Authors:
CAVE H
BAKKUS M
SUCIU S
GUIDAL C
FOURNIER M
ROBERT A
BOUTARD P
MECHINAUD F
PLOUVIER E
FERSTER A
NELKEN B
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THIELEMANS K
GRANDCHAMP B
VILMER E
Citation: H. Cave et al., SIGNIFICANCE OF THE QUANTITATION OF MINIMAL RESIDUAL DISEASE BY PCR AMPLIFICATION OF IGH AND TCR GENE REARRANGEMENTS IN CHILDHOOD ALL - AN EORTC - PROSPECTIVE MULTICENTER STUDY, Blood, 86(10), 1995, pp. 699-699
Authors:
RAYNAUD SD
CAVE H
BAENS M
BASTARD C
CACHEUX V
GROSGEORGE J
VILMER E
MARYNEN P
GRANDCHAMP B
Citation: Sd. Raynaud et al., THE T(12-21) TRANSLOCATION AND DELETIONS OF CHROMOSOME 12P12-13 - A 2HITS ALTERATION OF TEL FREQUENTLY INVOLVED IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIAS, Blood, 86(10), 1995, pp. 2379-2379
Authors:
CAVE H
GERARD B
MARTIN E
GUIDAL C
DEVAUX I
WEISSENBACH J
ELION J
VILMER E
GRANDCHAMP B
Citation: H. Cave et al., LOSS OF HETEROZYGOSITY IN THE CHROMOSOMAL REGION 12P12-13 IS VERY COMMON IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA AND PERMITS THE PRECISE LOCALIZATION OF A TUMOR-SUPPRESSOR GENE DISTINCT FROM P7(KIP1), Blood, 86(10), 1995, pp. 3869-3875
Citation: Mh. Delfaularue et al., COPROPORPHYRINOGENE OXIDASE - GENE ORGANIZATION AND DESCRIPTION OF A MUTATION LEADING TO EXON-6 SKIPPING, Human molecular genetics, 3(8), 1994, pp. 1325-1330
Citation: P. Martasek et al., HOMOZYGOUS HEREDITARY COPROPORPHYRIA CAUSED BY AN ARGININE TO TRYPTOPHANE SUBSTITUTION IN COPROPORPHYRINOGEN OXIDASE AND COMMON INTRAGENIC POLYMORPHISMS, Human molecular genetics, 3(3), 1994, pp. 477-480
Authors:
CACHEUX V
MARTASEK P
FOUGEROUSSE F
DELFAU MH
DRUART L
TACHDJIAN G
GRANDCHAMP B
Citation: V. Cacheux et al., LOCALIZATION OF THE HUMAN COPROPORPHYRINOGEN OXIDASE GENE TO CHROMOSOME BAND 3Q12, Human genetics, 94(5), 1994, pp. 557-559
Authors:
GU XF
DEROOIJ F
VOORTMAN G
VELDE KT
DEYBACH JC
NORDMANN Y
GRANDCHAMP B
Citation: Xf. Gu et al., DETECTION OF 11 MUTATIONS CAUSING ACUTE INTERMITTENT PORPHYRIA USING DENATURING GRADIENT GEL-ELECTROPHORESIS, Human genetics, 93(1), 1994, pp. 47-52
Authors:
MARTASEK P
CAMADRO JM
DELFAULARUE MH
DUMAS JB
MONTAGNE JJ
DEVERNEUIL H
LABBE P
GRANDCHAMP B
Citation: P. Martasek et al., MOLECULAR-CLONING, SEQUENCING, AND FUNCTIONAL EXPRESSION OF A CDNA-ENCODING HUMAN COPROPORPHYRINOGEN OXIDASE, Proceedings of the National Academy of Sciences of the United Statesof America, 91(8), 1994, pp. 3024-3028
Authors:
BEAUMONT C
SEYHAN A
YACHOU AK
GRANDCHAMP B
JONES R
Citation: C. Beaumont et al., MOUSE FERRITIN-H SUBUNIT GENE - FUNCTIONAL-ANALYSIS OF THE PROMOTER AND IDENTIFICATION OF AN UPSTREAM REGULATORY ELEMENT ACTIVE IN ERYTHYROID CELLS, The Journal of biological chemistry, 269(32), 1994, pp. 20281-20288
Authors:
LECOMTE MC
NICOLAS G
PEDRONI S
GAUTERO H
FOURNIER C
DHERMY D
GRANDCHAMP B
Citation: Mc. Lecomte et al., STUDIES OF THE TETRAMERIZATION SITE USING RECOMBINANT ALPHA AND BETA-SPECTRIN PEPTIDES - EFFECT OF 2 BETA-SPECTRIN MUTATIONS ASSOCIATED WITH HEREDITARY ELLIPTOCYTOSIS (HE), Blood, 84(10), 1994, pp. 10000004-10000004
Citation: N. Elkassar et al., CLONALITY ANALYSIS OF DIFFERENT HEMATOPOIETIC-CELL LINEAGES IN ESSENTIAL THROMBOCYTHEMIA, Blood, 84(10), 1994, pp. 10000055-10000055
Citation: Y. Li et al., ROLE OF PROTOONCOGENE C-MPL IN SPONTANEOUS MEGAKARYOCYTOPOIESIS IN ESSENTIAL THROMBOCYTHEMIA, Blood, 84(10), 1994, pp. 10000055-10000055
Authors:
GUIDAL C
GERARD B
CAVE H
ELION J
VILMER E
GRANDCHAMP B
Citation: C. Guidal et al., ABSENCE OF MUTATION OF THE P16INK4 GENE IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA EVEN WHEN BLASTS DISPLAY LOSS OF HETEROZYGOSITY IN THE 9P21 CHROMOSOMIC REGION, Blood, 84(10), 1994, pp. 10000297-10000297
Authors:
CAVE H
GUIDAL C
ROHRLICH P
DELFAU MH
BROYART A
LESCOEUR B
RAHIMY C
FENNETEAU O
MONPLAISIR N
DAURIOL L
ELION J
VILMER E
GRANDCHAMP B
Citation: H. Cave et al., PROSPECTIVE MONITORING AND QUANTITATION OF RESIDUAL BLASTS IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA BY POLYMERASE CHAIN-REACTION STUDY OF DELTA-T-CELL AND GAMMA-T-CELL RECEPTOR GENES, Blood, 83(7), 1994, pp. 1892-1902
Authors:
GU XF
DEROOIJ F
DEBAAR E
BRUYLAND M
LISSENS W
NORDMANN Y
GRANDCHAMP B
Citation: Xf. Gu et al., 2 NOVEL MUTATIONS OF THE PORPHOBILINOGEN DEAMINASE GENE IN ACUTE INTERMITTENT PORPHYRIA, Human molecular genetics, 2(10), 1993, pp. 1735-1736
Authors:
GRANDCHAMP B
GU XF
ROOIJ F
VOORTMAN G
NORDMANN Y
Citation: B. Grandchamp et al., DETECTION OF 13 MUTATIONS CAUSING ACUTE INTERMITTENT PORPHYRIA USING DENATURING GRADIENT GEL-ELECTROPHORESIS, American journal of human genetics, 53(3), 1993, pp. 904-904