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    1. Fanelli, F; Themmen, APN; Puett, D
      Lutropin receptor function: Insights from natural, engineered, and computer-simulated mutations

      IUBMB LIFE
    2. Shotelersuk, V; Ittiwut, C; Shotelersuk, K; Triratanachat, S; Poovorawan, Y; Mutirangura, A
      Fibroblast growth factor receptor 3 S249C mutation in virus associated squamous cell carcinomas

      ONCOLOGY REPORTS
    3. Sibley, K; Cuthbert-Heavens, D; Knowles, MA
      Loss of heterozygosity at 4p16.3 and mutation of FGFR3 in transitional cell carcinoma

      ONCOGENE
    4. Peace, BE; Hughes, MJ; Degen, SJF; Waltz, SE
      Point mutations and overexpression of Ron induce transformation, tumor formation, and metastasis

      ONCOGENE
    5. Karoui, M; Hofmann-Radvanyi, H; Zimmermann, U; Couvelard, A; Degott, C; Faridoni-Laurens, L; Ahomadegbe, JC; Gazzeri, S; Brambilla, E; Clerici, T; Charbonnier, P; Tresallet, C; Mitry, E; Penna, C; Rougier, P; Boileau, C; Thiery, JP; Nordlinger, B; Franc, B; Radvanyi, F
      No evidence of somatic FGFR3 mutation in various types of carcinoma

      ONCOGENE
    6. Sibley, K; Stern, P; Knowles, MA
      Frequency of fibroblast growth factor receptor 3 mutations in sporadic tumours

      ONCOGENE
    7. Ronchetti, D; Greco, A; Compasso, S; Colombo, G; Dell'Era, P; Otsuki, T; Lombardi, L; Neri, A
      Deregulated FGFR3 mutants in multiple myeloma cell lines with t(4;14): comparative analysis of Y373C, K650E and the novel G384D mutations

      ONCOGENE
    8. Wang, O; Green, RP; Zhao, GY; Ornitz, DM
      Differential regulation of endochondral bone growth and joint development by FGFR1 and FGFR3 tyrosine kinase domains

      DEVELOPMENT
    9. Cheung, WC; Van Ness, B
      The bone marrow stromal microenvironment influences myeloma therapeutic response in vitro

      LEUKEMIA
    10. Danilkovitch-Miagkova, A; Leonard, EJ
      Cross-talk between RON receptor tyrosine kinase and other transmembrane receptors

      HISTOLOGY AND HISTOPATHOLOGY
    11. Keijser, LCM; Van Tienen, TG; Schreuder, HWB; Lemmens, JAM; Pruszczynski, M; Veth, RPH
      Fibrous dysplasia of bone: Management and outcome of 20 cases

      JOURNAL OF SURGICAL ONCOLOGY
    12. Hayward, BE; Barlier, A; Korbonits, M; Grossman, AB; Jacquet, P; Enjalbert, A; Bonthron, DT
      Imprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegaly

      JOURNAL OF CLINICAL INVESTIGATION
    13. Coutant, R; Lumbroso, S; Rey, R; Lahlou, N; Venara, M; Rouleau, S; Sultan, C; Limal, JM
      Macroorchidism due to autonomous hyperfunction of Sertoli cells and G(s)alpha gene mutation: An unusual expression of McCune-Albright syndrome in a prepubertal boy

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    14. Lane, JM; Khan, SN; O'Connor, WJ; Nydick, M; Hommen, JP; Schneider, R; Tomin, E; Brand, J; Curtin, J
      Bisphosphonate therapy in fibrous dysplasia

      CLINICAL ORTHOPAEDICS AND RELATED RESEARCH
    15. Jang, JH; Shin, KH; Park, JG
      Mutations in fibroblast growth factor receptor 2 and fibroblast growth factor receptor 3 genes associated with human gastric and colorectal cancers

      CANCER RESEARCH
    16. Kimura, T; Suzuki, H; Ohashi, T; Asano, K; Kiyota, H; Eto, Y
      The incidence of thanatophoric dysplasia mutations in FGFR3 gene is higherin low-grade or superficial bladder carcinomas

      CANCER
    17. Intini, D; Baldini, L; Fabris, S; Lombardi, L; Ciceri, G; Maiolo, AT; Neri, A
      Analysis of FGFR3 gene mutations in multiple myeloma patients with t(4;14)

      BRITISH JOURNAL OF HAEMATOLOGY
    18. Kalakonda, N; Rothwell, DG; Scarffe, JH; Norton, JD
      Detection of N-Ras codon 61 mutations in subpopulations of tumor cells in multiple myeloma at presentation

      BLOOD
    19. Li, ZH; Zhu, YX; Plowright, EE; Bergsagel, PL; Chesi, M; Patterson, B; Hawley, TS; Hawley, RG; Stewart, AK
      The myeloma-associated oncogene fibroblast growth factor receptor 3 is transforming in hematopoietic cells

      BLOOD
    20. Billerey, C; Chopin, D; Aubriot-Lorton, MH; Ricol, D; de Medina, SGD; Van Rhijn, B; Bralet, MP; Lefrere-Belda, MA; Lahaye, JB; Abbou, CC; Bonaventure, J; Zafrani, ES; van der Kwast, T; Thiery, JP; Radvanyi, F
      Frequent FGFR3 mutations in papillary non-invasive bladder (pTa) tumors

      AMERICAN JOURNAL OF PATHOLOGY
    21. Sakamoto, A; Oda, Y; Iwamoto, Y; Tsuneyoshi, M
      A comparative study of fibrous dysplasia and osteofibrous dysplasia with regard to G(s)alpha mutation at the Arg(201) codon - Polymerase chain reaction-restriction fragment length polymorphism analysis of paraffin-embedded tissues

      JOURNAL OF MOLECULAR DIAGNOSTICS
    22. Chapurlat, RD; Meunier, PJ
      Fibrous dysplasia of bone

      BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY
    23. Ehrhard, KN; Jacoby, JJ; Fu, XY; Jahn, R; Dohlman, HG
      Use of G-protein fusions to monitor integral membrane protein-protein interactions in yeast

      NATURE BIOTECHNOLOGY
    24. Kirschner, LS; Carney, JA; Pack, SD; Taymans, SE; Giatzakis, C; Cho, YS; Cho-Chung, YS; Stratakis, CA
      Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex

      NATURE GENETICS
    25. Camacho, P; Gordon, D; Chiefari, E; Yong, S; DeJong, S; Pitale, S; Russo, D; Filetti, S
      A Phe 486 thyrotropin receptor mutation in an autonomously functioning follicular carcinoma that was causing hyperthyroidism

      THYROID
    26. Ashman, LK; Ferrao, P; Cole, SR; Cambareri, AC
      Effects of mutant c-Kit in early myeloid cells (vol 34, pg 451, 1997)

      LEUKEMIA & LYMPHOMA
    27. Iwata, T; Chen, L; Li, CI; Ovchinnikov, DA; Behringer, RR; Francomano, CA; Deng, CX
      A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos

      HUMAN MOLECULAR GENETICS
    28. Ziyaie, D; Hupp, TR; Thompson, AM
      p53 and breast cancer

      BREAST
    29. Bugalho, MJM; Li, X; Rao, CV; Soares, J; Sobrinho, LG
      Presence of a Gs alpha mutation in an adrenal tumor expressing LH/hCG receptors and clinically associated with Cushing's syndrome

      GYNECOLOGICAL ENDOCRINOLOGY
    30. Wu, R; Connolly, D; Ngelangel, C; Bosch, FX; Munoz, N; Cho, KR
      Somatic mutations of fibroblast growth factor receptor 3 (FGFR3) are uncommon in carcinomas of the uterine cervix

      ONCOGENE
    31. Nakaigawa, N; Weirich, G; Schmidt, L; Zbar, B
      Tumorigenesis mediated by MET mutant M1268T is inhibited by dominant-negative Src

      ONCOGENE
    32. Yamada, K; Ariyoshi, K; Onishi, M; Miyajima, A; Hayakawa, F; Towatari, M; Saito, H; Oka, Y; Asano, S; Nosaka, T; Kitamura, T
      Constitutively active STAT5A and STAT5B in vitro and in vivo: Mutation of STAT5 is not a frequent cause of leukemogenesis

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    33. Ignacak, M; Hilczer, M; Zarzycki, J; Trzeciak, WH
      Substitution of M398T in the second transmembrane helix of the LH receptorin a patient with familial male-limited precocious puberty

      ENDOCRINE JOURNAL
    34. Giordano, S; Maffe, A; Williams, TA; Artigiani, S; Gual, P; Bardelli, A; Basilico, C; Michieli, P; Comoglio, PM
      Different point mutations in the met oncogene elicit distinct biological properties

      FASEB JOURNAL
    35. Hsu, SY; Kudo, M; Chen, T; Nakabayashi, K; Bhalla, A; van der Spek, PJ; van Duin, M; Hsueh, AJW
      The three subfamilies of leucine-rich repeat-containing G protein-coupled receptors (LGR): Identification of LGR6 and LGR7 and the signaling mechanism for LGR7

      MOLECULAR ENDOCRINOLOGY
    36. Lala, R; Matarazzo, P; Bertelloni, S; Buzi, F; Rigon, F; de Sanctis, C
      Pamidronate treatment of bone fibrous dysplasia in nine children with McCune-Albright syndrome

      ACTA PAEDIATRICA
    37. Boissan, M; Feger, F; Guillosson, JJ; Arock, M
      c-Kit and c-kit mutations in mastocytosis and other hematological diseases

      JOURNAL OF LEUKOCYTE BIOLOGY
    38. Beck-Peccoz, P; Romoli, R; Persani, L
      Mutations of LH and FSH receptors

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    39. Raff, SB; Carney, JA; Krugman, D; Doppman, JL; Stratakis, CA
      Prolactin secretion abnormalities in patients with the "syndrome of spottyskin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex)

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    40. Silva, ES; Lumbroso, S; Medina, M; Gillerot, Y; Sultan, C; Sokal, EM
      Demonstration of McCune-Albright mutations in the liver of children with high gamma GT progressive cholestasis

      JOURNAL OF HEPATOLOGY
    41. Zacharin, M; O'Sullivan, M
      Intravenous pamidronate treatment of polyostotic fibrous dysplasia associated with the McCune Albright syndrome

      JOURNAL OF PEDIATRICS
    42. Malchoff, CD
      Editorial: Carney complex - Clarity and complexity

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    43. Mircescu, H; Jilwan, J; N'Diaye, N; Bourdeau, I; Tremblay, J; Hamet, P; Lacroix, A
      Are ectopic or abnormal membrane hormone receptors frequently present in adrenal Cushing's syndrome?

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    44. Pack, SD; Kirschner, LS; Pak, E; Zhuang, ZP; Carney, JA; Stratakis, CA
      Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex)

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    45. Jensen, AA; Spalding, TA; Burstein, ES; Sheppard, PO; O'Hara, PJ; Brann, MR; Krogsgaard-Larsen, P; Brauner-Osborne, H
      Functional importance of the Ala(116)-Pro(136) region in the calcium-sensing receptor - Constitutive activity and inverse agonism in a family C G-protein-coupled receptor

      JOURNAL OF BIOLOGICAL CHEMISTRY
    46. Naimi, B; Latil, A; Berthon, P; Cussenot, O
      No evidence for fibroblast growth factor receptor 3 (FGFR-3) R248C/S249C mutations in human prostate cancer

      INTERNATIONAL JOURNAL OF CANCER
    47. Batista, MC; Kohek, MBF; Frazzatto, EST; Fragoso, MCV; Mendonca, BB; Latronico, AC
      Mutation analysis of the follicle-stimulating hormone receptor gene in girls with gonadotropin-independent precocious puberty resulting from autonomous cystic ovaries

      FERTILITY AND STERILITY
    48. Hongyo, T; Li, T; Syaifudin, M; Baskar, R; Ikeda, H; Kanakura, Y; Aozasa, K; Nomura, T
      Specific c-kit mutations in sinonasal natural killer/T-cell lymphoma in China and Japan

      CANCER RESEARCH
    49. Frederick, L; Wang, XY; Eley, G; James, CD
      Diversity and frequency of Epidermal Growth Factor Receptor mutations in human glioblastomas

      CANCER RESEARCH
    50. Rowley, M; Liu, PC; Van Ness, B
      Heterogeneity in therapeutic response of genetically altered myeloma cell lines to interleukin 6, dexamethasone, doxorubicin, and melphalan

      BLOOD
    51. Beghini, A; Peterlongo, P; Ripamonti, CB; Larizza, L; Cairoli, R; Morra, E; Mecucci, C
      C-kit mutations in core binding factor leukemias

      BLOOD
    52. Xie, DW; Shu, XO; Deng, ZL; Wen, WQ; Creek, KE; Dai, Q; Gao, YT; Jin, F; Zheng, W
      Population-based, case-control study of HER2 genetic polymorphism and breast cancer risk

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    53. Ye, QO; Lu, QJ; Zhang, S; Huang, JJ; Wang, HL; Su, GF; Huang, PT; Huang, CF
      Existence of multiple novel Gs alpha splice variants in acute leukemia patients

      IUBMB LIFE
    54. Ross, JA; Nesnow, S
      Polycyclic aromatic hydrocarbons: correlations between DNA adducts and rasoncogene mutations

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    55. Wu, SM; Leschek, EW; Brain, C; Chan, WY
      A novel luteinizing hormone receptor mutation in a patient with familial male-limited precocious puberty: Effect of the size of a critical amino acidon receptor activity

      MOLECULAR GENETICS AND METABOLISM
    56. Kreisman, SH; Jackson, IMD
      Gonadotroph adenomas

      ENDOCRINOLOGIST
    57. Ashman, LK; Ferrao, P; Cole, SR; Cambareri, AC
      Effects of mutant c-Kit in early myeloid cells

      LEUKEMIA & LYMPHOMA
    58. Bareille, P; Azcona, C; Stanhope, R
      Multiple neonatal endocrinopathies in McCune-Albright syndrome

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    59. Michieli, P; Basilico, C; Pennacchietti, S; Maffe, A; Tamagnone, L; Giordano, S; Bardelli, A; Comoglio, PM
      Mutant Met-mediated transformation is ligand-dependent and can be inhibited by HGF antagonists

      ONCOGENE
    60. Schmidt, L; Junker, K; Nakaigawa, N; Kinjerski, T; Weirich, G; Miller, M; Lubensky, I; Neumann, HPH; Brauch, H; Decker, J; Vocke, C; Brown, JA; Jenkins, R; Richard, S; Bergerheim, U; Gerrard, B; Dean, M; Linehan, WM; Zbar, B
      Novel mutations of the MET proto-oncogene in papillary renal carcinomas

      ONCOGENE
    61. Hwang, SL; Hong, YR; Sy, WD; Chai, CY; Lin, HJ; Howng, SL
      Expression and mutation analysis of the p53 gene in astrocytoma

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    62. Esapa, CT; Harris, PE
      Mutation analysis of protein kinase A catalytic subunit in thyroid adenomas and pituitary tumours

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    63. Ozsaran, AA; Turker, S; Dikmen, Y; Erhan, Y; Itil, I; Terek, C; Ozdemir, N
      p53 staining as a prognostic indicator in endometrial carcinoma

      EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY
    64. Cetani, F; Tonacchera, M; Pinchera, A; Barsacchi, R; Basolo, F; Miccoli, P; Pacini, F
      Genetic analysis of the TSH receptor gene in differentiated human thyroid carcinomas

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    65. Kairemo, KJA; Verho, S; Dunkel, L
      Imaging of McCune-Albright syndrome using bone single photon emission computed tomography

      EUROPEAN JOURNAL OF PEDIATRICS
    66. de Sanctis, C; Lala, R; Matarazzo, P; Balsamo, A; Bergamaschi, R; Cappa, M; Cisternino, M; de Sanctis, V; Lucci, M; Franzese, A; Ghizzoni, L; Pasquino, AM; Segni, M; Rigon, F; Saggese, G; Bertelloni, S; Buzi, F
      McCune-Albright syndrome: A longitudinal clinical study of 32 patients

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    67. Eugster, EA; Shankar, R; Feezle, LK; Pescovitz, OH
      Tamoxifen treatment of progressive precocious puberty in a patient with McCune-Albright syndrome

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    68. Johnson, MC; Codner, E; Eggers, M; Mosso, L; Rodriguez, JA; Cassorla, F
      gps Mutations in Chilean patients harboring growth hormone-secreting pituitary tumors

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    69. Siegel, PM; Ryan, ED; Cardiff, RD; Muller, WJ
      Elevated expression of activated forms of Neu/ErbB-2 and ErbB-3 are involved in the induction of mammary tumors in transgenic mice: implications for human breast cancer

      EMBO JOURNAL
    70. Yavuzer, R; Khilnani, R; Jackson, IT; Audet, B
      A case of atypical McCune-Albright syndrome requiring optic nerve decompression

      ANNALS OF PLASTIC SURGERY
    71. Farfel, Z; Bourne, HR; Iiri, T
      The expanding spectrum of G protein diseases

      NEW ENGLAND JOURNAL OF MEDICINE
    72. Kitoh, H; Yamada, Y; Nogami, H
      Different genotype of periosteal and endosteal cells of a patient with polyostotic fibrous dysplasia

      JOURNAL OF MEDICAL GENETICS
    73. Eugster, EA; Pescovitz, ORH
      Commentary - Gigantism

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    74. Cohen, PA; Hupp, TR; Lane, DP; Daniels, DA
      Biochemical characterization of different conformational states of the Sf9cell-purified p53His175 mutant protein

      FEBS LETTERS
    75. Bradbury, FA; Menon, KMJ
      Evidence that constitutively active luteinizing hormone human chorionic gonadotropin receptors are rapidly internalized

      BIOCHEMISTRY
    76. MORRIS JC
      THE CLINICAL EXPRESSION OF THYROTROPIN RECEPTOR MUTATIONS

      The Endocrinologist
    77. ROMITI A; MORETTI A; VECCHIONE A; MURARO R; FEUDI ML; RINALDI V; MANCINI R; VALLI C; MOZZICAFREDDO A; FRATI L; TOMAO S
      ANALYSIS OF P53 EXPRESSION IN PRECANCEROUS AND MALIGNANT GASTRIC-MUCOSA

      Oncology Reports
    78. SUGAMURA K; MAKINO M; KAIBARA N
      APOPTOSIS AS A PROGNOSTIC FACTOR IN COLORECTAL-CARCINOMA

      SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY
    79. AFONJA O; AMOROSI E; ASHMAN L; TAKESHITA K
      MULTILINEAGE INVOLVEMENT AND ERYTHROPOIETIN-INDEPENDENT ERYTHROID PROGENITOR CELLS IN A PATIENT WITH SYSTEMIC MASTOCYTOSIS

      Annals of hematology
    80. ONISHI M
      USAGE OF ACTIVATING MUTATIONS IN THE ANALYSIS OF CYTOKINE SIGNAL-TRANSDUCTION PATHWAYS

      International journal of hematology
    81. KWONG KY; HUNG MC
      A NOVEL SPLICE VARIANT OF HER2 WITH INCREASED TRANSFORMATION ACTIVITY

      Molecular carcinogenesis (Print)
    82. ZHANG ZH; DIWAN BA; ANDERSON LM; LOGSDON D; OLIVERO OA; HAINES DC; RICE JM; YUSPA SH; POIRIER MC
      SKIN TUMORIGENESIS AND KI-RAS AND HA-RAS MUTATIONS IN TUMORS FROM ADULT MICE EXPOSED IN-UTERO TO 3'-AZIDO-2',3'-DIDEOXYTHYMIDINE

      Molecular carcinogenesis
    83. KANAGASUNDARAM V; CHRISTY E; HAMILTON JA; JAWOROWSKI A
      DIFFERENT PATHWAYS OF COLONY-STIMULATING FACTOR-1 DEGRADATION IN MACROPHAGE POPULATIONS REVEALED BY WORTMANNIN SENSITIVITY

      Biochemical journal
    84. Luque, EA; Tang, LH; Bortecen, KH; Kidd, M; Miu, K; Efstathiou, JA; Modlin, IM
      Gastrin-regulated expression of p53 in transformed enterochromaffin-like cells in the African rodent mastomys

      JOURNAL OF CLINICAL GASTROENTEROLOGY
    85. KHAN S; DO KA; KUHNERT P; PILLAY SP; PAPADIMOS D; CONRAD R; JASS JR
      DIAGNOSTIC-VALUE OF P53 IMMUNOHISTOCHEMISTRY IN BARRETTS-ESOPHAGUS - AN ENDOSCOPIC STUDY

      Pathology
    86. PIKIS A; DONKERSLOOT JA; RODRIGUEZ WJ; KEITH JM
      A CONSERVATIVE AMINO-ACID MUTATION IN THE CHROMOSOME-ENCODED DIHYDROFOLATE-REDUCTASE CONFERS TRIMETHOPRIM RESISTANCE IN STREPTOCOCCUS-PNEUMONIAE

      The Journal of infectious diseases
    87. BIANCO P; KUZNETSOV SA; RIMINUCCI M; FISHER LW; SPIEGEL AM; ROBEY PG
      REPRODUCTION OF HUMAN FIBROUS DYSPLASIA OF BONE IN IMMUNOCOMPROMISED MICE BY TRANSPLANTED MOSAICS OF NORMAL AND GS-ALPHA-MUTATED SKELETAL PROGENITOR CELLS

      The Journal of clinical investigation
    88. CHABRE O; LIAKOS P; VIVIER J; CHAFFANJON P; LABATMOLEUR F; MARTINIE M; BOTTARI SP; BACHELOT I; CHAMBAZ EM; DEFAYE G; FEIGE JJ
      CUSHINGS-SYNDROME DUE TO A GASTRIC-INHIBITORY POLYPEPTIDE-DEPENDENT ADRENAL ADENOMA - INSIGHTS INTO HORMONAL-CONTROL OF ADRENOCORTICAL TUMORIGENESIS

      The Journal of clinical endocrinology and metabolism
    89. NAMNOUM AB; MERRIAM GR; MOSES AM; LEVINE MA
      REPRODUCTIVE DYSFUNCTION IN WOMEN WITH ALBRIGHTS HEREDITARY OSTEODYSTROPHY

      The Journal of clinical endocrinology and metabolism
    90. STRATAKIS CA; KIRSCHNER LS
      CLINICAL AND GENETIC-ANALYSIS OF PRIMARY BILATERAL ADRENAL DISEASES (MICRO-AND MACRONODULAR DISEASE) LEADING TO CUSHING-SYNDROME

      Hormone and Metabolic Research
    91. WOROBEC AS; SEMERE T; NAGATA H; METCALFE DD
      CLINICAL CORRELATES OF THE PRESENCE OF THE ASP816VAL C-KIT MUTATION IN THE PERIPHERAL-BLOOD MONONUCLEAR-CELLS OF PATIENTS WITH MASTOCYTOSIS

      Cancer
    92. CANDELIERE GA; ROUGHLEY PJ; GLORIEUX FH
      POLYMERASE CHAIN REACTION-BASED TECHNIQUE FOR THE SELECTIVE ENRICHMENT AND ANALYSIS OF MOSAIC ARG(201) MUTATIONS IN G-ALPHA(S) FROM PATIENTS WITH FIBROUS DYSPLASIA OF BONE

      Bone
    93. COLUCCI S; ELGEHANI R; FLINT S; MOTHERSILL C
      P53 MUTATIONS AND PROTEIN EXPRESSION IN PRIMARY CULTURES OF NORMAL ORAL-MUCOSA IN SMOKERS AND NONSMOKERS

      Oral Oncology
    94. SHEKHAR PVM; WELTE R; CHRISTMAN JK; WANG H; WERDELL J
      ALTERED P53 CONFORMATION - A NOVEL MECHANISM OF WILD-TYPE P53 FUNCTIONAL INACTIVATION IN A MODEL FOR EARLY HUMAN BREAST-CANCER

      International journal of oncology
    95. COLUCCI S; MOTHERSILL C; HARNEY J; GAMBLE SC; SEYMOUR C; ARRAND JE
      INDUCTION OF MULTIPLE PCR-SSCPE MOBILITY SHIFTS IN P53 EXONS IN CULTURES OF NORMAL HUMAN UROTHELIUM EXPOSED TO LOW-DOSE GAMMA-RADIATION

      International journal of radiation biology
    96. MAGAE J; ILLENYE S; TEJIMA T; CHANG YC; MITSUI Y; TANAKA K; OMURA S; HEINTZ NH
      TRANSCRIPTIONAL SQUELCHING BY ECTOPIC EXPRESSION OF E2F-1 AND P53 IS ALLEVIATED BY PROTEASOME INHIBITORS MG-132 AND LACTACYSTIN

      Oncogene
    97. BLAGOSKLONNY MV
      LOSS OF FUNCTION AND P53 PROTEIN STABILIZATION

      Oncogene
    98. WHITESELL L; SUTPHIN P; AN WG; SCHULTE T; BLAGOSKLONNY MV; NECKERS L
      GELDANAMYCIN-STIMULATED DESTABILIZATION OF MUTATED P53 IS MEDIATED BYTHE PROTEASOME IN-VIVO

      Oncogene
    99. TENTLER JJ; HADCOCK JR; GUTIERREZHARTMANN A
      SOMATOSTATIN ACTS BY INHIBITING THE CYCLIC-3',5'-ADENOSINE-MONOPHOSPHATE (CAMP) PROTEIN-KINASE-A PATHWAY, CAMP RESPONSE ELEMENT-BINDING PROTEIN (CREB) PHOSPHORYLATION, AND CREB TRANSCRIPTION POTENCY

      Molecular endocrinology
    100. PIENKOWSKI C; LUMBROSO S; BIETH E; SULTAN C; ROCHICCIOLI P; TAUBER M
      RECURRENT OVARIAN-CYST AND MUTATION OF THE GS-ALPHA GENE IN OVARIAN-CYST FLUID CELLS - WHAT IS THE LINK WITH MCCUNE-ALBRIGHT-SYNDROME

      Acta paediatrica


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Documento generato il 04/06/20 alle ore 12:47:08