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La ricerca find articoli where soggetti phrase all words 'NECDIN GENE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 32 riferimenti
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    1. Salpekar, A; Huntriss, J; Bolton, V; Monk, M
      The use of amplified cDNA to investigate the expression of seven imprintedgenes in human oocytes and preimplantation embryos

      MOLECULAR HUMAN REPRODUCTION
    2. Bressler, J; Tsai, TF; Wu, MY; Tsai, SF; Ramirez, MA; Armstrong, D; Beaudet, AL
      The SNRPN promoter is not required for genomic imprinting of the PraderWilli/Angelman domain in mice

      NATURE GENETICS
    3. 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
    4. Fulmer-Smentek, SB; Francke, U
      Association of acetylated histones with paternally expressed genes in the Prader-Willi deletion region

      HUMAN MOLECULAR GENETICS
    5. Chai, JH; Locke, DP; Ohta, T; Greally, JM; Nicholls, RD
      Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site

      MAMMALIAN GENOME
    6. Chamberlain, SJ; Brannan, CI
      The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a

      GENOMICS
    7. Stone, B; Schummer, M; Paley, PJ; Crawford, M; Ford, M; Urban, N; Nelson, BH
      MAGE-F1, a novel ubiquitously expressed member of the MAGE superfamily

      GENE
    8. Hanel, ML; Wevrick, R
      Establishment and maintenance of DNA methylation patterns in mouse Ndn: Implications for maintenance of imprinting in target genes of the imprinting center

      MOLECULAR AND CELLULAR BIOLOGY
    9. Forslund, KO; Nordqvist, K
      The melanoma antigen genes - Any clues to their functions in normal tissues?

      EXPERIMENTAL CELL RESEARCH
    10. Hanel, ML; Wevrick, R
      The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome

      CLINICAL GENETICS
    11. Chomez, P; De Backer, O; Bertrand, M; De Plaen, E; Boon, T; Lucas, S
      An overview of the MAGE gene family with the identification of all human members of the family

      CANCER RESEARCH
    12. Fridman, C; Koiffmann, CP
      Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes

      GENETICS AND MOLECULAR BIOLOGY
    13. Fridman, C; Varela, MC; Kok, F; Setian, N; Koiffmann, CP
      Prader-Willi syndrome: Genetic tests and clinical findings

      GENETIC TESTING
    14. Bielinska, B; Blaydes, SM; Buiting, K; Yang, T; Krajewska-Walasek, M; Horsthemke, B; Brannan, CI
      De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

      NATURE GENETICS
    15. Lee, S; Kozlov, S; Hernandez, L; Chamberlain, SJ; Brannan, CI; Stewart, CL; Wevrick, R
      Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype

      HUMAN MOLECULAR GENETICS
    16. Salehi, AH; Roux, PP; Kubu, CJ; Zeindler, C; Bhakar, A; Tannis, LL; Verdi, JM; Barker, PA
      NRAGE, a novel MAGE protein, interacts with the p75 neurotrophin receptor and facilitates nerve growth factor-dependent apoptosis

      NEURON
    17. Farber, C; Gross, S; Neesen, J; Buiting, K; Horsthemke, B
      Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15

      GENOMICS
    18. Glenn, CC; Deng, G; Michaelis, RC; Tarleton, J; Phelan, MC; Surh, L; Yang, TP; Driscoll, DJ
      DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting

      PRENATAL DIAGNOSIS
    19. Yoshikawa, K
      Cell cycle regulators in neural stem cells and postmitotic neurons

      NEUROSCIENCE RESEARCH
    20. Pold, M; Pold, A; Ma, HJ; Sjak-Shie, NN; Vescio, RA; Berenson, JR
      Cloning of the first invertebrate MAGE paralogue: an epitope that activates T-cells in humans is highly conserved in evolution

      DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
    21. Hennuy, B; Reiter, E; Cornet, A; Bruyninx, M; Daukandt, M; Houssa, P; N'Guyen, VH; Closset, J; Hennen, G
      A novel messenger ribonucleic acid homologous to human MAGE-D is strongly expressed in rat Sertoli cells and weakly in Leydig cells and is regulated by follitropin, lutropin, and prolactin

      ENDOCRINOLOGY
    22. de los Santos, T; Schweizer, J; Rees, CA; Francke, U
      Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which is highly expressed in brain

      AMERICAN JOURNAL OF HUMAN GENETICS
    23. Lee, S; Wevrick, R
      Identification of novel imprinted transcripts in the Prader-Willi syndromeand Angelman syndrome deletion region: Further evidence for regional imprinting control

      AMERICAN JOURNAL OF HUMAN GENETICS
    24. Muralidhar, B; Marney, A; Butler, MG
      Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities

      GENETICS IN MEDICINE
    25. Jong, MTC; Gray, TA; Ji, YG; Glenn, CC; Saitoh, S; Driscoll, DJ; Nicholls, RD
      A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region

      HUMAN MOLECULAR GENETICS
    26. Jong, MTC; Carey, AH; Caldwell, KA; Lau, MH; Handel, MA; Driscoll, DJ; Stewart, CL; Rinchik, EM; Nicholls, RD
      Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region

      HUMAN MOLECULAR GENETICS
    27. 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
    28. Mann, MRW; Bautolomei, MS
      Towards a molecular understanding of Prader-Willi and Angelman syndromes

      HUMAN MOLECULAR GENETICS
    29. Gabriel, JM; Merchant, M; Ohta, T; Ji, Y; Caldwell, RG; Ramsey, MJ; Tucker, JD; Longnecker, R; Nicholls, RD
      A transgene insertion creating a heritable chromosome deletion mouse modelof Prader-Willi and Angelman syndromes

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    30. Lucas, S; Brasseur, F; Boon, T
      A new MAGE gene with ubiquitous expression does not code for known MAGE antigens recognized by T cells

      CANCER RESEARCH
    31. GABRIEL JM; GRAY TA; STUBBS L; SAITOH S; OHTA T; NICHOLLS RD
      STRUCTURE AND FUNCTION CORRELATIONS AT THE IMPRINTED MOUSE SNRPN LOCUS

      Mammalian genome
    32. 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


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 00:58:56