BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 16575193)

  • 41. Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader-Willi syndrome.
    Kim Y; Lee HM; Xiong Y; Sciaky N; Hulbert SW; Cao X; Everitt JI; Jin J; Roth BL; Jiang YH
    Nat Med; 2017 Feb; 23(2):213-222. PubMed ID: 28024084
    [TBL] [Abstract][Full Text] [Related]  

  • 42. The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome.
    Hanel ML; Wevrick R
    Clin Genet; 2001 Mar; 59(3):156-64. PubMed ID: 11260224
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Disruption of the bipartite imprinting center in a family with Angelman syndrome.
    Buiting K; Barnicoat A; Lich C; Pembrey M; Malcolm S; Horsthemke B
    Am J Hum Genet; 2001 May; 68(5):1290-4. PubMed ID: 11283796
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region.
    Sutcliffe JS; Jiang YH; Galijaard RJ; Matsuura T; Fang P; Kubota T; Christian SL; Bressler J; Cattanach B; Ledbetter DH; Beaudet AL
    Genome Res; 1997 Apr; 7(4):368-77. PubMed ID: 9110176
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
    Schulze A; Hansen C; Skakkebaek NE; Brøndum-Nielsen K; Ledbeter DH; Tommerup N
    Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR.
    Raca G; Buiting K; Das S
    Genet Test; 2004; 8(4):387-94. PubMed ID: 15684868
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
    Nicholls RD
    Am J Med Genet; 1993 Apr; 46(1):16-25. PubMed ID: 8388169
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The imprinting mechanism of the Prader-Willi/Angelman regional control center.
    Perk J; Makedonski K; Lande L; Cedar H; Razin A; Shemer R
    EMBO J; 2002 Nov; 21(21):5807-14. PubMed ID: 12411498
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions.
    Matsubara K; Itoh M; Shimizu K; Saito S; Enomoto K; Nakabayashi K; Hata K; Kurosawa K; Ogata T; Fukami M; Kagami M
    Clin Epigenetics; 2019 Feb; 11(1):36. PubMed ID: 30819260
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site.
    Chai JH; Locke DP; Ohta T; Greally JM; Nicholls RD
    Mamm Genome; 2001 Nov; 12(11):813-21. PubMed ID: 11845283
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region.
    Robinson WP; Lalande M
    Hum Mol Genet; 1995 May; 4(5):801-6. PubMed ID: 7633438
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Prader-Willi and Angelman syndromes: sister imprinted disorders.
    Cassidy SB; Dykens E; Williams CA
    Am J Med Genet; 2000; 97(2):136-46. PubMed ID: 11180221
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene.
    Watrin F; Le Meur E; Roeckel N; Ripoche MA; Dandolo L; Muscatelli F
    BMC Genet; 2005 Jan; 6():1. PubMed ID: 15634360
    [TBL] [Abstract][Full Text] [Related]  

  • 54. DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting.
    Glenn CC; Deng G; Michaelis RC; Tarleton J; Phelan MC; Surh L; Yang TP; Driscoll DJ
    Prenat Diagn; 2000 Apr; 20(4):300-6. PubMed ID: 10740202
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Allelic dropout can cause false-positive results for Prader-Willi and Angelman syndrome testing.
    Hussain Askree S; Hjelm LN; Ali Pervaiz M; Adam M; Bean LJ; Hedge M; Coffee B
    J Mol Diagn; 2011 Jan; 13(1):108-12. PubMed ID: 21227401
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Evolution of genomic imprinting with biparental care: implications for Prader-Willi and Angelman syndromes.
    Ubeda F
    PLoS Biol; 2008 Aug; 6(8):e208. PubMed ID: 18752349
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
    Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
    Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Genomic imprinting and its role in Prader-Willi and Angelman syndromes].
    Mglinets VA; Levina LIa; Konstantinova LM
    Genetika; 1996 Dec; 32(12):1605-15. PubMed ID: 9102354
    [TBL] [Abstract][Full Text] [Related]  

  • 59. DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region.
    Mowery-Rushton PA; Driscoll DJ; Nicholls RD; Locker J; Surti U
    Am J Med Genet; 1996 Jan; 61(2):140-6. PubMed ID: 8669440
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain.
    Wu MY; Tsai TF; Beaudet AL
    Genes Dev; 2006 Oct; 20(20):2859-70. PubMed ID: 17043311
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.