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    1. Harada, H; Nagai, NH; Tsuneizumi, M; Mikami, I; Sugano, S; Emi, M
      Identification of DMC1, a novel gene in the TOC region on 17q25.1 that shows loss of expression in multiple human cancers

      JOURNAL OF HUMAN GENETICS
    2. O'Neill, S; Ekstrom, L; Lastowska, M; Roberts, P; Brodeur, GM; Kees, UR; Schwab, M; Bown, N
      MYCN amplification and 17q in neuroblastoma: Evidence for structural association

      GENES CHROMOSOMES & CANCER
    3. Plantaz, D
      Neuroblastoma, one century after Pepper: Which genes?

      ARCHIVES DE PEDIATRIE
    4. Mikami, I; Harada, H; Nagai, H; Tsuneizumi, M; Nobe, Y; Koizumi, K; Sugano, S; Tanaka, S; Emi, M
      Down-regulation in multiple human cancers of a novel gene, DMHC, from 17q25.1 that encodes an integral membrane protein

      JAPANESE JOURNAL OF CANCER RESEARCH
    5. Krygier, S; Djakiew, D
      Molecular characterization of the loss of p75(NTR) expression in human prostate tumor cells

      MOLECULAR CARCINOGENESIS
    6. Lastowska, M; Cullinane, C; Variend, S; Cotterill, S; Bown, N; O'Neill, S; Mazzocco, K; Roberts, P; Nicholson, J; Ellershaw, C; Pearson, ADJ; Jackson, MS
      Comprehensive genetic and histopathologic study reveals three types of neuroblastoma tumors

      JOURNAL OF CLINICAL ONCOLOGY
    7. Tajiri, T; Tanaka, S; Shono, K; Kinoshita, Y; Fujii, Y; Suita, S; Ihara, K; Hara, T
      Quick quantitative analysis of gene dosages associated with prognosis in neuroblastoma

      CANCER LETTERS
    8. McConville, CM; Dyer, S; Rees, SA; Luttikhuis, MEMO; McMullan, DJ; Vickers, SJ; Ramani, P; Redfern, D; Morland, BJ
      Molecular cytogenetic characterization of two non-MYCN amplified neuroblastoma cell lines with complex t(11;17)

      CANCER GENETICS AND CYTOGENETICS
    9. Morerio, C; Russo, I; Rosanda, C; Rapella, A; Leszl, A; Basso, G; Maserati, E; Pasquali, F; Panarello, C
      17q21-qter trisomy is an indicator of poor prognosis in acute myelogenous leukemia

      CANCER GENETICS AND CYTOGENETICS
    10. Bown, N; Lastowska, M; Cotterill, S; O'Neill, S; Ellershaw, C; Roberts, P; Lewis, L; Pearson, ADJ
      17q gain in neuroblastoma predicts adverse clinical outcome

      MEDICAL AND PEDIATRIC ONCOLOGY
    11. Lastowska, M; Van Roy, N; Bown, N; Speleman, F; Roberts, P; Lunec, J; Strachan, T; Pearson, ADJ; Jackson, MS
      Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma

      MEDICAL AND PEDIATRIC ONCOLOGY
    12. Reid, A; Gribble, SM; Huntly, BJP; Andrews, KM; Campbell, L; Grace, CD; Wood, ME; Green, AR; Nacheva, EP
      Variant Philadelphia translocations in chronic myeloid leukaemia can mimictypical blast crisis chromosome abnormalities or classic t(9;22): a reportof two cases

      BRITISH JOURNAL OF HAEMATOLOGY
    13. Udayakumar, AM; Sundareshan, TS; Goud, TM; Biswas, S; Devi, MG; Kumari, BSA; Appaji, L
      Cytogenetics of neuroblastoma: A study using fine needle aspiration cultures

      ANNALES DE GENETIQUE
    14. Gordon, AT; Brinkschmidt, C; Anderson, J; Coleman, N; Dockhorn-Dworniczak, B; Pritchard-Jones, K; Shipley, J
      A novel and consistent amplicon at 13q31 associated with alveolar rhabdomyosarcoma

      GENES CHROMOSOMES & CANCER
    15. Kuhlenbaumer, G; Stogbauer, F; Timmerman, V; De Jonghe, P
      Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection

      NEUROMUSCULAR DISORDERS
    16. Britton, RA; Chen, SM; Wallis, D; Koeuth, T; Powell, BS; Shaffer, LG; Largaespada, D; Jenkins, NA; Copeland, NG; Court, DL; Lupski, JR
      Isolation and preliminary characterization of the human and mouse homologues of the bacterial cell cycle gene era

      GENOMICS
    17. Pestonjamasp, PH; Mittra, I
      Analysis of BRCA1 involvement in breast cancer in Indian women

      JOURNAL OF BIOSCIENCES
    18. Panarello, C; Morerio, C; Russo, I; Pasquali, F; Rapella, A; Corrias, MV; Morando, A; Rosanda, C
      Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation

      CANCER GENETICS AND CYTOGENETICS
    19. Islam, A; Kageyama, H; Hashizume, K; Kaneko, Y; Nakagawara, A
      Role of survivin, whose gene is mapped to 17q25, in human neuroblastoma and identification of a novel dominant-negative isoform, survivin-beta/2B

      MEDICAL AND PEDIATRIC ONCOLOGY
    20. McManus, K; Lupe, K; Coghlan, G; Zelinski, T
      An amino acid substitution in the putative second extracellular loop of RBC band 3 accounts for the Froese blood group polymorphism

      TRANSFUSION
    21. Stogbauer, F; Young, P; Kuhlenbaumer, G; De Jonghe, P; Timmerman, V
      Hereditary recurrent focal neuropathies - Clinical and molecular features

      NEUROLOGY
    22. van Alfen, N; van Engelen, BGM; Reinders, JWC; Kremer, H; Gabreels, FJM
      The natural history of hereditary neuralgic amyotrophy in the Dutch population - Two distinct types?

      BRAIN
    23. Risk, JM; Mills, HS; Garde, J; Dunn, JR; Evans, KE; Hollstein, M; Field, JK
      The tylosis esophageal cancer (TOC) locus: more than just a familial cancer gene

      DISEASES OF THE ESOPHAGUS
    24. Vassilakis, DA; Sourvinos, G; Markatos, M; Psathakis, K; Spandidos, DA; Siafakas, NM; Bouros, D
      Microsatellite DNA instability and loss of heterozygosity in pulmonary sarcoidosis

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    25. Hirai, M; Yoshida, S; Kashiwagi, H; Kawamura, T; Ishikawa, T; Kaneko, M; Ohkawa, H; Nakagawara, A; Miwa, M; Uchida, K
      1q23 gain is associated with progressive neuroblastoma resistant to aggressive treatment

      GENES CHROMOSOMES & CANCER
    26. Orsetti, B; Courjal, F; Cuny, M; Rodriguez, C; Theillet, C
      17q21-q25 aberrations in breast cancer: combined allelotyping and CGH analysis reveals 5 regions of allelic imbalance among which two correspond to DNA amplification

      ONCOGENE
    27. Risk, JM; Ruhrberg, C; Hennies, HC; Mills, HS; Di Colandrea, T; Evans, KE; Ellis, A; Watt, FM; Bishop, DT; Spurr, NK; Stevens, HP; Leigh, IM; Reis, A; Kelsell, DP; Field, JK
      Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): The integration of genetic and physical maps of the TOC region on 17q25

      GENOMICS
    28. Maris, JM; Matthay, KK
      Molecular biology of neuroblastoma

      JOURNAL OF CLINICAL ONCOLOGY
    29. Zhang, K; Howes, KA; He, W; Bronson, JD; Pettenati, MJ; Chen, CK; Palczewski, K; Wensel, TG; Baehr, W
      Structure, alternative splicing, and expression of the human RGS9 gene

      GENE
    30. Nastiuk, KL; Mansukhani, M; Terry, MB; Kularatne, P; Rubin, MA; Melamed, J; Gammon, MD; Ittmann, M; Krolewski, JJ
      Common mutations in BRCA1 and BRCA2 do not contribute to early prostate cancer in Jewish men

      PROSTATE
    31. Quezado, MM; Moskaluk, CA; Bryant, B; Mills, SE; Merino, MJ
      Incidence of loss of heterozygosity at p53 and BRCA1 loci in serous surface carcinoma

      HUMAN PATHOLOGY
    32. Higgins, JJ; Adler, RL; Loveless, JM
      Mutational analysis of the tau gene in progressive supranuclear palsy

      NEUROLOGY
    33. Park, SJ; Chan, PJ; Seraj, IM; King, A
      Denaturing gradient cel electrophoresis screening of the BRCA1 gene in cells from precancerous cervical lesions

      JOURNAL OF REPRODUCTIVE MEDICINE
    34. Toyota, M; Ho, C; Ohe-Toyota, M; Baylin, SB; Issa, JPJ
      Inactivation of CACNA1G, a T-type calcium channel gene, by aberrant methylation of its 5 ' CpG island in human tumors

      CANCER RESEARCH
    35. LASTOWSKA M; VANROY N; BROWN N; SPELEMAN F; LUNEC J; STRACHAN T; PEARSON ADJ; JACKSON MS
      MOLECULAR CYTOGENETIC DELINEATION OF 17Q TRANSLOCATION BREAKPOINTS INNEUROBLASTOMA CELL-LINES

      Genes, chromosomes & cancer
    36. VANDESOMPELE J; VANROY N; VANGELE M; LAUREYS G; AMBROS P; HEIMANN P; DEVALCK C; SCHUURING E; BROCK P; OTTEN J; GYSELINCK J; DEPAEPE A; SPELEMAN F
      GENETIC-HETEROGENEITY OF NEUROBLASTOMA STUDIED BY COMPARATIVE GENOMICHYBRIDIZATION

      Genes, chromosomes & cancer
    37. Abujiang, P; Mori, TJ; Takahashi, T; Tanaka, F; Kasyu, I; Hitomi, S; Hiai, H
      Loss of heterozygosity (LOH) at 17q and 14q in human lung cancers

      ONCOGENE
    38. SLENTZKESLER KA; HALE LP; KAUFMAN RE
      IDENTIFICATION AND CHARACTERIZATION OF K12 (SECTM1), A NOVEL HUMAN GENE THAT ENCODES A GOLGI-ASSOCIATED PROTEIN WITH TRANSMEMBRANE AND SECRETED ISOFORMS

      Genomics
    39. STOGBAUER F; YOUNG P; KUHLENBAUMER G; MEULEMAN J; TIMMERMAN V; VANBROECKHOVEN C; KURLEMANN G; RINGELSTEIN EB
      HEREDITARY NEURALGIC AMYOTROPHY (HNA) - C LINICAL FINDINGS AND MOLECULAR-GENETICS

      Fortschritte der Neurologie, Psychiatrie
    40. GIORDANA MT; MIGHELI A; PAVANELLI E
      ISOCHROMOSOME 17Q IS A CONSTANT FINDING IN MEDULLOBLASTOMA - AN INTERPHASE CYTOGENETIC STUDY ON TISSUE-SECTIONS

      Neuropathology and applied neurobiology
    41. DIAKOUMIS E; SOURVINOS G; KIARIS H; DELAKAS D; CRANIDIS A; SPANDIDOS DA
      GENETIC INSTABILITY IN RENAL-CELL CARCINOMA

      European urology
    42. GARCIAPATINO E; GOMENDIO B; LLEONART M; SILVA JM; GARCIA JM; PROVENCIO M; CUBEDO R; ESPANA P; CAJAL SRY; BONILLA F
      LOSS OF HETEROZYGOSITY IN THE REGION INCLUDING THE BRCA1 GENE ON 17Q IN COLON-CANCER

      Cancer genetics and cytogenetics
    43. WALTZ MR; PANDELIDIS SM; PRATT W; BARNES D; SWALLOW DM; GENDLER SJ; COHEN EP
      A MICROSATELLITE WITHIN THE MUC1 LOCUS AT 1Q21 IS ALTERED IN THE NEOPLASTIC-CELLS OF BREAST-CANCER PATIENTS

      Cancer genetics and cytogenetics
    44. ESTERLING LE; YOSHIKAWA T; TURNER G; BADNER JA; BENGEL D; GERSHON ES; BERRETTINI WH; DETERAWADLEIGH SD
      SEROTONIN TRANSPORTER (5-HTT) GENE AND BIPOLAR AFFECTIVE-DISORDER

      American journal of medical genetics
    45. LEHRER S; FODOR F; STOCK RG; STONE NN; ENG C; SONG HK; MCGOVERN M
      ABSENCE OF 185DELAG MUTATION OF THE BRCA1 GENE AND 6174DELT MUTATION OF THE BRCA2 GENE IN ASHKENAZI JEWISH MEN WITH PROSTATE-CANCER

      British Journal of Cancer
    46. Kuhlenbaeumer, G; Meuleman, J; Schirmacher, A; Stoegbauer, F; Ringelstein, EB; Wehnert, M; Hoeltzenbein, M; Van Broeckhoven, C; Timmerman, V
      Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicingfactor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA)

      ANNALS OF HUMAN GENETICS
    47. BERGA SL
      EARLY OVARIAN-CANCER - A REVIEW OF ITS GENETIC AND BIOLOGICAL FACTORS, DETECTION, AND TREATMENT

      Current problems in obstetrics, gynecology and fertility
    48. DEVILEE P; HERMANS J; EYFJORD J; BORRESEN AL; LIDEREAU R; SOBOL H; BORG A; CLETONJANSEN AM; OLAH E; COHEN B; SCHERNECK S; HAMANN U; PETERLIN B; CALIGO M; BIGNON YL; MAUGARD C; ANDERSEN TI; ODEGAND AEM; BIECHE I; BIRNBAUM D; CORNELISSE CJ; SZTAN M; STEEL MR; SEITZ S; LOGAR N; GOLOUH R; GHIMENTI C; BRUELLE S; JOALLAND MP
      LOSS OF HETEROZYGOSITY AT 7Q31 IN BREAST-CANCER - RESULTS FROM AN INTERNATIONAL COLLABORATIVE STUDY-GROUP

      Genes, chromosomes & cancer
    49. GOMENDIO B; SILVA JM; PROVENCIO M; GARCIA JM; GARCIAPATINO E; GARCIAANDRADE C; CARRETERO L; ESPANA P; BONILLA F
      PROGNOSTIC IMPLICATIONS OF LOSS OF HETEROZYGOSITY IN THE 17Q21 REGIONIN BREAST-CANCER

      International journal of oncology
    50. SOURVINOS G; KIARIS H; TSIKKINIS A; VASSILAROS S; SPANDIDOS DA
      MICROSATELLITE INSTABILITY AND LOSS OF HETEROZYGOSITY IN PRIMARY BREAST-TUMORS

      Tumor biology
    51. ROBINSON RL; MONNIER N; WOLZ W; JUNG M; REIS A; NUERNBERG G; CURRAN JL; MONSIEURS K; STIEGLITZ P; HEYTENS L; FRICKER R; VANBROECKHOVEN C; DEUFEL T; HOPKINS PM; LUNARDI J; MUELLER CR
      A GENOME WIDE SEARCH FOR SUSCEPTIBILITY LOCI IN 3 EUROPEAN MALIGNANT HYPERTHERMIA PEDIGREES

      Human molecular genetics
    52. LASTOWSKA M; COTTERILL S; PEARSON ADJ; ROBERTS P; MCGUCKIN A; LEWIS I; BOWN N
      GAIN OF CHROMOSOME ARM 17Q PREDICTS UNFAVORABLE OUTCOME IN NEUROBLASTOMA PATIENTS

      European journal of cancer
    53. KALIKIN LM; FRANK TS; SVOBODANEWMAN SM; WETZEL JC; COONEY KA; PETTY EM
      A REGION OF INTERSTITIAL 17Q25 ALLELIC LOSS IN OVARIAN-TUMORS COINCIDES WITH A DEFINED REGION OF LOSS IN BREAST-TUMORS

      Oncogene
    54. VISSCHER DW; SARKAR FH; CRISSMAN JD
      MOLECULAR-GENETIC ANALYSIS IN THE PATHOLOGICAL EVALUATION OF SOLID TUMORS - THEORY AND PRACTICE

      Journal of clinical laboratory analysis
    55. BODEY B; BODEY B; GROGER AM; SIEGEL SE; KAISER HE
      NM23 NUCLEOSIDE DIPHOSPHATE (NDP) KINASE EXPRESSION IN HUMAN-MALIGNANT MELANOMAS - SIGNIFICANCE AND IMPLICATIONS IN TUMOR BIOLOGY/

      Anticancer research
    56. LARSON JS; TONKINSON JL; LAI MT
      A BRCA1 MUTANT ALTERS G(2)-M CELL-CYCLE CONTROL IN HUMAN MAMMARY EPITHELIAL-CELLS

      Cancer research
    57. SPANDIDOS DA; SOURVINOS G; KIARIS H; TSAMPARLAKIS J
      MICROSATELLITE INSTABILITY AND LOSS OF HETEROZYGOSITY IN HUMAN PTERYGIA

      British journal of ophthalmology
    58. MONNIER N; PROCACCIO V; STIEGLITZ P; LUNARDI J
      MALIGNANT-HYPERTHERMIA SUSCEPTIBILITY IS ASSOCIATED WITH A MUTATION OF THE ALPHA(1)-SUBUNIT OF THE HUMAN DIHYDROPYRIDINE-SENSITIVE L-TYPE VOLTAGE-DEPENDENT CALCIUM-CHANNEL RECEPTOR IN SKELETAL-MUSCLE

      American journal of human genetics
    59. KALIKIN LM; QU XA; FRANK TS; CADUFF RF; SVOBODA SM; LAW DJ; PETTY EM
      DETAILED DELETION ANALYSIS OF SPORADIC BREAST-TUMORS DEFINES AN INTERSTITIAL REGION OF ALLELIC LOSS ON 17Q25

      Genes, chromosomes & cancer
    60. XU CF; SOLOMON E
      MUTATIONS OF THE BRCA1 GENE IN HUMAN CANCER

      Seminars in cancer biology
    61. TUNNY TJ; XU L; RICHARDSON KA; STOWASSER M; GARTSIDE M; GORDON RD
      INSERTION DELETION POLYMORPHISM OF THE ANGIOTENSIN-CONVERTING ENZYME GENE AND LOSS OF THE INSERTION ALLELE IN ALDOSTERONE-PRODUCING ADENOMA/

      Journal of human hypertension
    62. FEUNTEUN J; LENOIR GM
      BRCA1, A GENE INVOLVED IN INHERITED PREDISPOSITION TO BREAST AND OVARIAN-CANCER

      Biochimica et biophysica acta, CR. Reviews on cancer
    63. CHEN TP; DHINGRA K; SAHIN A; SNEIGE N; HORTOBAGYI G; ALDAZ CM
      TECHNICAL APPROACH FOR THE STUDY OF THE GENETIC EVOLUTION OF BREAST-CANCER FROM PARAFFIN-EMBEDDED TISSUE-SECTIONS

      Breast cancer research and treatment
    64. CANNONALBRIGHT LA; SKOLNICK MH
      THE GENETICS OF FAMILIAL BREAST-CANCER

      Seminars in oncology
    65. HEALY JMS; QUANE KA; KEATING KE; LEHANE M; HEFFRON JJA; MCCARTHY TV
      DIAGNOSIS OF MALIGNANT HYPERTHERMIA - A COMPARISON OF THE IN-VITRO CONTRACTURE TEST WITH THE MOLECULAR-GENETIC DIAGNOSIS IN A LARGE PEDIGREE

      Journal of Medical Genetics
    66. FUJII H; SZUMEL R; MARSH C; ZHOU WB; GABRIELSON E
      GENETIC PROGRESSION, HISTOLOGICAL GRADE, AND ALLELIC LOSS IN DUCTAL CARCINOMA IN-SITU OF THE BREAST

      Cancer research
    67. MUNN KE; WALKER RA; MENASCE L; VARLEY JM
      ALLELIC IMBALANCE IN THE REGION OF THE BRCA1 GENE IN DUCTAL CARCINOMAIN-SITU OF THE BREAST

      British Journal of Cancer
    68. BECKMANN MW; PICARD F; AN HX; VANROEYEN CRC; DOMINIK SI; MOSNY DS; SCHNURCH HG; BENDER HG; NIEDERACHER D
      CLINICAL IMPACT OF DETECTION OF LOSS OF HETEROZYGOSITY OF BRCA1 AND BRCA2 MARKERS IN SPORADIC BREAST-CANCER

      British Journal of Cancer
    69. SERFAS KD; BOSE D; PATEL L; WROGEMANN K; PHILLIPS MS; MACLENNAN DH; GREENBERG CR
      COMPARISON OF THE SEGREGATION OF THE RYR1 C1840T MUTATION WITH SEGREGATION OF THE CAFFEINE HALOTHANE CONTRACTURE TEST-RESULTS FOR MALIGNANTHYPERTHERMIA SUSCEPTIBILITY IN A LARGE MANITOBA MENNONITE FAMILY

      Anesthesiology
    70. WALLACE AJ; WOOLDRIDGE W; KINGSTON IIM; HARRISON MJ; ELLIS FR; FORD PM
      MALIGNANT HYPERTHERMIA - A LARGE KINDRED LINKED TO THE RYR1 GENE

      Anaesthesia
    71. MACLENNAN DH
      DISCORDANCE BETWEEN PHENOTYPE AND GENOTYPE IN MALIGNANT HYPERTHERMIA

      Current opinion in neurology
    72. CORNELIS RS; NEUHAUSEN SL; JOHANSSON O; ARASON A; KELSELL D; PONDER BAJ; TONIN P; HAMANN U; LINDBLOM A; LALLE P; LONGY M; OLAH E; SCHERNECK S; BIGNON YJ; SOBOL H; CHANGCLAUDE J; LARSSON C; SPURR N; BORG A; BARKARDOTTIR RB; NAROD S; DEVILEE P
      HIGH ALLELE LOSS RATES AT 17Q12-Q21 IN BREAST AND OVARIAN-TUMORS FROMBRCA1-LINKED FAMILIES

      Genes, chromosomes & cancer
    73. BERNARDGALLON D; GOSSE S; ESSIOUX L; LAURENTPUIG P; RALLIERE C; CURE H; BAY JO; SCHRAUB S; BONAITIPELLIE C; SOBOL H; BIGNON YJ
      ANALYSES OF LINKAGE TO 17Q11-Q23 IN 3 FRENCH HEREDITARY NONPOLYPOSIS COLON-CANCER FAMILIES

      International journal of oncology
    74. MATSUSHIMA M; KOBAYASHI K; EMI M; SAITO H; SAITO J; SUZUMORI K; NAKAMURA Y
      MUTATION ANALYSIS OF THE BRCA1 GENE IN 76 JAPANESE OVARIAN-CANCER PATIENTS - 4 GERMLINE MUTATIONS, BUT NO EVIDENCE OF SOMATIC MUTATION

      Human molecular genetics
    75. LAW DJ; PRASAD MA; KING SE; SPRANGER KD; LEE YH; FOX RE; COLLINS EE; GEBUHR TC; MILLER DE; PETTY EM
      LOCALIZATION OF THE HUMAN ESTROGEN-RESPONSIVE FINGER PROTEIN (EFP) GENE (ZNF147) WITHIN A YAC CONTIG CONTAINING THE MYELOPEROXIDASE (MPO) GENE

      Genomics
    76. BISHOP DT
      THE GAW9 BREAST-CANCER LINKAGE DATA SET

      Genetic epidemiology
    77. LEVIN ML; SHAFFER LG; LEWIS RA; GRESIK MV; LUPSKI JR
      UNIQUE DE-NOVO INTERSTITIAL DELETION OF CHROMOSOME-17, DEL(17) (Q23.2Q24.3) IN A FEMALE NEWBORN WITH MULTIPLE CONGENITAL-ANOMALIES

      American journal of medical genetics
    78. PURDIE CA; PIRIS J; BIRD CC; WYLLIE AH
      17Q ALLELE LOSS IS ASSOCIATED WITH LYMPH-NODE METASTASIS IN LOCALLY AGGRESSIVE HUMAN COLORECTAL-CANCER

      Journal of pathology
    79. RADFORD DM; FAIR KL; PHILLIPS NJ; RITTER JH; STEINBRUECK T; HOLT MS; DONISKELLER H
      ALLELOTYPING OF DUCTAL CARCINOMA IN-SITU OF THE BREAST - DELETION OF LOCI ON 8P, 13Q, 16Q, 17P AND 17Q

      Cancer research
    80. TAKAHASHI H; BEHBAKHT K; MCGOVERN PE; CHIU HC; COUCH FJ; WEBER BL; FRIEDMAN LS; KING MC; FURUSATO M; LIVOLSI VA; MENZIN AW; LIU PC; BENJAMIN I; MORGAN MA; KING SA; REBANE BA; CARDONICK A; MIKUTA JJ; RUBIN SC; BOYD J
      MUTATION ANALYSIS OF THE BRCA1 GENE IN OVARIAN CANCERS

      Cancer research
    81. VIEL A; DALLAGNESE L; CANZONIERI V; SOPRACORDEVOLE F; CAPOZZI E; CARBONE A; VISENTIN MC; BOIOCCHI M
      SUPPRESSIVE ROLE OF THE METASTASIS-RELATED NM23-H1 GENE IN HUMAN OVARIAN CARCINOMAS - ASSOCIATION OF HIGH MESSENGER-RNA EXPRESSION WITH LACK OF LYMPH-NODE METASTASIS

      Cancer research
    82. MANDAI M; KONISHI I; KOMATSU T; MORI T; ARAO S; NOMURA H; KANDA Y; HIAI H; FUKUMOTO M
      MUTATION OF THE NM23 GENE, LOSS OF HETEROZYGOSITY AT THE NM23 LOCUS AND K-RAS MUTATION IN OVARIAN-CARCINOMA - CORRELATION WITH TUMOR PROGRESSION AND NM23 GENE-EXPRESSION

      British Journal of Cancer
    83. SCHILDKRAUT JM; COLLINS NK; DENT GA; TUCKER JA; BARRETT JC; BERCHUCK A; BOYD J
      LOSS OF HETEROZYGOSITY ON CHROMOSOME 17Q11-21 IN CANCERS OF WOMEN WHOHAVE BOTH BREAST AND OVARIAN-CANCER

      American journal of obstetrics and gynecology
    84. FUTREAL PA; COCHRAN C; ROSENTHAL J; MIKI Y; SWENSON J; HOBBS M; BENNETT LM; HAUGENSTRANO A; MARKS J; BARRETT JC; TAVTIGIAN SV; SHATTUCKEIDENS D; KAMB A; SKOLNICK M; WISEMAN RW
      ISOLATION OF A DIVERGED HOMEOBOX GENE, MOX1, FROM THE BRCA1 REGION ON17Q21 BY SOLUTION HYBRID CAPTURE

      Human molecular genetics
    85. KEATING KE; QUANE KA; MANNING BM; LEHANE M; HARTUNG E; CENSIER K; URWYLER A; KLAUSNITZER M; MULLER CR; HEFFRON JJA; MCCARTHY TV
      DETECTION OF A NOVEL RYR1 MUTATION IN 4 MALIGNANT HYPERTHERMIA PEDIGREES

      Human molecular genetics
    86. KAMB A; FUTREAL PA; ROSENTHAL J; COCHRAN C; HARSHMAN KD; LIU QY; PHELPS RS; TAVTIGIAN SV; TRAN T; HUSSEY C; BELL R; MIKI Y; SWENSEN J; HOBBS MR; MARKS J; BENNETT LM; BARRETT JC; WISEMAN RW; SHATTUCKEIDENS D
      LOCALIZATION OF THE VHR PHOSPHATASE CANE AND ITS ANALYSIS AS A CANDIDATE FOR BRCA1

      Genomics
    87. KRAINER M
      GENETIC PREDISPOSITION FOR BREAST-CANCER - FROM EPIDEMIOLOGIC STUDIESTO MOLECULAR-GENETICS

      Onkologie
    88. ZELADAHEDMAN M; TORROELLA M; MESQUITA R; NORDENSKJOLD M; SKOOG L; LINDBLOM A
      LOSS OF HETEROZYGOSITY STUDIES IN TUMORS FROM FAMILIES WITH BREAST-OVARIAN CANCER SYNDROME

      Human genetics
    89. VOGELSTEIN B; KINZLER KW
      HAS THE BREAST-CANCER GENE BEEN FOUND

      Cell
    90. OSTERMEYER EA; FRIEDMAN LS; LYNCH ED; SZABO CI; DOWD P; LEE MK; ROWELL SE; KING MC
      GREEN PIGS, RED HERRINGS, AND A GOLDEN HOE - A RETROSPECTIVE ON THE IDENTIFICATION OF BRCA1 AND THE BEGINNING OF ITS CHARACTERIZATION

      Cold Spring Harbor Symposia on Quantitative Biology
    91. ROTHUIZEN J; WOLFSWINKEL J; LENSTRA JA; FRANTS RR
      THE INCIDENCE OF MINI-SATELLITE AND MICRO-SATELLITE REPETITIVE DNA INTHE CANINE GENOME

      Theoretical and Applied Genetics
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/05/20 alle ore 08:17:16