316 related articles for article (PubMed ID: 1303277)
1. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.
Ozçelik T; Leff S; Robinson W; Donlon T; Lalande M; Sanjines E; Schinzel A; Francke U
Nat Genet; 1992 Dec; 2(4):265-9. PubMed ID: 1303277
[TBL] [Abstract][Full Text] [Related]
2. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region.
Leff SE; Brannan CI; Reed ML; Ozçelik T; Francke U; Copeland NG; Jenkins NA
Nat Genet; 1992 Dec; 2(4):259-64. PubMed ID: 1303276
[TBL] [Abstract][Full Text] [Related]
3. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome.
Reed ML; Leff SE
Nat Genet; 1994 Feb; 6(2):163-7. PubMed ID: 7512861
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Deletion of small nuclear ribonucleoprotein polypeptide N (SNRPN) in Prader-Willi syndrome detected by fluorescence in situ hybridization: two sibs with the typical phenotype without a cytogenetic deletion in chromosome 15q.
Ishikawa T; Kibe T; Wada Y
Am J Med Genet; 1996 Apr; 62(4):350-2. PubMed ID: 8723064
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression.
Cattanach BM; Barr JA; Evans EP; Burtenshaw M; Beechey CV; Leff SE; Brannan CI; Copeland NG; Jenkins NA; Jones J
Nat Genet; 1992 Dec; 2(4):270-4. PubMed ID: 1303278
[TBL] [Abstract][Full Text] [Related]
8. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene.
Dittrich B; Buiting K; Korn B; Rickard S; Buxton J; Saitoh S; Nicholls RD; Poustka A; Winterpacht A; Zabel B; Horsthemke B
Nat Genet; 1996 Oct; 14(2):163-70. PubMed ID: 8841186
[TBL] [Abstract][Full Text] [Related]
9. Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
Kubota T; Sutcliffe JS; Aradhya S; Gillessen-Kaesbach G; Christian SL; Horsthemke B; Beaudet AL; Ledbetter DH
Am J Med Genet; 1996 Dec; 66(1):77-80. PubMed ID: 8957518
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.
Bressler J; Tsai TF; Wu MY; Tsai SF; Ramirez MA; Armstrong D; Beaudet AL
Nat Genet; 2001 Jul; 28(3):232-40. PubMed ID: 11431693
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
Wiriyaukaradecha S; Patmasiriwat P; Wasant P; Tantiniti P
Southeast Asian J Trop Med Public Health; 2003 Dec; 34(4):881-6. PubMed ID: 15115105
[TBL] [Abstract][Full Text] [Related]
15. Diagnostic test for the Prader-Willi syndrome by SNRPN expression in blood.
Wevrick R; Francke U
Lancet; 1996 Oct; 348(9034):1068-9. PubMed ID: 8874459
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
Buiting K; Saitoh S; Gross S; Dittrich B; Schwartz S; Nicholls RD; Horsthemke B
Nat Genet; 1995 Apr; 9(4):395-400. PubMed ID: 7795645
[TBL] [Abstract][Full Text] [Related]
18. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
[TBL] [Abstract][Full Text] [Related]
19. Methylation-sensitive high-resolution melting-curve analysis of the SNRPN gene as a diagnostic screen for Prader-Willi and Angelman syndromes.
White HE; Hall VJ; Cross NC
Clin Chem; 2007 Nov; 53(11):1960-2. PubMed ID: 17890436
[TBL] [Abstract][Full Text] [Related]
20. Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndrome.
White HE; Durston VJ; Harvey JF; Cross NC
Clin Chem; 2006 Jun; 52(6):1005-13. PubMed ID: 16574761
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
