pham‐Dinh, G. Chazot, M. Mattei, 1993, Human molecular genetics.

Mutations in the myelin protein zero gene associated with Charcot‐Marie‐Tooth disease type 1B

C. van Broeckhoven, D. Pham‐Dinh, G. Chazot, 1995, Human mutation.

Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation.

E. Bertini, D. Pham‐Dinh, R. Surtees, 2001, American journal of human genetics.

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

D. Pham‐Dinh, D. Baker, S. Amor, 2002, Journal of Neuroimmunology.

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

D. Pham‐Dinh, T. Olsson, M. Jagodic, 2003, Neuroscience Letters.

Autoimmunity Against Myelin Oligodendrocyte Glycoprotein Is Dispensable for the Initiation Although Essential for the Progression of Chronic Encephalomyelitis in Common Marmosets

D. Pham‐Dinh, B. '. ’t Hart, J. Laman, 2008, Journal of neuropathology and experimental neurology.

X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene

D. Pham‐Dinh, P. Latour, F. Sturtz, 1996, Human Genetics.

Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease.

D. Pham‐Dinh, D. Rodriguez, O. Boespflug-Tanguy, 2007, Experimental cell research.

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene

C. Broeckhoven, D. Pham‐Dinh, V. Timmerman, 1994, Human Genetics.

Charcot‐Marie‐Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein P0 gene

D. Pham‐Dinh, G. Chazot, P. Latour, 1995 .

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

D. Pham‐Dinh, B. Nait-Oumesmar, F. Lachapelle, 2007, Revue neurologique.

Characterization and Expression of the cDNA Coding for the Human Myelin/Oligodendrocyte Glycoprotein

M. Ruberg, D. Pham‐Dinh, B. Allinquant, 1994, Journal of neurochemistry.

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

D. Pham‐Dinh, B. '. ’t Hart, C. Delarasse, 2005, European journal of immunology.

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

D. Pham‐Dinh, J. Honnorat, M. Ghandour, 2012, International Journal of Developmental Neuroscience.

Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex.

K. Artzt, D. Pham‐Dinh, M. Mattei, 1993, Proceedings of the National Academy of Sciences of the United States of America.

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

D. Pham‐Dinh, R. Reynolds, L. Ewans, 2006, Molecular and cellular neurosciences.

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

D. Pham‐Dinh, J. Popot, J. Deleuze, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Linkage analysis of candidate myelin genes in familial multiple sclerosis

J. Haines, M. Pericak-Vance, G. Gyapay, 1999, Neurogenetics.

Identification of a Val I 45 IIe substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis

J. Hauw, D. Pham‐Dinh, B. Zalc, 1997 .

Alexander disease: putative mechanisms of an astrocytic encephalopathy

D. Pham‐Dinh, D. Rodriguez, O. Boespflug-Tanguy, 2004, Cellular and Molecular Life Sciences CMLS.

Developmental regulation ofcalmodulin gene expression inratbrain andskeletal muscle

D. Pham‐Dinh, H. Nojima, J. Weinman, 1991 .

The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome

D. Pham‐Dinh, M. Mattei, P. Jollès, 1986, Human Genetics.

Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two cases

D. Pham‐Dinh, D. Rodriguez, G. Ponsot, 1999, Acta Neuropathologica.

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

D. Pham‐Dinh, P. Villoslada, C. Delarasse, 2006, Proceedings of the National Academy of Sciences of the United States of America.

The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice

D. Simon, P. Avner, D. Pham‐Dinh, 1986, Nature.

Biology of Demyelinating Diseases

N. Baumann, D. Pham‐Dinh, 2011 .

Evidence for Cytokine Dysregulation in Multiple Sclerosis: Peripheral Blood Mononuclear Cell Production of Pro-inflammatory and Anti-inflammatory Cytokines During Relapse and Remission

D. Pham‐Dinh, L. Harbige, M. Sharief, 2003, Autoimmunity.

Complex alternative splicing of the myelin oligodendrocyte glycoprotein gene is unique to human and non‐human primates

D. Pham‐Dinh, D. Rodriguez, A. Gelot, 2006, Journal of neurochemistry.

Structure of the human myelin/oligodendrocyte glycoprotein gene and multiple alternative spliced isoforms.

D. Pham‐Dinh, N. Kerlero de Rosbo, A. Dautigny, 1995, Genomics.

Proteolipid DM-20 predominates over PLP in peripheral nervous system.

D. Pham‐Dinh, G. Roussel, M. Birling, 1991, Neuroreport.

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

L. Hertz-Pannier, D. Pham‐Dinh, D. Rodriguez, 2009, Brain and Development.

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

D. Pham‐Dinh, R. Reynolds, D. Papadopoulos, 2006, Experimental Neurology.

The large neurofilament subunit (NF-H) of the rat: cDNA cloning and in situ detection.

D. Pham‐Dinh, P. Jollès, J. Nussbaum, 1988, Biochemical and biophysical research communications.

Myelin Oligodendrocyte Glycoprotein Gene

D. Pham‐Dinh, C. Linington, A. Dautigny, 2003 .

Physical mapping of the human and mouse MOG gene at the distal end of the MHC class Ib region

D. Paslier, J. Mallet, D. Pham‐Dinh, 2004, Immunogenetics.

Myelin/oligodendrocyte glycoprotein-deficient (MOG-deficient) mice reveal lack of immune tolerance to MOG in wild-type mice.

D. Pham‐Dinh, A. Dierich, R. Liblau, 2003, The Journal of clinical investigation.

Upregulation of α-synuclein in neurons and glia in inflammatory demyelinating disease

D. Pham‐Dinh, R. Reynolds, L. Ewans, 2006, Molecular and Cellular Neuroscience.

Myelin proteolipid protein (PLP and DM‐20) transcripts are deleted in jimpy mutant mice.

D. Pham‐Dinh, P. Jollès, D. Morello, 1986, The EMBO journal.

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

D. Pham‐Dinh, O. Boespflug-Tanguy, G. Giraud, 1993, Human molecular genetics.

Development of Myelin Oligodendrocyte Glycoprotein Autoreactive Transgenic B Lymphocytes: Receptor Editing In Vivo After Encounter of a Self-Antigen Distinct from Myelin Oligodendrocyte Glycoprotein

D. Pham‐Dinh, H. Wekerle, H. Blüthmann, 2000, The Journal of Immunology.

New mutations in the X-linked form of Charcot-Marie-Tooth disease.

D. Pham‐Dinh, G. Chazot, P. Calvas, 1997, European neurology.

Charcot‐Marie‐Tooth type 1B neuropathy: A mutation at the single glycosylation site in the major peripheral myelin glycoprotein P0

D. Pham‐Dinh, G. Chazot, F. Chapon, 1996 .

In situ localization of NF-H neurofilament subunit mRNAs in rat brain.

D. Pham‐Dinh, P. Jollès, G. Roussel, 1991, Developmental neuroscience.

Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po.

D. Pham‐Dinh, G. Chazot, F. Chapon, 1996, Human mutation.

Membrane topology of the myelin/oligodendrocyte glycoprotein.

D. Pham‐Dinh, G. Roussel, J. Nussbaum, 1998, European journal of biochemistry.

Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO gene.

D. Pham‐Dinh, G. Chazot, P. Latour, 1995, Clinical Genetics.

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

D. Pham‐Dinh, N. Fazilleau, J. Kanellopoulos, 2006, European journal of immunology.

The gene encoding the large human neurofilament subunit (NF-H) maps to the q121–q131 region on human chromosome 22

D. Pham‐Dinh, M. Mattei, J. Mattéi, 1988, Human Genetics.

Myelin Oligodendrocyte Glycoprotein Encounter of a Self-Antigen Distinct from Lymphocytes : Receptor Editing In Vivo After Glycoprotein Autoreactive Transgenic B Development of Myelin Oligodendrocyte

D. Pham‐Dinh, H. Wekerle, H. Blüthmann, 2000 .

T Cell Repertoire Diversity Is Required for Relapses in Myelin Oligodendrocyte Glycoprotein-Induced Experimental Autoimmune Encephalomyelitis1

D. Pham‐Dinh, N. Fazilleau, P. Kourilsky, 2007, The Journal of Immunology.

Autoimmune Encephalomyelitis Glycoprotein-Induced Experimental Relapses in Myelin Oligodendrocyte T Cell Repertoire Diversity Is Required for

D. Pham‐Dinh, N. Fazilleau, P. Kourilsky, 2007 .