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Journal Abstract Search

197 related items for PubMed ID: 9365529

  • 1. Structure and function of the human chromosome 15 imprinting center.
    Horsthemke B.
    J Cell Physiol; 1997 Nov; 173(2):237-41. PubMed ID: 9365529
    [Abstract] [Full Text] [Related]

  • 2. The imprinting box of the Prader-Willi/Angelman syndrome domain.
    Shemer R, Hershko AY, Perk J, Mostoslavsky R, Tsuberi B, Cedar H, Buiting K, Razin A.
    Nat Genet; 2000 Dec; 26(4):440-3. PubMed ID: 11101841
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

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

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Control elements within the PWS/AS imprinting box and their function in the imprinting process.
    Kantor B, Makedonski K, Green-Finberg Y, Shemer R, Razin A.
    Hum Mol Genet; 2004 Apr 01; 13(7):751-62. PubMed ID: 14962980
    [Abstract] [Full Text] [Related]

  • 7. Imprint switch mechanism indicated by mutations in Prader-Willi and Angelman syndromes.
    Kelsey G, Reik W.
    Bioessays; 1997 May 01; 19(5):361-5. PubMed ID: 9174400
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 12(4):452-4. PubMed ID: 8630505
    [Abstract] [Full Text] [Related]

  • 9. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
    Camprubí C, Coll MD, Villatoro S, Gabau E, Kamli A, Martínez MJ, Poyatos D, Guitart M.
    Eur J Med Genet; 2007 Apr 01; 50(1):11-20. PubMed ID: 17095305
    [Abstract] [Full Text] [Related]

  • 10. 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 23; 93(15):7811-5. PubMed ID: 8755558
    [Abstract] [Full Text] [Related]

  • 11. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene.
    Dittrich B, Buiting K, Korn B, Rickard S, Buxton J, Saitoh S, Nicholls RD, Poustka A, Winterpacht A, Zabel B, Horsthemke B.
    Nat Genet; 1996 Oct 23; 14(2):163-70. PubMed ID: 8841186
    [Abstract] [Full Text] [Related]

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  • 13. Maternal methylation imprints on human chromosome 15 are established during or after fertilization.
    El-Maarri O, Buiting K, Peery EG, Kroisel PM, Balaban B, Wagner K, Urman B, Heyd J, Lich C, Brannan CI, Walter J, Horsthemke B.
    Nat Genet; 2001 Mar 23; 27(3):341-4. PubMed ID: 11242121
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  • 16. 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 23; 63(1):170-80. PubMed ID: 9634532
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  • 18. 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 23; 3(4):321-32. PubMed ID: 9237260
    [Abstract] [Full Text] [Related]

  • 19. Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain.
    Brant JO, Riva A, Resnick JL, Yang TP.
    Epigenetics; 2014 Nov 23; 9(11):1540-56. PubMed ID: 25482058
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