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La ricerca find articoli where authors phrase all words ' Highsmith, WE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 20 riferimenti
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    1. Karp, JE; Lancet, JE; Kaufmann, SH; End, DW; Wright, JJ; Bol, K; Horak, I; Tidwell, ML; Liesveld, J; Kottke, TJ; Ange, D; Buddharaju, L; Gojo, I; Highsmith, WE; Belly, RT; Hohl, RJ; Rybak, ME; Thibault, A; Rosenblatt, J
      Clinical and biologic activity of the farnesyltransferase inhibitor R115777 in adults with refractory and relapsed acute leukemias: a phase 1 clinical-laboratory correlative trial

      BLOOD
    2. King, JC; Treanor, J; Fast, PE; Wolff, M; Yan, LH; Iacuzio, D; Readmond, B; O'Brien, D; Mallon, K; Highsmith, WE; Lambert, JS; Belshe, RB
      Comparison of the safety, vaccine virus shedding, and immunogenicity of influenza virus vaccine, trivalent, types A and B, live cold-adapted, administered to human immunodeficiency virus (HIV)-infected and non-HIV-infected adults

      JOURNAL OF INFECTIOUS DISEASES
    3. Nataraj, AJ; Olivos-Glander, I; Kusukawa, N; Highsmith, WE
      Single-strand conformation polymorphism and heteroduplex analysis for gel-based mutation detection

      ELECTROPHORESIS
    4. Highsmith, WE; Jin, Q; Nataraj, AJ; O'Connor, JM; Burland, VD; Baubonis, WR; Curtis, FP; Kusukawa, N; Garner, MM
      Use of a DNA toolbox for the characterization of mutation scanning methods. I: Construction of the toolbox and evaluation of heteroduplex analysis

      ELECTROPHORESIS
    5. Highsmith, WE; Nataraj, AJ; Jin, Q; O'Connor, JM; El-Nabi, SH; Kusukawa, N; Garner, MM
      Use of DNA toolbox for the characterization of mutation scanning methods. II: Evaluation of single-strand conformation polymorphism analysis

      ELECTROPHORESIS
    6. STROVEL JW; ABRUZZO LV; HIGHSMITH WE; STAMBERG J
      QUANTITATIVE MEASUREMENT OF TELOMERASE ACTIVITY IN LYMPHADENOPATHY - CORRELATION WITH HISTOLOGIC FEATURES AND HUMAN IMMUNODEFICIENCY VIRUS-1 INFECTION

      Modern pathology
    7. HSU IC; HIGHSMITH WE; XU JF; KONG DH
      MISMATCH CLEAVAGE DETECTS BASE DELETION IN CYSTIC-FIBROSIS GENE

      BioTechniques
    8. OCONNOR JM; JIAN Q; NATARAJ A; BURLAND VD; BAUBONIS WH; CURTIS FP; GARNER MM; HIGHSMITH WE
      SENSITIVITY OF HETERODUPLEX ANALYSIS AND SSCP AS A FUNCTION OF DNA CHARACTERISTICS AND ELECTROPHORESIS CONDITIONS

      Biophysical journal
    9. HIGHSMITH WE; BURCH LH; ZHOU ZQ; OLSEN JC; STRONG TV; SMITH T; FRIEDMAN KJ; SILVERMAN LM; BOUCHER RC; COLLINS FS; KNOWLES MR
      IDENTIFICATION OF A SPLICE-SITE MUTATION (2789-G-GREATER-THAN-A) ASSOCIATED WITH SMALL AMOUNTS OF NORMAL CFTR MESSENGER-RNA AND MILD CYSTIC-FIBROSIS(5)

      Human mutation
    10. JIN Q; OCONNOR JM; BURLAND VD; BAUBONIS WR; CURTIS FP; GARNER MM; HIGHSMITH WE
      THE EFFECTS OF BASE CHANGE, FRAGMENT LENGTH AND BASE CONTENT ON THE DETECTION OF POINT MUTATIONS BY HETERODUPLEX ANALYSIS AND SSCP

      American journal of human genetics
    11. HIGHSMITH WE; SILVERMAN L
      EVOLUTION OF AUTOMATED MOLECULAR DIAGNOSTICS

      Clinical chemistry
    12. STOERKER J; HURWITZ C; ROSE NC; SILBERSTEIN LE; HIGHSMITH WE
      HETERODUPLEX GENERATOR IN ANALYSIS OF RH BLOOD-GROUP ALLELES

      Clinical chemistry
    13. FRIEDMAN KJ; TEICHTAHL H; DEKRETSER DM; TEMPLESMITH P; SOUTHWICK GJ; SILVERMAN LM; HIGHSMITH WE; BOUCHER RC; KNOWLES MR
      SCREENING YOUNG-SYNDROME PATIENTS FOR CFTR MUTATIONS

      American journal of respiratory and critical care medicine
    14. ROSE NC; HURWITZ C; HIGHSMITH WE; BECKER J; STOERKER J
      PRENATAL ANALYSIS OF RHESUS CCDEE BLOOD-GROUPS BY HETERODUPLEX GENERATOR

      American journal of human genetics
    15. HIGHSMITH WE; BURCH LH; ZHOU ZQ; OLSEN JC; BOAT TE; SPOCK A; GORVOY JD; QUITTELL L; FRIEDMAN KJ; SILVERMAN LM; BOUCHER RC; KNOWLES MR
      A NOVEL MUTATION IN THE CYSTIC-FIBROSIS GENE IN PATIENTS WITH PULMONARY-DISEASE BUT NORMAL SWEAT CHLORIDE CONCENTRATIONS

      The New England journal of medicine
    16. KIESEWETTER S; MACEK M; DAVIS C; CURRISTIN SM; CHU CS; GRAHAM C; SHRIMPTON AE; CASHMAN SM; TSUI LC; MICKLE J; AMOS J; HIGHSMITH WE; SHUBER A; WITT DR; CRYSTAL RG; CUTTING GR
      A MUTATION IN CFTR PRODUCES DIFFERENT PHENOTYPES DEPENDING ON CHROMOSOMAL BACKGROUND

      Nature genetics
    17. HIGHSMITH WE
      CARRIER SCREENING FOR CYSTIC-FIBROSIS

      Clinical chemistry
    18. KIESEWETTER S; MACEK M; CURRISTIN S; CHU C; GRAHAM C; SHRIMPTON AE; DEARCE M; ZIELENSKI J; MICKLE J; AMOS J; HIGHSMITH WE; SHUBER A; WITT D; CRYSTAL RG; CUTTING GR
      THE CFTR MUTATION R117H PRODUCES DIFFERENT PHENOTYPES DEPENDING ON GENETIC BACKGROUND

      American journal of human genetics
    19. HIGHSMITH WE; POFF H; DOHERTY T; YE S
      TOWARDS A 2ND TIER TEST FOR CYSTIC-FIBROSIS CARRIER TESTING - SIMULTANEOUS DETECTION OF CFTR MUTATIONS COMMON IN THE ASHKENAZIC POPULATION USING MDE ELECTROPHORESIS

      American journal of human genetics
    20. FRIEDMAN KJ; BURCH LH; WOOD BM; HIGHSMITH WE; HEIM RA; KNOWLES MR; SILVERMAN LM
      DETECTION OF NOVEL MUTATIONS AND SEQUENCE VARIATIONS WITHIN THE CFTR GENE BY HETERODUPLEX SCREENING ON ACRYLAMIDE AND MDE

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 23/01/21 alle ore 22:32:35