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    1. Gianfrancesco, F; Sanges, R; Esposito, T; Tempesta, S; Rao, E; Rappold, G; Archidiacono, N; Graves, JAM; Forabosco, A; D'Urso, M
      Differential divergence of three human pseudoautosomal genes and their mouse homologs: Implications for sex chromosome evolution

      GENOME RESEARCH
    2. Miano, MG; Testa, F; Filippini, F; Trujillo, M; Conte, I; Lanzara, C; Millan, JM; De Bernardo, C; Grammatico, B; Mangino, M; Torrente, I; Carrozzo, R; Simonelli, F; Rinaldi, E; Ventruto, V; D'Urso, M; Ayuso, C; Ciccodicola, A
      Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains

      HUMAN MUTATION
    3. Filippini, F; Rossi, V; Galli, T; Budillon, A; D'Urso, M; D'Esposito, M
      Longins: a new evolutionary conserved VAMP family sharing a novel SNARE domain

      TRENDS IN BIOCHEMICAL SCIENCES
    4. Aradhya, S; Bardaro, T; Galgoczy, P; Yamagata, T; Esposito, T; Patlan, H; Ciccodicola, A; Munnich, A; Kenwrick, S; Platzer, M; D'Urso, M; Nelson, DL
      Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes

      HUMAN MOLECULAR GENETICS
    5. Aradhya, S; Woffendin, H; Jakins, T; Bardaro, T; Esposito, T; Smahi, A; Shaw, C; Levy, M; Munnich, A; D'Urso, M; Lewis, RA; Kenwrick, S; Nelson, DL
      A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations

      HUMAN MOLECULAR GENETICS
    6. Vacca, M; Filippini, F; Budillon, A; Rossi, V; Mercadante, G; Manzati, E; Gualandi, F; Bigoni, S; Trabanelli, C; Pini, G; Calzolari, E; Ferlini, A; Meloni, I; Hayek, G; Zappella, M; Renieri, A; D'Urso, M; D'Esposito, M; MacDonald, F; Kerr, A; Dhanjal, S; Hulten, M
      Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females

      JOURNAL OF MOLECULAR MEDICINE-JMM
    7. Fusaro, M; Munaretto, G; Urso, M; Bonadonna, A; Mastrosimone, S; Virga, G; Piccoli, A
      Severe obesity in haemodialysis: the utility of bioimpedance vector analysis

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    8. Gianfrancesco, F; Falco, G; Esposito, T; Rocchi, M; D'Urso, M
      Characterization of the murine orthologue of a novel human subtelomeric multigene family

      CYTOGENETICS AND CELL GENETICS
    9. Landoni, F; Dell'Anna, T; Urso, M; Fiana, L; Villa, A; Ratti, M
      Randomised trial of neoadjuvant chemotherapy in locally advanced squamous cell cervical cancer comparison of cisplatin, ifosfamide, paclitaxel (TIP) versus cisplatin, paclitaxel (TP)

      TUMORI
    10. Maneo, A; Villa, A; Dell'Anna, T; Ratti, M; Fiana, L; Urso, M
      Optimal treatment for stage IIIB cervical cancer. A comparison between radiotherapy, concurrent chemo-radiotherapy and neoadjuvant chemotherapy followed by surgery

      TUMORI
    11. Zanetta, G; Dell'Anna, T; Urso, M; Fiana, L; Villa, A; Ratti, M
      Randomised multicentric trial of neoadjuvant chemotherapy in locally advanced squamous cell cervical cancer. Comparison of cisplatin, ifosfamide (IP)versus paclitaxel, cispaltin, ifosfamide (TIP)

      TUMORI
    12. Pautas, E; Siguret, V; d'Urso, M; Laurent, M; Gaussem, P; Fevrier, M; Durand-Gasselin, B
      Monitoring of tinzaparin treatment at treatment dose of 10 days in elderlypatients

      REVUE DE MEDECINE INTERNE
    13. Kenwrick, S; Woffendin, H; Jakins, T; Shuttleworth, SG; Mayer, E; Greenhalgh, L; Whittaker, J; Rugolotto, S; Bardaro, T; Esposito, T; D'Urso, M; Soli, F; Turco, A; Smahi, A; Hamel-Teillac, D; Lyonnet, S; Bonnefont, JP; Munnich, A; Aradhya, S; Kashork, CD; Shaffer, LG; Nelson, DL; Levy, M; Lewis, RA
      Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    14. Di Iorio, G; Cappa, V; Ciccodicola, A; Sampaolo, S; Ammendola, A; Sanges, G; Giugliano, R; D'Urso, M
      A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease

      NEUROLOGICAL SCIENCES
    15. Ciccodicola, A; D'Esposito, M; Esposito, T; Gianfrancesco, F; Migliaccio, C; Miano, MG; Matarazzo, MR; Vacca, M; Franze, A; Cuccurese, M; Cocchia, M; Curci, A; Terracciano, A; Torino, A; Cocchia, S; Mercadante, G; Pannone, E; Archidiacono, N; Rocchi, M; Schlessinger, D; D'Urso, M
      Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region

      HUMAN MOLECULAR GENETICS
    16. Palmieri, G; de Franciscis, V; Casamassimi, A; Romano, G; Torino, A; Pingitore, P; Califano, D; Santelli, G; Eva, A; Vecchio, G; D'Urso, M; Ciccodicola, A
      Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site

      GENE
    17. Siguret, V; Pautas, E; Fevrier, M; Wipff, C; Durand-Gasselin, B; Laurent, M; Andreux, JP; d'Urso, M; Gaussem, P
      Elderly patients treated with tinzaparin (Innohep (R)) administered once daily (175 anti-Xa IU/kg): Anti-Xa and anti-IIa activities over 10 days

      THROMBOSIS AND HAEMOSTASIS
    18. Aradhya, S; Ahobila, P; Lewis, RA; Nelson, DL; Esposito, T; Ciccodicola, A; Bardaro, T; D'Urso, M; Woffendin, H; Kenwrick, S; Smahi, A; Heuertz, S; Munnich, A; Heiss, NS; Poustka, A; Chishti, AH
      Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2

      AMERICAN JOURNAL OF MEDICAL GENETICS
    19. Aradhya, S; Nelson, DL; Heiss, NS; Poustka, A; Woffendin, H; Kenwrick, S; Esposito, T; Ciccodicola, A; Bardaro, T; D'Urso, M; Smahi, A; Munnich, A; Herman, GE; Lewis, RA
      Human homologue of the murine Bare patches/Striated gene is not mutated inIncontinentia Pigmenti type 2

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Simonelli, F; Testa, F; de Crecchio, G; Rinaldi, E; Hutchinson, A; Atkinson, A; Dean, M; D'Urso, M; Allikmets, R
      New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    21. De Brasi, D; Esposito, T; Rossi, M; Parenti, G; Sperandeo, MP; Zuppaldi, A; Bardaro, T; Ambruzzi, MA; Zelante, L; Ciccodicola, A; Sebastio, G; D'Urso, M; Andria, G
      Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of Delta7-sterol reductase in Italy and report of three novel mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    22. Miano, MG; Testa, F; Strazzullo, M; Trujillo, M; De Bernardo, C; Grammatico, B; Simonelli, F; Mangino, M; Torrente, I; Ruberto, G; Beneyto, M; Antinolo, G; Rinaldi, E; Danesino, C; Ventruto, V; D'Urso, M; Ayuso, C; Baiget, M; Ciccodicola, A
      Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa

      EUROPEAN JOURNAL OF HUMAN GENETICS
    23. Esposito, T; Gianfrancesco, F; Ciccodicola, A; Montanini, L; Mumm, S; D'Urso, M; Forabosco, A
      A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases

      HUMAN MOLECULAR GENETICS
    24. Vacca, M; Matarazzo, MR; Jones, J; Spalluto, C; Archidiacono, N; Ma, P; Rocchi, M; D'Urso, M; Chen, EY; D'Esposito, M; Mumm, S
      Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region

      GENOMICS
    25. Matarazzo, MR; Cuccurese, M; Strazzullo, M; Vacca, M; Curci, A; Miano, MG; Cocchia, M; Mercadante, G; Torino, A; D'Urso, M; Ciccodicola, A; D'Esposito, M
      Human and mouse SYBL1 gene structure and expression

      GENE
    26. Gianfrancesco, F; Esposito, T; Ciccodicola, A; D'Esposito, M; Mazzarella, R; D'Urso, M; Forabosco, A
      Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene

      CYTOGENETICS AND CELL GENETICS
    27. Canetti, M; Urso, M; Sadocco, P
      Influence of the morphology and of the supermolecular structure on the enzymatic degradation of bacterial poly(3-hydroxybutyrate)

      POLYMER
    28. Huber, R; Hansen, RS; Strazzullo, M; Pengue, G; Mazzarella, R; D'Urso, M; Schlessinger, D; Pilia, G; Gartler, SM; D'Esposito, M
      DNA methylation in transcriptional repression of two differentially expressed X-linked genes, GPC3 and SYBL1

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    29. Heiss, NS; Poustka, A; Knight, SW; Aradhya, S; Nelson, DL; Lewis, RA; Esposito, T; Ciccodicola, A; D'Urso, M; Smahi, A; Heuertz, S; Munnich, A; Vabres, P; Woffendin, H; Kenwrick, S
      Mutation analysis of the DKC1 gene in incontinentia pigmenti

      JOURNAL OF MEDICAL GENETICS
    30. D'Esposito, M; Strazzullo, M; Cuccurese, M; Spalluto, C; Rocchi, M; D'Urso, M; Ciccodicola, A
      Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22

      CYTOGENETICS AND CELL GENETICS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/05/20 alle ore 12:52:51