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La ricerca find articoli where soggetti phrase all words 'BANNAYAN-ZONANA SYNDROME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 51 riferimenti
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    1. Marsh, DJ; Theodosopoulos, G; Howell, V; Richardson, AL; Benn, DE; Proos, AL; Eng, C; Robinson, BG
      Rapid mutation scanning of genes associated with familial cancer syndromesusing denaturing high-performance liquid chromatography

      NEOPLASIA
    2. Scheid, MP; Woodgett, JR
      Phosphatidylinositol 3' kinase signaling in mammary tumorigenesis

      JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
    3. Eng, C
      To be or not to BMP

      NATURE GENETICS
    4. Weng, LP; Brown, JL; Eng, C
      PTEN coordinates G(1) arrest by down-regulating cyclin D1 via its protein phosphatase activity and up-regulating p27 via its lipid phosphatase activity in a breast cancer model

      HUMAN MOLECULAR GENETICS
    5. Weng, LP; Smith, WM; Brown, JL; Eng, C
      PTEN inhibits insulin-stimulated MEK/MAPK activation and cell growth by blocking IRS-1 phosphorylation and 1RS-1/Grb-2/Sos complex formation in a breast cancer model

      HUMAN MOLECULAR GENETICS
    6. Weng, LP; Brown, JL; Eng, C
      PTEN induces apoptosis and cell cycle arrest through phosphoinositol-3-kinase/Akt-dependent and -independent pathways

      HUMAN MOLECULAR GENETICS
    7. Naidich, JJ; Rofsky, NM; Rosen, R; Karp, N
      Arteriovenous malformation in a patient with Bannayan-Zonana syndrome

      CLINICAL IMAGING
    8. Marsh, DJ; Stratakis, CA
      Hamartoma and lentiginosis syndromes: Clinical and molecular aspects

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    9. Maehama, T; Taylor, GS; Dixon, JE
      PTEN and myotubularin: Novel phosphoinositide phosphatases

      ANNUAL REVIEW OF BIOCHEMISTRY
    10. Padwa, BL; Mulliken, JB
      Facial infiltrating lipomatosis

      PLASTIC AND RECONSTRUCTIVE SURGERY
    11. Corredor, J; Wambach, J; Barnard, J
      Gastrointestinal polyps in children: Advances in molecular genetics, diagnosis, and management

      JOURNAL OF PEDIATRICS
    12. Fackenthal, JD; Marsh, DJ; Richardson, AL; Cummings, SA; Eng, C; Robinson, BG; Olopade, OI
      Male breast cancer in Cowden syndrome patients with germline PTEN mutations

      JOURNAL OF MEDICAL GENETICS
    13. Simpson, L; Parsons, R
      PTEN: Life as a tumor suppressor

      EXPERIMENTAL CELL RESEARCH
    14. Niendorf, KB; Shannon, KM
      The role of genetic testing and effect on patient care

      ARCHIVES OF DERMATOLOGY
    15. Kurose, K; Zhou, XP; Araki, T; Cannistra, SA; Maher, ER; Eng, C
      Frequent loss of PTEN expression is linked to elevated phosphorylated Akt levels, but not associated with p27 and cyclin D1 expression, in primary epithelial ovarian carcinomas

      AMERICAN JOURNAL OF PATHOLOGY
    16. Bonneau, D; Longy, M
      Mutations of the human PTEN gene

      HUMAN MUTATION
    17. Kurose, K; Zhou, XP; Araki, T; Eng, C
      Biallelic inactivating mutations and an occult germline mutation of PTEN in primary cervical carcinomas

      GENES CHROMOSOMES & CANCER
    18. Parisi, MA; Sybert, VP
      Molecular genetics in pediatric dermatology

      CURRENT OPINION IN PEDIATRICS
    19. Zhou, XP; Marsh, DJ; Hampel, H; Mulliken, JB; Gimm, O; Eng, C
      Germline and germline mosaic PTEN mutations associated with a Proteus-likesyndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis

      HUMAN MOLECULAR GENETICS
    20. Guanti, G; Resta, N; Simone, C; Cariola, F; Demma, I; Fiorente, P; Gentile, M
      Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesis

      HUMAN MOLECULAR GENETICS
    21. Gimm, O; Attie-Bitach, T; Lees, JA; Vekemans, M; Eng, C
      Expression of the PTEN tumour suppressor protein during human development

      HUMAN MOLECULAR GENETICS
    22. Zhang, CL; Tada, M; Kobayashi, H; Nozaki, M; Moriuchi, T; Abe, H
      Detection of PTEN nonsense mutation and psi PTEN expression in central nervous system high-grade astrocytic tumors by a yeast-based stop codon assay

      ONCOGENE
    23. Fujiwara, Y; Hoon, DSB; Yamada, T; Umeshita, K; Gotoh, M; Sakon, M; Nishisho, I; Monden, M
      PTEN/MMAC1 mutation and frequent loss of heterozygosity identified in chromosome 10q in a subset of hepatocellular carcinomas

      JAPANESE JOURNAL OF CANCER RESEARCH
    24. Celebi, JT; Ping, XL; Zhang, H; Remington, T; Sulica, VI; Tsou, HC; Peacocke, M
      Germline PTEN mutations in three families with Cowden syndrome

      EXPERIMENTAL DERMATOLOGY
    25. Celebi, JT; Wanner, M; Ping, XL; Zhang, H; Peacocke, M
      Association of splicing defects in PTEN leading to exon skipping or partial intron retention in Cowden syndrome

      HUMAN GENETICS
    26. Trapasso, F; Iuliano, R; Boccia, A; Stella, A; Visconti, R; Bruni, P; Baldassarre, G; Santoro, M; Viglietto, G; Fusco, A
      Rat protein tyrosine phosphatase eta suppresses the neoplastic phenotype of retrovirally transformed thyroid cells through the stabilization of p27(Kip1)

      MOLECULAR AND CELLULAR BIOLOGY
    27. Robinson, S; Cohen, AR
      Cowden disease and Lhermitte-Duclos disease: Characterization of a new phakomatosis

      NEUROSURGERY
    28. Bussaglia, E; del Rio, E; Matias-Guiu, X; Prat, J
      PTEN mutations in endometrial carcinomas: A molecular and clinicopathologic analysis of 38 cases

      HUMAN PATHOLOGY
    29. De Vivo, I; Gertig, DM; Nagase, S; Hankinson, SE; O'Brien, R; Speizer, FE; Parsons, R; Hunter, DJ
      Novel germline mutations in the PTEN tumour suppressor gene found in womenwith multiple cancers

      JOURNAL OF MEDICAL GENETICS
    30. Eng, C
      Will the real Cowden syndrome please stand up: revised diagnostic criteria

      JOURNAL OF MEDICAL GENETICS
    31. 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
    32. Stambolic, V; Tsao, MS; Macpherson, D; Suzuki, A; Chapman, WR; Mak, TW
      High incidence of breast and endometrial neoplasia resembling human Cowdensyndrome in pten(+/-) mice

      CANCER RESEARCH
    33. Perren, A; Komminoth, P; Saremaslani, P; Matter, C; Feurer, S; Lees, JA; Heitz, PU; Eng, C
      Mutation and expression analyses reveal differential subcellular compartmentalization of PTEN in endocrine pancreatic tumors compared to normal isletcells

      AMERICAN JOURNAL OF PATHOLOGY
    34. Zhou, XP; Gimm, O; Hampel, H; Niemann, T; Walker, MJ; Eng, C
      Epigenetic PTEN silencing in malignant melanomas without PTEN mutation

      AMERICAN JOURNAL OF PATHOLOGY
    35. Hu, YC; Lam, KY; Tang, JCO; Srivastava, G
      Mutational analysis of the PTEN/MMAC1 gene in primary oesophageal squamouscell carcinomas

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    36. Nelen, MR; Kremer, H; Konings, IBM; Schoute, F; van Essen, AJ; Koch, R; Woods, CG; Fryns, JP; Hamel, B; Hoefsloot, LH; Peeters, EAJ; Padberg, GW
      Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    37. Stambolic, V; Mak, TW; Woodgett, JR
      Modulation of cellular apoptotic potential: contributions to oncogenesis

      ONCOGENE
    38. Yao, YJ; Ping, XL; Zhang, H; Chen, FF; Lee, PK; Ahsan, H; Chen, CJ; Lee, PH; Pleacocke, M; Santella, RM; Tsou, HC
      PTEN/MMAC1 mutations in hepatocellular carcinomas

      ONCOGENE
    39. Celebi, JT; Chen, FF; Zhang, H; Ping, XL; Tsou, HC; Peacocke, M
      Identification of PTEN mutations in five families with Bannayan-Zonana syndrome

      EXPERIMENTAL DERMATOLOGY
    40. Sanson, M; Zhou, XP; Brault, JL; Hoang-Xuan, K; Hamelin, R
      A novel germline mutation of the PTEN/MMAC1 gene in a patient with Cowden disease

      ACTA ONCOLOGICA
    41. Chen, ST; Yu, SY; Tsai, M; Yeh, KT; Wang, JC; Kao, MC; Shih, MC; Chang, JG
      Mutation analysis of the putative tumor suppression gene PTEN/MMAC1 in sporadic breast cancer

      BREAST CANCER RESEARCH AND TREATMENT
    42. 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
    43. Celebi, JT; Tsou, HC; Chen, FF; Zhang, H; Ping, XL; Lebwohl, MG; Kezis, J; Peacocke, M
      Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN

      JOURNAL OF MEDICAL GENETICS
    44. Weng, LP; Smith, WM; Dahia, PLM; Ziebold, U; Gil, E; Lees, JA; Eng, C
      PTEN suppresses breast cancer cell growth by phosphatase activity-dependent G(1) arrest followed by cell death

      CANCER RESEARCH
    45. Cina, SJ; Radentz, SS; Smialek, JE
      A case of familial angiolipomatosis with Lisch nodules

      ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
    46. Ali, IU; Schriml, LM; Dean, M
      Mutational spectra of PTEN/MMAC1 gene: a tumor suppressor with lipid phosphatase activity

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    47. CAMPIGLIO GL; DIGIUSEPPE P; GRAPPOLINI S
      MACROCEPHALY WITH MULTIPLE SOFT-TISSUE AND VISCERAL HAMARTOMAS (BANNAYAN-ZONANA-SYNDROME) - CASE-REPORT

      Scandinavian journal of plastic and reconstructive surgery and hand surgery
    48. DILIBERTI JH
      INHERITED MACROCEPHALY-HAMARTOMA SYNDROMES

      American journal of medical genetics
    49. Zori, RT; Marsh, DJ; Graham, GE; Marliss, EB; Eng, C
      Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    50. NG SCY; KHOO BS; HO NK
      PROTEUS SYNDROME

      Journal of paediatrics and child health
    51. ARCH EM; GOODMAN BK; VANWESEP RA; LIAW D; CLARKE K; PARSONS R; MCKUSICK VA; GERAGHTY MT
      DELETION OF PTEN IN A PATIENT WITH BANNAYAN-RILEY-RUVALCABA-SYNDROME SUGGESTS ALLELISM WITH COWDEN-DISEASE

      American journal of medical genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/10/20 alle ore 10:04:08