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La ricerca find articoli where authors phrase all words ' Dautigny, A' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 24 riferimenti
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    1. 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
      Infantile Alexander disease: Spectrum of GFAP mutations and genotype-phenotype correlation

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Litzenburger, T; Bluthmann, H; Morales, P; Pham-Dinh, D; Dautigny, A; Wekerle, H; Iglesias, A
      Development of myelin oligodendrocyte glycoprotein autoreactive transgenicB lymphocytes: Receptor editing in vivo after encounter of a self-antigen distinct from myelin oligodendrocyte glycoprotein

      JOURNAL OF IMMUNOLOGY
    3. Rodriguez, D; Gelot, A; della Gaspera, B; Robain, O; Ponsot, G; Sarlieve, LL; Ghandour, S; Pompidou, A; Dautigny, A; Aubourg, P; Pham-Dinh, D
      Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two cases

      ACTA NEUROPATHOLOGICA
    4. RESSOT C; GOMES D; DAUTIGNY A; PHAMDINH D; BRUZZONE R
      CONNEXIN32 MUTATIONS ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTH DISEASE SHOW 2 DISTINCT BEHAVIORS - LOSS OF FUNCTION AND ALTERED GATING PROPERTIES

      The Journal of neuroscience
    5. Della Gaspera, B; Pham-Dinh, D; Roussel, G; Nussbaum, JL; Dautigny, A
      Membrane topology of the myelin/oligodendrocyte glycoprotein

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    6. RODRIGUEZ D; DELLAGASPERA B; ZALC B; HAUW JJ; FONTAINE B; EDAN G; CLANET M; DAUTIGNY A; PHAMDINH D
      IDENTIFICATION OF A VAL-145-ILE SUBSTITUTION IN THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN - LACK OF ASSOCIATION WITH MULTIPLE-SCLEROSIS

      Multiple sclerosis
    7. PHAMDINH D; BLANQUETGROSSARD F; RESSOT C; BRUZZONE R; DAUTIGNY A
      3 GENES, 4 DEMYELINATING PERIPHERAL NEUROPATHIES - FIRST GENOTYPE PHENOTYPE CORRELATIONS/

      MS. Medecine sciences
    8. SOLLY SK; DAUBAS P; MONGE M; DAUTIGNY A; ZALC B
      FUNCTIONAL-ANALYSIS OF THE MOUSE MYELIN OLIGODENDROCYTE GLYCOPROTEIN GENE PROMOTER IN THE OLIGODENDROGLIAL CG4 CELL-LINE/

      Journal of neurochemistry
    9. LATOUR P; FABREGUETTE A; RESSOT C; BLANQUETGROSSARD F; ANTOINE JC; CALVAS P; CHAPON F; CORBILLON E; OLLAGNON E; STURTZ F; BOUCHERAT M; CHAZOT G; DAUTIGNY A; PHAMDINH D; VANDENBERGHE A
      NEW MUTATIONS IN THE X-LINKED FORM OF CHARCOT-MARIE-TOOTH DISEASE

      European neurology
    10. BLANQUETGROSSARD E; PHAMDINH D; DAUTIGNY A; LATOUR P; BONNEBOUCHE C; DIRAISON P; CHAPON F; CHAZOT G; VANDENBERGHE A
      CHARCOT-MARIE-TOOTH TYPE-1B NEUROPATHY - A MUTATION AT THE SINGLE GLYCOSYLATION SITE IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN-P0

      Human mutation
    11. RESSOT C; GOMES D; DAUTIGNY A; PHAMDINH D; BRUZZONE R
      FUNCTIONAL-ANALYSIS OF CONNEXIN32 MUTATIONS ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTH DISEASE

      Molecular biology of the cell
    12. RESSOT C; LATOUR P; BLANQUETGROSSARD F; STURTZ F; DUTHEL S; BATTIN J; CORBILLON E; OLLAGNON E; SERVILLE F; VANDENBERGHE A; DAUTIGNY A; PHAMDINH D
      X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY (CMTX) - NEW MUTATIONS IN THE CONNEXIN32 GENE

      Human genetics
    13. SEBOUN E; CARSIQUE R; PAHMDINH D; BOESPFLUGTANGUY O; GOODKIN DE; LATHROP M; RIMMLER J; HAINES JL; OKSENBERG J; FIZAMES C; LINCOLN R; PERICAKVANCE MA; GUSELLA JF; ROSES AD; WEISSENBACH J; DAUTIGNY A; HAUSER SL
      GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP, AND PLP

      Neurology
    14. LATOUR P; BLANQUET F; NELIS E; BONNEBOUCHE C; CHAPON F; DIRAISON P; OLLAGNON E; DAUTIGNY A; PHAMDINH D; CHAZOT G; BOUCHERAT M; VANBROECKHOVEN C; VANDENBERGHE A
      MUTATIONS IN THE MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 1B

      Human mutation
    15. PHAMDINH D; DELLAGASPERA B; DEROSBO NK; DAUTIGNY A
      STRUCTURE OF THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN GENE AND MULTIPLE ALTERNATIVE SPLICED ISOFORMS

      Genomics
    16. PHAMDINH D; JONES EP; PITIOT G; DELLAGASPERA B; DAUBAS P; MALLET J; LEPASLIER D; LINDAHL KF; DAUTIGNY A
      PHYSICAL MAPPING OF THE HUMAN AND MOUSE MOG GENE AT THE DISTAL END OFTHE MHC CLASS IB REGION

      Immunogenetics
    17. BLANQUETGROSSARD F; PHAMDINH D; DAUTIGNY A; LATOUR P; BONNEBOUCHE C; CORBILLON E; CHAZOT G; VANDENBERGHE A
      CHARCOT-MARIE-TOOTH TYPE 1B NEUROPATHY - 3RD MUTATION OF SERINE-63 CODON IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN P0 GENE

      Clinical genetics
    18. CARSIQUE R; PHAMDINH D; BOESPFLUGTANGUY O; GOODKIN DE; LATHROP M; RIMMLER J; HAINES JL; OKSENBERG J; FIZAMES C; LINCOLN R; PERICAKVANCE MA; GUSELLA JF; ROSES AD; WEISSENBACH J; DAUTIGNY A; HAUSER SL; SEBOUN E
      GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP AND PLP

      American journal of human genetics
    19. DAUBAS P; PHAMDINH D; DAUTIGNY A
      STRUCTURE AND POLYMORPHISM OF THE MOUSE MYELIN OLIGODENDROCYTE GLYCOPROTEIN GENE/

      Genomics
    20. NELIS E; TIMMERMAN V; DEJONGHE P; VANDENBERGHE A; PHAMDINH D; DAUTIGNY A; MARTIN JJ; VANBROECKHOVEN C
      RAPID SCREENING OF MYELIN GENES IN CMT1 PATIENTS BY SSCP ANALYSIS - IDENTIFICATION OF NEW MUTATIONS AND POLYMORPHISMS IN THE P-0 GENE

      Human genetics
    21. PHAMDINH D; ALLINQUANT B; RUBERG M; DELLAGASPERA B; NUSSBAUM JL; DAUTIGNY A
      CHARACTERIZATION AND EXPRESSION OF THE CDNA CODING FOR THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN/

      Journal of neurochemistry
    22. BOESPFLUGTANGUY O; MIMAULT C; MELKI J; CAVAGNA A; GIRAUD G; DINH DP; DASTUGUE B; DAUTIGNY A; AICARDI J; GOUTTIERES F; BAUMANN N; BERTINI E; DAVID A; HENOCQ A; LANDRIEU P; TARDIEU M; LEBERRE C; LEMAREC B; LYON G; MAYER M; PINARD JM; PONSOT G; MATHIEU M; SAINTIVE JP; SAURA R; VALLEE L
      GENETIC HOMOGENEITY OF PELIZAEUS-MERZBACHER-DISEASE - TIGHT LINKAGE TO THE PROTEOLIPOPROTEIN LOCUS IN 16 AFFECTED FAMILIES

      American journal of human genetics
    23. PHAMDINH D; FOURBIL Y; BLANQUET F; MATTEI MG; ROECKEL N; LATOUR P; CHAZOT G; VANDENBERGHE A; DAUTIGNY A
      THE MAJOR PERIPHERAL MYELIN PROTEIN ZERO GENE - STRUCTURE AND LOCALIZATION IN THE CLUSTER OF FC-GAMMA RECEPTOR GENES ON HUMAN-CHROMOSOME 1Q21.3-Q23

      Human molecular genetics
    24. PHAMDINH D; MATTEI MG; NUSSBAUM JL; ROUSSEL G; PONTAROTTI P; ROECKEL N; MATHER IH; ARTZT K; LINDAHL KF; DAUTIGNY A
      MYELIN OLIGODENDROCYTE GLYCOPROTEIN IS A MEMBER OF A SUBSET OF THE IMMUNOGLOBULIN SUPERFAMILY ENCODED WITHIN THE MAJOR HISTOCOMPATIBILITY COMPLEX

      Proceedings of the National Academy of Sciences of the United Statesof America


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 01:05:24