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Results: 1-13 |
Results: 13
2 DISTINCT TRUNCATED VARIANTS OF ANKYRIN ASSOCIATED WITH HEREDITARY SPHEROCYTOSIS
Authors: HAYETTE S CARRE G BOZON M ALLOISIO N MAILLET P WILMOTTE R PASCAL O REYNAUD J REMAN O STEPHAN JL MORLE L DELAUNAY J
Citation: S. Hayette et al., 2 DISTINCT TRUNCATED VARIANTS OF ANKYRIN ASSOCIATED WITH HEREDITARY SPHEROCYTOSIS, American journal of hematology, 58(1), 1998, pp. 36-41
MYCOBACTERIUM-AVIUM COMPLEX STRAINS FROM AIDS PATIENTS BELONG TO A HOMOGENEOUS GROUP ASCRIBED BY RIBOSOMAL-RNA TYPING METHODS
Authors: PEILLON R DROUET E WILMOTTE R COTTE L PANTEIX G DEMONTCLOS H
Citation: R. Peillon et al., MYCOBACTERIUM-AVIUM COMPLEX STRAINS FROM AIDS PATIENTS BELONG TO A HOMOGENEOUS GROUP ASCRIBED BY RIBOSOMAL-RNA TYPING METHODS, Research in microbiology, 148(8), 1997, pp. 683-690
DETECTION OF PNEUMOCYSTIS-CARINII DNA BY PCR AMPLIFICATION IN VARIOUSRAT ORGANS IN EXPERIMENTAL PNEUMOCYSTOSIS
Authors: RABODONIRINA M WILMOTTE R DANNAOUI E PERSAT F BAYLE G MOJON M
Citation: M. Rabodonirina et al., DETECTION OF PNEUMOCYSTIS-CARINII DNA BY PCR AMPLIFICATION IN VARIOUSRAT ORGANS IN EXPERIMENTAL PNEUMOCYSTOSIS, Journal of Medical Microbiology, 46(8), 1997, pp. 665-668
EXON 46-ENCODED SEQUENCE IS ESSENTIAL FOR STABILITY OF HUMAN ERYTHROID ALPHA-SPECTRIN AND HETERODIMER FORMATION
Authors: WILMOTTE R HARPER SL URSITTI JA MARECHAL J DELAUNAY J SPEICHER DW
Citation: R. Wilmotte et al., EXON 46-ENCODED SEQUENCE IS ESSENTIAL FOR STABILITY OF HUMAN ERYTHROID ALPHA-SPECTRIN AND HETERODIMER FORMATION, Blood, 90(10), 1997, pp. 4188-4196
MOLECULAR-GENETICS OF HEREDITARY ELLIPTOCYTOSIS AND HEREDITARY SPHEROCYTOSIS
Authors: DELAUNAY J ALLOISIO N MORLE L BAKLOUTI F DALLAVENEZIA N MAILLET P WILMOTTE R
Citation: J. Delaunay et al., MOLECULAR-GENETICS OF HEREDITARY ELLIPTOCYTOSIS AND HEREDITARY SPHEROCYTOSIS, Annales de genetique, 39(4), 1996, pp. 209-221
BAND-4.2 KOMATSU - 523 GAT-]TAT (175 ASP-]TYR) IN EXON-4 OF THE BAND-4.2 GENE ASSOCIATED WITH TOTAL DEFICIENCY OF BAND-4.2, HEMOLYTIC-ANEMIA WITH OVALOSTOMATOCYTOSIS AND MARKED DISRUPTION OF THE CYTOSKELETAL NETWORK
Authors: KANZAKI A YAWATA Y YAWATA A INOUE T OKAMOTO N WADA H HARANO T HARANO K WILMOTTE R HAYETTE S NAKAMURA Y NIKI T KAWAMURA Y NAKAMURA S MATSUDA T
Citation: A. Kanzaki et al., BAND-4.2 KOMATSU - 523 GAT-]TAT (175 ASP-]TYR) IN EXON-4 OF THE BAND-4.2 GENE ASSOCIATED WITH TOTAL DEFICIENCY OF BAND-4.2, HEMOLYTIC-ANEMIA WITH OVALOSTOMATOCYTOSIS AND MARKED DISRUPTION OF THE CYTOSKELETAL NETWORK, International journal of hematology, 61(4), 1995, pp. 165-178
THE QUIET YET DANGEROUS ALPHA(LELY) ALLEL E OF RED RED-CELL SPECTRIN
Authors: DELAUNAY J WILMOTTE R ALLOISIO N MARECHAL J
Citation: J. Delaunay et al., THE QUIET YET DANGEROUS ALPHA(LELY) ALLEL E OF RED RED-CELL SPECTRIN, MS. Medecine sciences, 11(5), 1995, pp. 752-754
ETHNIC DISTRIBUTION OF ALLELE ALPHA(LELY), A LOW-EXPRESSION ALLELE OFRED-CELL SPECTRIN ALPHA-GENE
Authors: MARECHAL J WILMOTTE R KANZAKI A DHERMY D GARBARZ M GALAND C TANG TK 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
HEREDITARY ELLIPTOCYTOSIS ASSOCIATED WITH SPECTRIN LE PUY IN A JAPANESE FAMILY - ULTRASTRUCTURAL ASPECT OF THE RED-CELL SKELETON
Authors: MARECHAL J WADA H KOFFA T KANZAKI A WILMOTTE R IKOMA K YAWATA A INOUE T TAKANASHI K MIURA A ALLOISIO N DELAUNAY J YAWATA Y
Citation: J. Marechal et al., HEREDITARY ELLIPTOCYTOSIS ASSOCIATED WITH SPECTRIN LE PUY IN A JAPANESE FAMILY - ULTRASTRUCTURAL ASPECT OF THE RED-CELL SKELETON, European journal of haematology, 52(2), 1994, pp. 92-98
A DELETIONAL FRAMESHIFT MUTATION IN SPECTRIN BETA-GENE ASSOCIATED WITH HEREDITARY ELLIPTOCYTOSIS IN SPECTRIN NAPOLI
Authors: WILMOTTE R DELGIUDICE EM MARECHAL J PERROTTA S DEMATTIA D DELAUNAY J IOLASCON A
Citation: R. Wilmotte et al., A DELETIONAL FRAMESHIFT MUTATION IN SPECTRIN BETA-GENE ASSOCIATED WITH HEREDITARY ELLIPTOCYTOSIS IN SPECTRIN NAPOLI, British Journal of Haematology, 88(2), 1994, pp. 437-439
A 2ND-ALLELE OF SPECTRIN ALPHA-GENE ASSOCIATED WITH THE ALPHA-1 65-PHENOTYPE (ALLELE ALPHA(PONTE-DE-SOR))/
Authors: BOULANGER L DHERMY D GARBARZ M SILVA C RANDON J WILMOTTE R DELAUNAY J
Citation: L. Boulanger et al., A 2ND-ALLELE OF SPECTRIN ALPHA-GENE ASSOCIATED WITH THE ALPHA-1 65-PHENOTYPE (ALLELE ALPHA(PONTE-DE-SOR))/, Blood, 84(6), 1994, pp. 2056-2057
LOW EXPRESSION ALLELE-ALPHA(LELY) OF RED-CELL SPECTRIN IS ASSOCIATED WITH MUTATIONS IN EXON-40 (ALPHA(V 41)-POLYMORPHISM) AND INTRON-45 ANDWITH PARTIAL SKIPPING OF EXON-46/
Authors: WILMOTTE R MARECHAL J MORLE L BAKLOUTI F PHILIPPE N KASTALLY R KOTULA L DELAUNAY J ALLOISIO N
Citation: R. Wilmotte et al., LOW EXPRESSION ALLELE-ALPHA(LELY) OF RED-CELL SPECTRIN IS ASSOCIATED WITH MUTATIONS IN EXON-40 (ALPHA(V 41)-POLYMORPHISM) AND INTRON-45 ANDWITH PARTIAL SKIPPING OF EXON-46/, The Journal of clinical investigation, 91(5), 1993, pp. 2091-2096
A SPLICE SITE MUTATION OF ALPHA-SPECTRIN GENE CAUSING SKIPPING OF EXON-18 IN HEREDITARY ELLIPTOCYTOSIS
Authors: ALLOISIO N WILMOTTE R MARECHAL J TEXIER P DENOROY L FEO C BENHADJIZOUAOUI Z DELAUNAY J
Citation: N. Alloisio et al., A SPLICE SITE MUTATION OF ALPHA-SPECTRIN GENE CAUSING SKIPPING OF EXON-18 IN HEREDITARY ELLIPTOCYTOSIS, Blood, 81(10), 1993, pp. 2791-2798
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