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    1. CHENEVIXTRENCH G; SPURDLE A; VENTER D; SOUTHEY M; HOPPER J
      USING LARGE CASE-CONTROL STUDIES TO FIND LOW-RISK GENES FOR BREAST AND OVARIAN-CANCER

      European journal of human genetics
    2. WRIGHT K; WILSON PJ; KERR J; DO K; HURST T; KHOO SK; WARD B; CHENEVIXTRENCH G
      FREQUENT LOSS OF HETEROZYGOSITY AND 3 CRITICAL REGIONS ON THE SHORT ARM OF CHROMOSOME-8 IN OVARIAN ADENOCARCINOMAS

      Oncogene
    3. WICKING C; SIMMS LA; EVANS T; WALSH M; CHAWENGSAKSOPHAK K; BECK F; CHENEVIXTRENCH G; YOUNG J; JASS J; LEGGETT B; WAINWRIGHT B
      CDX2, A HUMAN HOMOLOG OF DROSOPHILA CAUDAL, IS MUTATED IN BOTH ALLELES IN A REPLICATION ERROR POSITIVE COLORECTAL-CANCER

      Oncogene
    4. WICKING C; EVANS T; HENK B; HAYWARD N; SIMMS LA; CHENEVIXTRENCH G; PIETSCH T; WAINWRIGHT B
      NO EVIDENCE FOR THE H133Y MUTATION IN SONIC HEDGEHOG IN A COLLECTION OF COMMON TUMOR TYPES

      Oncogene
    5. SMYTH I; WICKING C; WAINWRIGHT B; CHENEVIXTRENCH G
      THE EFFECTS OF SPLICE-SITE MUTATIONS IN PATIENTS WITH NEVOID BASAL-CELL CARCINOMA SYNDROME

      Human genetics
    6. KOHONENCORISH M; YOUNG J; CHENEVIXTRENCH G; DOE WF
      UROKINASE RECEPTOR GENOTYPES IN COLORECTAL-CANCER

      Carcinogenesis (New York. Print)
    7. SHI YC; KERR J; HURST TG; KHOO SK; WARD BG; CHENEVIXTRENCH G
      NO EVIDENCE FOR MICROSATELLITE INSTABILITY FROM ALLELOTYPE ANALYSIS OF BENIGN AND LOW MALIGNANT POTENTIAL OVARIAN NEOPLASMS

      Gynecologic oncology (Print)
    8. OBATA K; MORLAND SJ; WATSON RH; HITCHCOCK A; CHENEVIXTRENCH G; THOMAS EJ; CAMPBELL IG
      FREQUENT PTEN MMAC MUTATIONS IN ENDOMETRIOID BUT NOT SEROUS OR MUCINOUS EPITHELIAL OVARIAN-TUMORS/

      Cancer research
    9. WEBB PM; GREEN A; CUMMINGS MC; PURDIE DM; WALSH MD; CHENEVIXTRENCH G
      RELATIONSHIP BETWEEN NUMBER OF OVULATORY CYCLES AND ACCUMULATION OF MUTANT P53 IN EPITHELIAL OVARIAN-CANCER

      Journal of the National Cancer Institute
    10. CHOI C; CHO SH; HORIKAWA I; BERCHUCK A; WANG N; CEDRONE E; JHUNG SW; LEE JB; KERR J; CHENEVIXTRENCH G; KIM SY; BARRETT JC; KOI M
      LOSS OF HETEROZYGOSITY AT CHROMOSOME SEGMENT XQ25-26.1 IN ADVANCED HUMAN OVARIAN CARCINOMAS

      Genes, chromosomes & cancer
    11. CHENEVIXTRENCH G; KERR J; HURST T; SHIH YC; PURDIE D; BERGMAN L; FRIEDLANDER M; SANDERSON B; ZOURNAZI A; COOMBS T; LEARY JA; CRAWFORD E; SHELLING AN; COOKE I; GANESAN TS; SEARLE J; CHOI C; BARRETT JC; KHOO SK; WARD B
      ANALYSIS OF LOSS OF HETEROZYGOSITY AND KRAS2 MUTATIONS IN OVARIAN NEOPLASMS - CLINICOPATHOLOGICAL CORRELATIONS

      Genes, chromosomes & cancer
    12. SIMMS LA; ZOU TT; YOUNG J; SHI YQ; LEI JY; APPEL R; RHYU MG; SUGIMURA H; CHENEVIXTRENCH G; SOUZA RF; MELTZER SJ; LEGGETT BA
      APPARENT PROTECTION FROM INSTABILITY OF REPEAT SEQUENCES IN CANCER-RELATED GENES IN REPLICATION ERROR POSITIVE GASTROINTESTINAL CANCERS

      Oncogene
    13. WICKING C; GILLIES S; SMYTH I; SHANLEY S; FOWLES L; RATCLIFFE J; WAINWRIGHT B; CHENEVIXTRENCH G
      DE-NOVO MUTATIONS OF THE PATCHED GENE IN NEVOID BASAL-CELL CARCINOMA SYNDROME HELP TO DEFINE THE CLINICAL PHENOTYPE

      American journal of medical genetics
    14. SHIH YC; KERR J; LIU J; HURST T; KHOO SK; WARD B; WAINWRIGHT B; CHENEVIXTRENCH G
      RARE MUTATIONS AND NO HYPERMETHYLATION AT THE CDKN2A LOCUS IN EPITHELIAL OVARIAN-TUMORS

      International journal of cancer
    15. RADFORD G; SMITH I; BUTTENSHAW R; BIDEN K; SIMMS L; CHENEVIXTRENCH G; YOU J; LEGGETT B
      FREQUENCY OF P53-MUTATIONS IN 64 RER-SPORADIC AND RER-SPORADIC COLORECTAL CANCERS - FURTHER EVIDENCE FOR SEPARATE PATHWAYS IN TUMORIGENESIS()

      Gastroenterology
    16. PIETSCH T; WAHA A; KOCH A; KRAUS J; ALBRECHT S; TONN J; SORENSEN N; BERTHOLD F; HENK B; SCHMANDT N; WOLF HK; VONDEIMLING A; WAINWRIGHT B; CHENEVIXTRENCH G; WIESTLER OD; WICKING C
      MEDULLOBLASTOMAS OF THE DESMOPLASTIC VARIANT CARRY MUTATIONS OF THE HUMAN HOMOLOG OF DROSOPHILA PATCHED

      Cancer research
    17. WICKING C; SMYTH I; GILLIES S; EVANS T; PIETSCH T; FIETZ M; CHENEVIXTRENCH G; WAINWRIGHT B
      THE INVOLVEMENT OF THE HEDGEHOG PATCHED SIGNALING PATHWAY IN NBCCS AND TUMORIGENESIS

      American journal of human genetics
    18. WICKING C; SHANLEY S; SMYTH I; GILLIES S; NEGUS K; GRAHAM S; SUTHERS G; HAITES N; EDWARDS M; WAINWRIGHT B; CHENEVIXTRENCH G
      MOST GERM-LINE MUTATIONS IN THE NEVOID BASAL-CELL CARCINOMA SYNDROME LEAD TO A PREMATURE TERMINATION OF THE PATCHED PROTEIN, AND NO GENOTYPE-PHENOTYPE CORRELATIONS ARE EVIDENT

      American journal of human genetics
    19. CHENEVIXTRENCH G; COOMBS T; KERR J; PURDIE D; GREEN A; CUMMINGS MC
      FERTILITY AND INCIDENCE OF KRAS2 MUTATIONS IN BORDERLINE OVARIAN ADENOCARCINOMAS

      Journal of the National Cancer Institute
    20. KERR J; LEARY JA; HURST T; SHIH YC; ANTALIS TM; FRIEDLANDER M; CRAWFORD E; KHOO SK; WARD B; CHENEVIXTRENCH G
      ALLELIC LOSS ON CHROMOSOME 7Q IN OVARIAN ADENOCARCINOMAS - 2 CRITICALREGIONS AND A REARRANGEMENT OF THE PLANH1 LOCUS

      Oncogene
    21. HAHN H; WICKING C; ZAPHIROPOULOS PG; GAILANI MR; SHANLEY S; CHIDAMBARAM A; VORECHOVSKY I; HOLMBERG E; UNDEN AB; GILLIES S; NEGUS K; SMYTH I; PRESSMAN C; LEFFELL DJ; GERRARD B; GOLDSTEIN AM; DEAN M; TOFTGARD R; CHENEVIXTRENCH G; WAINWRIGHT B; BALE AE
      MUTATIONS OF THE HUMAN HOMOLOG OF DROSOPHILA PATCHED IN THE NEVOID BASAL-CELL CARCINOMA SYNDROME

      Cell
    22. GUSTAFSON CE; WILSON PJ; LUKEIS R; BAKER E; WOOLLATT E; ANNAB L; HAWKE L; BARRETT JC; CHENEVIXTRENCH G
      FUNCTIONAL EVIDENCE FOR A COLORECTAL-CANCER TUMOR-SUPPRESSOR GENE AT CHROMOSOME 8P22-23 BY MONOCHROMOSOME TRANSFER

      Cancer research
    23. FOSTER KA; HARRINGTON P; KERR J; RUSSELL P; DICIOCCIO RA; SCOTT IV; JACOBS I; CHENEVIXTRENCH G; PONDER BAJ; GAYTHER SA
      SOMATIC AND GERMLINE MUTATIONS OF THE BRCA2 GENE IN SPORADIC OVARIAN-CANCER

      Cancer research
    24. DUFFY DL; HEALEY SC; CHENEVIXTRENCH G; MARTIN NG; WEGER J; LICHTER J
      ATOPY IN AUSTRALIA

      Nature genetics
    25. YOUNG J; SEARLE J; BUTTENSHAW R; THOMAS L; WARD M; CHENEVIXTRENCH G; LEGGETT B
      AN ALU VPA MARKER ON CHROMOSOME-I DEMONSTRATES THAT REPLICATION ERRORS MANIFEST AT THE ADENOMA CARCINOMA TRANSITION IN SPORADIC COLORECTAL TUMORS

      Genes, chromosomes & cancer
    26. SHANLEY SM; DAWKINS H; WAINWRIGHT BJ; WICKING C; HEENAN P; ELDON M; SEARLE J; CHENEVIXTRENCH G
      FINE DELETION MAPPING ON THE LONG ARM OF CHROMOSOME-9 IN SPORADIC ANDFAMILIAL BASAL-CELL CARCINOMAS

      Human molecular genetics
    27. WICKING C; BREEN M; NEGUS K; BERKMAN J; EVDOKIOU A; COWLED P; CHENEVIXTRENCH G; WAINWRIGHT B
      THE HUMAN GROWTH-ARREST-SPECIFIC GENE GAS 1 MAPS OUTSIDE THE CANDIDATE REGION OF THE GENE FOR NEVOID BASAL-CELL CARCINOMA SYNDROME

      Cytogenetics and cell genetics
    28. SHANLEY SM; CHENEVIXTRENCH G; PALMER J; HAYWARD N
      GLUTATHIONE-S-TRANSFERASE GSTM1 NULL GENOTYPE IS NOT OVERREPRESENTED IN AUSTRALIAN PATIENTS WITH NEVOID BASAL-CELL CARCINOMA SYNDROME OR SPORADIC MELANOMA

      Carcinogenesis
    29. CHENEVIXTRENCH G; YOUNG J; COGGAN M; BOARD P
      GLUTATHIONE-S-TRANSFERASE M1 AND T1 POLYMORPHISMS - SUSCEPTIBILITY TOCOLON-CANCER AND AGE-OF-ONSET

      Carcinogenesis
    30. LEARY JA; KERR J; CHENEVIXTRENCH G; DORIS CP; HURST T; ROGERS C; HOUGHTON CRS; FRIEDLANDER ML
      INCREASED EXPRESSION OF THE NME1 GENE IS ASSOCIATED WITH METASTASIS IN EPITHELIAL OVARIAN-CANCER

      International journal of cancer
    31. LEGGETT BA; CORNWELL M; THOMAS LR; BUTTENSHAW RL; CHENEVIXTRENCH G; SEARLE J; YOUNG J; WARD M
      REPLICATION ERROR STATUS OF COLORECTAL CARCINOMAS AND PREDICTION OF RISK OF METACHRONOUS CARCINOMA WHILE ON A COLONOSCOPY FOLLOW-UP PROGRAM

      Gastroenterology
    32. RATCLIFFE JF; SHANLEY S; CHENEVIXTRENCH G
      THE PREVALENCE OF CERVICAL AND THORACIC CONGENITAL SKELETAL ABNORMALITIES IN BASAL-CELL NEVUS SYNDROME - A REVIEW OF CERVICAL AND CHEST RADIOGRAPHS IN 80 PATIENTS WITH BCNS

      British journal of radiology
    33. RATCLIFFE JF; SHANLEY S; FERGUSON J; CHENEVIXTRENCH G
      THE DIAGNOSTIC-IMPLICATION OF FALCINE CALCIFICATION ON PLAIN SKULL RADIOGRAPHS OF PATIENTS WITH BASAL-CELL NEVUS SYNDROME AND THE INCIDENCEOF FALCINE CALCIFICATION IN THEIR RELATIVES AND 2 CONTROL-GROUPS

      British journal of radiology
    34. LEGGETT B; YOUNG J; BUTTENSHAW R; THOMAS L; YOUNG B; CHENEVIXTRENCH G; SEARLE J; WARD M
      COLORECTAL CARCINOMAS SHOW FREQUENT ALLELIC LOSS ON THE LONG ARM OF CHROMOSOME-17 WITH EVIDENCE FOR A SPECIFIC TARGET REGION

      British Journal of Cancer
    35. MITCHELL LE; HEALEY SC; CHENEVIXTRENCH G
      EVIDENCE FOR AN ASSOCIATION BETWEEN NONSYNDROMIC CLEFT-LIP WITH OR WITHOUT CLEFT-PALATE AND A GENE LOCATED ON THE LONG ARM OF CHROMOSOME-4

      American journal of human genetics
    36. CHENEVIXTRENCH G; GUSTAFSON CE; ANNAB L; BARRETT C
      FUNCTIONAL EVIDENCE FOR A TUMOR-SUPPRESSOR GENE ON CHROMOSOME-8 BY MONOCHROMOSOME TRANSFER INTO COLORECTAL-CANCER CELL-LINES

      American journal of human genetics
    37. WICKING C; GILLIES S; NEGUS K; SMYTH I; BERKMAN J; SHANLEY S; CHENEVIXTRENCH G; WAINWRIGHT B
      GENETIC AND PHYSICAL MAPPING OF THE GENE FOR NEVOID BASAL-CELL CARCINOMA SYNDROME

      American journal of human genetics
    38. BERKMAN J; ARMOUR JAL; CHENEVIXTRENCH G; WICKING C; WAINWRIGHT B
      SIMPLE REPEAT POLYMORPHISM AT THE D9S151 LOCUS

      Human molecular genetics
    39. YOUNG J; BUTTENSHAW R; BUTTERWORTH L; WARD M; SEARLE J; LEGGETT B; CHENEVIXTRENCH G
      ASSOCIATION OF THE SS GENOTYPE OF THE L-MYC GENE AND LOSS OF 18Q SEQUENCES WITH A WORSE CLINICAL PROGNOSIS IN COLORECTAL CANCERS

      Oncogene
    40. WICKING C; BERKMAN J; WAINWRIGHT B; CHENEVIXTRENCH G
      FINE GENETIC-MAPPING OF THE GENE FOR NEVOID BASAL-CELL CARCINOMA SYNDROME

      Genomics
    41. HEALEY S; POWELL F; BATTERSBY M; CHENEVIXTRENCH G; MCGILL J
      DISTINCT PHENOTYPE IN MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME-14

      American journal of medical genetics
    42. SHANLEY S; RATCLIFFE J; HOCKEY A; HAAN E; OLEY C; RAVINE D; MARTIN N; WICKING C; CHENEVIXTRENCH G
      NEVOID BASAL-CELL CARCINOMA SYNDROME - REVIEW OF 118 AFFECTED INDIVIDUALS

      American journal of medical genetics
    43. WILSON L; BURN J; CURTIS A; KORENBERG J; CHENEVIXTRENCH G; ALLAN L; GOODSHIP J
      EXCLUSION OF ATRIOVENTRICULAR SEPTAL-DEFECT IN A LARGE DOMINANT PEDIGREE FROM THE DOWNS-SYNDROME REGION

      Journal of Medical Genetics
    44. GUSTAFSON CE; YOUNG J; LEGGETT B; SEARLE J; CHENEVIXTRENCH G
      LOSS OF HETEROZYGOSITY ON THE LONG ARM OF CHROMOSOME-11 IN COLORECTALTUMORS

      British Journal of Cancer
    45. CHENEVIXTRENCH G; KERR J; FRIEDLANDER M; HURST T; SANDERSON B; COGLAN M; WARD B; LEARY J; KHOO SK
      HOMOZYGOUS DELETIONS ON THE SHORT ARM OF CHROMOSOME-9 IN OVARIAN ADENOCARCINOMA CELL-LINES AND LOSS OF HETEROZYGOSITY IN SPORADIC TUMORS

      American journal of human genetics
    46. YOUNG J; LEGGETT B; GUSTAFSON C; WARD M; SEARLE J; THOMAS L; BUTTENSHAW R; CHENEVIXTRENCH G
      GENOMIC INSTABILITY OCCURS IN COLORECTAL CARCINOMAS BUT NOT IN ADENOMAS

      Human mutation
    47. WICKING C; BERKMAN J; SHARPE H; WAINWRIGHT B; CHENEVIXTRENCH G
      FURTHER CHARACTERIZATION OF THE GORLIN SYNDROME LOCUS

      Cytogenetics and cell genetics
    48. REEDER JA; DICKINSON JL; CHENEVIXTRENCH G; ANTALIS TM
      SODIUM-BUTYRATE DIFFERENTIALLY MODULATES PLASMINOGEN-ACTIVATOR INHIBITOR TYPE-1, UROKINASE PLASMINOGEN-ACTIVATOR, AND ITS RECEPTOR IN A HUMAN COLON-CARCINOMA CELL

      Teratogenesis, carcinogenesis, and mutagenesis
    49. LEGGETT BA; THOMAS LR; KNIGHT N; HEALEY S; CHENEVIXTRENCH G; SEARLE J
      EXCLUSION OF APC AND MCC AS THE GENE DEFECT IN ONE FAMILY WITH FAMILIAL JUVENILE POLYPOSIS

      Gastroenterology
    50. WILSON L; CURTIS A; KORENBERG JR; SCHIPPER RD; ALLAN L; CHENEVIXTRENCH G; STEPHENSON A; GOODSHIP J; BURN J
      A LARGE, DOMINANT PEDIGREE OF ATRIOVENTRICULAR SEPTAL-DEFECT (AVSD) -EXCLUSION FROM THE DOWN-SYNDROME CRITICAL REGION ON CHROMOSOME-21

      American journal of human genetics
    51. LEGGETT B; YOUNG J; BUTTENSHAW R; BUTTERWORTH L; CHENEVIXTRENCH G
      THE SS GENOTYPE OF L-MYC IS ASSOCIATED WITH THE OCCURRENCE OF DISTANTMETASTASES AND LOSS OF HETEROZYGOSITY OF 17P AND 18Q IN COLORECTAL CANCERS

      American journal of human genetics
    52. WICKING C; BERKMAN J; SHARPE H; NEGUS K; WAINWRIGHT BJ; CHENEVIXTRENCH G
      FURTHER CHARACTERIZATION OF THE GORLIN SYNDROME LOCUS

      American journal of human genetics
    53. CHENEVIXTRENCH G; WICKING C; BERKMAN J; SHARPE H; HOCKEY A; HAAN E; OLEY C; RAVINE D; TURNER A; GOLDGAR D; SEARLE J; WAINWRIGHT B
      FURTHER LOCALIZATION OF THE GENE FOR NEVOID BASAL-CELL CARCINOMA SYNDROME (NBCCS) IN 15 AUSTRALASIAN FAMILIES - LINKAGE AND LOSS OF HETEROZYGOSITY

      American journal of human genetics


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Documento generato il 04/08/20 alle ore 02:50:00