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La ricerca find articoli where authors phrase all words ' Kum, JB' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 9 riferimenti
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    1. 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
    2. Mutter, GL; Lin, MC; Fitzgerald, JT; Kum, JB; Eng, C
      Changes in endometrial PTEN expression throughout the human menstrual cycle

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    3. Mutter, GL; Lin, MC; Fitzgerald, JT; Kum, JB; Baak, JPA; Lees, JA; Weng, LP; Eng, C
      Altered PTEN expression as a diagnostic marker for the earliest endometrial precancers

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    4. Sarraf, P; Mueller, E; Smith, WM; Wright, HM; Kum, JB; Aaltonen, LA; de la Chapelle, A; Spiegelman, BM; Eng, C
      Loss-of-function mutations in PPAR gamma associated with human colon cancer

      MOLECULAR CELL
    5. Marsh, DJ; Kum, JB; Lunetta, KL; Bennett, MJ; Gorlin, RJ; Ahmed, SF; Bodurtha, J; Crowe, C; Curtis, MA; Dasouki, M; Dunn, T; Feit, H; Geraghty, MT; Graham, JM; Hodgson, SV; Hunter, A; Korf, BR; Manchester, D; Miesfeldt, S; Murday, VA; Nathanson, KL; Parisi, M; Pober, B; Romano, C; Tolmie, JL; Trembath, R; Winter, RM; Zackai, EH; Zori, RT; Weng, LP; Dahia, PLM; Eng, C
      PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

      HUMAN MOLECULAR GENETICS
    6. Dahia, PLM; Aguiar, RCT; Alberta, J; Kum, JB; Caron, S; Sill, H; Marsh, DJ; Ritz, J; Freedman, A; Stiles, C; Eng, C
      PTEN is inversely correlated with the cell survival factor Akt/PKB and is inactivated via multiple mechanisms in haematological malignancies

      HUMAN MOLECULAR GENETICS
    7. Otto, LR; Boriack, RL; Marsh, DJ; Kum, JB; Eng, C; Burlina, AB; Bennett, MJ
      Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (ERRS)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Duerr, EM; Gimm, O; Neuberg, DS; Kum, JB; Clifford, SC; Toledo, SPA; Maher, ER; Dahia, PLM; Eng, C
      Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    9. MARSH DJ; DAHIA PLM; CARON S; KUM JB; FRAYLING IM; TOMLINSON IPM; HUGHES KS; EELES RA; HODGSON SV; MURDAY VA; HOULSTON R; ENG C
      GERMLINE PTEN MUTATIONS IN COWDEN-SYNDROME-LIKE FAMILIES

      Journal of Medical Genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/10/20 alle ore 21:02:08