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.
209 related articles for article (PubMed ID: 22578325)
1. Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity. Williams SR; Zies D; Mullegama SV; Grotewiel MS; Elsea SH Am J Hum Genet; 2012 Jun; 90(6):941-9. PubMed ID: 22578325 [TBL] [Abstract][Full Text] [Related]
2. Smith-Magenis syndrome protein RAI1 regulates body weight homeostasis through hypothalamic BDNF-producing neurons and neurotrophin downstream signalling. Javed S; Chang YT; Cho Y; Lee YJ; Chang HC; Haque M; Lin YC; Huang WH Elife; 2023 Nov; 12():. PubMed ID: 37956053 [No Abstract] [Full Text] [Related]
3. Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder. Poisson A; Nicolas A; Bousquet I; Raverot V; Gronfier C; Demily C Int J Mol Sci; 2019 Jul; 20(14):. PubMed ID: 31330985 [TBL] [Abstract][Full Text] [Related]
4. Comparative analyses of the Smith-Magenis syndrome protein RAI1 in mice and common marmoset monkeys. Chang YT; Lee YJ; Haque M; Chang HC; Javed S; Lin YC; Cho Y; Abramovitz J; Chin G; Khamis A; Raja R; Murai KK; Huang WH J Comp Neurol; 2024 Jan; 532(1):e25589. PubMed ID: 38289192 [TBL] [Abstract][Full Text] [Related]
5. Case Report: A Case of a Patient with Smith-Magenis Syndrome and Early-Onset Parkinson's Disease. Stern T; Hussein Y; Cordeiro D; Sadis H; Garin-Shkolnik T; Spiegel R; Cohen S; Harari R; Schlesinger I; Stern S Int J Mol Sci; 2024 Aug; 25(15):. PubMed ID: 39126013 [TBL] [Abstract][Full Text] [Related]
6. A case of Smith-Magenis syndrome with skin manifestations caused by a novel locus mutation in the RAI1 gene. Wu X; Zhang L; Chen S; Li Y J Int Med Res; 2023 Sep; 51(9):3000605231190553. PubMed ID: 37756600 [TBL] [Abstract][Full Text] [Related]
7. Falco M; Amabile S; Acquaviva F Appl Clin Genet; 2017; 10():85-94. PubMed ID: 29138588 [TBL] [Abstract][Full Text] [Related]
8. Psychiatric and neurological manifestations in adults with Smith-Magenis syndrome: A scoping review. Korteling D; Musch JLI; Zinkstok JR; Boot E Am J Med Genet B Neuropsychiatr Genet; 2024 Mar; 195(2):e32956. PubMed ID: 37584268 [TBL] [Abstract][Full Text] [Related]
9. First Case Report of Smith-Magenis Syndrome (SMS) Among the Arab Community in Nazareth: View and Overview. Nijim Y; Adawi A; Bisharat B; Bowirrat A Medicine (Baltimore); 2016 Jan; 95(3):e2362. PubMed ID: 26817868 [TBL] [Abstract][Full Text] [Related]
10. Behavior and physiology in female Zhu H; Wu M; Mou J; Yang X; Xu Q; Zhang Y; Zhang H; Wang X; Xue H; Xu J; Chen L; Xu L Front Endocrinol (Lausanne); 2023; 14():1281617. PubMed ID: 38374960 [TBL] [Abstract][Full Text] [Related]
11. Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike. Yan J; Bi W; Lupski JR Am J Hum Genet; 2007 Mar; 80(3):518-25. PubMed ID: 17273973 [TBL] [Abstract][Full Text] [Related]
12. Core circadian protein CLOCK is a positive regulator of NF-κB-mediated transcription. Spengler ML; Kuropatwinski KK; Comas M; Gasparian AV; Fedtsova N; Gleiberman AS; Gitlin II; Artemicheva NM; Deluca KA; Gudkov AV; Antoch MP Proc Natl Acad Sci U S A; 2012 Sep; 109(37):E2457-65. PubMed ID: 22895791 [TBL] [Abstract][Full Text] [Related]
14. Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion. Boudreau EA; Johnson KP; Jackman AR; Blancato J; Huizing M; Bendavid C; Jones M; Chandrasekharappa SC; Lewy AJ; Smith AC; Magenis RE Am J Med Genet A; 2009 Jul; 149A(7):1382-91. PubMed ID: 19530184 [TBL] [Abstract][Full Text] [Related]
15. Yin-yang actions of histone methylation regulatory complexes in the brain. Garay PM; Wallner MA; Iwase S Epigenomics; 2016 Dec; 8(12):1689-1708. PubMed ID: 27855486 [TBL] [Abstract][Full Text] [Related]
16. Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndrome. Cogliati F; Straniero L; Rimoldi V; Masciadri M; Perego S; Rinaldi B; Milani D; Gentilini D; Larizza L; Asselta R; Russo S; Bedeschi MF Am J Med Genet B Neuropsychiatr Genet; 2024 Sep; 195(6):e32976. PubMed ID: 38385826 [TBL] [Abstract][Full Text] [Related]