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    1. Han, S; Cooper, DN; Upadhyaya, M
      Evaluation of denaturing high performance liquid chromatography (DHPLC) for the mutational analysis of the neurofibromatosis type 1 (NF1) gene

      HUMAN GENETICS
    2. Winter, H; Langbein, L; Krawczak, M; Cooper, DN; Jave-Suarez, LF; Rogers, MA; Praetzel, S; Heidt, PJ; Schweizer, J
      Human type I keratin pseudogene phi hHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergence

      HUMAN GENETICS
    3. Al-Jader, LN; Harper, PS; Krawczak, M; Palmer, SR; Johansen, BN; Cooper, DN
      The frequency of inherited disorders database

      HUMAN GENETICS
    4. Martin, MA; Rubio, JC; Garcia, A; Fernandez, MA; Campos, Y; Krawczak, M; Cooper, DN; Arenas, J
      Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease

      CLINICAL GENETICS
    5. Krawczak, M; Cooper, DN; Schmidtke, J
      Estimating the efficacy and efficiency of cascade genetic screening

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Evans, RJ; Mareels, IMY; Sciacca, LJ; Cooper, DN; Middleton, RH; Betz, RE; Kennedy, RA
      Adaptive servo control of large antenna structures

      MODEL INDENTIFICATION AND ADAPTIVE CONTROL: FROM WINDSURFING TO TELECOMMUNICATIONS
    7. Krawczak, M; Ball, EV; Fenton, I; Stenson, PD; Abeysinghe, S; Thomas, N; Cooper, DN
      Human gene mutation database - A biomedical information and research resource

      HUMAN MUTATION
    8. Cheadle, JP; Gill, H; Fleming, N; Maynard, J; Kerr, A; Leonard, H; Krawczak, M; Cooper, DN; Lynch, S; Thomas, N; Hughes, H; Hulten, M; Ravine, D; Sampson, JR; Clarke, A
      Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location

      HUMAN MOLECULAR GENETICS
    9. Cheadle, JP; Gill, H; Fleming, N; Maynard, J; Kerr, A; Leonard, H; Krawczak, M; Cooper, DN; Lynch, S; Thomas, N; Hughes, H; Hulten, M; Ravine, D; Sampson, JR; Clarke, A
      Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location (vol 9, pg 1119, 2000)

      HUMAN MOLECULAR GENETICS
    10. Symons, A; Cooper, DN; Barclay, AN
      Characterization of the interaction between galectin-1 and lymphocyte glycoproteins CD45 and Thy-1

      GLYCOBIOLOGY
    11. Chuzhanova, NA; Krawczak, M; Nemytikova, LA; Gusev, VD; Cooper, DN
      Promoter shuffling has occurred during the evolution of the vertebrate growth hormone gene

      GENE
    12. Shamsher, MK; Chuzhanova, NA; Friedman, B; Scopes, DA; Alhaq, A; Millar, DS; Cooper, DN; Berg, LP
      Identification of an intronic regulatory element in the human protein C (PROC) gene

      HUMAN GENETICS
    13. Millar, DS; Kemball-Cook, G; McVey, JH; Tuddenham, EGD; Mumford, AD; Attock, GB; Reverter, JC; Lanir, N; Parapia, LA; Reynaud, J; Meili, E; von Felton, A; Martinowitz, U; Prangnell, DR; Krawczak, M; Cooper, DN
      Molecular analysis of the genotype-phenotype relationship in factor VII deficiency

      HUMAN GENETICS
    14. Krawczak, M; Chuzhanova, NA; Stenson, PD; Johansen, BN; Ball, EV; Cooper, DN
      Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regions

      HUMAN GENETICS
    15. Horan, MP; Cooper, DN; Upadhyaya, M
      Hypermethylation of the neurofibromatosis type 1 (NF1) gene promoter is not a common event in the inactivation of the NF1 gene in NF1-specific tumours

      HUMAN GENETICS
    16. Millar, DS; Johansen, B; Berntorp, E; Minford, A; Bolton-Maggs, P; Wensley, R; Kakkar, V; Schulman, S; Torres, A; Bosch, N; Cooper, DN
      Molecular genetic analysis of severe protein C deficiency

      HUMAN GENETICS
    17. Millar, DS; Elliston, L; Deex, P; Krawczak, M; Wacey, AI; Reynaud, J; Nieuwenhuis, HK; Bolton-Maggs, P; Mannucci, PM; Reverter, JC; Cachia, P; Pasi, KJ; Layton, DM; Cooper, DN
      Molecular analysis of the genotype-phenotype relationship in factor X deficiency

      HUMAN GENETICS
    18. Gandrille, S; Borgel, D; Sala, N; Espinosa-Parrilla, Y; Simmonds, R; Rezende, S; Lind, B; Mannhalter, C; Pabinger, I; Reitsma, PH; Formstone, C; Cooper, DN; Saito, H; Suzuki, K; Bernardi, F; Aiach, M
      Protein S deficiency: A database of mutations - Summary of the first update

      THROMBOSIS AND HAEMOSTASIS
    19. Antonarakis, SE; Krawczak, M; Cooper, DN
      Disease-causing mutations in the human genome

      EUROPEAN JOURNAL OF PEDIATRICS
    20. Osborn, M; Cooper, DN; Upadhyaya, M
      Molecular analysis of the 5 '-flanking region of the neurofibromatosis type 1 (NF1) gene: identification of five sequence variants

      CLINICAL GENETICS
    21. Krawczak, M; Chuzhanova, NA; Cooper, DN
      Evolution of the proximal promoter region of the mammalian growth hormone gene

      GENE
    22. Wacey, AI; Cooper, DN; Liney, D; Hovig, E; Krawczak, M
      Disentangling the perturbational effects of amino acid substitutions in the DNA-binding domain of p53

      HUMAN GENETICS
    23. PROCTER AM; PHILLIPS JA; COOPER DN
      THE MOLECULAR-GENETICS OF GROWTH-HORMONE DEFICIENCY

      Human genetics
    24. MILLAR DS; KRAWCZAK M; COOPER DN
      VARIATION OF SITE-SPECIFIC METHYLATION PATTERNS IN THE FACTOR-VIII (F8C) GENE IN HUMAN SPERM DNA

      Human genetics
    25. UPADHYAYA M; RUGGIERI M; MAYNARD J; OSBORN M; HARTOG C; MUDD S; PENTTINEN M; CORDEIRO I; PONDER M; PONDER BAJ; KRAWCZAK M; COOPER DN
      GROSS DELETIONS OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ARE PREDOMINANTLY OF MATERNAL ORIGIN AND COMMONLY ASSOCIATED WITH A LEARNING-DISABILITY, DYSMORPHIC FEATURES AND DEVELOPMENTAL DELAY

      Human genetics
    26. COOPER DN; BALL EV; KRAWCZAK M
      THE HUMAN GENE MUTATION DATABASE

      Nucleic acids research
    27. KRAWCZAK M; COOPER DN
      P53 MUTATIONS, BENZO[A]PYRENE AND LUNG-CANCER

      Mutagenesis
    28. HALLAM PJ; MANNUCCI P; TRIPODI A; BEVAN D; LAURSEN B; TENGBORN L; WACEY A; COOPER DN
      3 NOVEL PROC GENE LESIONS CAUSING PROTEIN-C DEFICIENCY

      Clinical genetics
    29. KRAWCZAK M; BALL EV; COOPER DN
      NEIGHBORING-NUCLEOTIDE EFFECTS ON THE RATES OF GERM-LINE SINGLE-BASE-PAIR SUBSTITUTION IN HUMAN GENES

      American journal of human genetics
    30. RAVINE D; COOPER DN
      ADULT-ONSET GENETIC-DISEASE - MECHANISMS, ANALYSIS AND PREDICTION

      Quarterly Journal of Medicine
    31. COOPER DN
      THE FUTURE OF WORK IN THE DIGITAL DIASPORA - ECONOMIC RESTRUCTURING AND EDUCATION

      Journal of organisational change management
    32. UPADHYAYA M; OSBORN MJ; MAYNARD J; KIM MR; TAMANOI F; COOPER DN
      MUTATIONAL AND FUNCTIONAL-ANALYSIS OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE

      Human genetics
    33. WACEY AI; KRAWCZAK M; KEMBALLCOOK G; COOPER DN
      HOMOLOGY MODELING OF THE CATALYTIC DOMAIN OF EARLY MAMMALIAN PROTEIN-C - EVOLUTION OF STRUCTURAL FEATURES

      Human genetics
    34. COOPER DN; MILLAR DS; WACEY A; BANNER DW; TUDDENHAM EGD
      INHERITED FACTOR-VII DEFICIENCY - MOLECULAR-GENETICS AND PATHOPHYSIOLOGY

      Thrombosis and haemostasis
    35. COOPER DN; MILLAR DS; WACEY A; PEMBERTON S; TUDDENHAM EGD
      INHERITED FACTOR-X DEFICIENCY - MOLECULAR-GENETICS AND PATHOPHYSIOLOGY

      Thrombosis and haemostasis
    36. GANDRILLE S; BORGEL D; IRELAND H; LANE DA; SIMMONDS R; REITSMA PH; MANNHALTER C; PABINGER I; SAITO H; SUZUKI K; FORMSTONE C; COOPER DN; ESPINOSA Y; SALA N; BERNARDI F; ALACH M
      PROTEIN-S DEFICIENCY - A DATABASE OF MUTATIONS - FOR THE PLASMA COAGULATION INHIBITORS SUBCOMMITTEE OF THE SCIENTIFIC AND STANDARDIZATION COMMITTEE OF THE INTERNATIONAL-SOCIETY-ON-THROMBOSIS-AND-HEMOSTASIS

      Thrombosis and haemostasis
    37. LANE DA; BAYSTON T; OLDS RJ; FITCHES AC; COOPER DN; MILLAR DS; JOCHMANS K; PERRY DJ; OKAJIMA K; THEIN SL; EMMERICH J
      ANTITHROMBIN MUTATION DATABASE - 2ND (1997) UPDATE - FOR THE PLASMA COAGULATION INHIBITORS SUBCOMMITTEE OF THE SCIENTIFIC AND STANDARDIZATION COMMITTEE OF THE INTERNATIONAL-SOCIETY-ON-THROMBOSIS-AND-HEMOSTASIS

      Thrombosis and haemostasis
    38. SHAMSHER MK; SCOPES D; KAKKAR VV; COOPER DN; BERG LP
      INTERAGENIC ELEMENTS IN PROTEIN-C GENE-EXPRESSION

      Thrombosis and haemostasis
    39. KRAWCZAK M; COOPER DN
      THE HUMAN-GENE-MUTATION-DATABASE

      Trends in genetics
    40. MILLAR DS; TUDDENHAM EGD; WACEY AL; COOPER DN
      MOLECULAR-GENETIC ANALYSIS OF FACTOR-VII DEFICIENCY

      Journal of Medical Genetics
    41. MILLAR DS; DEEX P; ELLISTON L; WACEY AL; COOPER DN
      MOLECULAR-GENETIC ANALYSIS OF FACTOR-X DEFICIENCY

      Journal of Medical Genetics
    42. COOPER DN; TUDDENHAM EGD; WACEY AI; MILLAR DS
      MOLECULAR-GENETIC ANALYSIS OF FACTOR-VII DEFICIENCY

      American journal of human genetics
    43. MILLAR DS; DEEX P; ELLISTON L; WACEY AI; COOPER DN
      MOLECULAR-GENETIC ANALYSIS OF FACTOR-X DEFICIENCY

      American journal of human genetics
    44. UPADHYAYA M; MAYNARD J; RUGGIERI M; HUSON S; PONDER M; KRAWCZAK M; PONDER BAJ; COOPER DN
      A SEX BIAS IN THE ORIGIN OF NEW MUTATIONS IN THE NF1 GENE - THE NATURE OF MUTATIONS AND THEIR POSSIBLE MOLECULAR MECHANISMS

      American journal of human genetics
    45. KRAWCZAK M; COOPER DN
      SINGLE BASE-PAIR SUBSTITUTIONS IN PATHOLOGY AND EVOLUTION - 2 SIDES TO THE SAME COIN

      Human mutation
    46. BERG LP; SORIA JM; FORMSTONE CJ; MORELL M; KAKKAR VV; ESTIVILL X; SALA N; COOPER DN
      ABERRANT RNA SPLICING OF THE PROTEIN-C AND PROTEIN-S GENES IN HEALTHY-INDIVIDUALS

      Blood coagulation & fibrinolysis
    47. COOPER DN; KRAWCZAK M
      HUMAN GENE MUTATION DATABASE

      Human genetics
    48. KRAWCZAK M; WACEY A; COOPER DN
      MOLECULAR RECONSTRUCTION AND HOMOLOGY MODELING OF THE CATALYTIC DOMAIN OF THE COMMON ANCESTOR OF THE HEMOSTATIC VITAMIN-K-DEPENDENT SERINE PROTEINASES

      Human genetics
    49. SORIA JM; BERG LP; FONTCUBERTA J; KAKKAR VV; ESTIVILL X; COOPER DN; SALA N
      ECTOPIC TRANSCRIPT ANALYSIS INDICATES THAT ALLELIC EXCLUSION IS AN IMPORTANT CAUSE OF TYPE-I PROTEIN-C DEFICIENCY IN PATIENTS WITH NONSENSEAND FRAMESHIFT MUTATIONS IN THE PROC GENE

      Thrombosis and haemostasis
    50. BENZAKOUR O; KANTHOU C; KANSE SM; SCULLY MF; KAKKAR VV; COOPER DN
      EVIDENCE FOR CULTURED HUMAN VASCULAR SMOOTH-MUSCLE CELL HETEROGENEITY- ISOLATION OF CLONAL CELLS AND STUDY OF THEIR GROWTH-CHARACTERISTICS

      Thrombosis and haemostasis
    51. SIMIONI P; KALAFATIS M; MILLAR DS; HENDERSON SC; LUNI S; COOPER DN; GIROLAMI A
      COMPOUND HETEROZYGOUS PROTEIN-C DEFICIENCY RESULTING IN THE PRESENCE OF ONLY THE BETA-FORM OF PROTEIN-C IN PLASMA

      Blood
    52. FORMSTONE CJ; HALLAM PJ; TUDDENHAM EGD; VOKE J; LAYTON M; NICOLAIDES K; HANN IM; COOPER DN
      SEVERE PERINATAL THROMBOSIS IN DOUBLE AND TRIPLE HETEROZYGOUS OFFSPRING OF A FAMILY SEGREGATING 2 INDEPENDENT PROTEIN-S MUTATIONS AND A PROTEIN-C MUTATION

      Blood
    53. KRAWCZAK M; SMITHSORENSEN B; SCHMIDTKE J; KAKKAR VV; COOPER DN; HOVIG E
      SOMATIC SPECTRUM OF CANCER-ASSOCIATED SINGLE BASEPAIR SUBSTITUTIONS IN THE TP53 GENE IS DETERMINED MAINLY BY ENDOGENOUS MECHANISMS OF MUTATION AND BY SELECTION

      Human mutation
    54. WINTER PC; SCOPES DA; BERG LP; MILLAR DS; KAKKAR VV; MAYNE EE; KRAWCZAK M; COOPER DN
      FUNCTIONAL-ANALYSIS OF AN UNUSUAL LENGTH POLYMORPHISM IN THE HUMAN ANTITHROMBIN-III (AT3) GENE PROMOTER

      Blood coagulation & fibrinolysis
    55. SCOPES D; BERG LP; KRAWCZAK M; KAKKAR VV; COOPER DN
      POLYMORPHIC VARIATION IN THE HUMAN PROTEIN-C (PROC) GENE PROMOTER CANINFLUENCE TRANSCRIPTIONAL EFFICIENCY IN-VITRO

      Blood coagulation & fibrinolysis
    56. MILLAR DS; BEVAN D; CHITOLIE A; REYNAUD J; CHISHOLM M; KAKKAR VV; COOPER DN
      3 NOVEL MUTATIONS IN THE PROTEIN-C (PROC) GENE CAUSING VENOUS THROMBOSIS

      Blood coagulation & fibrinolysis
    57. BENZAKOUR O; KANTHOU C; LUPU F; DENNEHY U; GOODWIN C; SCULLY MF; KAKKAR VV; COOPER DN
      PROTHROMBIN CLEAVAGE BY HUMAN VASCULAR SMOOTH-MUSCLE CELLS - A POTENTIAL ALTERNATIVE PATHWAY TO THE COAGULATION CASCADE

      Journal of cellular biochemistry
    58. KRAWCZAK M; REITSMA PH; COOPER DN
      THE MUTATIONAL DEMOGRAPHY OF PROTEIN-C DEFICIENCY

      Human genetics
    59. HALLAM PJ; WACEY AI; MANNUCCI PM; LEGNANI C; KUHNAU W; KRAWCZAK M; KAKKAR VV; COOPER DN
      A NOVEL MISSENSE MUTATION (THR176-]ILE) AT THE PUTATIVE HINGE OF THE NEO N-TERMINUS OF ACTIVATED PROTEIN-C

      Human genetics
    60. TUDDENHAM EGD; PEMBERTON S; COOPER DN
      INHERITED FACTOR-VII DEFICIENCY - GENETICS AND MOLECULAR PATHOLOGY

      Thrombosis and haemostasis
    61. BENZAKOUR O; FORMSTONE C; RAHMAN S; KANTHOU C; DENNEHY U; SCULLY MF; COOPER DN; KAKKAR VV
      EVIDENCE FOR PROTEIN-S RECEPTOR(S) ON HUMAN VASCULAR SMOOTH-MUSCLE CELLS - ANALYSIS OF THE BINDING CHARACTERISTICS AND MITOGENIC PROPERTIESOF PROTEIN-S ON HUMAN VASCULAR SMOOTH-MUSCLE CELLS

      Thrombosis and haemostasis
    62. FORMSTONE CJ; WACEY AI; BERG LP; BEVAN D; ROWLEY M; VOKE J; BERNARDI F; LEGNANI C; SIMIONI P; GIROLAMI A; TIDDENHAM EGD; COOPER DN
      DETECTION AND CHARACTERIZATION OF 6 NOVEL PROTEIN-S (PROS) GENE LESIONS - EVALUATION OF RT-PCR AS A MUTATION SCREENING STRATEGY

      Thrombosis and haemostasis
    63. WINTER PC; SCOPES DA; BERG LP; MILLAR DS; MAYNE EE; KAKKAR VV; COOPER DN
      INVESTIGATION OF THE FUNCTIONAL-SIGNIFICANCE OF A FREQUENT LENGTH POLYMORPHISM IN THE PROMOTER OF THE HUMAN ANTITHROMBIN-III GENE

      Thrombosis and haemostasis
    64. BERG LP; SCOPES DA; GREENGARD JS; GRIFFIN JH; COOPER DN
      THE -1511 MUTATION IN THE PROTEIN-C GENE PROMOTER DISRUPTS THE BINDING-SITE FOR THE TRANSCRIPTIONAL ACTIVATOR, HEPATOCYTE NUCLEAR FACTOR-I (HNF-1)

      Thrombosis and haemostasis
    65. SORIA JM; BERG LP; FONTCUBERTA J; ESTIVILL X; COOPER DN; SALA N
      MESSENGER-RNA ANALYSIS OF 3 PROTEIN-C GENE-MUTATIONS THAT GENERATE PREMATURE STOP CODONS

      Thrombosis and haemostasis
    66. REITSMA PH; BERNARDI F; DOIG RG; GANDRILLE S; GREENGARD JS; IRELAND H; KRAWCZAK M; LIND B; LONG GL; POORT SR; SAITO H; SALA N; WITT I; COOPER DN
      PROTEIN-C DEFICIENCY - A DATABASE OF MUTATIONS, 1995 UPDATE

      Thrombosis and haemostasis
    67. BENZAKOUR O; KANTHOU C; DENNEHY U; ALHAQ A; BERG LP; KAKKAR VV; COOPER DN
      EVALUATION OF THE USE OF THE LUCIFERASE-REPORTER-GENE SYSTEM FOR GENE-REGULATION STUDIES INVOLVING CYCLIC AMP-ELEVATING AGENTS

      Biochemical journal
    68. BENZAKOUR O; FORMSTONE C; RAHMAN S; KANTHOU C; DENNEHY U; SCULLY MF; KAKKAR VV; COOPER DN
      EVIDENCE FOR A PROTEIN-S RECEPTOR(S) ON HUMAN VASCULAR SMOOTH-MUSCLE CELLS - ANALYSIS OF THE BINDING CHARACTERISTICS AND MITOGENIC PROPERTIES OF PROTEIN-S ON HUMAN VASCULAR SMOOTH-MUSCLE CELLS

      Biochemical journal
    69. KRAWCZAK M; COOPER DN
      CORE DATABASE

      Nature
    70. HALLAM PJ; MILLAR DS; KRAWCZAK M; KAKKAR VV; COOPER DN
      POPULATION DIFFERENCES IN THE FREQUENCY OF THE FACTOR-V LEIDEN VARIANT AMONG PEOPLE WITH CLINICALLY SYMPTOMATIC PROTEIN-C DEFICIENCY

      Journal of Medical Genetics
    71. FORMSTONE CJ; WACEY AI; BERG LP; RAHMAN S; BEVAN D; ROWLEY M; VOKE J; BERNARDI F; LEGNANI C; SIMIONI P; GIROLAMI A; TUDDENHAM EGD; KAKKAR VV; COOPER DN
      DETECTION AND CHARACTERIZATION OF 7 NOVEL PROTEIN-S (PROS) GENE LESIONS - EVALUATION OF REVERSE TRANSCRIPT-POLYMERASE CHAIN-REACTION AS A MUTATION SCREENING STRATEGY

      Blood
    72. ANTONARAKIS SE; ROSSITER JP; YOUNG M; HORST J; DEMOERLOOSE P; SOMMER SS; KETTERLING RP; KAZAZIAN HH; NEGRIER C; VINCIGUERRA C; GITSCHIER J; GOOSSENS M; GIRODON E; GHANEM N; PLASSA F; LAVERGNE JM; VIDAUD M; COSTA JM; LAURIAN Y; LIN SW; LIN SR; SHEN MC; LILLICRAP D; TAYLOR SAM; WINDSOR S; VALLEIX SV; NAFA K; SULTAN Y; DELPECH M; VNENCAKJONES CL; PHILLIPS JA; LJUNG RCR; KOUMBARELIS E; GIALERAKI A; MANDALAKI T; JENKINS PV; COLLINS PW; PASI KJ; GOODEVE A; PEAKE I; PRESTON FE; SCHWARTZ M; SCHEIBEL E; INGERSLEV J; COOPER DN; MILLAR DS; KAKKAR VV; GIANNELLI F; NAYLOR JA; TIZZANO EF; BAIGET M; DOMENECH M; ALTISENT C; TUSELL J; BENEYTO M; LORENZO JI; GAUCHER C; MAZURIER C; PEERLINCK K; MATTHIJS G; CASSIMAN JJ; VERMYLEN J; MORI PG; ACQUILA M; CAPRINO D; INABA H
      FACTOR-VIII GENE INVERSIONS IN SEVERE HEMOPHILIA-A - RESULTS OF AN INTERNATIONAL CONSORTIUM STUDY

      Blood
    73. BERG LP; SCOPES DA; ALHAQ A; KAKKAR VV; COOPER DN
      DISRUPTION OF A BINDING-SITE FOR HEPATOCYTE NUCLEAR FACTOR-1 IN THE PROTEIN-C GENE PROMOTER IS ASSOCIATED WITH HEREDITARY THROMBOPHILIA

      Human molecular genetics
    74. MILLAR DS; ALLGROVE J; RODECK C; KAKKAR VV; COOPER DN
      A HOMOZYGOUS DELETION INSERTION MUTATION IN THE PROTEIN-C (PROC) GENECAUSING NEONATAL PURPURA FULMINANS - PRENATAL-DIAGNOSIS IN AN AT-RISKPREGNANCY/

      Blood coagulation & fibrinolysis
    75. MILLAR DS; KAKKAR VV; COOPER DN
      SCREENING FOR INVERSIONS IN THE FACTOR-VIII (F8) GENE CAUSING SEVERE HEMOPHILIA-A

      Blood coagulation & fibrinolysis
    76. BERG LP; VARON D; MARTINOWITZ U; WIELAND K; KAKKAR VV; COOPER DN
      COMBINED FACTOR-VIII FACTOR-XI DEFICIENCY MAY CAUSE INTRA-FAMILIAL CLINICAL VARIABILITY IN HEMOPHILIA-A AMONG ASHKENAZI JEWS

      Blood coagulation & fibrinolysis
    77. COOPER DN
      THE MOLECULAR-GENETICS OF FAMILIAL VENOUS THROMBOSIS

      Bailliere's clinical haematology
    78. COOPER DN; BERG LP; KAKKAR VV; REISS J
      ECTOPIC (ILLEGITIMATE) TRANSCRIPTION - NEW POSSIBILITIES FOR THE ANALYSIS AND DIAGNOSIS OF HUMAN GENETIC-DISEASE

      Annals of medicine
    79. WACEY AI; KRAWCZAK M; KAKKAR VV; COOPER DN
      DETERMINANTS OF THE FACTOR-IX MUTATIONAL SPECTRUM IN HEMOPHILIA-B - AN ANALYSIS OF MISSENSE MUTATIONS USING A MULTIDOMAIN MOLECULAR-MODEL OF THE ACTIVATED

      Human genetics
    80. MILLAR DS; WACEY AI; RIBANDO J; MELISSARI E; LAURSEN B; WOODS P; KAKKAR VV; COOPER DN
      3 NOVEL MISSENSE MUTATIONS IN THE ANTITHROMBIN-III (AT3) GENE CAUSINGRECURRENT VENOUS THROMBOSIS

      Human genetics
    81. TUDDENHAM EGD; SCHWAAB R; SEEHAFER J; MILLAR DS; GITSCHIER J; HIGUCHI M; BIDICHANDANI S; CONNOR JM; HOYER LW; YOSHIOKA A; PEAKE IR; OLEK K; KAZAZIAN HH; LAVERGNE JM; GIANNELLI F; ANTONARAKIS SE; COOPER DN
      HEMOPHILIA-A - DATABASE OF NUCLEOTIDE SUBSTITUTIONS, DELETIONS, INSERTIONS AND REARRANGEMENTS OF THE FACTOR-VIII GENE, 2ND EDITION (VOL 22,PG 3511, 1994)

      Nucleic acids research
    82. TUDDENHAM EGD; SCHWAAB R; SEEHAFER J; MILLAR DS; GITSCHIER J; HIGUCHI M; BIDICHANDANI S; CONNOR JM; HOYER LW; YOSHIOKA A; PEAKE IR; OLEK K; KAZAZIAN HH; LAVERGNE JM; GIANNELLI F; ANTONARAKIS SE; COOPER DN
      HEMOPHILIA-A - DATABASE OF NUCLEOTIDE SUBSTITUTIONS, DELETIONS, INSERTIONS AND REARRANGEMENTS OF THE FACTOR-VIII GENE, 2ND EDITION

      Nucleic acids research
    83. COOPER DN
      NET INVESTMENT IN AGRICULTURAL TRACTORS

      Journal of agricultural economics
    84. COOPER DN; TUDDENHAM EGD
      MOLECULAR-GENETICS OF FAMILIAL VENOUS THROMBOSIS

      British Medical Bulletin
    85. RAYNER AJ; COOPER DN
      COINTEGRATION ANALYSIS AND THE UK DEMAND FOR NITROGEN-FERTILIZER

      Applied economics
    86. COOPER DN
      MAPPING THE HUMAN GENOME

      Annales de genetique
    87. MILLAR DS; LOPEZ A; WHITE D; ABRAHAM G; LAURSEN B; HOLDING S; REVERTER JC; REYNAUD J; MARTINOWITZ U; HAYES JPLA; KAKKAR VV; COOPER DN
      SCREENING FOR MUTATIONS IN THE ANTITHROMBIN-III GENE CAUSING RECURRENT VENOUS THROMBOSIS BY SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS

      Human mutation
    88. TAKAMIYA O; KEMBALLCOOK G; MARTIN DMA; COOPER DN; VONFELTEN A; MEILI E; HANN I; PRANGNELL DR; LUMLEY H; TUDDENHAM EGD; MCVEY JH
      DETECTION OF MISSENSE MUTATIONS BY SINGLE-STRAND CONFORMATIONAL POLYMORPHISM (SSCP) ANALYSIS IN 5 DYSFUNCTIONAL VARIANTS OF COAGULATION FACTOR-VII

      Human molecular genetics
    89. MILLAR DS; WACEY AI; VOKE J; KAKKAR VV; COOPER DN
      A NOVEL POINT MUTATION (VAL 297-]MET) IN THE SERINE PROTEINASE DOMAINOF PROTEIN-C IN A PATIENT WITH BOTH VENOUS AND ARTERIAL THROMBOEMBOLIC DISEASE

      Blood coagulation & fibrinolysis
    90. COOPER DN; SCHMIDTKE J
      DIAGNOSIS OF HUMAN GENETIC-DISEASE USING RECOMBINANT-DNA .4.

      Human genetics
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      Thrombosis and haemostasis
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      MOLECULAR-GENETIC ANALYSIS OF PROTEIN-S DEFICIENCY BY RT-PCR

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    98. FORMSTONE CJ; VOKE J; TUDDENHAM EGD; JENKINS E; CLARK J; LAYTON M; NICOLAIDES K; KAKKAR VV; COOPER DN
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      Thrombosis and haemostasis
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/12/20 alle ore 19:40:30