These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
322 related articles for article (PubMed ID: 9973278)
81. Angelman syndrome imprinting center encodes a transcriptional promoter. Lewis MW; Brant JO; Kramer JM; Moss JI; Yang TP; Hansen PJ; Williams RS; Resnick JL Proc Natl Acad Sci U S A; 2015 Jun; 112(22):6871-5. PubMed ID: 25378697 [TBL] [Abstract][Full Text] [Related]
82. Association of acetylated histones with paternally expressed genes in the Prader--Willi deletion region. Fulmer-Smentek SB; Francke U Hum Mol Genet; 2001 Mar; 10(6):645-52. PubMed ID: 11230184 [TBL] [Abstract][Full Text] [Related]
83. 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]
84. Imprinting defects on human chromosome 15. Horsthemke B; Buiting K Cytogenet Genome Res; 2006; 113(1-4):292-9. PubMed ID: 16575192 [TBL] [Abstract][Full Text] [Related]
85. 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]
86. 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]
87. Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient. Sun Y; Nicholls RD; Butler MG; Saitoh S; Hainline BE; Palmer CG Hum Mol Genet; 1996 Apr; 5(4):517-24. PubMed ID: 8845846 [TBL] [Abstract][Full Text] [Related]
88. A modified MS-PCR approach to diagnose patients with Prader-Willi and Angelman syndrome. Dos Santos JF; Mota LR; Rocha PH; Ferreira de Lima RL Mol Biol Rep; 2016 Nov; 43(11):1221-1225. PubMed ID: 27535666 [TBL] [Abstract][Full Text] [Related]
89. A mouse model of Angelman syndrome imprinting defects. Lewis MW; Vargas-Franco D; Morse DA; Resnick JL Hum Mol Genet; 2019 Jan; 28(2):220-229. PubMed ID: 30260400 [TBL] [Abstract][Full Text] [Related]
90. 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]
91. Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions. Matsubara K; Itoh M; Shimizu K; Saito S; Enomoto K; Nakabayashi K; Hata K; Kurosawa K; Ogata T; Fukami M; Kagami M Clin Epigenetics; 2019 Feb; 11(1):36. PubMed ID: 30819260 [TBL] [Abstract][Full Text] [Related]
92. 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]
93. 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]
94. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Shemer R; Birger Y; Riggs AD; Razin A Proc Natl Acad Sci U S A; 1997 Sep; 94(19):10267-72. PubMed ID: 9294199 [TBL] [Abstract][Full Text] [Related]
95. 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]
96. Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect. Schulze A; Hansen C; Baekgaard P; Blichfeldt S; Petersen MB; Tommerup N; Brøndum-Nielsen K Acta Paediatr; 1997 Aug; 86(8):906-10. PubMed ID: 9307178 [TBL] [Abstract][Full Text] [Related]
97. Expression of the Snurf-Snrpn IC transcript in the oocyte and its putative role in the imprinting establishment of the mouse 7C imprinting domain. Mapendano CK; Kishino T; Miyazaki K; Kondo S; Yoshiura KI; Hishikawa Y; Koji T; Niikawa N; Ohta T J Hum Genet; 2006; 51(3):236-243. PubMed ID: 16429232 [TBL] [Abstract][Full Text] [Related]
98. Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site. Chai JH; Locke DP; Ohta T; Greally JM; Nicholls RD Mamm Genome; 2001 Nov; 12(11):813-21. PubMed ID: 11845283 [TBL] [Abstract][Full Text] [Related]
99. 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]