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La ricerca find articoli where authors phrase all words ' KWAN SP' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 24 riferimenti
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    1. Hagemann, TL; Mares, D; Kwan, SP
      Gene regulation of Wiskott-Aldrich syndrome protein and the human homolog of the Drosophila Su(var)3-9: WASP and SUV39H1, two adjacent genes at Xp11.23

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    2. Vihinen, M; Kwan, SP; Lester, T; Ochs, HD; Resnick, I; Valiaho, J; Conley, ME; Smith, CIE
      Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia

      HUMAN MUTATION
    3. Hagemann, TL; Kwan, SP
      The identification and characterization of two promoters and the complete genomic sequence for the Wiskott-Aldrich syndrome gene

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    4. SNAPPER SB; ROSEN FS; MIZOGUCHI E; COHEN P; KHAN W; LIU CH; HAGEMANN TL; KWAN SP; FERRINI R; DAVIDSON L; BHAN AK; ALT FW
      WISKOTT-ALDRICH-SYNDROME PROTEIN-DEFICIENT MICE REVEAL A ROLE FOR WASP IN T-CELL BUT NOT B-CELL ACTIVATION

      Immunity (Cambridge, Mass.)
    5. VIHINEN M; BRANDAU O; BRANDEN LJ; KWAN SP; LAPPALAINEN I; LESTER T; NOORDZIJ JG; OCHS HD; OLLILA J; PIENAAR SM; RIIKONEN P; SAHA BK; SMITH CIE
      BTKBASE, MUTATION DATABASE FOR X-LINKED AGAMMAGLOBULINEMIA (XLA)

      Nucleic acids research
    6. VIHINEN M; BELOHRADSKY BH; HAIRE RN; HOLINSKIFEDER E; KWAN SP; LAPPALAINEN I; LEHVASLAIHO H; LESTER T; MEINDL A; OCHS H; OLLILA J; VORECHOVSKY I; WEISS M; SMITH CIE
      BTKBASE, MUTATION DATABASE FOR X-LINKED AGAMMAGLOBULINEMIA (VOL 25, PG 166, 1997)

      Nucleic acids research
    7. VIHINEN M; BELOHRADSKY BH; HAIRE RN; HOLINSKIFEDER E; KWAN SP; LAPPALAINEN I; LEHVASLAIHO H; LESTER T; MEINDL A; OCHS HD; OLLILA J; VORECHOVSKY I; WEISS M; SMITH CIE
      BTKBASE, MUTATION DATABASE FOR X-LINKED AGAMMAGLOBULINEMIA (XLA)

      Nucleic acids research
    8. REMOLDODONNELL E; COOLEY J; SHCHERBINA A; HAGEMANN TL; KWAN SP; KENNEY DM; ROSEN FS
      VARIABLE EXPRESSION OF WASP IN B-CELL LINES OF WISKOTT-ALDRICH-SYNDROME PATIENTS

      The Journal of immunology
    9. VIHINEN M; IWATA T; KINNON C; KWAN SP; OCHS HD; VORECHOVSKY I; SMITH CIE
      BTKBASE, MUTATION DATABASE FOR X-LINKED AGAMMAGLOBULINEMIA (XLA)

      Nucleic acids research
    10. HAGEMANN TL; ROSEN FS; KWAN SP
      CHARACTERIZATION OF GERMLINE MUTATIONS OF THE GENE ENCODING BRUTONS TYROSINE KINASE IN FAMILIES WITH X-LINKED AGAMMAGLOBULINEMIA

      Human mutation
    11. KWAN SP; HAGEMANN TL; BLAESE RM; KNUTSEN A; ROSEN FS
      SCANNING OF THE WISKOTT-ALDRICH SYNDROME (WAS) GENE - IDENTIFICATION OF 18 NOVEL ALTERATIONS INCLUDING A POSSIBLE MUTATION HOTSPOT AT ARG86RESULTING IN THROMBOCYTOPENIA, A MILD WAS PHENOTYPE

      Human molecular genetics
    12. KWAN SP; HAGEMANN TL; BLAESE RM; ROSEN FS
      A HIGH-RESOLUTION MAP OF GENES, MICROSATELLITE MARKERS, AND NEW DINUCLEOTIDE REPEATS FROM UBE1 TO THE GATA LOCUS IN THE REGION XP11.23

      Genomics
    13. VIHINEN M; COOPER MD; DESAINTBASILE G; FISCHER A; GOOD RA; HENDRIKS RW; KINNON C; KWAN SP; LITMAN GW; NOTARANGELO LD; OCHS HD; ROSEN FS; VETRIE D; WEBSTER ADB; ZEGERS BJM; SMITH CIE
      BTKBASE - A DATABASE OF XLA-CAUSING MUTATIONS

      Immunology today
    14. HAGEMANN TL; ASSAAD AH; KWAN SP
      MUTATION ANALYSIS OF THE GENE ENCODING BRUTON TYROSINE KINASE IN A FAMILY WITH A SPORADIC CASE OF X-LINKED AGAMMAGLOBULINEMIA REVEALS 3 FEMALE CARRIERS

      American journal of medical genetics
    15. KWAN SP; HAGEMANN TL; RADTKE BE; BLAESE RM; ROSEN FS
      IDENTIFICATION OF MUTATIONS IN THE WISKOTT-ALDRICH SYNDROME GENE AND CHARACTERIZATION OF A POLYMORPHIC DINUCLEOTIDE REPEAT AT DXS6940, ADJACENT TO THE DISEASE GENE

      Proceedings of the National Academy of Sciences of the United Statesof America
    16. HAGEMANN TL; CHEN YX; ROSEN FS; KWAN SP
      GENOMIC ORGANIZATION OF THE BTK GENE AND EXON SCANNING FOR MUTATIONS IN PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA

      Human molecular genetics
    17. HAGEMANN T; SUROSKY R; MONACO AP; LEHRACH H; ROSEN FS; KWAN SP
      PHYSICAL MAPPING IN A YAC CONTIG OF 11 MARKERS ON THE HUMAN X-CHROMOSOME IN XP11.23

      Genomics
    18. KWAN SP; HAGEMANN T; DOLGANOV G; ROSEN FS
      DIRECT SELECTION OF CODING SEQUENCES WITH YACS IN THE REGION OF XP11.23

      Cytogenetics and cell genetics
    19. KWAN SP; WALKER AP; HAGEMANN T; GUPTA S; VAYUVEGULA B; OCHS HD
      NEW RFLP MARKER, SP282, AT THE BTK LOCUS FOR GENETIC-ANALYSIS IN X-LINKED AGAMMAGLOBULINEMIA FAMILIES

      Prenatal diagnosis
    20. ZHU O; ZHANG M; HAGEMANN T; RAWLINGS DJ; SAFFRAN DC; CHEN SH; KWAN SP; WITTE ON; OCHS HD
      MUTATION AFFECTING THE SH3 DOMAIN OF THE B-CELL TYROSINE KINASE (BTK)IN A FAMILY WITH X-LINKED AGAMMAGLOBULINEMIA

      Pediatric research
    21. ZHU QL; ZHANG M; RAWLINGS DJ; VIHINEN M; HAGEMANN T; SAFFRAN DC; KWAN SP; NILSSON L; SMITH CIE; WITTE ON; CHEN SH; OCHS HD
      DELETION WITHIN THE SRC HOMOLOGY DOMAIN-3 OF BRUTON TYROSINE KINASE RESULTING IN X-LINKED AGAMMAGLOBULINEMIA (XLA)

      The Journal of experimental medicine
    22. ZHU O; ZHANG M; KWAN SP; CHEN SH; OCHS HD
      SPLICE JUNCTION POINT MUTATION OF B-CELL TYROSINE KINASE (BTK) IN A FAMILY WITH X-LINKED AGAMMAGLOBULINEMIA

      Clinical research
    23. HAGEMANN T; KWAN SP
      BSTNI POLYMORPHISM AT THE BTK LOCUS IN XQ21.3 - XQ22

      Human molecular genetics
    24. KWAN SP; HAGEMANN T; GUAN L; ROSEN FS; MONACO AP; LEHRACH H
      YAC MAPPING OF THE WISKOTT-ALDRICH SYNDROME LOCUS IN XP11.31-]P11.22

      Cytogenetics and cell genetics


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Documento generato il 30/10/20 alle ore 04:02:35