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Results: 1-20 |
Results: 20
CONNEXIN32 MUTATIONS ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTH DISEASE SHOW 2 DISTINCT BEHAVIORS - LOSS OF FUNCTION AND ALTERED GATING PROPERTIES
Authors: RESSOT C GOMES D DAUTIGNY A PHAMDINH D BRUZZONE R
Citation: C. Ressot et al., 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, 18(11), 1998, pp. 4063-4075
IDENTIFICATION OF A VAL-145-ILE SUBSTITUTION IN THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN - LACK OF ASSOCIATION WITH MULTIPLE-SCLEROSIS
Authors: RODRIGUEZ D DELLAGASPERA B ZALC B HAUW JJ FONTAINE B EDAN G CLANET M DAUTIGNY A PHAMDINH D
Citation: D. Rodriguez et al., IDENTIFICATION OF A VAL-145-ILE SUBSTITUTION IN THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN - LACK OF ASSOCIATION WITH MULTIPLE-SCLEROSIS, Multiple sclerosis, 3(6), 1997, pp. 377-381
3 GENES, 4 DEMYELINATING PERIPHERAL NEUROPATHIES - FIRST GENOTYPE PHENOTYPE CORRELATIONS/
Authors: PHAMDINH D BLANQUETGROSSARD F RESSOT C BRUZZONE R DAUTIGNY A
Citation: D. Phamdinh et al., 3 GENES, 4 DEMYELINATING PERIPHERAL NEUROPATHIES - FIRST GENOTYPE PHENOTYPE CORRELATIONS/, MS. Medecine sciences, 13(10), 1997, pp. 1113-1122
STUDIES ON MUTATED PLP IN IMMORTALIZED JIMPY OLIGODENDROCYTE CELL-LINES
Authors: GHANDOUR MS FEUTZ AC HUSS Y PHAMDINH D ALLINQUANT B MIEHE MM
Citation: Ms. Ghandour et al., STUDIES ON MUTATED PLP IN IMMORTALIZED JIMPY OLIGODENDROCYTE CELL-LINES, Journal of neurochemistry, 69, 1997, pp. 100-100
NEW MUTATIONS IN THE X-LINKED FORM OF CHARCOT-MARIE-TOOTH DISEASE
Authors: 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
Citation: P. Latour et al., NEW MUTATIONS IN THE X-LINKED FORM OF CHARCOT-MARIE-TOOTH DISEASE, European neurology, 37(1), 1997, pp. 38-42
CHARCOT-MARIE-TOOTH TYPE-1B NEUROPATHY - A MUTATION AT THE SINGLE GLYCOSYLATION SITE IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN-P0
Authors: BLANQUETGROSSARD E PHAMDINH D DAUTIGNY A LATOUR P BONNEBOUCHE C DIRAISON P CHAPON F CHAZOT G VANDENBERGHE A
Citation: E. Blanquetgrossard et al., CHARCOT-MARIE-TOOTH TYPE-1B NEUROPATHY - A MUTATION AT THE SINGLE GLYCOSYLATION SITE IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN-P0, Human mutation, 8(2), 1996, pp. 185-186
FUNCTIONAL-ANALYSIS OF CONNEXIN32 MUTATIONS ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTH DISEASE
Authors: RESSOT C GOMES D DAUTIGNY A PHAMDINH D BRUZZONE R
Citation: C. Ressot et al., FUNCTIONAL-ANALYSIS OF CONNEXIN32 MUTATIONS ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTH DISEASE, Molecular biology of the cell, 7, 1996, pp. 2681-2681
X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY (CMTX) - NEW MUTATIONS IN THE CONNEXIN32 GENE
Authors: RESSOT C LATOUR P BLANQUETGROSSARD F STURTZ F DUTHEL S BATTIN J CORBILLON E OLLAGNON E SERVILLE F VANDENBERGHE A DAUTIGNY A PHAMDINH D
Citation: C. Ressot et al., X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY (CMTX) - NEW MUTATIONS IN THE CONNEXIN32 GENE, Human genetics, 98(2), 1996, pp. 172-175
MUTATIONS IN THE MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 1B
Authors: 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
Citation: P. Latour et al., MUTATIONS IN THE MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 1B, Human mutation, 6(1), 1995, pp. 50-54
STRUCTURE OF THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN GENE AND MULTIPLE ALTERNATIVE SPLICED ISOFORMS
Authors: PHAMDINH D DELLAGASPERA B DEROSBO NK DAUTIGNY A
Citation: D. Phamdinh et al., STRUCTURE OF THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN GENE AND MULTIPLE ALTERNATIVE SPLICED ISOFORMS, Genomics, 29(2), 1995, pp. 345-352
PHYSICAL MAPPING OF THE HUMAN AND MOUSE MOG GENE AT THE DISTAL END OFTHE MHC CLASS IB REGION
Authors: PHAMDINH D JONES EP PITIOT G DELLAGASPERA B DAUBAS P MALLET J LEPASLIER D LINDAHL KF DAUTIGNY A
Citation: D. Phamdinh et al., PHYSICAL MAPPING OF THE HUMAN AND MOUSE MOG GENE AT THE DISTAL END OFTHE MHC CLASS IB REGION, Immunogenetics, 42(5), 1995, pp. 386-391
CHARCOT-MARIE-TOOTH TYPE 1B NEUROPATHY - 3RD MUTATION OF SERINE-63 CODON IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN P0 GENE
Authors: BLANQUETGROSSARD F PHAMDINH D DAUTIGNY A LATOUR P BONNEBOUCHE C CORBILLON E CHAZOT G VANDENBERGHE A
Citation: F. Blanquetgrossard et al., CHARCOT-MARIE-TOOTH TYPE 1B NEUROPATHY - 3RD MUTATION OF SERINE-63 CODON IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN P0 GENE, Clinical genetics, 48(6), 1995, pp. 281-283
GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP AND PLP
Authors: 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
Citation: R. Carsique et al., GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP AND PLP, American journal of human genetics, 57(4), 1995, pp. 1872-1872
STRUCTURE AND POLYMORPHISM OF THE MOUSE MYELIN OLIGODENDROCYTE GLYCOPROTEIN GENE/
Authors: DAUBAS P PHAMDINH D DAUTIGNY A
Citation: P. Daubas et al., STRUCTURE AND POLYMORPHISM OF THE MOUSE MYELIN OLIGODENDROCYTE GLYCOPROTEIN GENE/, Genomics, 23(1), 1994, pp. 36-41
RAPID SCREENING OF MYELIN GENES IN CMT1 PATIENTS BY SSCP ANALYSIS - IDENTIFICATION OF NEW MUTATIONS AND POLYMORPHISMS IN THE P-0 GENE
Authors: NELIS E TIMMERMAN V DEJONGHE P VANDENBERGHE A PHAMDINH D DAUTIGNY A MARTIN JJ VANBROECKHOVEN C
Citation: E. Nelis et al., RAPID SCREENING OF MYELIN GENES IN CMT1 PATIENTS BY SSCP ANALYSIS - IDENTIFICATION OF NEW MUTATIONS AND POLYMORPHISMS IN THE P-0 GENE, Human genetics, 94(6), 1994, pp. 653-657
CHARACTERIZATION AND EXPRESSION OF THE CDNA CODING FOR THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN/
Authors: PHAMDINH D ALLINQUANT B RUBERG M DELLAGASPERA B NUSSBAUM JL DAUTIGNY A
Citation: D. Phamdinh et al., CHARACTERIZATION AND EXPRESSION OF THE CDNA CODING FOR THE HUMAN MYELIN OLIGODENDROCYTE GLYCOPROTEIN/, Journal of neurochemistry, 63(6), 1994, pp. 2353-2356
THE MAJOR PERIPHERAL MYELIN PROTEIN ZERO GENE - STRUCTURE AND LOCALIZATION IN THE CLUSTER OF FC-GAMMA RECEPTOR GENES ON HUMAN-CHROMOSOME 1Q21.3-Q23
Authors: PHAMDINH D FOURBIL Y BLANQUET F MATTEI MG ROECKEL N LATOUR P CHAZOT G VANDENBERGHE A DAUTIGNY A
Citation: D. Phamdinh et al., 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, 2(12), 1993, pp. 2051-2054
THE ESCHERICHIA-COLI ENVY GENE ENCODES A HIGH-AFFINITY OPIOID BINDING-SITE
Authors: CABON F MORSER J PARMANTIER E SOLLY SK PHAMDINH D ZALC B
Citation: F. Cabon et al., THE ESCHERICHIA-COLI ENVY GENE ENCODES A HIGH-AFFINITY OPIOID BINDING-SITE, Neurochemical research, 18(7), 1993, pp. 795-800
INFANTILE NEUROPATHY WITH UNSTABLE MYELIN - STUDY OF THE PO PROTEIN
Authors: PEUDENIER S DELEUZE JF PHAMDINH D LACROIX C BOULLOCHE J LANDRIEU P
Citation: S. Peudenier et al., INFANTILE NEUROPATHY WITH UNSTABLE MYELIN - STUDY OF THE PO PROTEIN, Journal of neurology, 240(5), 1993, pp. 291-294
MYELIN OLIGODENDROCYTE GLYCOPROTEIN IS A MEMBER OF A SUBSET OF THE IMMUNOGLOBULIN SUPERFAMILY ENCODED WITHIN THE MAJOR HISTOCOMPATIBILITY COMPLEX
Authors: PHAMDINH D MATTEI MG NUSSBAUM JL ROUSSEL G PONTAROTTI P ROECKEL N MATHER IH ARTZT K LINDAHL KF DAUTIGNY A
Citation: D. Phamdinh et al., 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, 90(17), 1993, pp. 7990-7994
Risultati: 1-20 |