339 related articles for article (PubMed ID: 10626556)
1. Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.
Nicholls RD; Ohta T; Gray TA
Acta Paediatr Suppl; 1999 Dec; 88(433):99-104. PubMed ID: 10626556
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.
Brøndum-Nielsen K
Acta Paediatr Suppl; 1997 Nov; 423():55-7. PubMed ID: 9401540
[TBL] [Abstract][Full Text] [Related]
5. Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.
Cassidy SB; Schwartz S
Medicine (Baltimore); 1998 Mar; 77(2):140-51. PubMed ID: 9556704
[TBL] [Abstract][Full Text] [Related]
6. Structure and function correlations at the imprinted mouse Snrpn locus.
Gabriel JM; Gray TA; Stubbs L; Saitoh S; Ohta T; Nicholls RD
Mamm Genome; 1998 Oct; 9(10):788-93. PubMed ID: 9745031
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Imprinting in Angelman and Prader-Willi syndromes.
Jiang Y; Tsai TF; Bressler J; Beaudet AL
Curr Opin Genet Dev; 1998 Jun; 8(3):334-42. PubMed ID: 9691003
[TBL] [Abstract][Full Text] [Related]
9. Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.
Conroy JM; Grebe TA; Becker LA; Tsuchiya K; Nicholls RD; Buiting K; Horsthemke B; Cassidy SB; Schwartz S
Am J Hum Genet; 1997 Aug; 61(2):388-94. PubMed ID: 9311744
[TBL] [Abstract][Full Text] [Related]
10. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
Nicholls RD
Am J Med Genet; 1993 Apr; 46(1):16-25. PubMed ID: 8388169
[TBL] [Abstract][Full Text] [Related]
11. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
Kalsner L; Chamberlain SJ
Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome.
Tsai TF; Jiang YH; Bressler J; Armstrong D; Beaudet AL
Hum Mol Genet; 1999 Aug; 8(8):1357-64. PubMed ID: 10400982
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).
Nakao M; Sutcliffe JS; Durtschi B; Mutirangura A; Ledbetter DH; Beaudet AL
Hum Mol Genet; 1994 Feb; 3(2):309-15. PubMed ID: 8004100
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Prader-Willi syndrome and Angelman syndrome.
Buiting K
Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):365-76. PubMed ID: 20803659
[TBL] [Abstract][Full Text] [Related]
19. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.
Wevrick R; Kerns JA; Francke U
Hum Mol Genet; 1994 Oct; 3(10):1877-82. PubMed ID: 7849716
[TBL] [Abstract][Full Text] [Related]
20. Deletion of SNURF/SNRPN U1B and U1B* upstream exons in a child with developmental delay and excessive weight.
Koufaris C; Alexandrou A; Papaevripidou I; Alexandrou I; Christophidou-Anastasiadou V; Sismani C
J Genet; 2016 Sep; 95(3):621-4. PubMed ID: 27659333
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
