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La ricerca find articoli where soggetti phrase all words 'OLIGONUCLEOTIDE LIGATION ASSAY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 36 riferimenti
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    1. Syvanen, AC
      Accessing genetic variation: Genotyping single nucleotide polymorphisms

      NATURE REVIEWS GENETICS
    2. Gut, IG
      Automation in genotyping of single nucleotide polymorphisms

      HUMAN MUTATION
    3. Fries, R; Ewald, D; Thaller, G; Buitkamp, J
      Assessment of the nucleotide sequence variability in the bovine T-cell receptor alpha delta joining gene region

      ANIMAL BIOTECHNOLOGY
    4. Feriotto, G; Corradini, R; Sforza, S; Bianchi, N; Mischiati, C; Marchelli, R; Gambari, R
      Peptide nucleic acids and biosensor technology for real-time detection of the cystic fibrosis W1282X mutation by surface plasmon resonance

      LABORATORY INVESTIGATION
    5. China, B; Evrard, V; Noirfalise, R; Clinquart, A; Daube, G
      Tracability in meat processing. The genetic markers.

      ANNALES DE MEDECINE VETERINAIRE
    6. Bijlsma, FJ; Bruggink, AH; Hartman, M; Gmelig-Meyling, FHJ; Tilanus, MGJ; de Jonge, N; de Weger, RA
      No association between IL-10 promoter gene polymorphism and heart failure or rejection following cardiac transplantation

      TISSUE ANTIGENS
    7. Larsen, LA; Christiansen, M; Vuust, J; Andersen, PS
      High throughput mutation screening by automated capillary electrophoresis

      COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING
    8. Nickerson, DA; Taylor, SL; Fullerton, SM; Weiss, KM; Clark, AG; Stengard, JH; Salomaa, V; Boerwinkle, E; Sing, CF
      Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene

      GENOME RESEARCH
    9. Lampe, JW; Bigler, J; Bush, AC; Potter, JD
      Prevalence of polymorphisms in the human UDP-glucuronosyltransferase 2B family: UGT2B4((DE)-E-458), UGT2B7((HY)-Y-268), and UGT2B15((DY)-Y-85)

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    10. Pecheniuk, NM; Walsh, TP; Marsh, NA
      DNA technology for the detection of common genetic variants that predispose to thrombophilia

      BLOOD COAGULATION & FIBRINOLYSIS
    11. Pecheniuk, NM; Marsh, NA; Walsh, TP
      Multiple analysis of three common genetic alterations associated with thrombophilia

      BLOOD COAGULATION & FIBRINOLYSIS
    12. Karim, L; Coppieters, W; Grobet, L; Valentini, A; Georges, M
      Convenient genotyping of six myostatin mutations causing double-muscling in cattle using a multiplex oligonucleotide ligation assay

      ANIMAL GENETICS
    13. Iannone, MA; Taylor, JD; Chen, JW; Li, MS; Rivers, P; Slentz-Kesler, KA; Weiner, MP
      Multiplexed single nucleotide polymorphism genotyping by oligonucleotide ligation and flow cytometry

      CYTOMETRY
    14. Shi, MM; Bleavins, MR; de la Iglesia, FA
      Technologies for detecting genetic polymorphisms in pharmacogenomics

      MOLECULAR DIAGNOSIS
    15. Linder, MW; Valdes, R
      Pharmacogenetics in the practice of laboratory medicine

      MOLECULAR DIAGNOSIS
    16. Chen, C; Cook, LS; Li, XY; Hallagan, S; Madeleine, MM; Daling, JR; Weiss, NS
      CYP2D6 genotype and the incidence of anal and vulvar cancer

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    17. Seelig, B; Jaschke, A
      Ternary conjugates of guanosine monophosphate as initiator nucleotides forthe enzymatic synthesis of 5 '-modified RNAs

      BIOCONJUGATE CHEMISTRY
    18. Gasparini, P; Arbustini, E; Restagno, G; Zelante, L; Stanziale, P; Gatta, L; Sbaiz, L; Sedita, AM; Banchieri, N; Sapone, L; Fiorucci, GC; Brinson, E; Shulse, E; Rappaport, E; Fortina, P
      Analysis of 31 CFTR mutations by polymerase chain reaction oligonucleotideligation assay in a pilot screening of 4476 newborns for cystic fibrosis

      JOURNAL OF MEDICAL SCREENING
    19. Khanna, M; Park, P; Zirvi, M; Cao, WG; Picon, A; Day, J; Paty, P; Barany, F
      Multiplex PCR/LDR for detection of K-ras mutations in primary colon tumors

      ONCOGENE
    20. Morin, PA; Saiz, R; Monjazeb, A
      High-throughput single nucleotide polymorphism genotyping by fluorescent 5' exonuclease assay

      BIOTECHNIQUES
    21. Chataway, J; Sawcer, S; Sherman, D; Hobart, M; Fernie, B; Coraddu, F; Feakes, R; Broadley, S; Gray, J; Hywel, BJD; Jones, HB; Clayton, D; Goodfellow, PN; Compston, A
      No evidence for association of multiple sclerosis with the complement factors C6 and C7

      JOURNAL OF NEUROIMMUNOLOGY
    22. Ravine, D
      Automated mutation analysis

      JOURNAL OF INHERITED METABOLIC DISEASE
    23. Wilde, JT; O'Sullivan, JJ; Roper, JL; Aerts, P; Horowitz, M; Navot, N
      A novel ELISA-based primer extension assay for the detection of the factorV Leiden mutation

      BRITISH JOURNAL OF HAEMATOLOGY
    24. Van Landeghem, GF; Tabatabaie, P; Kucinskas, V; Saha, N; Beckman, G
      Ethnic variation in the mitochondrial targeting sequence polymorphism of MnSOD

      HUMAN HEREDITY
    25. LANDEGREN U; NILSSON M; KWOK PY
      READING BITS OF GENETIC INFORMATION - METHODS FOR SINGLE-NUCLEOTIDE POLYMORPHISM ANALYSIS

      PCR methods and applications
    26. NELSON NC
      RAPID DETECTION OF GENETIC MUTATIONS USING THE CHEMILUMINESCENT HYBRIDIZATION PROTECTION ASSAY (HPA) - OVERVIEW AND COMPARISON WITH OTHER METHODS

      Critical reviews in clinical laboratory sciences
    27. TRUETT GE; WALKER JA; WILSON JB; REDMANN SM; TULLEY RT; ECKARDT GR; PLASTOW G; LEFEVRE M
      ELISA DETECTION OF RESTRICTION SITE POLYMORPHISMS IN THE PIG RYANODINE RECEPTOR LOCUS

      Mammalian genome
    28. SCHUSTER H; LAMPRECHT A; JUNGHANS C; DIETZ B; BARON H; NOTHNAGEL M; MULLERMYHSOK B; LUFT FC
      APPROACHES TO THE GENETICS OF CARDIOVASCULAR-DISEASE THROUGH GENETIC FIELD WORK

      Kidney international
    29. ROSEN SB; STURK A
      ACTIVATED PROTEIN-C RESISTANCE - A MAJOR RISK FACTOR FOR THROMBOSIS

      European journal of clinical chemistry and clinical biochemistry
    30. ROTHSCHILD CB; BREWER CS; LOGGIE B; BEARD GA; TRISCOTT MX
      DETECTION OF COLORECTAL-CANCER K-RAS MUTATIONS USING A SIMPLIFIED OLIGONUCLEOTIDE LIGATION ASSAY

      Journal of immunological methods
    31. ZOTZ RB; GIERS G; MARUHNDEBOWSKI B; SCHARF RE
      GENETIC TYPING OF HUMAN PLATELET ANTIGEN-1 (HPA-1) BY OLIGONUCLEOTIDELIGATION ASSAY IN A SPECIFIC AND RELIABLE SEMIAUTOMATED SYSTEM

      British Journal of Haematology
    32. ROSS PL; LEE K; BELGRADER P
      DISCRIMINATION OF SINGLE-NUCLEOTIDE POLYMORPHISMS IN HUMAN DNA USING PEPTIDE NUCLEIC-ACID PROBES DETECTED BY MALDI-TOF MASS-SPECTROMETRY

      Analytical chemistry
    33. ADCOCK DM; FINK L; MARLAR RA
      A LABORATORY APPROACH TO THE EVALUATION OF HEREDITARY HYPERCOAGULABILITY

      American journal of clinical pathology
    34. BARON H; FUNG S; AYDIN A; BAHRING S; LUFT FC; SCHUSTER H
      OLIGONUCLEOTIDE LIGATION ASSAY (OLA) FOR THE DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA

      Nature biotechnology
    35. LUO JY; BERGSTROM DE; BARANY F
      IMPROVING THE FIDELITY OF THERMUS-THERMOPHILUS DNA-LIGASE

      Nucleic acids research
    36. BENSON JM; PHILLIPS DJ; HOLLOWAY BP; EVATT BL; HOOPER WC
      OLIGONUCLEOTIDE LIGATION ASSAY FOR DETECTION OF THE FACTOR-V MUTATION(ARG(506)-]GLN) CAUSING PROTEIN-C RESISTANCE

      Thrombosis research


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/02/20 alle ore 03:06:49