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    1. Shimizu, Y; Ikeda, S; Fujimori, M; Kodama, S; Nakahara, M; Okajima, M; Asahara, T
      Frequent alterations in the Wnt signaling pathway in colorectal cancer with microsatellite instability

      GENES CHROMOSOMES & CANCER
    2. Strippoli, P; Sarchielli, S; Santucci, R; Bagnara, GP; Brandi, G; Biasco, G
      Cold single-strand conformation polymorphism analysis: Optimization for detection of APC gene mutations in patients with familial adenomatous polyposis

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    3. Sekine, M; Nagata, H; Tsuji, S; Hirai, Y; Fujimoto, S; Hatae, M; Kobayashi, I; Fujii, T; Nagata, I; Ushijima, K; Obata, K; Suzuki, M; Yoshinaga, M; Umesaki, N; Satoh, S; Enomoto, T; Motoyama, S; Tanaka, K
      Mutational analysis of BRCA1 and BRCA2 and clinicopathologic analysis of ovarian cancer in 82 ovarian cancer families: Two common founder mutations of BRCA1 in Japanese population

      CLINICAL CANCER RESEARCH
    4. Wirtzfeld, DA; Petrelli, NJ; Rodriguez-Bigas, MA
      Hamartomatous polyposis syndromes: Molecular genetics, neoplastic risk, and surveillance recommendations

      ANNALS OF SURGICAL ONCOLOGY
    5. Hashemi, J; Bendahl, PO; Sandberg, T; Platz, A; Linder, S; Stierner, U; Olsson, H; Ingvar, C; Hansson, J; Borg, A
      Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families

      GENES CHROMOSOMES & CANCER
    6. Bruder, CEG; Hirvela, C; Tapia-Paez, I; Fransson, I; Segraves, R; Hamilton, G; Zhang, XX; Evans, DG; Wallace, AJ; Baser, ME; Zucman-Rossi, J; Hergersberg, M; Boltshauser, E; Papi, L; Rouleau, GA; Poptodorov, G; Jordanova, A; Rask-Andersen, H; Kluwe, L; Mautner, V; Sainio, M; Hung, G; Mathiesen, T; Moller, C; Pulst, SM; Harder, H; Heiberg, A; Honda, M; Miimura, M; Sahlen, S; Blennow, E; Albertson, DG; Pinkel, D; Dumanski, JP
      High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

      HUMAN MOLECULAR GENETICS
    7. Gutmann, DH; Hirbe, AC; Haipek, CA
      Functional analysis of neurofibromatosis 2 (NF2) missense mutations

      HUMAN MOLECULAR GENETICS
    8. Okai, T; Yamaguchi, Y; Sakai, J; Ohtsubo, K; Mouri, H; Sawabu, N
      Complete regression of colonic adenomas after treatment with sulindac in Gardner's syndrome: a 4-year follow-up

      JOURNAL OF GASTROENTEROLOGY
    9. Peshkin, BN; DeMarco, TA; Brogan, BM; Lerman, C; Isaacs, C
      BRCA1/2 testing: Complex themes in result interpretation

      JOURNAL OF CLINICAL ONCOLOGY
    10. Olschwang, S
      Digestive polyposes : genetic aspects

      GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE
    11. Werness, BA; Eltabbakh, GH
      Familial ovarian cancer and early ovarian cancer: Biologic, pathologic, and clinical features

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
    12. Andreassen, A; Vikse, R; Steffensen, IL; Paulsen, JE; Alexander, J
      Intestinal tumours induced by the food carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in multiple intestinal neoplasia mice have truncation mutations as well as loss of the wild-type Apc(+) allele

      MUTAGENESIS
    13. Tutt, A; Bertwistle, D; Valentine, J; Gabriel, A; Swift, S; Ross, G; Griffin, C; Thacker, J; Ashworth, A
      Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences

      EMBO JOURNAL
    14. Chang, J; Elledge, RM
      Clinical management of women with genomic BRCA1 and BRCA2 mutations

      BREAST CANCER RESEARCH AND TREATMENT
    15. Filipitsch, T; Wolf, B; Karner-Hanusch, J
      Results of molecular diagnosis in 30 Austrian families with familial adenomatous polyposis

      WIENER KLINISCHE WOCHENSCHRIFT
    16. Patronas, NJ; Courcoutsakis, N; Bromley, CM; Katzman, GL; MacCollin, M; Parry, DM
      Intramedullary and spinal canal tumors in patients with neurofibromatosis 2: MR imaging findings and correlation with genotype

      RADIOLOGY
    17. Hedenfalk, I; Duggan, D; Chen, YD; Radmacher, M; Bittner, M; Simon, R; Meltzer, P; Gusterson, B; Esteller, M; Kallioniemi, OP; Wilfond, B; Borg, A; Trent, J
      Gene-expression profiles in hereditary breast cancer.

      NEW ENGLAND JOURNAL OF MEDICINE
    18. Najera, C; Sanchez, F; Mateu, E; Prieto, F; Beneyto, M
      Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations

      MEDICINA CLINICA
    19. Saldanha, G
      The Hedgehog signalling pathway and cancer

      JOURNAL OF PATHOLOGY
    20. Bergthorsson, JT; Ejlertsen, B; Olsen, JH; Borg, A; Nielsen, KV; Barkardottir, RB; Klausen, S; Mouridsen, HT; Winther, K; Fenger, K; Niebuhr, A; Harboe, TL; Niebuhr, E
      BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age

      JOURNAL OF MEDICAL GENETICS
    21. Baser, ME; Friedman, JM; Evans, DGR
      Maternal gene effect in neurofibromatosis 2: fact or artefact?

      JOURNAL OF MEDICAL GENETICS
    22. Cetta, F; Curia, MC; Montalto, G; Gori, M; Cama, A; Battista, P; Barbarisi, A
      Thyroid carcinoma usually occurs in patients with familial adenomatous polyposis in the absence of biallelic inactivation of the adenomatous polyposis coli gene

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    23. Galea, MA; Eleftheriou, A; Henderson, BR
      ARM domain-dependent nuclear import of adenomatous polyposis coli protein is stimulated by the B56 alpha subunit of protein phosphatase 2A

      JOURNAL OF BIOLOGICAL CHEMISTRY
    24. Friedl, W; Caspari, R; Uhlhaas, S; Lamberti, C; Jungck, M; Kadmon, M; Wolf, M; Fahnenstich, J; Gebert, J; Moslein, G; Mangold, E; Propping, P
      Can APC: mutation analysis contribute to therapeutic decisions in familialadenomatous polyposis? Experience from 680 FAP families

      GUT
    25. Giardiello, FM; Brensinger, JD; Petersen, GM
      AGA technical review on hereditary colorectal cancer and genetic testing

      GASTROENTEROLOGY
    26. Della Torre, G; Pasini, B; Frigerio, S; Donghi, R; Rovini, D; Delia, D; Peters, G; Huot, TJG; Bianchi-Scarra, G; Lantieri, F; Rodolfo, M; Parmiani, G; Pierotti, MA
      CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation

      BRITISH JOURNAL OF CANCER
    27. Allen, RC; Webster, AR; Sui, R; Brown, J; Taylor, CM; Stone, EM
      Molecular characterization and ophthalmic investigation of a large family with type 2A Von Hippel-Lindau disease

      ARCHIVES OF OPHTHALMOLOGY
    28. Harbour, JW
      Molecular basis of low-penetrance retinoblastoma

      ARCHIVES OF OPHTHALMOLOGY
    29. Olschwang, S
      Intestinal polyposis

      ANNALES DE MEDECINE INTERNE
    30. Lasota, J; Fetsch, JF; Wozniak, A; Wasag, B; Sciot, R; Miettinen, M
      The neurofibromatosis type 2 gene is mutated in perineurial cell tumors - A molecular genetic study of eight cases

      AMERICAN JOURNAL OF PATHOLOGY
    31. Loman, N; Johannsson, O; Kristoffersson, U; Olsson, H; Borg, A
      Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutationsin a population-based series of early-onset breast cancer

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    32. Phay, JE; Moley, JF; Lairmore, TC
      Multiple endocrine neoplasias

      SEMINARS IN SURGICAL ONCOLOGY
    33. Chong, JM; Koshiishi, N; Kurihara, K; Kubono, S; Kawai, T; Fukayama, M
      Aspiration and imprint cytopathology of thyroid carcinoma associated with familial adenomatous polyposis

      DIAGNOSTIC CYTOPATHOLOGY
    34. de Leon, MP; Roncucci, L
      The cause of colorectal cancer

      DIGESTIVE AND LIVER DISEASE
    35. Crow, JF
      The origins patterns and implications of human spontaneous mutation

      NATURE REVIEWS GENETICS
    36. Crawford, R; Everest, S; Mackay, J
      Familial ovarian malignancy

      HOSPITAL MEDICINE
    37. Russell, LB; Hunsicker, PR; Kerley, MK; Johnson, DK; Shelby, MD
      Bleomycin, unlike other male-mouse mutagens, is most effective in spermatogonia, inducing primarily deletions

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    38. Sieber, OM; Tomlinson, IP; Lamlum, H
      The adenomatous polyposis coli (APC) tumour suppressor - genetics, function and disease

      MOLECULAR MEDICINE TODAY
    39. Dipple, KM; McCabe, ERB
      Modifier genes convert "simple" Mendelian disorders to complex traits

      MOLECULAR GENETICS AND METABOLISM
    40. Grzybowska, E; Zientek, H; Jasinska, A; Rusin, M; Kozlowski, P; Sobczak, K; Sikorska, A; Kwiatkowska, E; Gorniak , L; Kalinowska, E; Utracka-Hutka, B; Wloch, J; Chmielik, E; Krzyzosiak, WJ
      High frequency of recurrent mutations in BRCA1 and BRCA2 genes in Polish families with breast and ovarian cancer

      HUMAN MUTATION
    41. Koul, A; Malander, S; Loman, N; Pejovic, T; Heim, S; Willen, R; Johannson, O; Olsson, H; Ridderheim, M; Borg, A
      BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER
    42. Paunu, N; Sallinen, SL; Karhu, R; Miettinen, H; Sallinen, P; Kononen, J; Laippala, P; Simola, KOJ; Helen, P; Haapasalo, H
      Chromosome imbalances in familial gliomas detected by comparative genomic hybridization

      GENES CHROMOSOMES & CANCER
    43. DiCiommo, D; Gallie, BL; Bremner, R
      Retinoblastoma: the disease, gene and protein provide critical leads to understand cancer

      SEMINARS IN CANCER BIOLOGY
    44. Aaltonen, LA
      Hereditary intestinal cancer

      SEMINARS IN CANCER BIOLOGY
    45. Aunoble, B; Sanches, R; Didier, E; Bignon, YJ
      Major oncogenes and tumor suppressor genes involved in epithelial ovarian cancer (Review)

      INTERNATIONAL JOURNAL OF ONCOLOGY
    46. Kuschel, B; Lux, MP; Goecke, TO; Beckmann, MW
      Prevention and therapy for BRCA1/2 mutation carriers and women at high risk for breast and ovarian cancer

      EUROPEAN JOURNAL OF CANCER PREVENTION
    47. Ravid, A; Barschack, I; Hirsh-Yechezkel, G; Goldberg, I; Bar-Sade, RB; Chetrit, A; Reder, I; Ben-Baruch, C; Gotlieb, WH; Koplovic, J; Friedman, E
      Immunohistochemical analyses of sporadic and familial (185delAG carriers) ovarian cancer in Israel

      EUROPEAN JOURNAL OF CANCER
    48. Vasen, HFA
      Clinical diagnosis and management of hereditary colorectal cancer syndromes

      JOURNAL OF CLINICAL ONCOLOGY
    49. Ogiso, Y; Ueno, M; Fujimori, M; Fukushima, Y; Katsuyama, T
      A novel non-pathogenetic polymorphism of the APC gene in a patient with familial adenomatous polyposis coli

      JAPANESE JOURNAL OF CLINICAL ONCOLOGY
    50. Sestini, R; Vivarelli, R; Balestri, P; Ammannati, F; Montali, E; Papi, L
      Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene

      HUMAN GENETICS
    51. Grobbelaar, JJ; Fortuin, R; Scholtz, CL; Zikind, A; Langenhoven, E; Wyllie, AH; Bubb, VJ; Kotze, MJ
      Familial adenomatous polyposis coli in South Africa - Molecular basis and diagnosis

      SOUTH AFRICAN MEDICAL JOURNAL
    52. Tsao, H
      Update on familial cancer syndromes and the skin

      JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
    53. Lim, DJ; Rubenstein, AE; Evans, DG; Jacks, T; Seizinger, BG; Baser, ME; Beebe, D; Brackmann, DE; Chiocca, EA; Fehon, RG; Giovannini, M; Glazer, R; Gusella, JF; Gutmann, DH; Korf, B; Lieberman, F; Martuza, R; McClatchey, AI; Parry, DM; Pulst, SM; Ramesh, V; Ramsey, WJ; Ratner, N; Rutkowski, JL; Ruttledge, M; Weinstein, DE
      Advances in neurofibromatosis 2 (NF2): A workshop report

      JOURNAL OF NEUROGENETICS
    54. Boyd, J; Sonoda, Y; Federici, MG; Bogomolniy, F; Rhei, E; Maresco, DL; Saigo, PE; Almadrones, LA; Barakat, RR; Brown, CL; Chi, DS; Curtin, JP; Poynor, EA; Hoskins, WJ
      Clinicopathologic features of BRCA-linked and sporadic ovarian cancer

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    55. Sainio, M; Jaaskelainen, J; Pihlaja, H; Carpen, O
      Mild familial neurofibromatosis 2 associates with expression of merlin with altered COOH-terminus

      NEUROLOGY
    56. Kainu, T; Juo, SHH; Desper, R; Schaffer, AA; Gillanders, E; Rozenblum, E; Freas-Lutz, D; Weaver, D; Stephan, D; Bailey-Wilson, J; Kallioniemi, OP; Tirkkonen, M; Syrjakoski, K; Kuukasjarvi, T; Koivisto, P; Karhu, R; Holli, K; Arason, A; Johannesdottir, G; Bergthorsson, JT; Johannsdottir, H; Egilsson, V; Barkardottir, RB; Johannsson, O; Haraldsson, K; Sandberg, T; Holmberg, E; Gronberg, H; Olsson, H; Borg, A; Vehmanen, P; Eerola, H; Heikkila, P; Pyrhonen, S; Nevanlinna, H
      Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    57. Bolk, S; Pelet, A; Hofstra, RMW; Angrist, M; Salomon, R; Croaker, D; Buys, CHCM; Lyonnet, S; Chakravarti, A
      A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    58. Lamszus, K; Vahldiek, F; Mautner, VF; Schichor, C; Tonn, J; Stavrou, D; Fillbrandt, R; Westphal, M; Kluwe, L
      Allelic losses in neurofibromatosis 2-associated meningiomas

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    59. Evans, DGR; Sainio, M; Baser, ME
      Neurofibromatosis type 2

      JOURNAL OF MEDICAL GENETICS
    60. Evans, DGR; Newton, V; Neary, W; Baser, ME; Wallace, A; Macleod, R; Jenkins, JPR; Gillespie, J; Ramsden, RT
      Use of MRI and audiological tests in presymptomatic diagnosis of type 2 neurofibromatosis (NF2)

      JOURNAL OF MEDICAL GENETICS
    61. Kluwe, L; Friedrich, RE; Hagel, C; Lindenau, M; Mautner, VF
      Mutations and allelic loss of the NF2 gene in neurofibromatosis 2-associated skin tumors

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    62. Barreto, DC; Gomez, RS; Bale, AE; Boson, WL; De Marco, L
      PTCH gene mutations in odontogenic keratocysts

      JOURNAL OF DENTAL RESEARCH
    63. Peelen, T; de Leeuw, W; van Lent, K; Morreau, H; van Eijk, R; van Vliet, M; Wijnen, J; Ligtenberg, M; Ginjaar, HB; Zweemer, R; Menko, F; Fodde, R; van Ommen, GJB; Vasen, HFA; Cornelisse, CJ; Devilee, P
      Genetic analysis of a breast-ovarian cancer family, with 7 cases of colorectal cancer linked to BRCA1, fails to support a role for BRCA1 in colorectal tumorigenesis

      INTERNATIONAL JOURNAL OF CANCER
    64. Woodford-Richens, K; Bevan, S; Churchman, M; Dowling, B; Jones, D; Norbury, CG; Hodgson, SV; Desai, D; Neale, K; Phillips, RKS; Young, J; Leggett, B; Dunlop, M; Rozen, P; Eng, C; Markie, D; Rodriguez-Bigas, MA; Sheridan, E; Iwama, T; Eccles, D; Smith, GT; Kim, JC; Kim, KM; Sampson, JR; Evans, G; Tejpar, S; Bodmer, WF; Tomlinson, IPM; Houlston, RS
      Analysis of genetic and phenotypic heterogeneity in juvenile polyposis

      GUT
    65. Roijers, JFM; de Wit, MJ; van der Luijt, RB; van Amstel, HKP; Hoppener, JWM; Lips, CJM
      Criteria for mutation analysis in MEN 1-suspected patients: MEN 1 case-finding

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    66. Umetani, N; Watanabe, T; Sasaki, S; Nagawa, H
      Rectosigmoidal adenomatous polyposis: A novel entity of polyposis? Report of a case

      DISEASES OF THE COLON & RECTUM
    67. Savithri, HS; Murthy, HSV; Baskaran, G; Rao, NA; Kool, D; Edkins, E; Wang, W; Bittles, AH
      Predictive testing for familial adenomatous polyposis in a rural South Indian community

      CLINICAL GENETICS
    68. Huang, SC; Chen, CR; Lavine, JE; Taylor, SF; Newbury, RO; Pham, TTT; Ricciardiello, L; Carethers, JM
      Genetic heterogeneity in familial juvenile polyposis

      CANCER RESEARCH
    69. Kauraniemi, P; Hedenfalk, I; Persson, K; Duggan, DJ; Tanner, M; Johannsson, O; Olsson, H; Trent, JM; Isola, J; Borg, A
      MYB oncogene amplification in hereditary BRCA1 breast cancer

      CANCER RESEARCH
    70. Yazici, H; Bitisik, O; Akisik, E; Cabioglu, N; Saip, P; Muslumanoglu, M; Glendon, G; Bengisu, E; Ozbilen, S; Dincer, M; Turkmen, S; Andrulis, IL; Dalay, N; Ozcelik, H
      BRCA1 and BRCA2 mutations in Turkish breast/ovarian families and young breast cancer patients

      BRITISH JOURNAL OF CANCER
    71. Singh, AD; Santos, MCM; Shields, CL; Shields, JA; Eagle, RC
      Observations on 17 patients with retinocytoma

      ARCHIVES OF OPHTHALMOLOGY
    72. Miyaki, M; Iijima, T; Ishii, R; Hishima, T; Mori, T; Yoshinaga, K; Takami, H; Kuroki, T; Iwama, T
      Molecular evidence for multicentric development of thyroid carcinomas in patients with familial adenomatous polyposis

      AMERICAN JOURNAL OF PATHOLOGY
    73. Gorski, B; Byrski, T; Huzarski, T; Jakubowska, A; Menkiszak, J; Gronwald, J; Pluzanska, A; Bebenek, M; Fischer-Maliszewska, L; Grzybowska, E; Narod, SA; Lubinski, J
      Founder mutations in the BRCA1 gene in polish families with breast-ovariancancer

      AMERICAN JOURNAL OF HUMAN GENETICS
    74. McGuire, V; Whittemore, AS; Norris, R; Oakley-Girvan, I
      Survival in epithelial ovarian cancer patients with prior breast cancer

      AMERICAN JOURNAL OF EPIDEMIOLOGY
    75. Yasui, W; Yokozaki, H; Shimamoto, F; Tahara, H; Tahara, E
      Molecular-pathological diagnosis of gastrointestinal tissues and its contribution to cancer histopathology

      PATHOLOGY INTERNATIONAL
    76. Lohmann, DR
      RB1 gene mutations in retinoblastoma

      HUMAN MUTATION
    77. Legoix, P; Legrand, MF; Ollagnon, E; Lenoir, G; Thomas, G; Zucman-Rossi, J
      Characterisation of 16 polymorphic markers in the NF2 gene: Application tohemizygosity detection

      HUMAN MUTATION
    78. Giarola, M; Stagi, L; Presciuttini, S; Mondini, P; Radice, MT; Sala, P; Pierotti, MA; Bertario, L; Radice, P
      Screening for mutations of the APC gene in 66 Italian familial adenomatouspolyposis patients: Evidence for phenotypic differences in cases with and without identified mutation

      HUMAN MUTATION
    79. Poncin, J; Mulkens, J; Arends, JW; de Goeij, A
      Optimizing the APC gene mutation analysis in archival colorectal tumor tissue

      DIAGNOSTIC MOLECULAR PATHOLOGY
    80. Bruder, CEG; Ichimura, K; Blennow, E; Ikeuchi, T; Yamaguchi, T; Yuasa, Y; Collins, VP; Dumanski, JP
      Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: Possible localization of a neurofibromatosis type 2 modifier gene?

      GENES CHROMOSOMES & CANCER
    81. Balci, A; Huusko, P; Paakkonen, K; Launonen, V; Uner, A; Ekmekci, A; Winqvist, R
      Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414de14 found in male breast cancer

      EUROPEAN JOURNAL OF CANCER
    82. Phillips, HA
      The role of the p53 tumour suppressor gene in human breast cancer

      CLINICAL ONCOLOGY
    83. Rapallo, A; Sciutto, A; Geido, E; Orecchia, R; Infusini, E; Pujic, N; d'Amore, ESG; Monaco, R; Risio, M; Rossini, FP; Giaretti, W
      K-ras2 activation and genome instability increase proliferation and size of FAP adenomas

      ANALYTICAL CELLULAR PATHOLOGY
    84. Iwama, T; Konishi, M; Iijima, T; Yoshinaga, K; Tominaga, T; Koike, M; Miyaki, M
      Somatic mutation of the APC gene in thyroid carcinoma associated with familial adenomatous polyposis

      JAPANESE JOURNAL OF CANCER RESEARCH
    85. Cohen, MM
      Nevoid basal cell carcinoma syndrome: molecular biology and new hypotheses

      INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY
    86. Giovannini, M; Robanus-Maandag, E; Niwa-Kawakita, M; van der Valk, M; Woodruff, JM; Goutebroze, L; Merel, P; Berns, A; Thomas, G
      Schwann cell hyperplasia and tumors in transgenic mice expressing a naturally occurring mutant NF2 protein

      GENES & DEVELOPMENT
    87. Kulaylat, MN; Karakousis, CP; Keaney, CM; McCorvey, D; Bem, J; Ambrus, JL
      Desmoid tumour: a pleomorphic lesion

      EUROPEAN JOURNAL OF SURGICAL ONCOLOGY
    88. Li, G; Tamura, K; Yamamoto, Y; Sashio, H; Utsunomiya, J; Yamamura, T; Shimoyama, T; Furuyama, J
      Molecular and clinical study of familial adenomatous polyposis for genetictesting and management

      JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH
    89. Sagawa, T; Yamashita, Y; Fujimoto, T; Yamada, H; Hoshi, N; Sakuragi, N; Fujimoto, S
      Clinicopathological comparisons of familial and sporadic cases in 219 consecutive Japanese epithelial ovarian cancer patients

      JAPANESE JOURNAL OF CLINICAL ONCOLOGY
    90. Schuyer, M; Berns, EMJJ
      Is TP53 dysfunction required for BRCA1-associated carcinogenesis?

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    91. Yamashita, Y; Sagawa, T; Fujimoto, T; Sugawara, T; Yamada, H; Hoshi, N; Sakuragi, N; Ishioka, C; Fujimoto, S
      BRCA1 mutation testing for Japanese patients with ovarian cancer in breastcancer screening

      BREAST CANCER RESEARCH AND TREATMENT
    92. Fidalgo, PO; Maia, LC; Cravo, ML; Albuquerque, CM; Suspiro, A; Ramalho, E; Nobre-Leitao, C
      Seven novel mutations in the APC gene of Portuguese families with familialadenomatous polyposis: Correlation with phenotype

      CANCER GENETICS AND CYTOGENETICS
    93. Hahn, M; Kruppa, C; Pistorius, S; Schackert, HK
      Predictive molecular diagnosis and preventive surgical treatment of colorectal carcinoma. A new field of interest for surgical research

      ZENTRALBLATT FUR CHIRURGIE
    94. Harbour, JW
      Tumor suppressor genes in ophthalmology

      SURVEY OF OPHTHALMOLOGY
    95. Smardova, J
      FASAY: a simple functional assay in yeast for identification of p53 mutation in tumors

      NEOPLASMA
    96. Spain, BH; Larson, CJ; Shihabuddin, LS; Gage, FH; Verma, IM
      Truncated BRCA2 is cytoplasmic: Implications for cancer-linked mutations

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    97. Evans, DGR; Lye, R; Neary, W; Black, G; Strachan, T; Wallace, A; Ramsden, RT
      Probability of bilateral disease in people presenting with a unilateral vestibular schwannoma

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    98. Wallis, YL; Morton, DG; McKeown, CM; Macdonald, F
      Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition

      JOURNAL OF MEDICAL GENETICS
    99. Tonin, PN; Mes-Masson, AM; Narod, SA; Ghadirian, P; Provencher, D
      Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history

      CLINICAL GENETICS
    100. Petersen, GM; Brensinger, JD; Johnson, KA; Giardiello, FM
      Genetic testing and counseling for hereditary forms of colorectal cancer

      CANCER


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/10/20 alle ore 13:00:23