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 *

210 related articles for article (PubMed ID: 17236194)

  • 1. Whole genome microarray analysis of gene expression in Prader-Willi syndrome.
    Bittel DC; Kibiryeva N; Sell SM; Strong TV; Butler MG
    Am J Med Genet A; 2007 Mar; 143A(5):430-42. PubMed ID: 17236194
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD.
    Bittel DC; Kibiryeva N; Talebizadeh Z; Butler MG
    J Med Genet; 2003 Aug; 40(8):568-74. PubMed ID: 12920063
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.
    Bittel DC; Kibiryeva N; McNulty SG; Driscoll DJ; Butler MG; White RA
    Am J Med Genet A; 2007 Mar; 143A(5):422-9. PubMed ID: 17036336
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array.
    Morandi A; Bonnefond A; Lobbens S; Carotenuto M; Del Giudice EM; Froguel P; Maffeis C
    Am J Med Genet A; 2015 Nov; 167A(11):2720-6. PubMed ID: 26109092
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities.
    Muralidhar B; Marney A; Butler MG
    Genet Med; 1999; 1(4):141-5. PubMed ID: 11258349
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.
    Jiang YH; Wauki K; Liu Q; Bressler J; Pan Y; Kashork CD; Shaffer LG; Beaudet AL
    BMC Genomics; 2008 Jan; 9():50. PubMed ID: 18226259
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. 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]  

  • 13. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.
    Bittel DC; Kibiryeva N; Butler MG
    Pediatrics; 2006 Oct; 118(4):e1276-83. PubMed ID: 16982806
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Insulin resistance and obesity-related factors in Prader-Willi syndrome: comparison with obese subjects.
    Talebizadeh Z; Butler MG
    Clin Genet; 2005 Mar; 67(3):230-9. PubMed ID: 15691361
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.
    Wang JC; Vaccarello-Cruz M; Ross L; Owen R; Pratt VM; Lightman K; Liu Y; Hafezi K; Cherif D; Sahoo T
    Am J Med Genet A; 2013 Jul; 161A(7):1695-701. PubMed ID: 23686718
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
    Milner KM; Craig EE; Thompson RJ; Veltman MW; Thomas NS; Roberts S; Bellamy M; Curran SR; Sporikou CM; Bolton PF
    J Child Psychol Psychiatry; 2005 Oct; 46(10):1089-96. PubMed ID: 16178933
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.
    Zilina O; Kahre T; Talvik I; Oiglane-Shlik E; Tillmann V; Ounap K
    Eur J Med Genet; 2014; 57(6):279-83. PubMed ID: 24704109
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome.
    Zhang K; Liu S; Feng B; Yang Y; Zhang H; Dong R; Liu Y; Gai Z
    PLoS One; 2016; 11(2):e0147824. PubMed ID: 26841067
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.