332 related articles for article (PubMed ID: 9302265)
21. A mouse model for Prader-Willi syndrome imprinting-centre mutations.
Yang T; Adamson TE; Resnick JL; Leff S; Wevrick R; Francke U; Jenkins NA; Copeland NG; Brannan CI
Nat Genet; 1998 May; 19(1):25-31. PubMed ID: 9590284
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival.
Kuwako K; Hosokawa A; Nishimura I; Uetsuki T; Yamada M; Nada S; Okada M; Yoshikawa K
J Neurosci; 2005 Jul; 25(30):7090-9. PubMed ID: 16049186
[TBL] [Abstract][Full Text] [Related]
26. A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.
Kanber D; Giltay J; Wieczorek D; Zogel C; Hochstenbach R; Caliebe A; Kuechler A; Horsthemke B; Buiting K
Eur J Hum Genet; 2009 May; 17(5):582-90. PubMed ID: 19066619
[TBL] [Abstract][Full Text] [Related]
27. Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
Saitoh S; Buiting K; Rogan PK; Buxton JL; Driscoll DJ; Arnemann J; König R; Malcolm S; Horsthemke B; Nicholls RD
Proc Natl Acad Sci U S A; 1996 Jul; 93(15):7811-5. PubMed ID: 8755558
[TBL] [Abstract][Full Text] [Related]
28. Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences.
Matarazzo V; Muscatelli F
Rare Dis; 2013; 1():e27228. PubMed ID: 25003016
[TBL] [Abstract][Full Text] [Related]
29. Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.
Rodriguez-Jato S; Shan J; Khadake J; Heggestad AD; Ma X; Johnstone KA; Resnick JL; Yang TP
PLoS One; 2013; 8(2):e52390. PubMed ID: 23390487
[TBL] [Abstract][Full Text] [Related]
30. Necdin gene, respiratory disturbances and Prader-Willi syndrome.
Zanella S; Barthelemy M; Muscatelli F; Hilaire G
Adv Exp Med Biol; 2008; 605():159-64. PubMed ID: 18085265
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Necdin: a multi functional protein with potential tumor suppressor role?
Chapman EJ; Knowles MA
Mol Carcinog; 2009 Nov; 48(11):975-81. PubMed ID: 19626646
[TBL] [Abstract][Full Text] [Related]
33. Unique maternal deletion of 15q in a patient with some symptoms of Prader-Willi syndrome.
Ninomiya S; Yokoyama Y; Kawakami M; Une T; Maruyama H; Morishima T
Pediatr Int; 2005 Oct; 47(5):541-5. PubMed ID: 16190961
[TBL] [Abstract][Full Text] [Related]
34. Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice.
Ren J; Lee S; Pagliardini S; Gérard M; Stewart CL; Greer JJ; Wevrick R
J Neurosci; 2003 Mar; 23(5):1569-73. PubMed ID: 12629158
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy?
Smith A
Acta Genet Med Gemellol (Roma); 1996; 45(1-2):179-89. PubMed ID: 8872029
[TBL] [Abstract][Full Text] [Related]
38. Necdin downregulates CDC2 expression to attenuate neuronal apoptosis.
Kurita M; Kuwajima T; Nishimura I; Yoshikawa K
J Neurosci; 2006 Nov; 26(46):12003-13. PubMed ID: 17108174
[TBL] [Abstract][Full Text] [Related]
39. Imprinted genes in the Prader-Willi deletion.
Francke U
Novartis Found Symp; 1998; 214():264-75; discussion 275-9. PubMed ID: 9601023
[TBL] [Abstract][Full Text] [Related]
40. Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains.
Rabinovitz S; Kaufman Y; Ludwig G; Razin A; Shemer R
Proc Natl Acad Sci U S A; 2012 May; 109(19):7403-8. PubMed ID: 22529396
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
