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La ricerca find articoli where authors phrase all words ' Muscatelli, F' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 19 riferimenti
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    1. Runte, M; Farber, C; Lich, C; Zeschnigk, M; Buchholz, T; Smith, A; Van Maldergem, L; Burger, J; Muscatelli, F; Gillessen-Kaesbach, G; Horsthemke, B; Buiting, K
      Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

      EUROPEAN JOURNAL OF HUMAN GENETICS
    2. Muscatelli, F; Abrous, DN; Massacrier, A; Boccaccio, I; La Moal, M; Cau, P; Cremer, H
      Disruption of the mouse Necdin gene results in hypothalamic and behavioralalterations reminiscent of the human Prader-Willi syndrome

      HUMAN MOLECULAR GENETICS
    3. Boccaccio, I; Glatt-Deeley, H; Watrin, F; Roeckel, N; Lalande, M; Muscatelli, F
      The human MAGEL2 gene and its mouse homologue are paternally expressed andmapped to the Prader-Willi region

      HUMAN MOLECULAR GENETICS
    4. JAY P; ROUGEULLE C; MASSACRIER A; MONCLA A; MATTEI MG; MALZAC P; ROECKEL N; TAVIAUX S; LEFRANC JLB; CAU P; BERTA P; LALANDE M; MUSCATELLI F
      THE HUMAN NECDIN GENE, NDN, IS MATERNALLY IMPRINTED AND LOCATED IN THE PRADER-WILLI-SYNDROME CHROMOSOMAL REGION

      Nature genetics
    5. WATRIN F; ROECKEL N; LACROIX L; MIGNON C; MATTEI MG; DISTECHE C; MUSCATELLI F
      THE MOUSE NECDIN GENE IS EXPRESSED FROM THE PATERNAL ALLELE ONLY AND LIES IN THE 7C REGION OF THE MOUSE-CHROMOSOME-7, A REGION OF CONSERVEDSYNTENY TO THE HUMAN PRADER-WILLI-SYNDROME REGION

      European journal of human genetics
    6. LURQUIN C; DESMET C; BRASSEUR F; MUSCATELLI F; MARTELANGE V; DEPLAEN E; BRASSEUR R; MONACO AP; BOON T
      2 MEMBERS OF THE HUMAN MAGEB GENE FAMILY LOCATED IN XP21.3 ARE EXPRESSED IN TUMORS OF VARIOUS HISTOLOGICAL ORIGINS

      Genomics
    7. WALKER AP; MUSCATELLI F; STAFFORD AN; CHELLY J; DAHL N; BLOMQUIST HK; DELANGHE J; WILLEMS PJ; STEINMANN B; MONACO AP
      MUTATIONS AND PHENOTYPE IN ISOLATED GLYCEROL KINASE-DEFICIENCY

      American journal of human genetics
    8. MUSCATELLI F; WALKER AP; DEPLAEN E; STAFFORD AN; MONACO AP
      ISOLATION AND CHARACTERIZATION OF A MAGE GENE FAMILY IN THE XP21.3 REGION

      Proceedings of the National Academy of Sciences of the United Statesof America
    9. TAMAGNONE L; LAHTINEN I; MUSTONEN T; VIRTANEVA K; FRANCIS F; MUSCATELLI F; ALITALO R; SMITH CIE; LARSSON C; ALITALO K
      BMX, A NOVEL NONRECEPTOR TYROSINE KINASE GENE OF THE BTK ITK/TEC/TXK FAMILY LOCATED IN CHROMOSOME XP22.2/

      Oncogene
    10. MATFIN G; SHEAVES R; MUSCATELLI F; WALKER A; MONACO A; GRANT D; NWOSE O; WASS JAH
      GENE DELETION CAUSING ADRENAL HYPOPLASIA CONGENITA AND HYPOGONADOTROPIC HYPOGONADISM

      Clinical endocrinology
    11. ZANARIA E; MUSCATELLI F; BARDONI B; STROM TM; GUIOLI S; GUO WW; LALLI E; MOSER C; WALKER AP; MCCABE ERB; MEITINGER T; MONACO AP; SASSONECORSI P; CAMERINO G
      AN UNUSUAL MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY RESPONSIBLE FOR X-LINKED ADRENAL HYPOPLASIA CONGENITA

      Nature
    12. MUSCATELLI F; STROM TM; WALKER AP; ZANARIA E; RECAN D; MEINDL A; BARDONI B; GUIOLI S; ZEHETNER G; RABL W; SCHWARZ HP; KAPLAN JC; CAMERINO G; MEITINGER T; MONACO AP
      MUTATIONS IN THE DAX-1 GENE GIVE RISE TO BOTH X-LINKED ADRENAL HYPOPLASIA CONGENITA AND HYPOGONADOTROPIC HYPOGONADISM

      Nature
    13. RONSIN C; MUSCATELLI F; MATTEI MG; BREATHNACH R
      A NOVEL PUTATIVE RECEPTOR PROTEIN TYROSINE KINASE OF THE MET FAMILY

      Oncogene
    14. CHELLY J; RIDER S; FAIRWEATHER N; ISHIKAWABRUSH Y; MUSCATELLI F; MONACO AP
      PHYSICAL AND GENETIC-MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XCEN-]Q21

      Cytogenetics and cell genetics
    15. WALKER AP; HO MF; MUSCATELLI F; CHELLY J; CLARKE E; ISHIKAWABRUSH Y; MONACO AP
      PHYSICAL MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XP21

      Cytogenetics and cell genetics
    16. SCHURMANS S; MUSCATELLI F; MIOT F; MATTEI MG; VASSART G; PARMENTIER M
      THE OLFR1 GENE ENCODING THE HGMP07E PUTATIVE OLFACTORY RECEPTOR MAPS TO THE 17P13-]P12 REGION OF THE HUMAN GENOME AND REVEALS AN MSPI RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM

      Cytogenetics and cell genetics
    17. PIARROUX R; AZAIEZ R; LOSSI AM; REYNIER P; MUSCATELLI F; GAMBARELLI F; FONTES M; DUMON H; QUILICI M
      ISOLATION AND CHARACTERIZATION OF A REPETITIVE DNA-SEQUENCE FROM LEISHMANIA-INFANTUM - DEVELOPMENT OF A VISCERAL LEISHMANIASIS POLYMERASE CHAIN-REACTION

      The American journal of tropical medicine and hygiene
    18. MUSCATELLI F; WALKER AP; MEITINGER T; MONACO AP
      ISOLATION OF CANDIDATE GENE(S) FOR ADRENOCORTICAL HYPOPLASIA-CONGENITA AND (OR) HYPOGONADOTROPIC HYPOGONADISM X-LINKED DISEASES

      American journal of human genetics
    19. MUSCATELLI F; VERNA JM; PHILIP N; MONCLA A; MATTEI MG; MATTEI JF; FONTES M
      PHYSICAL MAPPING OF AN XQ-PROXIMAL INTERSTITIAL DUPLICATION IN A MALE

      Human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/20 alle ore 03:26:20