BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

394 related articles for article (PubMed ID: 32961075)

  • 1. Prader-Willi syndrome: reflections on seminal studies and future therapies.
    Chung MS; Langouët M; Chamberlain SJ; Carmichael GG
    Open Biol; 2020 Sep; 10(9):200195. PubMed ID: 32961075
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 9(11):1540-56. PubMed ID: 25482058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.
    Hassan M; Butler MG
    Eur J Med Genet; 2016 Nov; 59(11):584-589. PubMed ID: 27659713
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.
    Lee S; Wevrick R
    Am J Hum Genet; 2000 Mar; 66(3):848-58. PubMed ID: 10712201
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.
    Wu MY; Jiang M; Zhai X; Beaudet AL; Wu RC
    PLoS One; 2012; 7(4):e34348. PubMed ID: 22496793
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
    Bittel DC; Butler MG
    Expert Rev Mol Med; 2005 Jul; 7(14):1-20. PubMed ID: 16038620
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An Atypical 15q11.2 Microdeletion Not Involving
    Crenshaw MM; Graw SL; Slavov D; Boyle TA; Piqué DG; Taylor M; Baker P
    Case Rep Genet; 2023; 2023():4225092. PubMed ID: 37736297
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
    Hartin SN; Hossain WA; Weisensel N; Butler MG
    Am J Med Genet A; 2018 Apr; 176(4):886-895. PubMed ID: 29437285
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. [Prader-Willi syndrome and genomic imprinting].
    Wang W; Wang DF; Cui YF; Ni JH; Dong ZY; Fu MF; Fu HM; Lu GQ; Chen FS
    Zhonghua Er Ke Za Zhi; 2003 Jun; 41(6):453-6. PubMed ID: 14749005
    [TBL] [Abstract][Full Text] [Related]  

  • 14. R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation.
    Powell WT; Coulson RL; Gonzales ML; Crary FK; Wong SS; Adams S; Ach RA; Tsang P; Yamada NA; Yasui DH; Chédin F; LaSalle JM
    Proc Natl Acad Sci U S A; 2013 Aug; 110(34):13938-43. PubMed ID: 23918391
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region.
    Mim RA; Soorajkumar A; Kosaji N; Rahman MM; Sarker S; Karuvantevida N; Eshaque TB; Rahaman MA; Islam A; Chowdhury MSJ; Shams N; Uddin KMF; Akter H; Uddin M
    Brain Behav; 2024 Apr; 14(4):e3437. PubMed ID: 38616334
    [TBL] [Abstract][Full Text] [Related]  

  • 17. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
    Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA
    Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD.
    Muthusamy K; Macke EL; Klee EW; Tebben PJ; Hand JL; Hasadsri L; Marcou CA; Schimmenti LA
    Am J Med Genet A; 2020 Oct; 182(10):2442-2449. PubMed ID: 32815268
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect.
    Schulze A; Hansen C; Baekgaard P; Blichfeldt S; Petersen MB; Tommerup N; Brøndum-Nielsen K
    Acta Paediatr; 1997 Aug; 86(8):906-10. PubMed ID: 9307178
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prader-Willi Syndrome: Molecular Mechanism and Epigenetic Therapy.
    Mian-Ling Z; Yun-Qi C; Chao-Chun Z
    Curr Gene Ther; 2020; 20(1):36-43. PubMed ID: 32329685
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.