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Results:
1-7
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Results: 7
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
Authors:
BRUZZONE R
RESSOT C
Citation: R. Bruzzone et C. Ressot, CONNEXINS, GAP-JUNCTIONS AND CELL-CELL SIGNALING IN THE NERVOUS-SYSTEM, European journal of neuroscience, 9(1), 1997, pp. 1-6
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
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
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
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
Authors:
LASSAGNE H
RESSOT C
MATTEI MG
GACHON AMF
Citation: H. Lassagne et al., ASSIGNMENT OF THE HUMAN TEAR LIPOCALIN GENE (LCN1) TO 9Q34 BY IN-SITUHYBRIDIZATION, Genomics, 18(1), 1993, pp. 160-161
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1-7
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