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La ricerca find articoli where authors phrase all words ' WILMOTTE R' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 16 riferimenti
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    1. Klug, SJ; Wilmotte, R; Santos, C; Almonte, M; Herrero, R; Guerrero, I; Caceres, E; Peixoto-Guimaraes, D; Lenoir, G; Hainaut, P; Walboomers, JMM; Munoz, N
      TP53 polymorphism, HPV infection, and risk of cervical cancer

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    2. Guimaraes, DP; Lu, SH; Snijders, P; Wilmotte, R; Herrero, R; Lenoir, G; Montesano, R; Meijer, CJLM; Walboomers, J; Hainaut, P
      Absence of association between HPV DNA, TP53 codon 72 polymorphism, and risk of oesophageal cancer in a high-risk area of China

      CANCER LETTERS
    3. Wilmotte, R; Marechal, J; Delaunay, J
      Mutation at position -12 of intron 45 (c -> t) plays a prevalent role in the partial skipping of exon 46 from the transcript of allele alpha(LELY) inerythroid cells

      BRITISH JOURNAL OF HAEMATOLOGY
    4. HAYETTE S; CARRE G; BOZON M; ALLOISIO N; MAILLET P; WILMOTTE R; PASCAL O; REYNAUD J; REMAN O; STEPHAN JL; MORLE L; DELAUNAY J
      2 DISTINCT TRUNCATED VARIANTS OF ANKYRIN ASSOCIATED WITH HEREDITARY SPHEROCYTOSIS

      American journal of hematology
    5. PEILLON R; DROUET E; WILMOTTE R; COTTE L; PANTEIX G; DEMONTCLOS H
      MYCOBACTERIUM-AVIUM COMPLEX STRAINS FROM AIDS PATIENTS BELONG TO A HOMOGENEOUS GROUP ASCRIBED BY RIBOSOMAL-RNA TYPING METHODS

      Research in microbiology
    6. RABODONIRINA M; WILMOTTE R; DANNAOUI E; PERSAT F; BAYLE G; MOJON M
      DETECTION OF PNEUMOCYSTIS-CARINII DNA BY PCR AMPLIFICATION IN VARIOUSRAT ORGANS IN EXPERIMENTAL PNEUMOCYSTOSIS

      Journal of Medical Microbiology
    7. WILMOTTE R; HARPER SL; URSITTI JA; MARECHAL J; DELAUNAY J; SPEICHER DW
      EXON 46-ENCODED SEQUENCE IS ESSENTIAL FOR STABILITY OF HUMAN ERYTHROID ALPHA-SPECTRIN AND HETERODIMER FORMATION

      Blood
    8. DELAUNAY J; ALLOISIO N; MORLE L; BAKLOUTI F; DALLAVENEZIA N; MAILLET P; WILMOTTE R
      MOLECULAR-GENETICS OF HEREDITARY ELLIPTOCYTOSIS AND HEREDITARY SPHEROCYTOSIS

      Annales de genetique
    9. 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
      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
    10. DELAUNAY J; WILMOTTE R; ALLOISIO N; MARECHAL J
      THE QUIET YET DANGEROUS ALPHA(LELY) ALLEL E OF RED RED-CELL SPECTRIN

      MS. Medecine sciences
    11. MARECHAL J; WILMOTTE R; KANZAKI A; DHERMY D; GARBARZ M; GALAND C; TANG TK; YAWATA Y; DELAUNAY J
      ETHNIC DISTRIBUTION OF ALLELE ALPHA(LELY), A LOW-EXPRESSION ALLELE OFRED-CELL SPECTRIN ALPHA-GENE

      British Journal of Haematology
    12. 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
      HEREDITARY ELLIPTOCYTOSIS ASSOCIATED WITH SPECTRIN LE PUY IN A JAPANESE FAMILY - ULTRASTRUCTURAL ASPECT OF THE RED-CELL SKELETON

      European journal of haematology
    13. WILMOTTE R; DELGIUDICE EM; MARECHAL J; PERROTTA S; DEMATTIA D; DELAUNAY J; IOLASCON A
      A DELETIONAL FRAMESHIFT MUTATION IN SPECTRIN BETA-GENE ASSOCIATED WITH HEREDITARY ELLIPTOCYTOSIS IN SPECTRIN NAPOLI

      British Journal of Haematology
    14. BOULANGER L; DHERMY D; GARBARZ M; SILVA C; RANDON J; WILMOTTE R; DELAUNAY J
      A 2ND-ALLELE OF SPECTRIN ALPHA-GENE ASSOCIATED WITH THE ALPHA-1 65-PHENOTYPE (ALLELE ALPHA(PONTE-DE-SOR))/

      Blood
    15. WILMOTTE R; MARECHAL J; MORLE L; BAKLOUTI F; PHILIPPE N; KASTALLY R; KOTULA L; DELAUNAY J; ALLOISIO N
      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
    16. ALLOISIO N; WILMOTTE R; MARECHAL J; TEXIER P; DENOROY L; FEO C; BENHADJIZOUAOUI Z; DELAUNAY J
      A SPLICE SITE MUTATION OF ALPHA-SPECTRIN GENE CAUSING SKIPPING OF EXON-18 IN HEREDITARY ELLIPTOCYTOSIS

      Blood


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/10/20 alle ore 02:43:45