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 *

115 related articles for article (PubMed ID: 15779004)

  • 1. Imprinting centers, chromatin structure, and disease.
    Soejima H; Wagstaff J
    J Cell Biochem; 2005 May; 95(2):226-33. PubMed ID: 15779004
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 13(7):751-62. PubMed ID: 14962980
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Genomic imprinting and hereditary diseases].
    Orstavik KH
    Tidsskr Nor Laegeforen; 1999 Feb; 119(6):835-8. PubMed ID: 10101947
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic imprinting: the paradigm of Prader-Willi and Angelman syndromes.
    Gurrieri F; Accadia M
    Endocr Dev; 2009; 14():20-8. PubMed ID: 19293572
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DNA methylation in genomic imprinting, development, and disease.
    Paulsen M; Ferguson-Smith AC
    J Pathol; 2001 Sep; 195(1):97-110. PubMed ID: 11568896
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Epigenetic modification of the genetic material. Genomic imprinting and its significance for disease in human beings].
    Brøndum-Nielsen K; Pedersen ML
    Ugeskr Laeger; 2001 Jun; 163(23):3218-22. PubMed ID: 11421188
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 50(1):11-20. PubMed ID: 17095305
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Epigenetics and development: genomic imprinting].
    Gabory A; Dandolo L
    Med Sci (Paris); 2005 Apr; 21(4):390-5. PubMed ID: 15811304
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomic imprinting relevant to genetic diseases.
    Niikawa N
    Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():46-57. PubMed ID: 9640600
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genomic imprinting].
    Kato R; Niikawa N
    Tanpakushitsu Kakusan Koso; 1996 Nov; 41(15 Suppl):2325-34. PubMed ID: 8952395
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.
    Murthy SK; Nygren AO; El Shakankiry HM; Schouten JP; Al Khayat AI; Ridha A; Al Ali MT
    Cytogenet Genome Res; 2007; 116(1-2):135-40. PubMed ID: 17268193
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures.
    Eggermann T
    Horm Res; 2009 Apr; 71 Suppl 2():30-5. PubMed ID: 19407494
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Methylation-specific multiplex ligation-dependent probe amplification in diagnosis of Prader-Willi syndrome and Angelman syndrome].
    Li MR; Wang XZ; Liu XY; Yang YL; Bao XH; Zhang YH; Xiong H; Zhong N; Qin J; Wu XR; Pan H
    Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3257-61. PubMed ID: 19159549
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genomic imprinting and human pathology].
    Polívková Z
    Cas Lek Cesk; 2005; 144(4):245-50; discussion 250-1. PubMed ID: 15945483
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromatin modification of the human imprinted NDN (necdin) gene detected by in vivo footprinting.
    Hanel ML; Lau JC; Paradis I; Drouin R; Wevrick R
    J Cell Biochem; 2005 Apr; 94(5):1046-57. PubMed ID: 15669020
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A review of known imprinting syndromes and their association with assisted reproduction technologies.
    Amor DJ; Halliday J
    Hum Reprod; 2008 Dec; 23(12):2826-34. PubMed ID: 18703582
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.