These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 10775525)

  • 41. Inhibitors of DNA methylation and histone deacetylation independently relieve AML1/ETO-mediated lysozyme repression.
    Claus R; Fliegauf M; Stock M; Duque JA; Kolanczyk M; Lübbert M
    J Leukoc Biol; 2006 Dec; 80(6):1462-72. PubMed ID: 17000900
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Angelman syndrome imprinting center encodes a transcriptional promoter.
    Lewis MW; Brant JO; Kramer JM; Moss JI; Yang TP; Hansen PJ; Williams RS; Resnick JL
    Proc Natl Acad Sci U S A; 2015 Jun; 112(22):6871-5. PubMed ID: 25378697
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells.
    Tsai TF; Bressler J; Jiang YH; Beaudet AL
    Genesis; 2003 Dec; 37(4):151-61. PubMed ID: 14666508
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mosaic de novo
    Huang Y; Grand K; Kimonis V; Butler MG; Jain S; Huang AY; Martinez-Agosto JA; Nelson SF; Sanchez-Lara PA
    J Med Genet; 2022 Jul; 59(7):719-722. PubMed ID: 34099539
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 but not intron 7.
    Balmer D; LaSalle JM
    Hum Genet; 2001 Feb; 108(2):116-22. PubMed ID: 11281449
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
    Kalsner L; Chamberlain SJ
    Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15.
    Runte M; Färber C; Lich C; Zeschnigk M; Buchholz T; Smith A; Van Maldergem L; Bürger J; Muscatelli F; Gillessen-Kaesbach G; Horsthemke B; Buiting K
    Eur J Hum Genet; 2001 Jul; 9(7):519-26. PubMed ID: 11464243
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A novel in vitro system for analyzing parental allele-specific histone acetylation in genomic imprinting.
    Yoshioka H; Shirayoshi Y; Oshimura M
    J Hum Genet; 2001; 46(11):626-32. PubMed ID: 11721881
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila.
    Lyko F; Buiting K; Horsthemke B; Paro R
    Proc Natl Acad Sci U S A; 1998 Feb; 95(4):1698-702. PubMed ID: 9465079
    [TBL] [Abstract][Full Text] [Related]  

  • 50. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.
    Brøndum-Nielsen K
    Acta Paediatr Suppl; 1997 Nov; 423():55-7. PubMed ID: 9401540
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. DNA demethylation reactivation of imprinted genes in cell lines from patients with Prader-Willi syndrome and a mouse model.
    Takano K; Okajima M; Saitoh S
    Am J Med Genet A; 2007 Jun; 143A(12):1386-90. PubMed ID: 17506103
    [No Abstract]   [Full Text] [Related]  

  • 53. Imprinting-mutation mechanisms in Prader-Willi syndrome.
    Ohta T; Gray TA; Rogan PK; Buiting K; Gabriel JM; Saitoh S; Muralidhar B; Bilienska B; Krajewska-Walasek M; Driscoll DJ; Horsthemke B; Butler MG; Nicholls RD
    Am J Hum Genet; 1999 Feb; 64(2):397-413. PubMed ID: 9973278
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes.
    Chotai KA; Payne SJ
    J Med Genet; 1998 Jun; 35(6):472-5. PubMed ID: 9643288
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.
    Ozçelik T; Leff S; Robinson W; Donlon T; Lalande M; Sanjines E; Schinzel A; Francke U
    Nat Genet; 1992 Dec; 2(4):265-9. PubMed ID: 1303277
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Familial Prader-Willi syndrome: case report and a literature review.
    McEntagart ME; Webb T; Hardy C; King MD
    Clin Genet; 2000 Sep; 58(3):216-23. PubMed ID: 11076044
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
    Stefan M; Portis T; Longnecker R; Nicholls RD
    Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis.
    Kubota T; Aradhya S; Macha M; Smith AC; Surh LC; Satish J; Verp MS; Nee HL; Johnson A; Christan SL; Ledbetter DH
    J Med Genet; 1996 Dec; 33(12):1011-4. PubMed ID: 9004133
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Establishing the epigenetic status of the Prader-Willi/Angelman imprinting center in the gametes and embryo.
    Kantor B; Kaufman Y; Makedonski K; Razin A; Shemer R
    Hum Mol Genet; 2004 Nov; 13(22):2767-79. PubMed ID: 15367489
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.