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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. Hruban, RH; Iacobuzio-Donahue, C; Wilentz, RE; Goggins, M; Kern, SE
      Molecular pathology of pancreatic cancer

      CANCER JOURNAL
    3. Klein, AP; Hruban, RH; Brune, KA; Petersen, GM; Goggins, M
      Familial pancreatic cancer

      CANCER JOURNAL
    4. Yao, QP; Wang, SJ; Glorioso, JC; Evans, CH; Robbins, PD; Ghivizzani, SC; Oligino, TJ
      Gene transfer of p53 to arthritic joints stimulates synovial apoptosis andinhibits inflammation

      MOLECULAR THERAPY
    5. Pei, Y
      A 'two-hit' model of cystogenesis in autosomal dominant polycystic kidney disease?

      TRENDS IN MOLECULAR MEDICINE
    6. Voswinkel, J; Weisgerber, K; Pfreundschuh, M; Gause, A
      B lymphocyte involvement in ankylosing spondylitis: the heavy chain variable segment gene repertoire of B lymphocytes from germinal center-like foci in the synovial membrane indicates antigen selection

      ARTHRITIS RESEARCH
    7. Esposito, I; Friess, H; Buchler, MW
      Carcinogenesis of cancer of the papilla and ampulla: pathophysiological facts and molecular biological mechanisms

      LANGENBECKS ARCHIVES OF SURGERY
    8. Druck, T; Podolski, J; Byrski, T; Wyrwicz, L; Zajaczek, S; Kata, G; Borowka, A; Lubinski, J; Huebner, K
      The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation

      JOURNAL OF HUMAN GENETICS
    9. Jackson, AL; Loeb, LA
      The contribution of endogenous sources of DNA damage to the multiple mutations in cancer

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    10. Grant, WF; Owens, ET
      Chromosome aberration assays in Pisum for the study of environmental mutagens

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    11. Bianchi, NO; Bianchi, MS; Richard, SM
      Mitochondrial genome instability in human cancers

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    12. Jeffries, S; Foulkes, WD
      Genetic mechanisms in squamous cell carcinoma of the head and neck

      ORAL ONCOLOGY
    13. Lindor, NM; Dechet, CB; Greene, MH; Jenkins, RB; Zincke, MT; Weaver, AL; Wilson, M; Zincke, H; Liu, WG
      Papillary renal cell carcinoma: Analysis of germline mutations in the MET proto-oncogene in a clinic-based population

      GENETIC TESTING
    14. Williams-Johnson, MM; Ashizawa, AE; De Rosa, CT
      Trichloroethylene in the environment: Public health concerns

      HUMAN AND ECOLOGICAL RISK ASSESSMENT
    15. Cogliano, VJ; Scott, CS; Caldwell, JC; Farland, WH
      Trichloroethylene: Using new information to improve the cancer characterization

      HUMAN AND ECOLOGICAL RISK ASSESSMENT
    16. Leach, FS
      Molecular genetics of urothelial malignancies: Mismatch repair genes as markers for detection and prognosis?

      UROLOGIC ONCOLOGY
    17. Virmani, AK; Rathi, A; Sathyanarayana, UG; Padar, A; Huang, CX; Cunnigham, HT; Farinas, AJ; Milchgrub, S; Euhus, DM; Gilcrease, M; Herman, J; Minna, JD; Gazdar, AF
      Aberrant methylation of the adenomatous polyposis coli (APC) gene promoter1A in breast and lung carcinomas

      CLINICAL CANCER RESEARCH
    18. Takayasu, H; Horie, H; Hiyama, E; Matsunaga, T; Hayashi, Y; Watanabe, Y; Suita, S; Kaneko, M; Sasaki, F; Hashizume, K; Ozaki, T; Furuuchi, K; Tada, M; Ohnuma, N; Nakagawara, A
      Frequent deletions and mutations of the beta-catenin gene are associated with overexpression of cyclin D1 and fibronectin and poorly differentiated histology in childhood hepatoblastoma

      CLINICAL CANCER RESEARCH
    19. Coller, HA; Khrapko, K; Bodyak, ND; Nekhaeva, E; Herrero-Jimenez, P; Thilly, WG
      High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection

      NATURE GENETICS
    20. Gottlieb, B; Beitel, LE; Trifiro, MA
      Variable expressivity and mutation databases: The androgen receptor gene mutations database

      HUMAN MUTATION
    21. Nickerson, ML; Warren, MB; Zbar, B; Schmidt, LS
      Random mutagenesis-PCR to introduce alterations into defined DNA sequencesfor validation of SNP and mutation detection methods

      HUMAN MUTATION
    22. Berry, SE; Kinsella, TJ
      Targeting DNA mismatch repair for radiosensitization

      SEMINARS IN RADIATION ONCOLOGY
    23. Amant, F; Dorfling, CM; Dreyer, L; Vergote, I; Lindeque, BG; Van Rensburg, EJ
      Microsatellite instability in uterine sarcomas

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER
    24. Moore, PS; Missiaglia, E; Antonello, D; Zamo, A; Zamboni, G; Corleto, V; Falconi, M; Scarpa, A
      Role of disease-causing genes in sporadic pancreatic endocrine tumors: MENI and VHL

      GENES CHROMOSOMES & CANCER
    25. Sunaga, N; Kohno, T; Kolligs, FT; Fearon, ER; Saito, R; Yokota, J
      Constitutive activation of the Wnt signaling pathway by CTNNBI (beta-catenin) mutations in a subset of human lung adenocarcinoma

      GENES CHROMOSOMES & CANCER
    26. Alsanea, O; Clark, OH
      Familial thyroid cancer

      CURRENT OPINION IN ONCOLOGY
    27. Park, YK; Cho, CH; Chi, SG; Han, CS; Ushigome, S; Unni, KK
      Low incidence of genetic alterations of the p16(CDKN2a) in clear cell chondrosarcoma

      INTERNATIONAL JOURNAL OF ONCOLOGY
    28. Van der Looij, M; Papp, J; Sztan, M; Pulay, T; Elfadil, I; Besznyak, I; Toth, J; Devilee, P; Olah, E
      Allelic imbalance and microsatellite instability in BRCA1 associated breast and ovarian tumors

      INTERNATIONAL JOURNAL OF ONCOLOGY
    29. Alexander, JM
      Tumor suppressor loss in pituitary tumors

      BRAIN PATHOLOGY
    30. Sourvinos, G; Miyakis, S; Liloglou, TL; Field, JK; Spandidos, DA
      Von Hippel-Lindau tumour suppressor gene is not involved in sporadic humanbreast cancer

      TUMOR BIOLOGY
    31. Sasaki, Y; Morimoto, I; Kusano, M; Hosokawa, M; Itoh, F; Yanagihara, K; Imai, K; Tokino, T
      Mutational analysis of the beta-catenin gene in gastric carcinomas

      TUMOR BIOLOGY
    32. Peltomaki, P
      Deficient DNA mismatch repair: a common etiologic factor for colon cancer

      HUMAN MOLECULAR GENETICS
    33. Weng, LP; Gimm, O; Kum, JB; Smith, WM; Zhou, XP; Wynford-Thomas, D; Leone, G; Eng, C
      Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell death

      HUMAN MOLECULAR GENETICS
    34. Magee, CJ; Greenhalf, W; Howes, N; Ghaneh, P; Neoptolemos, JP
      Molecular pathogenesis of pancreatic ductal adenocarcinoma and clinical implications

      SURGICAL ONCOLOGY-OXFORD
    35. Peace, BE; Hughes, MJ; Degen, SJF; Waltz, SE
      Point mutations and overexpression of Ron induce transformation, tumor formation, and metastasis

      ONCOGENE
    36. Suen, TC; Goss, PE
      Identification of a novel transcriptional repressor element located in thefirst intron of the human BRCA1 gene

      ONCOGENE
    37. Ma, X; Yang, K; Lindblad, P; Egevad, L; Hemminki, K
      VHL gene alterations in renal cell carcinoma patients: novel hotspot or founder mutations and linkage disequilibrium

      ONCOGENE
    38. Gayet, J; Zhou, XP; Duval, A; Rolland, S; Hoang, JM; Cottu, P; Hamelin, R
      Extensive characterization of genetic alterations in a series of human colorectal cancer cell lines

      ONCOGENE
    39. Baba, M; Hirai, S; Kawakami, S; Kishida, T; Sakai, N; Kaneko, S; Yao, M; Shuin, T; Kubota, Y; Hosaka, M; Ohno, S
      Tumor suppressor protein VHL is induced at high cell density and mediates contact inhibition of cell growth

      ONCOGENE
    40. Szutorisz, H; Palmqvist, R; Roos, G; Stenling, R; Schorderet, DF; Reddell, R; Lingner, J; Nabholz, M
      Rearrangements of minisatellites in the human telomerase reverse transcriptase gene are not correlated with its expression in colon carcinomas

      ONCOGENE
    41. Hadzija, MP; Kapitanovic, S; Radosevic, S; Cacev, T; Mirt, M; Kovacevic, D; Lukac, J; Hadzija, M; Spaventi, R; Pavelic, K
      Loss of heterozygosity of DPC4 tumor suppressor gene in human sporadic colon cancer

      JOURNAL OF MOLECULAR MEDICINE-JMM
    42. Kang, JH; Kim, SJ; Noh, DY; Choe, KJ; Lee, ES; Kang, HS
      The timing and characterization of p53 mutations in progression from atypical ductal hyperplasia to invasive lesions in the breast cancer

      JOURNAL OF MOLECULAR MEDICINE-JMM
    43. Trulzsch, B; Krohn, K; Wonerow, P; Chey, S; Holzapfel, HP; Ackermann, F; Fuhrer, D; Paschke, R
      Detection of thyroid-stimulating hormone receptor and G(s)alpha mutations:in 75 toxic thyroid nodules by denaturing gradient gel electrophoresis

      JOURNAL OF MOLECULAR MEDICINE-JMM
    44. Hashimoto, T; Takishita, M; Kosaka, M; Sano, T; Matsumoto, T
      Superantigens and autoantigens may be involved in the pathogenesis of gastric mucosa-associated lymphoid tissue lymphoma

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    45. Takano, T; Miyauchi, A; Yoshida, H; Hasegawa, Y; Kuma, K; Amino, N
      Large-scale analysis of mutations in RET exon 16 in sporadic medullary thyroid carcinomas in Japan

      JAPANESE JOURNAL OF CANCER RESEARCH
    46. Miwa, H; Takakuwa, T; Nakatsuka, S; Tomita, Y; Matsuzuka, F; Aozasa, K
      DNA sequence of immunoglobulin heavy chain variable region gene in thyroidlymphoma

      JAPANESE JOURNAL OF CANCER RESEARCH
    47. Laudanski, J; Niklinska, W; Burzykowski, T; Chyczewski, L; Niklinski, J
      Prognostic significance of p53 and bcl-2 abnormalities in operable nonsmall cell lung cancer

      EUROPEAN RESPIRATORY JOURNAL
    48. Peiro, G; Diebold, J; Mayr, D; Baretton, GB; Kimmig, R; Schmidt, M; Lohrs, U
      Prognostic relevance of hMLH1, hMSH2, and BAX protein expression in endometrial carcinoma

      MODERN PATHOLOGY
    49. Ryu, B; Song, J; Sohn, T; Hruban, RH; Kern, SE
      Frequent germline deletion polymorphism of chromosomal region 8p12-p21 identified as a recurrent homozygous deletion in human tumors

      GENOMICS
    50. Bessler, M; Schaefer, A; Keller, P
      Paroxysmal nocturnal hemoglobinuria: Insights from recent advances in molecular biology

      TRANSFUSION MEDICINE REVIEWS
    51. Alberti, L; Proverbio, MC; Costagliola, S; Weber, G; Beck-Peccoz, P; Chiumello, G; Persani, L
      A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    52. Chappuis, PO; Ghadirian, P; Foulkes, WD
      The role of genetic factors in the etiology of pancreatic adenocarcinoma: An update

      CANCER INVESTIGATION
    53. Tiede, A; Daniels, RJ; Higgs, DR; Mehrein, Y; Schmidt, RE; Schubert, J
      The human GPI1 gene is required for efficient glycosylphosphatidylinositolbiosynthesis

      GENE
    54. Chapusot, C; Assem, M; Martin, L; Chalabreyssse, L; Benhamiche, AM; Lignier, MA; Chauffert, B; Teyssier, JR; Faivre, J; Piard, F
      p21(WAF1/CIP1) expression in colorectal carcinomas: its correlation with p53 mutations and p53 and Ki67 immunohistochemistry.

      PATHOLOGIE BIOLOGIE
    55. Klein, E; Wierich, G; Brauch, H
      DHPLC-based germline mutation screening in the analysis of the VHL tumor suppressor gene: usefulness and limitations

      HUMAN GENETICS
    56. Delbanco, EH; Bolt, HM; Huber, WW; Beken, S; Geller, F; Philippou, S; Brands, FH; Bruning, T; Thier, R
      Glutathione transferase activities in renal carcinomas and adjacent normalrenal tissues: factors influencing renal carcinogenesis induced by xenobiotics

      ARCHIVES OF TOXICOLOGY
    57. Grabsch, H; Takeno, S; Noguchi, T; Hommel, G; Gabbert, HE; Mueller, W
      Different patterns of beta-catenin expression in gastric carcinomas: relationship with clinicopathological parameters and prognostic outcome

      HISTOPATHOLOGY
    58. Mokdad-Gargouri, R; Belhadj, K; Gargouri, A
      Translational control of human p53 expression in yeast mediated by 5 '-UTR-ORF structural interaction

      NUCLEIC ACIDS RESEARCH
    59. Nihal, M; Mikkola, D; Qian, Z; Remick, SC; Wood, GS
      The clonality of tumor-infiltrating lymphocytes in African Kaposi's sarcoma

      JOURNAL OF CUTANEOUS PATHOLOGY
    60. Gimm, O
      Multiple endocrine neoplasia type 2: Clinical aspects

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    61. Salvatori, R; Thakker, RV; Lopes, MB; Fan, XG; Eswara, JR; Ellison, D; Lees, P; Harding, B; Yang, IM; Levine, MA
      Absence of mutations in the growth hormone (GH)-releasing hormone receptorgene in GH-secreting pituitary adenomas

      CLINICAL ENDOCRINOLOGY
    62. Bullock, CM; Li, C; Li, M; Bermak, JC; Zhou, QY
      Sensitization of adenylate cyclase induced by a dopamine D2 receptor mutant: Inverse agonism by D2 receptor antagonists

      PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
    63. Zullo, SJ
      Gene therapy of mitochondrial DNA mutations: A brief, biased history of allotopic expression in mammalian cells

      SEMINARS IN NEUROLOGY
    64. Ziemer, LT; Pennica, D; Levine, AJ
      Identification of a mouse homolog of the human BTEB2 transcription factor as a beta-catenin-independent Wnt-1-responsive gene

      MOLECULAR AND CELLULAR BIOLOGY
    65. Stuart, GR; de Boer, JG; Haesevoets, R; Holcroft, J; Kangas, J; Sojonky, K; Thorleifson, E; Thornton, A; Walsh, DF; Yang, HY; Glickman, BW
      Mutations induced by 2-amino-1-methyl-6-phenylimidazo [4,5-b]pyridine (PhIP) in cecum and proximal and distal colon of lacI transgenic rats

      MUTAGENESIS
    66. Spink, KE; Fridman, SG; Weis, WI
      Molecular mechanisms of beta-catenin recognition by adenomatous polyposis coli revealed by the structure of an APC-beta-catenin complex

      EMBO JOURNAL
    67. Hruban, RH; Canto, MI; Yeo, CJ
      Prevention of pancreatic cancer and strategies for management of familial pancreatic cancer

      DIGESTIVE DISEASES
    68. Kersten, B; Niemann, B; Jahn, S
      Development of single-chain Fv fragments from a human anti-double-strandedDNA antibody to study the influence of somatic mutations on antigen binding

      EXPERIMENTAL AND CLINICAL IMMUNOGENETICS
    69. Sepulveda, AR
      Molecular testing of Helicobacter pylori-associated chronic gastritis and premalignant gastric lesions - Clinical implications

      JOURNAL OF CLINICAL GASTROENTEROLOGY
    70. McDoniels-Silvers, AL; Herzog, CR; Tyson, FL; Malkinson, AM; You, M
      Inactivation of both Rb and p53 pathways in mouse lung epithelial cell lines

      EXPERIMENTAL LUNG RESEARCH
    71. Kim, JC; Koo, KH; Lee, DH; Roh, SA; Kim, HC; Yu, CS; Kang, GH
      Mutations at the APC exon 15 in the colorectal neoplastic tissues of serial array

      INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
    72. Komura, K; Masuda, H; Esumi, M
      Distinct relationship between polypoid growth type and sporadic colorectalcarcinomas with microsatellite instability

      HEPATO-GASTROENTEROLOGY
    73. Devilee, P; Cleton-Jansen, AM; Cornelisse, CJ
      Ever since Knudson

      TRENDS IN GENETICS
    74. Corcoran, RB; Scott, MP
      A mouse model for medulloblastoma and basal cell nevus syndrome

      JOURNAL OF NEURO-ONCOLOGY
    75. Sprenger, SHE; Gijtenbeek, JMM; Wesseling, P; Sciot, R; Van Calenbergh, F; Lammens, M; Jeuken, JWM
      Characteristic chromosomal aberrations in sporadic cerebellar hemangioblastomas revealed by comparative genomic hybridization

      JOURNAL OF NEURO-ONCOLOGY
    76. Potocnik, U; Glavac, D; Golouh, R; Ravnik-Glavac, M
      Causes of microsatellite instability in colorectal tumors: implications for hereditary non-polyposis colorectal cancer screening

      CANCER GENETICS AND CYTOGENETICS
    77. Gross, E; Kiechle, M; Arnold, N
      Mutation analysis of p53 in ovarian rumors by DHPLC

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    78. Coupland, SE; Foss, HD; Bechrakis, NE; Hummel, M; Stein, H
      Secondary ocular involvement in systemic "memory" B-cell lymphocytic leukemia

      OPHTHALMOLOGY
    79. Southey, MC; Young, MA; Whitty, J; Mifsud, S; Keilar, M; Mead, L; Trute, L; Aittomaki, K; McLachlan, SA; Debinski, H; Venter, DJ; Armes, JE
      Molecular pathologic analysis enhances the diagnosis and management of Muir-Torre syndrome and gives insight into its underlying molecular pathogenesis

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    80. Peters, DJM; Breuning, MH
      Autosomal dominant polycystic kidney disease: modification of disease progression

      LANCET
    81. Trusolino, L; Bertotti, A; Comoglio, PM
      A signaling adapter function for alpha 6 beta 4 integrin in the control ofHGF-dependent invasive growth

      CELL
    82. Maeda, T; Kamihira, S
      Apoptosis, part II: The role of mutated Fas genes in tumorigenesis

      ADVANCES IN CLINICAL CHEMISTRY, VOL 36
    83. Clifford, SC; Maher, ER
      von Hippel-Lindau disease: Clinical and molecular perspectives

      ADVANCES IN CANCER RESEARCH, VOL 82
    84. Golden, TR; Melov, S
      Mitochondrial DNA mutations, oxidative stress, and aging

      MECHANISMS OF AGEING AND DEVELOPMENT
    85. Matias-Guiu, X; Catasus, L; Bussaglia, E; Lagarda, H; Garcia, A; Pons, C; Munoz, J; Arguelles, R; Machin, P; Prat, J
      Molecular pathology of endometrial hyperplasia and carcinoma

      HUMAN PATHOLOGY
    86. Hamazaki, S; Yoshida, M; Yao, M; Nagashima, Y; Taguchi, K; Nakashima, H; Okada, S
      Mutation of von Hippel-Lindau tumor suppressor gene in a sporadic endolymphatic sac tumor

      HUMAN PATHOLOGY
    87. Emmrich, P; Gauer, J; Mattig, H
      Unifocal autonomous thyroid nodule and carcinoma

      ZENTRALBLATT FUR CHIRURGIE
    88. Su, GH; Bansal, R; Murphy, KM; Montgomery, E; Yeo, CJ; Hruban, RH; Kern, SE
      ACVR1B (ALK4, activin receptor type 1B) gene mutations in pancreatic carcinoma

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    89. Haase, VH; Glickman, JN; Socolovsky, M; Jaenisch, R
      Vascular tumors in livers with targeted inactivation of the von Hippel-Lindau tumor suppressor

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    90. Cocca, BA; Seal, SN; D'Agnillo, P; Mueller, YM; Katsikis, PD; Rauch, J; Weigert, M; Radic, MZ
      Structural basis for autoantibody recognition of phosphatidylserine-beta 2glycoprotein I and apoptotic cells

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    91. Xie, JW; Aszterbaum, M; Zhang, XL; Bonifas, JM; Zachary, C; Epstein, E; McCormick, F
      A role of PDGFR alpha in basal cell carcinoma proliferation

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    92. Seeberger, H; Starostik, P; Schwarz, S; Knorr, C; Kalla, J; Ott, G; Muller-Hermelink, HK; Greiner, A
      Loss of Fas (CD95/APO-1) regulatory function is an important step in earlyMALT-type lymphoma development

      LABORATORY INVESTIGATION
    93. Suto, T; Habano, W; Sugai, T; Uesugi, N; Kanno, S; Saito, K; Nakamura, S
      Infrequent microsatellite instability in biliary tract cancer

      JOURNAL OF SURGICAL ONCOLOGY
    94. Park, WS; Oh, RR; Park, JY; Kim, PJ; Shin, MS; Lee, JH; Kim, HS; Lee, SH; Kim, SY; Park, YG; An, WG; Kim, HS; Jang, JJ; Yoo, NJ; Lee, JY
      Nuclear localization of beta-catenin is an important prognostic factor in hepatoblastoma

      JOURNAL OF PATHOLOGY
    95. Lagarda, H; Catasus, L; Arguelles, R; Matias-Guiu, X; Prat, J
      K-ras mutations in endometrial carcinomas with microsatellite instability

      JOURNAL OF PATHOLOGY
    96. Glasker, S; Bender, BU; Apel, TW; van Velthoven, V; Mulligan, LM; Zentner, J; Neumann, NPH
      Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    97. Olschwang, S; Boisson, C; Thomas, G
      Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma

      JOURNAL OF MEDICAL GENETICS
    98. Tomlinson, IPM; Roylance, R; Houlston, RS
      Two hits revisited again

      JOURNAL OF MEDICAL GENETICS
    99. Harwood, CA; Swale, VJ; Bataille, VA; Quinn, AG; Ghali, L; Patel, SV; Dove-Edwin, I; Cerio, R; McGregor, JM
      An association between sebaceous carcinoma and microsatellite instability in immunosuppressed organ transplant recipients

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    100. Parhami-Seren, B; Viswanathan, M; Strong, RK; Margolies, MN
      Structural analysis of mutants of high-affinity and low-affinity p-azophenylarsonate-specific antibodies generated by alanine scanning of heavy chaincomplementarity-determining region 2

      JOURNAL OF IMMUNOLOGY


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Documento generato il 25/10/20 alle ore 12:56:28