Citations for
1ANO1, ANO10, ANO4, ANO6
Differential effects of anoctamins on intracellular calcium signals.
Cabrita I, Benedetto R, Fonseca A, Wanitchakool P, Sirianant L, Skryabin BV, Schenk LK, Pavenstädt H, Schreiber R, Kunzelmann K.
FASEB J ASEB J. 2017 Feb 9. pii: fj.201600797RR. doi: 10.1096/fj.201600797RR. [Epub ahead of print] 2017
2ANO10, SCAR10
Executive and Attentional Disorders, Epilepsy and Porencephalic Cyst in Autosomal Recessive Cerebellar Ataxia Type 3 Due to ANO10 Mutation.
Chamard L, Sylvestre G, Koenig M, Magnin E.
Eur Neurol 75(3-4):186-90. doi: 10.1159/000445109. Epub 2016 Apr 6. 2016
3ANO1, ANO10, ANO6
Expression of anoctamins in retinal pigment epithelium (RPE).
Schreiber R, Kunzelmann K.
Pflugers Arch 468(11-12):1921-1929. Epub 2016 Nov 7. 2016
4ANO10
A Coding Variant of ANO10, Affecting Volume Regulation of Macrophages, Is Associated with Borrelia Seropositivity.
Hammer C, Wanitchakool P, Sirianant L, Papiol S, Monnheimer M, Faria D, Ousingsawat J, Schramek N, Schmitt C, Margos G, Michel A, Kraiczy P, Pawlita M, Schreiber R, Schulz TF, Fingerle V, Tumani H, Ehrenreich H, Kunzelmann K.
Mol Med 21:26-37. doi: 10.2119/molmed.2014.00219. 2015
5ANO10
Anoctamins support calcium-dependent chloride secretion by facilitating calcium signaling in adult mouse intestine.
Schreiber R, Faria D, Skryabin BV, Wanitchakool P, Rock JR, Kunzelmann K.
Pflugers Arch 467(6):1203-13. doi: 10.1007/s00424-014-1559-2. Epub 2014 Jul 1. 2015
6ANO10, EXOSC8, PCH1C, SCAR10
Respiratory chain deficiency in nonmitochondrial disease.
Pyle A, Nightingale HJ, Griffin H, Abicht A, Kirschner J, Baric I, Cuk M, Douroudis K, Feder L, Kratz M, Czermin B, Kleinle S, Santibanez-Koref M, Karcagi V, Holinski-Feder E, Chinnery PF, Horvath R.
Neurol Genet 1(1):e6. doi: 10.1212/NXG.0000000000000006. eCollection 2015 Jun. 2015
7ANO10, SCAR10
ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency.
Balreira A, Boczonadi V, Barca E, Pyle A, Bansagi B, Appleton M, Graham C, Hargreaves IP, Rasic VM, Lochmüller H, Griffin H, Taylor RW, Naini A, Chinnery PF, Hirano M, Quinzii CM, Horvath R.
J Neurol 261(11):2192-8. doi: 10.1007/s00415-014-7476-7. Epub 2014 Sep 3. 2014
8ANO10, SCAR10
Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study.
Renaud M, Anheim M, Kamsteeg EJ, Mallaret M, Mochel F, Vermeer S, Drouot N, Pouget J, Redin C, Salort-Campana E, Kremer HP, Verschuuren-Bemelmans CC, Muller J, Scheffer H, Durr A, Tranchant C, Koenig M.
JAMA Neurol 71(10):1305-10. doi: 10.1001/jamaneurol.2014.193. 2014
9ANO10, ANO3, ANO5, ANO6
Structure and function of TMEM16 proteins (anoctamins).
Pedemonte N, Galietta LJ.
Physiol Rev 94(2):419-59. doi: 10.1152/physrev.00039.2011. Review. 2014
10ANO10, SCAR10
Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia.
Maruyama H, Morino H, Miyamoto R, Murakami N, Hamano T, Kawakami H.
Clin Genet 85(3):296-7. doi: 10.1111/cge.12140. Epub 2013 Apr 4. No abstract available. 2014
11ANO10, RUBCN, SCAR10, SCAR11, SCAR15, SYT14
Recent advances in the genetics of cerebellar ataxias.
Sailer A, Houlden H.
Curr Neurol Neurosci Rep 12(3):227-36. doi: 10.1007/s11910-012-0267-6. Review. 2012
12ANO10, ANO9
Evolution and functional divergence of the anoctamin family of membrane proteins.
Milenkovic VM, Brockmann M, Stöhr H, Weber BH, Strauss O.
BMC Evol Biol 10:319.PMID: 20964844 2010
13ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9
Expression and function of epithelial anoctamins.
Schreiber R, Uliyakina I, Kongsuphol P, Warth R, Mirza M, Martins JR, Kunzelmann K.
J Biol Chem 285(10):7838-45. Epub 2010 Jan 7.PMID: 20056604 2010
14ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9, SCAR10
Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.
Vermeer S, Hoischen A, Meijer RP, Gilissen C, Neveling K, Wieskamp N, de Brouwer A, Koenig M, Anheim M, Assoum M, Drouot N, Todorovic S, Milic-Rasic V, Lochmüller H, Stevanin G, Goizet C, David A, Durr A, Brice A, Kremer B, van de Warrenburg BP, Schijvenaars MM, Heister A, Kwint M, Arts P, van der Wijst J, Veltman J, Kamsteeg EJ, Scheffer H, Knoers N.
Am J Hum Genet 87(6):813-9. Epub 2010 Nov 18.PMID: 21092923 2010
15ANO1, ANO10, ANO3, ANO6, ANO8
Expression patterns of the Tmem16 gene family during cephalic development in the mouse.
Gritli-Linde A, Vaziri Sani F, Rock JR, Hallberg K, Iribarne D, Harfe BD, Linde A.
Gene Expr Patterns 9(3):178-91. Epub 2008 Nov 25.PMID: 19059364 2009
16ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9, BEST1
Bestrophin and TMEM16-Ca(2+) activated Cl(-) channels with different functions.
Kunzelmann K, Kongsuphol P, Aldehni F, Tian Y, Ousingsawat J, Warth R, Schreiber R.
Cell Calcium 46(4):233-41. Epub 2009 Sep 26. Review.PMID: 19783045 2009
17ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9
Expression of TMEM16 paralogs during murine embryogenesis.
Rock JR, Harfe BD.
Dev Dyn 237(9):2566-74. 2008
18ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9
Identification and characterization of TMEM16E and TMEM16F genes in silico.
Katoh M, Katoh M.
Int J Oncol 24(5):1345-9. 2004