PubMed (OMIM) for id: 8622

Year	Number of Results
1998	1
2002	1
2004	1
2008	3
2010	1
2015	2
2024	0

1

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. Azuma R, et al. Mov Disord. 2015 Dec;30(14):1964-7. doi: 10.1002/mds.26345. Epub 2015 Oct 13. Mov Disord. 2015. PMID: 26769607

2

Familial striatal degeneration: New mutation and neuroimaging clues.

Barsottini OG, Martins Pde M, Chien HF, Raskin S, Nunes RH, da Rocha AJ, Pedroso JL. Barsottini OG, et al. Neurology. 2015 Nov 17;85(20):1816-8. doi: 10.1212/WNL.0000000000002128. Epub 2015 Oct 16. Neurology. 2015. PMID: 26475694 No abstract available.

3

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. Appenzeller S, et al. Am J Hum Genet. 2010 Jan;86(1):83-7. doi: 10.1016/j.ajhg.2009.12.003. Am J Hum Genet. 2010. PMID: 20085714 Free PMC article.

4

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.

Arnaud-Lopez L, Usala G, Ceresini G, Mitchell BD, Pilia MG, Piras MG, Sestu N, Maschio A, Busonero F, Albai G, Dei M, Lai S, Mulas A, Crisponi L, Tanaka T, Bandinelli S, Guralnik JM, Loi A, Balaci L, Sole G, Prinzis A, Mariotti S, Shuldiner AR, Cao A, Schlessinger D, Uda M, Abecasis GR, Nagaraja R, Sanna S, Naitza S. Arnaud-Lopez L, et al. Am J Hum Genet. 2008 Jun;82(6):1270-80. doi: 10.1016/j.ajhg.2008.04.019. Am J Hum Genet. 2008. PMID: 18514160 Free PMC article.

5

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. Horvath A, et al. Eur J Hum Genet. 2008 Oct;16(10):1245-53. doi: 10.1038/ejhg.2008.85. Epub 2008 Apr 23. Eur J Hum Genet. 2008. PMID: 18431404 Free PMC article.

6

Mutation in PDE8B, a cyclic AMP-specific phosphodiesterase in adrenal hyperplasia.

Horvath A, Mericq V, Stratakis CA. Horvath A, et al. N Engl J Med. 2008 Feb 14;358(7):750-2. doi: 10.1056/NEJMc0706182. N Engl J Med. 2008. PMID: 18272904 No abstract available.

7

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. Kuhlenbäumer G, et al. Neurology. 2004 Jun 22;62(12):2203-8. doi: 10.1212/01.wnl.0000130485.89814.10. Neurology. 2004. PMID: 15210883

8

Genomic organization, chromosomal localization, and alternative splicing of the human phosphodiesterase 8B gene.

Hayashi M, Shimada Y, Nishimura Y, Hama T, Tanaka T. Hayashi M, et al. Biochem Biophys Res Commun. 2002 Oct 11;297(5):1253-8. doi: 10.1016/s0006-291x(02)02371-9. Biochem Biophys Res Commun. 2002. PMID: 12372422

9

Molecular cloning and characterization of human PDE8B, a novel thyroid-specific isozyme of 3',5'-cyclic nucleotide phosphodiesterase.

Hayashi M, Matsushima K, Ohashi H, Tsunoda H, Murase S, Kawarada Y, Tanaka T. Hayashi M, et al. Biochem Biophys Res Commun. 1998 Sep 29;250(3):751-6. doi: 10.1006/bbrc.1998.9379. Biochem Biophys Res Commun. 1998. PMID: 9784418

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

9 results

Results by year