Citations for
1NME8
Association between NME8 locus polymorphism and cognitive decline, cerebrospinal fluid and neuroimaging biomarkers in Alzheimer's disease.
Liu Y, Yu JT, Wang HF, Hao XK, Yang YF, Jiang T, Zhu XC, Cao L, Zhang DQ, Tan L.
PLoS One 9(12):e114777. doi: 10.1371/journal.pone.0114777. eCollection 2014. 2014
2NME8, TXNDC2
Functional deletion of Txndc2 and Txndc3 increases the susceptibility of spermatozoa to age-related oxidative stress.
Smith TB, Baker MA, Connaughton HS, Habenicht U, Aitken RJ.
Free Radic Biol Med 65:872-81. doi: 10.1016/j.freeradbiomed.2013.05.021. Epub 2013 May 23. 2013
3DNAH11, DNAH5, DNAI1, ICS10, ICS2, ICS3, ICS6, ICS7, NME8
Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q.
Geremek M, Schoenmaker F, Zietkiewicz E, Pogorzelski A, Diehl S, Wijmenga C, Witt M.
Eur J Hum Genet 16(6):688-95. Epub 2008 Feb 13. 2008
4NME8, RHOB
Genetic association analysis of RHOB and TXNDC3 in osteoarthritis.
Loughlin J, Meulenbelt I, Min J, Mustafa Z, Sinsheimer JS, Carr A, Slagboom PE.
Am J Hum Genet 80(2):383-6; author reply 386-7. No abstract available. 2007
5ICS6, NME8
A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia.
Duriez B, Duquesnoy P, Escudier E, Bridoux AM, Escalier D, Rayet I, Marcos E, Vojtek AM, Bercher JF, Amselem S.
Proc Natl Acad Sci U S A 104(9):3336-41. Epub 2007 Feb 20. Erratum in: Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6490. 2007
6AK1, AK5, C14orf68, DNAH1, DNAH10, DNAH11, DNAH12, DNAH14, DNAH17, DNAH2, DNAH3, DNAH5, DNAH6, DNAH7, DNAH8, DNAH9, DNAI1, DNAI2, DNAL4, DYNC1H1, DYNC1I1, DYNC1I2, DYNC2H1, DYNLL1, DYNLL2, DYNLRB1, DYNLRB2, DYNLT1, DYNLT3, ICS5, ICS6, NME8, TCTE3, TCTEX1D1, TXNDC2, TXNDC6, WDR63, WDR78
Identification of predicted human outer dynein arm genes: candidates for primary ciliary dyskinesia genes.
Pazour GJ, Agrin N, Walker BL, Witman GB.
J Med Genet 43(1):62-73. Epub 2005 Jun 3. 2006
7NLRP3, NME8, RHOB
Cis- and trans-acting gene regulation is associated with osteoarthritis.
Mahr S, Burmester GR, Hilke D, Gobel U, Grutzkau A, Haupl T, Hauschild M, Koczan D, Krenn V, Neidel J, Perka C, Radbruch A, Thiesen HJ, Muller B.
Am J Hum Genet 78(5):793-803. Epub 2006 Mar 22. 2006
8NME8
Cloning and developmental analysis of murid spermatid-specific thioredoxin-2 (SPTRX-2), a novel sperm fibrous sheath protein and autoantigen.
Miranda-Vizuete A, Tsang K, Yu Y, Jimenez A, Pelto-Huikko M, Flickinger CJ, Sutovsky P, Oko R.
J Biol Chem 278(45):44874-85. Epub 2003 Aug 7. 2003
9NME8
Sptrx-2, a fusion protein composed of one thioredoxin and three tandemly repeated NDP-kinase domains is expressed in human testis germ cells.
Sadek CM, Damdimopoulos AE, Pelto-Huikko M, Gustafsson JA, Spyrou G,Miranda-Vizuete A.
Genes Cells 6(12):1077-90. 2001