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GALAND C
BOURNIER O
CYNOBER T
MECHINAUD F
TCHEMIA G
GARBARZ M
Citation: D. Dhermy et al., HEREDITARY SPHEROCYTOSIS WITH SPECTRIN DEFICIENCY RELATED TO NULL MUTATIONS OF THE BETA-SPECTRIN GENE, Blood cells, molecules, & diseases (Print), 24(12), 1998, pp. 251-261
Authors:
NICOLAS G
PEDRONI S
FOURNIER C
GAUTERO H
CRAESCU C
DHERMY D
LECOMTE MC
Citation: G. Nicolas et al., SPECTRIN SELF-ASSOCIATION SITE - CHARACTERIZATION AND STUDY OF BETA-SPECTRIN MUTATIONS ASSOCIATED WITH HEREDITARY ELLIPTOCYTOSIS, Biochemical journal, 332, 1998, pp. 81-89
Authors:
GARBARZ M
GALAND C
BIBAS D
BOURNIER O
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HAROUSSEAU JL
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DHERMY D
Citation: M. Garbarz et al., A 5'-SPLICE REGION G-]C MUTATION IN EXON-3 OF THE HUMAN BETA-SPECTRINGENE LEADS TO DECREASED LEVELS OF BETA-SPECTRIN MESSENGER-RNA AND IS RESPONSIBLE FOR DOMINANT HEREDITARY SPHEROCYTOSIS (SPECTRIN GUEMENE-PENFAO), British Journal of Haematology, 100(1), 1998, pp. 90-98
Authors:
DHERMY D
GALAND C
BOURNIER O
KING MJ
CYNOBER T
ROBERTS I
KANYIKE F
ADEKILE A
Citation: D. Dhermy et al., COINHERITANCE OF ALPHA-SPECTRIN AND BETA-SPECTRIN GENE-MUTATIONS IN ACASE OF HEREDITARY ELLIPTOCYTOSIS, Blood, 92(11), 1998, pp. 4481-4482
Authors:
DHERMY D
GALAND C
BOURNIER O
BOULANGER L
CYNOBER T
SCHISMANOFF PO
BURSAUX E
TCHERNIA G
BOIVIN P
GARBARZ M
Citation: D. Dhermy et al., HETEROGENOUS BAND-3 DEFICIENCY IN HEREDITARY SPHEROCYTOSIS RELATED TODIFFERENT BAND-3 GENE DEFECTS. (VOL 98, PG 32, 1997), British Journal of Haematology, 99(2), 1997, pp. 474-474
Authors:
DHERMY D
GALAND C
BOURNIER O
BOULANGER L
CYNOBER T
SCHISMANOFF PO
BURSAUX E
TCHERNIA G
BOIVIN P
GARBARZ M
Citation: D. Dhermy et al., HETEROGENOUS BAND-3 DEFICIENCY IN HEREDITARY SPHEROCYTOSIS RELATED TODIFFERENT BAND-3 GENE DEFECTS, British Journal of Haematology, 98(1), 1997, pp. 32-40
Authors:
FOURNIER CM
NICOLAS G
GALLAGHER PG
DHERMY D
GRANDCHAMP B
LECOMTE MC
Citation: Cm. Fournier et al., SPECTRIN ST CLAUDE, A SPLICING MUTATION OF THE HUMAN ALPHA-SPECTRIN GENE ASSOCIATED WITH SEVERE POIKILOCYTIC ANEMIA, Blood, 89(12), 1997, pp. 4584-4590
Authors:
SILVEIRA P
CYNOBER T
DHERMY D
MOHANDAS N
TCHERNIA G
Citation: P. Silveira et al., RED-BLOOD-CELL ABNORMALITIES IN HEREDITARY ELLIPTOCYTOSIS AND THEIR RELEVANCE TO VARIABLE CLINICAL EXPRESSION, American journal of clinical pathology, 108(4), 1997, pp. 391-399
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FOURNIER C
DEREGNAUCOURT C
GRELLIER P
DHERMY D
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SCHREVEL J
Citation: S. Lebonniec et al., HUMAN ERYTHROID SPECTRIN ALPHA-SUBUNIT AND ITS SH3 DOMAIN ARE SENSITIVE TO ACIDIC PLASMODIUM-FALCIPARUM PROTEOLYTIC ACTIVITY, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 319(11), 1996, pp. 1011-1017
Authors:
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BIBAS D
CYNOBER T
GALAND C
BOURNIER O
DEVAUX I
TCHERNIA G
DHERMY D
Citation: M. Garbarz et al., SEARCH FOR THE CANDIDATE GENES IN DOMINANT HEREDITARY SPHEROCYTOSIS USING LINKAGE ANALYSIS, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 319(10), 1996, pp. 913-919
Citation: Am. Maurer et al., INHIBITORY EFFECT OF PLATELET FACTOR-4 ON HUMAN ERYTHROLEUKEMIC CELLSIS DEPENDENT ON CELL-SURFACE HEPARAN-SULFATE, The Journal of laboratory and clinical medicine, 127(4), 1996, pp. 382-390
Authors:
JENKINS PB
ABOUALFA GK
DHERMY D
BURSAUX E
FEO C
SCARPA AL
LUX SE
GARBARZ M
FORGET BG
GALLAGHER PG
Citation: Pb. Jenkins et al., NONSENSE MUTATION IN THE ERYTHROCYTE BAND-3 GENE ASSOCIATED WITH DECREASED MESSENGER-RNA ACCUMULATION IN A KINDRED WITH DOMINANT HEREDITARYSPHEROCYTOSIS, The Journal of clinical investigation, 97(2), 1996, pp. 373-380
Authors:
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GARBARZ M
LECOMTE MC
LEBORGNE S
GALAND C
BOURNIER O
DEVAUX I
GAUTERO H
ZOHOUN I
GALLAGHER PG
FORGET BG
DHERMY D
Citation: C. Glelekakai et al., EPIDEMIOLOGIC STUDIES OF SPECTRIN MUTATIONS RELATED TO HEREDITARY ELLIPTOCYTOSIS AND SPECTRIN POLYMORPHISMS IN BENIN, British Journal of Haematology, 95(1), 1996, pp. 57-66
Authors:
GARBARZ M
DEVAUX I
BOURNIER O
GRANDCHAMP B
DHERMY D
Citation: M. Garbarz et al., PROTEIN-4.1-LILLE, A NOVEL MUTATION IN THE DOWNSTREAM INITIATION CODON OF PROTEIN-4.1 GENE ASSOCIATED WITH HETEROZYGOUS-4,1(-) HEREDITARY ELLIPTOCYTOSIS, Human mutation, 5(4), 1995, pp. 339-340
Authors:
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SEGUIN I
BOIVIN P
DHERMY D
Citation: Mj. Navarroprigent et al., STUDY OF HUMAN ERYTHROCYTE-MEMBRANE PROTEIN INTERACTIONS BY SELECTIVESOLUBILIZATION OF TRITON-SKELETONS, Biology of the cell, 83(1), 1995, pp. 33-38
Authors:
MARECHAL J
WILMOTTE R
KANZAKI A
DHERMY D
GARBARZ M
GALAND C
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YAWATA Y
DELAUNAY J
Citation: J. Marechal et al., ETHNIC DISTRIBUTION OF ALLELE ALPHA(LELY), A LOW-EXPRESSION ALLELE OFRED-CELL SPECTRIN ALPHA-GENE, British Journal of Haematology, 90(3), 1995, pp. 553-556
Authors:
HAYETTE S
DHERMY D
DOSSANTOS ME
BOZON M
DRENCKHAHN D
ALLOISIO N
TEXIER P
DELAUNAY J
MORLE L
Citation: S. Hayette et al., A DELETIONAL FRAMESHIFT MUTATION IN PROTEIN-4.2 GENE (ALLELE-4.2 LISBOA) ASSOCIATED WITH HEREDITARY HEMOLYTIC-ANEMIA, Blood, 85(1), 1995, pp. 250-256
Authors:
BOIVIN P
GALAND C
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GARBARZ M
DHERMY D
Citation: P. Boivin et al., SPECTRIN ALPHA-IIA VARIANT IN DOMINANT AND NONDOMINANT SPHEROCYTOSIS (VOL 92, PG 153, 1993), Human genetics, 93(5), 1994, pp. 614-614
Authors:
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RABETAFIKA E
BOURNIER O
BOIVIN P
DHERMY D
Citation: Mj. Navarroprigent et al., EFFECT OF OKADAIC ACID ON THE RHEOLOGICAL PROPERTIES OF HUMAN ERYTHROCYTE-MEMBRANES, Clinical hemorheology, 14(6), 1994, pp. 819-830
Authors:
FLORENT I
LEBONNIEC S
CARCY B
GRELLIER P
MERCEREAUPUIJALON O
BONNEFOY S
DHERMY D
MONSIGNY M
MAYER R
SCHREVEL J
Citation: I. Florent et al., PLASMODIUM-FALCIPARUM PROTEINASES - CLONING OF THE PUTATIVE GENE CODING FOR THE MEROZOITE PROTEINASE FOR ERYTHROCYTE INVASION (MPEI) AND DETERMINATION OF HYDROLYSIS SITES OF SPECTRIN BY PF37 PROTEINASE, Memorias do Instituto Oswaldo Cruz, 89, 1994, pp. 47-49
Authors:
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FLOYD P
GALLAGHER PG
DHERMY D
BURSAUX E
SCARPA A
GARBARZ M
FORGET BG
Citation: Gk. Aboualfa et al., BAND-3 NOIRTERRE - A NONSENSE MUTATION OF THE ERYTHROCYTE BAND-3 GENECAUSING DOMINANT HEREDITARY SPHEROCYTOSIS, Clinical research, 42(3), 1994, pp. 10000447-10000447
Authors:
RANDON J
BOULANGER L
MARECHAL J
GARBARZ M
VALLIER A
RIBEIRO L
TAMAGNINI G
DHERMY D
DELAUNAY J
Citation: J. Randon et al., A VARIANT OF SPECTRIN LOW-EXPRESSION ALLELE ALPHA(LELY) CARRYING A HEREDITARY ELLIPTOCYTOSIS MUTATION IN CODON-28, British Journal of Haematology, 88(3), 1994, pp. 534-540
Authors:
LI Y
HETET G
MAURER AM
CHAIT Y
DHERMY D
BRIERE J
Citation: Y. Li et al., SPONTANEOUS MEGAKARYOCYTE COLONY FORMATION IN MYELOPROLIFERATIVE DISORDERS IS NOT NEUTRALIZABLE BY ANTIBODIES AGAINST IL3, IL6, AND GM-CSF, British Journal of Haematology, 87(3), 1994, pp. 471-476