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 *

128 related articles for article (PubMed ID: 32152487)

  • 1. Common genetic variation in the Angelman syndrome imprinting centre affects the imprinting of chromosome 15.
    Beygo J; Grosser C; Kaya S; Mertel C; Buiting K; Horsthemke B
    Eur J Hum Genet; 2020 Jun; 28(6):835-839. PubMed ID: 32152487
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15.
    Zogel C; Böhringer S; Gross S; Varon R; Buiting K; Horsthemke B
    Eur J Hum Genet; 2006 Jun; 14(6):752-8. PubMed ID: 16596119
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion.
    Färber C; Dittrich B; Buiting K; Horsthemke B
    Hum Mol Genet; 1999 Feb; 8(2):337-43. PubMed ID: 9931342
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.
    Buiting K; Dittrich B; Gross S; Lich C; Färber C; Buchholz T; Smith E; Reis A; Bürger J; Nöthen MM; Barth-Witte U; Janssen B; Abeliovich D; Lerer I; van den Ouweland AM; Halley DJ; Schrander-Stumpel C; Smeets H; Meinecke P; Malcolm S; Gardner A; Lalande M; Nicholls RD; Friend K; Schulze A; Matthijs G; Kokkonen H; Hilbert P; Van Maldergem L; Glover G; Carbonell P; Willems P; Gillessen-Kaesbach G; Horsthemke B
    Am J Hum Genet; 1998 Jul; 63(1):170-80. PubMed ID: 9634532
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome.
    Runte M; Kroisel PM; Gillessen-Kaesbach G; Varon R; Horn D; Cohen MY; Wagstaff J; Horsthemke B; Buiting K
    Hum Genet; 2004 May; 114(6):553-61. PubMed ID: 15014980
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp.
    Buiting K; Lich C; Cottrell S; Barnicoat A; Horsthemke B
    Hum Genet; 1999 Dec; 105(6):665-6. PubMed ID: 10647904
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect.
    Buiting K; Gross S; Lich C; Gillessen-Kaesbach G; el-Maarri O; Horsthemke B
    Am J Hum Genet; 2003 Mar; 72(3):571-7. PubMed ID: 12545427
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC; Driscoll DJ; Yang TP; Nicholls RD
    Mol Hum Reprod; 1997 Apr; 3(4):321-32. PubMed ID: 9237260
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
    Saitoh S; Buiting K; Rogan PK; Buxton JL; Driscoll DJ; Arnemann J; König R; Malcolm S; Horsthemke B; Nicholls RD
    Proc Natl Acad Sci U S A; 1996 Jul; 93(15):7811-5. PubMed ID: 8755558
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
    Zeschnigk M; Schmitz B; Dittrich B; Buiting K; Horsthemke B; Doerfler W
    Hum Mol Genet; 1997 Mar; 6(3):387-95. PubMed ID: 9147641
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.
    Bürger J; Buiting K; Dittrich B; Gross S; Lich C; Sperling K; Horsthemke B; Reis A
    Am J Hum Genet; 1997 Jul; 61(1):88-93. PubMed ID: 9245988
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prader-Willi syndrome and Angelman syndrome.
    Buiting K
    Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):365-76. PubMed ID: 20803659
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Imprinting defects on human chromosome 15.
    Horsthemke B; Buiting K
    Cytogenet Genome Res; 2006; 113(1-4):292-9. PubMed ID: 16575192
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects.
    Johnstone KA; DuBose AJ; Futtner CR; Elmore MD; Brannan CI; Resnick JL
    Hum Mol Genet; 2006 Feb; 15(3):393-404. PubMed ID: 16368707
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mechanisms of imprinting of the Prader-Willi/Angelman region.
    Horsthemke B; Wagstaff J
    Am J Med Genet A; 2008 Aug; 146A(16):2041-52. PubMed ID: 18627066
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mouse imprinting defect mutations that model Angelman syndrome.
    Wu MY; Chen KS; Bressler J; Hou A; Tsai TF; Beaudet AL
    Genesis; 2006 Jan; 44(1):12-22. PubMed ID: 16397868
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Somatic mosaicism in patients with Angelman syndrome and an imprinting defect.
    Nazlican H; Zeschnigk M; Claussen U; Michel S; Boehringer S; Gillessen-Kaesbach G; Buiting K; Horsthemke B
    Hum Mol Genet; 2004 Nov; 13(21):2547-55. PubMed ID: 15385437
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
    Buiting K; Saitoh S; Gross S; Dittrich B; Schwartz S; Nicholls RD; Horsthemke B
    Nat Genet; 1995 Apr; 9(4):395-400. PubMed ID: 7795645
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic imprinting and human chromosome 15.
    Repetto GM
    Biol Res; 2001; 34(2):141-5. PubMed ID: 11715207
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.