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La ricerca find articoli where soggetti phrase all words 'IMPRINTED EXPRESSION' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 17 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. Bussey, KJ; Lawce, HJ; Himoe, E; Shu, XO; Heerema, NA; Perlman, EJ; Olson, SB; Magenis, RE
      SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development

      GENES CHROMOSOMES & CANCER
    3. Hitchins, MP; Monk, D; Bell, GM; Ali, Z; Preece, MA; Stanier, P; Moore, GE
      Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB70 in Silver-Russell syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Takai, D; Gonzales, FA; Tsai, YC; Thayer, MJ; Jones, PA
      Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer

      HUMAN MOLECULAR GENETICS
    5. Zhu, WG; Dai, ZY; Ding, HM; Srinivasan, K; Hall, J; Duan, WR; Villalona-Calero, MA; Plass, C; Otterson, GA
      Increased expression of unmethylated CDKN2D by 5-aza-2 '-deoxycytidine in human lung cancer cells

      ONCOGENE
    6. Schulze, A; Mogensen, H; Hamborg-Petersen, B; Graem, N; Ostergaard, JR; Brondum-Nielsen, K
      Fertility in Prader-Willi syndrome: a case report with Angelman syndrome in the offspring

      ACTA PAEDIATRICA
    7. Monk, M; Salpekar, A
      Expression of imprinted genes in human preimplantation development

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    8. Ohlsson, R; Renkawitz, R; Lobanenkov, V
      CTCF is a uniquely versatile transcription regulator linked to epigeneticsand disease

      TRENDS IN GENETICS
    9. Srivastava, R; Hsieh, S; Grinberg, A; Williams-Simons, L; Huang, SP; Pfeifer, K
      H19 and Igf2 monoallelic expression is regulated in two distinct ways by ashared cis acting regulatory region upstream of H19

      GENES & DEVELOPMENT
    10. Chan, MF; Liang, G; Jones, PA
      Relationship between transcription and DNA methylation

      DNA METHYLATION AND CANCER
    11. Lossie, AC; Driscoll, DJ
      Transmission of Angelman syndrome by an affected mother

      GENETICS IN MEDICINE
    12. Tsai, TF; Jiang, YH; Bressler, J; Armstrong, D; Beaudet, AL
      Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

      HUMAN MOLECULAR GENETICS
    13. Kim, JY; Lu, XC; Stubbs, L
      Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7

      HUMAN MOLECULAR GENETICS
    14. SURRALLES J; NATARAJAN AT
      POSITION EFFECT OF TRANSLOCATIONS INVOLVING THE INACTIVE X-CHROMOSOME- PHYSICAL LINKAGE TO XIC XIST DOES NOT LEAD TO LONG-RANGE DE-NOVO INACTIVATION IN HUMAN DIFFERENTIATED CELLS/

      Cytogenetics and cell genetics
    15. GOTO T; MONK M
      REGULATION OF X-CHROMOSOME INACTIVATION IN DEVELOPMENT IN MICE AND HUMANS

      Microbiology and molecular biology reviews
    16. LEE JT; JAENISCH R
      THE (EPI)GENETIC CONTROL OF MAMMALIAN X-CHROMOSOME INACTIVATION

      Current opinion in genetics & development
    17. HEARD E; CLERC P; AVNER P
      X-CHROMOSOME INACTIVATION IN MAMMALS

      Annual review of genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/05/20 alle ore 11:29:37