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Journal Abstract Search
131 related items for PubMed ID: 20085714
1. Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene. Appenzeller S, Schirmacher A, Halfter H, Bäumer S, Pendziwiat M, Timmerman V, De Jonghe P, Fekete K, Stögbauer F, Lüdemann P, Hund M, Quabius ES, Ringelstein EB, Kuhlenbäumer G. Am J Hum Genet; 2010 Jan; 86(1):83-7. PubMed ID: 20085714 [Abstract] [Full Text] [Related]
2. Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disorders. Ni J, Yi X, Liu Z, Sun W, Yuan Y, Yang J, Jiang H, Shen L, Tang B, Liu Y, Wang J. Parkinsonism Relat Disord; 2019 Dec; 69():94-98. PubMed ID: 31726290 [Abstract] [Full Text] [Related]
3. A novel mutation of PDE8B Gene in a Japanese family with autosomal-dominant striatal degeneration. Azuma R, Ishikawa K, Hirata K, Hashimoto Y, Takahashi M, Ishii K, Inaba A, Yokota T, Orimo S. Mov Disord; 2015 Dec; 30(14):1964-7. PubMed ID: 26769607 [Abstract] [Full Text] [Related]
4. A Novel PDE8B Gene Variant Associated with Autosomal Dominant Striatal Degeneration. Chunga N, Minks K, Sell DL, Shah N, Corcoran J, Barbano RL, Schneider RB. Mov Disord Clin Pract; 2024 Aug; 11(8):1044-1046. PubMed ID: 38818539 [No Abstract] [Full Text] [Related]
5. PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population. Fan TS, Wu RM, Lin HI, Cheng C, Lin CH. Neurobiol Aging; 2018 Nov; 71():265.e15-265.e16. PubMed ID: 29909144 [Abstract] [Full Text] [Related]
6. Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14. Kuhlenbäumer G, Lüdemann P, Schirmacher A, De Vriendt E, Hünermund G, Young P, Hund-Georgiadis M, Schuierer G, Möller H, Ringelstein EB, Van Broeckhoven C, Timmerman V, Stögbauer F. Neurology; 2004 Jun 22; 62(12):2203-8. PubMed ID: 15210883 [Abstract] [Full Text] [Related]
7. Tremor without parkinsonism: A new phenotype of autosomal-dominant striatal degeneration. Sun YM, Li HQ, Zhang Y. Parkinsonism Relat Disord; 2021 Jun 22; 87():122-123. PubMed ID: 34022587 [No Abstract] [Full Text] [Related]
10. A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex. Horvath A, Giatzakis C, Tsang K, Greene E, Osorio P, Boikos S, Libè R, Patronas Y, Robinson-White A, Remmers E, Bertherat J, Nesterova M, Stratakis CA. Eur J Hum Genet; 2008 Oct 22; 16(10):1245-53. PubMed ID: 18431404 [Abstract] [Full Text] [Related]
11. Transcriptional activation of phosphodiesterase 7B1 by dopamine D1 receptor stimulation through the cyclic AMP/cyclic AMP-dependent protein kinase/cyclic AMP-response element binding protein pathway in primary striatal neurons. Sasaki T, Kotera J, Omori K. J Neurochem; 2004 Apr 22; 89(2):474-83. PubMed ID: 15056290 [Abstract] [Full Text] [Related]
14. Genomic organization, chromosomal localization, and alternative splicing of the human phosphodiesterase 8B gene. Hayashi M, Shimada Y, Nishimura Y, Hama T, Tanaka T. Biochem Biophys Res Commun; 2002 Oct 11; 297(5):1253-8. PubMed ID: 12372422 [Abstract] [Full Text] [Related]