230 related articles for article (PubMed ID: 17303379)
1. Quantification of the methylation status of the PWS/AS imprinted region: comparison of two approaches based on bisulfite sequencing and methylation-sensitive MLPA.
Dikow N; Nygren AO; Schouten JP; Hartmann C; Krämer N; Janssen B; Zschocke J
Mol Cell Probes; 2007 Jun; 21(3):208-15. PubMed ID: 17303379
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Prader-Willi and Angelman syndromes: diagnosis with a bisulfite-treated methylation-specific PCR method.
Kosaki K; McGinniss MJ; Veraksa AN; McGinnis WJ; Jones KL
Am J Med Genet; 1997 Dec; 73(3):308-13. PubMed ID: 9415690
[TBL] [Abstract][Full Text] [Related]
4. An analytical method for the detection of methylation differences at specific chromosomal loci using primer extension and ion pair reverse phase HPLC.
Matin MM; Baumer A; Hornby DP
Hum Mutat; 2002 Oct; 20(4):305-11. PubMed ID: 12325026
[TBL] [Abstract][Full Text] [Related]
5. A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus.
Zeschnigk M; Lich C; Buiting K; Doerfler W; Horsthemke B
Eur J Hum Genet; 1997; 5(2):94-8. PubMed ID: 9195159
[TBL] [Abstract][Full Text] [Related]
6. A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms.
Baumer A; Wiedemann U; Hergersberg M; Schinzel A
Hum Mutat; 2001 May; 17(5):423-30. PubMed ID: 11317358
[TBL] [Abstract][Full Text] [Related]
7. Validation of a multiplex methylation-sensitive PCR assay for the diagnosis of Prader-Willi and Angelman's syndromes.
Buller A; Pandya A; Jackson-Cook C; Bodurtha J; Tekin M; Wilkinson DS; Garrett CT; Ferreira-Gonzalez A
Mol Diagn; 2000 Sep; 5(3):239-43. PubMed ID: 11070159
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA.
Velinov M; Gu H; Genovese M; Duncan C; Brown WT; Jenkins E
Mol Genet Metab; 2000 Jan; 69(1):81-3. PubMed ID: 10655162
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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
[TBL] [Abstract][Full Text] [Related]
15. Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.
Procter M; Chou LS; Tang W; Jama M; Mao R
Clin Chem; 2006 Jul; 52(7):1276-83. PubMed ID: 16690734
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region.
Mowery-Rushton PA; Driscoll DJ; Nicholls RD; Locker J; Surti U
Am J Med Genet; 1996 Jan; 61(2):140-6. PubMed ID: 8669440
[TBL] [Abstract][Full Text] [Related]
18. Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR.
Hung CC; Lin SY; Lin SP; Niu DM; Lee NC; Cheng WF; Chen CP; Lin WL; Lee CN; Su YN
Electrophoresis; 2009 Jan; 30(2):410-6. PubMed ID: 19137525
[TBL] [Abstract][Full Text] [Related]
19. DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting.
Glenn CC; Deng G; Michaelis RC; Tarleton J; Phelan MC; Surh L; Yang TP; Driscoll DJ
Prenat Diagn; 2000 Apr; 20(4):300-6. PubMed ID: 10740202
[TBL] [Abstract][Full Text] [Related]
20. Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.
Henkhaus RS; Kim SJ; Kimonis VE; Gold JA; Dykens EM; Driscoll DJ; Butler MG
Genet Test Mol Biomarkers; 2012 Mar; 16(3):178-86. PubMed ID: 21977908
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]