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Results: 1-25 | 26-50 | 51-73
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CLONALITY ANALYSIS OF HEMATOPOIESIS AND THROMBOPOIETIN LEVELS IN PATIENTS WITH ESSENTIAL THROMBOCYTHEMIA
Authors: ELKASSAR N HETET G BRIERE J GRANDCHAMP B
Citation: N. Elkassar et al., CLONALITY ANALYSIS OF HEMATOPOIESIS AND THROMBOPOIETIN LEVELS IN PATIENTS WITH ESSENTIAL THROMBOCYTHEMIA, Leukemia & lymphoma, 30(1-2), 1998, pp. 181-188
HIGH-RESOLUTION ALLELOTYPE ANALYSIS OF CHILDHOOD B-LINEAGE ACUTE LYMPHOBLASTIC-LEUKEMIA
Authors: CHAMBONPAUTAS C CAVE H GERARD B GUIDALGIROUX C DUVAL M VILMER E GRANDCHAMP B
Citation: C. Chambonpautas et al., HIGH-RESOLUTION ALLELOTYPE ANALYSIS OF CHILDHOOD B-LINEAGE ACUTE LYMPHOBLASTIC-LEUKEMIA, Leukemia, 12(7), 1998, pp. 1107-1113
CLINICAL-SIGNIFICANCE OF MINIMAL RESIDUAL DISEASE IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA
Authors: CAVE H TENBOSCH JV SUCIU S GUIDAL C WATERKEYN C OTTEN J BAKKUS M THIELEMANS K GRANDCHAMP B VILMER E
Citation: H. Cave et al., CLINICAL-SIGNIFICANCE OF MINIMAL RESIDUAL DISEASE IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA, The New England journal of medicine, 339(9), 1998, pp. 591-598
CYTOTOXIC T-CELL RESPONSE AGAINST THE CHIMERIC ETV6-AML1 PROTEIN IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA
Authors: YOTNDA P GARCIA F PEUCHMAUR M GRANDCHAMP B DUVAL M LEMONNIER F VILMER E LANGLADEDEMOYEN P
Citation: P. Yotnda et al., CYTOTOXIC T-CELL RESPONSE AGAINST THE CHIMERIC ETV6-AML1 PROTEIN IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA, The Journal of clinical investigation, 102(2), 1998, pp. 455-462
X-CHROMOSOME INACTIVATION IN HEALTHY FEMALES - INCIDENCE OF EXCESSIVELYONIZATION WITH AGE AND COMPARISON OF ASSAYS INVOLVING DNA METHYLATION AND TRANSCRIPT POLYMORPHISMS
Authors: ELKASSAR N HETET G BRIERE E GRANDCHAMP B
Citation: N. Elkassar et al., X-CHROMOSOME INACTIVATION IN HEALTHY FEMALES - INCIDENCE OF EXCESSIVELYONIZATION WITH AGE AND COMPARISON OF ASSAYS INVOLVING DNA METHYLATION AND TRANSCRIPT POLYMORPHISMS, Clinical chemistry, 44(1), 1998, pp. 61-67
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)
Authors: GARBARZ M GALAND C BIBAS D BOURNIER O DEVAUX I HAROUSSEAU JL GRANDCHAMP B 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
MICROSATELLITE INSTABILITY AND FRAMESHIFT MUTATIONS IN BAX AND TRANSFORMING-GROWTH-FACTOR-BETA RII GENES ARE VERY UNCOMMON IN ACUTE LYMPHOBLASTIC-LEUKEMIA IN-VIVO BUT NOT IN CELL-LINES
Authors: MOLENAAR JJ GERARD B CHAMBONPAUTAS C CAVE H DUVAL M VILMER E GRANDCHAMP B
Citation: Jj. Molenaar et al., MICROSATELLITE INSTABILITY AND FRAMESHIFT MUTATIONS IN BAX AND TRANSFORMING-GROWTH-FACTOR-BETA RII GENES ARE VERY UNCOMMON IN ACUTE LYMPHOBLASTIC-LEUKEMIA IN-VIVO BUT NOT IN CELL-LINES, Blood, 92(1), 1998, pp. 230-233
NEONATAL HEMOLYTIC-ANEMIA DUE TO INHERITED HARDEROPORPHYRIA - CLINICAL CHARACTERISTICS AND MOLECULAR-BASIS
Authors: LAMORIL J PUY H GOUYA L ROSIPAL R DASILVA V GRANDCHAMP B FOINT T BADERMEUNIER B DOMMERGUES JP DEYBACH JC NORDMANN Y
Citation: J. Lamoril et al., NEONATAL HEMOLYTIC-ANEMIA DUE TO INHERITED HARDEROPORPHYRIA - CLINICAL CHARACTERISTICS AND MOLECULAR-BASIS, Blood, 91(4), 1998, pp. 1453-1457
3 NOVEL MUTATIONS IN THE COPROPORPHYRINOGEN OXIDASE GENE
Authors: LAMORIL J DEYBACH JC PUY H GRANDCHAMP B NORDMANN Y
Citation: J. Lamoril et al., 3 NOVEL MUTATIONS IN THE COPROPORPHYRINOGEN OXIDASE GENE, Human mutation, 9(1), 1997, pp. 78-80
ETV6 IS THE TARGET OF CHROMOSOME 12P DELETIONS IN T(12-21) CHILDHOOD ACUTE LYMPHOCYTIC-LEUKEMIA
Authors: CAVE H CACHEUX V RAYNAUD S BRUNIE G BAKKUS M COCHAUX P PREUDHOMME C LAI JL VILMER E GRANDCHAMP B
Citation: H. Cave et al., ETV6 IS THE TARGET OF CHROMOSOME 12P DELETIONS IN T(12-21) CHILDHOOD ACUTE LYMPHOCYTIC-LEUKEMIA, Leukemia, 11(9), 1997, pp. 1459-1464
DELINEATION OF A 6 CM COMMONLY DELETED REGION IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA ON THE 6Q CHROMOSOMAL ARM
Authors: GERARD B CAVE H GUIDAL C DASTUGUE N VILMER E GRANDCHAMP B
Citation: B. Gerard et al., DELINEATION OF A 6 CM COMMONLY DELETED REGION IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA ON THE 6Q CHROMOSOMAL ARM, Leukemia, 11(2), 1997, pp. 228-232
STUDY OF THE THROMBOPOIETIN RECEPTOR IN ESSENTIAL THROMBOCYTHEMIA
Authors: KILADJIAN JJ ELKASSAR N HETET G BRIERE J GRANDCHAMP B GARDIN C
Citation: Jj. Kiladjian et al., STUDY OF THE THROMBOPOIETIN RECEPTOR IN ESSENTIAL THROMBOCYTHEMIA, Leukemia, 11(11), 1997, pp. 1821-1826
HUMAN COPROPORPHYRINOGEN OXIDASE - BIOCHEMICAL-CHARACTERIZATION OF RECOMBINANT NORMAL AND R231W MUTATED ENZYMES EXPRESSED IN ESCHERICHIA-COLI AS SOLUBLE, CATALYTICALLY ACTIVE HOMODIMERS
Authors: MARTASEK P CAMADRO JM RAMAN CS LECOMTE MC LECAER JP DEMELER B GRANDCHAMP B LABBE P
Citation: P. Martasek et al., HUMAN COPROPORPHYRINOGEN OXIDASE - BIOCHEMICAL-CHARACTERIZATION OF RECOMBINANT NORMAL AND R231W MUTATED ENZYMES EXPRESSED IN ESCHERICHIA-COLI AS SOLUBLE, CATALYTICALLY ACTIVE HOMODIMERS, Cellular and molecular biology, 43(1), 1997, pp. 47-58
ANALYSIS OF ETV6 AND ETV6-AML1 PROTEINS IN ACUTE LYMPHOBLASTIC-LEUKEMIA
Authors: AGAPE P GERARD B CAVE H DEVAUX I VILMER E LECOMTE MC GRANDCHAMP B
Citation: P. Agape et al., ANALYSIS OF ETV6 AND ETV6-AML1 PROTEINS IN ACUTE LYMPHOBLASTIC-LEUKEMIA, British Journal of Haematology, 98(1), 1997, pp. 234-239
X-CHROMOSOME INACTIVATION IN NORMAL FEMALES - COMPARISON OF ASSAYS USING DNA METHYLATION AND TRANSCRIPT POLYMORPHISMS
Authors: ELKASSAR N HETET G BRIERE J GRANDCHAMP B
Citation: N. Elkassar et al., X-CHROMOSOME INACTIVATION IN NORMAL FEMALES - COMPARISON OF ASSAYS USING DNA METHYLATION AND TRANSCRIPT POLYMORPHISMS, Blood, 90(10), 1997, pp. 3359-3359
CLONALITY ANALYSIS IN ESSENTIAL THROMBOCYTHEMIA
Authors: ELKASSAR N HETET G BRIERE J GRANDCHAMP B
Citation: N. Elkassar et al., CLONALITY ANALYSIS IN ESSENTIAL THROMBOCYTHEMIA, Blood, 90(10), 1997, pp. 1548-1548
SPECTRIN ST CLAUDE, A SPLICING MUTATION OF THE HUMAN ALPHA-SPECTRIN GENE ASSOCIATED WITH SEVERE POIKILOCYTIC ANEMIA
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
CLONALITY ANALYSIS OF HEMATOPOIESIS IN ESSENTIAL THROMBOCYTHEMIA - ADVANTAGES OF STUDYING T-LYMPHOCYTES AND PLATELETS
Authors: ELKASSAR N HETET G BRIERE J GRANDCHAMP B
Citation: N. Elkassar et al., CLONALITY ANALYSIS OF HEMATOPOIESIS IN ESSENTIAL THROMBOCYTHEMIA - ADVANTAGES OF STUDYING T-LYMPHOCYTES AND PLATELETS, Blood, 89(1), 1997, pp. 128-134
SYSTEMATIC SCREENING FOR FRAGILE-X-SYNDROME IN A COHORT OF 574 MENTALLY-RETARDED CHILDREN
Authors: GERARD B LEHEUZEY MF BRUNIE G LEWINE P SAIAG MC CACHEUX V DASILVA F DUGAS M MOURENSIMEONI MC ELION J GRANDCHAMP B
Citation: B. Gerard et al., SYSTEMATIC SCREENING FOR FRAGILE-X-SYNDROME IN A COHORT OF 574 MENTALLY-RETARDED CHILDREN, Annales de genetique, 40(3), 1997, pp. 139-144
MOLECULAR EPIDEMIOLOGY AND DIAGNOSIS OF PBG DEAMINASE GENE DEFECTS INACUTE INTERMITTENT PORPHYRIA
Authors: PUY H DEYBACH JC LAMORIL J ROBREAU AM DASILVA V GOUYA L GRANDCHAMP B NORDMANN Y
Citation: H. Puy et al., MOLECULAR EPIDEMIOLOGY AND DIAGNOSIS OF PBG DEAMINASE GENE DEFECTS INACUTE INTERMITTENT PORPHYRIA, American journal of human genetics, 60(6), 1997, pp. 1373-1383
PORPHOBILINOGEN DEAMINASE DEFICIENCY IN MICE CAUSES A NEUROPATHY RESEMBLING THAT OF HUMAN HEPATIC PORPHYRIA
Authors: LINDBERG RLP PORCHER C GRANDCHAMP B LEDERMANN B BURKI K BRANDNER S AGUZZI A MEYER UA
Citation: Rlp. Lindberg et al., PORPHOBILINOGEN DEAMINASE DEFICIENCY IN MICE CAUSES A NEUROPATHY RESEMBLING THAT OF HUMAN HEPATIC PORPHYRIA, Nature genetics, 12(2), 1996, pp. 195-199
MUTATIONS IN THE PROTOPORPHYRINOGEN OXIDASE GENE IN PATIENTS WITH VARIEGATE PORPHYRIA
Authors: DEYBACH JC PUY H ROBREAU AM LAMORIL J DASILVA V GRANDCHAMP B NORDMANN Y
Citation: Jc. Deybach et al., MUTATIONS IN THE PROTOPORPHYRINOGEN OXIDASE GENE IN PATIENTS WITH VARIEGATE PORPHYRIA, Human molecular genetics, 5(3), 1996, pp. 407-410
A LOW-RATE OF LOSS OF HETEROZYGOSITY IS FOUND AT MANY DIFFERENT LOCI IN CHILDHOOD B-LINEAGE ACUTE LYMPHOCYTIC-LEUKEMIA
Authors: CAVE H GUIDAL C ELION J VILMER E GRANDCHAMP B
Citation: H. Cave et al., A LOW-RATE OF LOSS OF HETEROZYGOSITY IS FOUND AT MANY DIFFERENT LOCI IN CHILDHOOD B-LINEAGE ACUTE LYMPHOCYTIC-LEUKEMIA, Leukemia, 10(9), 1996, pp. 1486-1491
REVIEW - MOLECULAR PATHOGENESIS OF HEPATIC ACUTE PORPHYRIAS
Authors: GRANDCHAMP B PUY H LAMORIL J DEYBACH JC NORDMANN Y
Citation: B. Grandchamp et al., REVIEW - MOLECULAR PATHOGENESIS OF HEPATIC ACUTE PORPHYRIAS, Journal of gastroenterology and hepatology, 11(11), 1996, pp. 1046-1052
EXPRESSION OF H-FERRITIN AND L-FERRITIN MESSENGER-RNAS IN MOUSE SMALL-INTESTINE
Authors: GERARD B FARMAN N RAJA KB EUGENE E GRANDCHAMP B BEAUMONT C
Citation: B. Gerard et al., EXPRESSION OF H-FERRITIN AND L-FERRITIN MESSENGER-RNAS IN MOUSE SMALL-INTESTINE, Experimental cell research, 228(1), 1996, pp. 8-13
Risultati: 1-25 | 26-50 | 51-73