Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where soggetti phrase all words '1q21-22' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 8 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Hegele, RA
      Molecular basis of partial lipodystrophy and prospects for therapy

      TRENDS IN MOLECULAR MEDICINE
    2. Mirnics, K; Middleton, FA; Stanwood, GD; Lewis, DA; Levitt, P
      Disease-specific changes in regulator of G-protein signaling 4 (RGS4) expression in schizophrenia

      MOLECULAR PSYCHIATRY
    3. Finelli, P; Cavalli, P; Giardino, D; Gottardi, G; Natacci, F; Savasta, S; Larizza, L
      FISH characterization of a supernumerary r(1)(:: cen -> q22 :: q22 -> sq21::) chromosome associated with multiple anomalies and bilateral cataracts

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Hegele, RA
      Familial partial lipodystrophy: A monogenic form of the insulin resistancesyndrome

      MOLECULAR GENETICS AND METABOLISM
    5. Matsuda, S; Miyazaki, K; Ichigotani, Y; Kurata, H; Takenouchi, Y; Yamamoto, T; Nimura, Y; Irimura, T; Nakatsugawa, S; Hamaguchi, M
      Molecular cloning and characterization of a novel human gene (NESCA) whichencodes a putative adapter protein containing SH3

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    6. Garg, A
      Gender differences in the prevalence of metabolic complications in familial partial lipodystrophy (Dunnigan variety)

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    7. Schaffler, A; Barth, N; Palitzsch, KD; Drobnik, W; Scholmerich, J; Schmitz, G
      Mutation analysis of the human adipocyte-specific apM-I gene

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    8. Speckman, RA; Garg, A; Du, FH; Bennett, L; Veile, R; Arioglu, E; Taylor, SI; Lovett, M; Bowcock, AM
      Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C

      AMERICAN JOURNAL OF HUMAN GENETICS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 02/12/20 alle ore 05:22:07