A. Dautigny

发表

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.

α1-microglobulin from normal and pathologigal urines

P. Jollès, I. Bernier, D. Gillessen, 1980 .

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.

Investigations on human leucocyte antigens (HLA) from urine

P. Jollès, I. Bernier, A. Dautigny, 1976, FEBS letters.

Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical Group.

J. Melki, B. Dastugue, O. Boespflug-Tanguy, 1994, American journal of human genetics.

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

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

Human urine as source of human leucocyte antigens. Purification and characterization of antigens from the first and second human leucocyte antigen locus, HLA-A9 and HLA-B12.

P. Jollès, I. Bernier, A. Dautigny, 1977, Biochimica et biophysica acta.

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 .

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

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

Molecular cloning and nucleotide sequence of a cDNA clone coding for rat brain myelin proteolipid

F. Galibert, P. Alliel, J. Nussbaum, 1985, FEBS letters.

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.

Human platelets as a source of HL-A antigens : a study of various solubilization techniques.

P. Jollès, I. Bernier, A. Dautigny, 1976, Biochimie.

Purification of HL‐A antigens from the urine of diseased and healthy individuals

P. Jollès, I. Bernier, A. Dautigny, 1974, FEBS letters.

Purification and characterization of HL-A antigens from human platelets, solubilized by the non-ionic detergent NP-40.

P. Jollès, I. Bernier, A. Dautigny, 1973, Biochimica et biophysica acta.

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.

Developmental expression of myelin proteolipid, basic protein, and 2′,3′-cyclic nucleotide 3′-phosphodiesterase transcripts in different rat brain regions

L. Bernier, A. Campagnoni, B. Zalc, 2008, Journal of Molecular Neuroscience.

Developmental expression of myelin proteolipid, basic protein, and 2′,3′-cyclic nucleotide 3′-phosphodiesterase transcripts in different rat brain regions

L. Bernier, A. Campagnoni, B. Zalc, 2008, Journal of Molecular Neuroscience.

Cell-free synthesis of hemocyanin from the scorpion Androctonus australis. Characterization of the translation products by monospecific antisera.

P. Jollès, P. Alliel, J. Lamy, 1983, European journal of biochemistry.

Detergent-solubilized HL-A antigens from human platelets: a comparative study of various purification techniques.

P. Jollès, I. Bernier, A. Dautigny, 1974, Biochimica et biophysica acta.

Major myelin proteolipid: The 4-α-helix topology

J. Popot, A. Dautigny, Danielle Pham Dinh, 1991, The Journal of Membrane Biology.

Immunological and serological data concerning human histocompatibility antigens (HLA) and alpha 1-microglobulin co-purified from urine.

P. Jollès, I. Bernier, A. Dautigny, 1979, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

Molecular data on urinary glycoproteins with human leucocyte antigen (HLA) activity.

P. Jollès, I. Bernier, J. Jollés, 1978, Biochimica et biophysica acta.

A molecular defect in thrombasthenic platelets.

N. Ardaillou, J. Brouet, L. Degos, 1975, The Journal of clinical investigation.

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.

Functional Analysis of the Mouse Myelin/Oligodendrocyte Glycoprotein Gene Promoter in the Oligodendroglial CG4 Cell Line

B. Zalc, P. Daubas, M. Monge, 1997, Journal of neurochemistry.

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

E. M. Prager, P. Jollès, B. Grinde, 1991, Journal of Molecular Evolution.

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

H. Nojima, J. Weinman, S. Weinman, 1991, Cell regulation.

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.

Spontaneous release of soluble HL-A antigens from platelets during conservation.

P. Jollès, I. Bernier, A. Dautigny, 1975, Immunological communications.

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.

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

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

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.

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

J. Popot, A. Dautigny, D. Pham Dinh, 1991, The Journal of membrane biology.

Characterization of α1-microglobulin in human colostrum and milk

P. Jollès, I. Bernier, A. Dautigny, 1980, Experientia.

alpha 1-Microglobulin from normal and pathological urines.

P. Jollès, I. Bernier, D. Gillessen, 1980, Biochimica et biophysica acta.

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.

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.

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.

Cell free synthesis of rat brain myelin proteolipids and their identification by immunoprecipitation.

P. Jollès, P. Alliel, J. Nussbaum, 1983, Biochemical and biophysical research communications.

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.

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 .