198 related articles for article (PubMed ID: 12971993)
41. Mouse models of Prader-Willi Syndrome: a systematic review.
Bervini S; Herzog H
Front Neuroendocrinol; 2013 Apr; 34(2):107-19. PubMed ID: 23391702
[TBL] [Abstract][Full Text] [Related]
42. Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15.
Färber C; Gross S; Neesen J; Buiting K; Horsthemke B
Genomics; 2000 Apr; 65(2):174-83. PubMed ID: 10783265
[TBL] [Abstract][Full Text] [Related]
43. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.
Jay P; Rougeulle C; Massacrier A; Moncla A; Mattei MG; Malzac P; Roëckel N; Taviaux S; Lefranc JL; Cau P; Berta P; Lalande M; Muscatelli F
Nat Genet; 1997 Nov; 17(3):357-61. PubMed ID: 9354807
[TBL] [Abstract][Full Text] [Related]
44. Prader-Willi Critical Region, a Non-Translated, Imprinted Central Regulator of Bone Mass: Possible Role in Skeletal Abnormalities in Prader-Willi Syndrome.
Khor EC; Fanshawe B; Qi Y; Zolotukhin S; Kulkarni RN; Enriquez RF; Purtell L; Lee NJ; Wee NK; Croucher PI; Campbell L; Herzog H; Baldock PA
PLoS One; 2016; 11(1):e0148155. PubMed ID: 26824232
[TBL] [Abstract][Full Text] [Related]
45. Imprinting in Prader-Willi and Angelman syndromes.
Nicholls RD; Saitoh S; Horsthemke B
Trends Genet; 1998 May; 14(5):194-200. PubMed ID: 9613204
[TBL] [Abstract][Full Text] [Related]
46. Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.
Rieusset A; Schaller F; Unmehopa U; Matarazzo V; Watrin F; Linke M; Georges B; Bischof J; Dijkstra F; Bloemsma M; Corby S; Michel FJ; Wevrick R; Zechner U; Swaab D; Dudley K; Bezin L; Muscatelli F
PLoS Genet; 2013; 9(9):e1003752. PubMed ID: 24039599
[TBL] [Abstract][Full Text] [Related]
47. Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain.
de los Santos T; Schweizer J; Rees CA; Francke U
Am J Hum Genet; 2000 Nov; 67(5):1067-82. PubMed ID: 11007541
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. An imprinted, mammalian bicistronic transcript encodes two independent proteins.
Gray TA; Saitoh S; Nicholls RD
Proc Natl Acad Sci U S A; 1999 May; 96(10):5616-21. PubMed ID: 10318933
[TBL] [Abstract][Full Text] [Related]
50. 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]
51. [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]
52. Novel paternally expressed intergenic transcripts at the mouse Prader-Willi/Angelman Syndrome locus.
Buettner VL; Walker AM; Singer-Sam J
Mamm Genome; 2005 Apr; 16(4):219-27. PubMed ID: 15965783
[TBL] [Abstract][Full Text] [Related]
53. Maternal transcription of non-protein coding RNAs from the PWS-critical region rescues growth retardation in mice.
Rozhdestvensky TS; Robeck T; Galiveti CR; Raabe CA; Seeger B; Wolters A; Gubar LV; Brosius J; Skryabin BV
Sci Rep; 2016 Feb; 6():20398. PubMed ID: 26848093
[TBL] [Abstract][Full Text] [Related]
54. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
Nicholls RD; Knepper JL
Annu Rev Genomics Hum Genet; 2001; 2():153-75. PubMed ID: 11701647
[TBL] [Abstract][Full Text] [Related]
55. Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes.
Ieda D; Negishi Y; Miyamoto T; Johmura Y; Kumamoto N; Kato K; Miyoshi I; Nakanishi M; Ugawa S; Oishi H; Saitoh S
PLoS One; 2020; 15(8):e0237814. PubMed ID: 32804975
[TBL] [Abstract][Full Text] [Related]
56. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region.
Sutcliffe JS; Nakao M; Christian S; Orstavik KH; Tommerup N; Ledbetter DH; Beaudet AL
Nat Genet; 1994 Sep; 8(1):52-8. PubMed ID: 7987392
[TBL] [Abstract][Full Text] [Related]
57. Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome.
Meader BN; Albano A; Sekizkardes H; Delaney A
J Clin Endocrinol Metab; 2020 Aug; 105(8):2732-9. PubMed ID: 32480405
[TBL] [Abstract][Full Text] [Related]
58. Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndrome.
Yazdi PG; Su H; Ghimbovschi S; Fan W; Coskun PE; Nalbandian A; Knoblach S; Resnick JL; Hoffman E; Wallace DC; Kimonis VE
Clin Transl Sci; 2013 Oct; 6(5):347-55. PubMed ID: 24127921
[TBL] [Abstract][Full Text] [Related]
59. The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous
Pellikaan K; van Woerden GM; Kleinendorst L; Rosenberg AGW; Horsthemke B; Grosser C; van Zutven LJCM; van Rossum EFC; van der Lely AJ; Resnick JL; Brüggenwirth HT; van Haelst MM; de Graaff LCG
Genes (Basel); 2021 Jun; 12(6):. PubMed ID: 34200226
[TBL] [Abstract][Full Text] [Related]
60. The imprinted gene Magel2 regulates normal circadian output.
Kozlov SV; Bogenpohl JW; Howell MP; Wevrick R; Panda S; Hogenesch JB; Muglia LJ; Van Gelder RN; Herzog ED; Stewart CL
Nat Genet; 2007 Oct; 39(10):1266-72. PubMed ID: 17893678
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
