Citations for
1OIXIV, TMEM38B
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta.
Rubinato E, Morgan A, D'Eustacchio A, Pecile V, Gortani G, Gasparini P, Faletra F.
Gene 545(2):290-2. doi: 10.1016/j.gene.2014.05.028. Epub 2014 May 14. 2014
2TMEM38A, TMEM38B
Trimeric intracellular cation channels and sarcoplasmic/endoplasmic reticulum calcium homeostasis.
Zhou X, Lin P, Yamazaki D, Park KH, Komazaki S, Chen SR, Takeshima H, Ma J.
Circ Res 114(4):706-16. doi: 10.1161/CIRCRESAHA.114.301816. Review. 2014
3OIXIV, TMEM38B
A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfecta.
Volodarsky M, Markus B, Cohen I, Staretz-Chacham O, Flusser H, Landau D, Shelef I, Langer Y, Birk OS.
Hum Mutat 34(4):582-6. doi: 10.1002/humu.22274. 2013
4OIXIV, TMEM38B
Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation.
Shaheen R, Alazami AM, Alshammari MJ, Faqeih E, Alhashmi N, Mousa N, Alsinani A, Ansari S, Alzahrani F, Al-Owain M, Alzayed ZS, Alkuraya FS.
J Med Genet 49(10):630-5. doi: 10.1136/jmedgenet-2012-101142. 2012
5TMEM38A, TMEM38B
Essential role of the TRIC-B channel in Ca2+ handling of alveolar epithelial cells and in perinatal lung maturation.
Yamazaki D, Komazaki S, Nakanishi H, Mishima A, Nishi M, Yazawa M, Yamazaki T, Taguchi R, Takeshima H.
Development 136(14):2355-61. doi: 10.1242/dev.036798. Epub 2009 Jun 10. 2009
6TMEM38A, TMEM38B
TRIC channels are essential for Ca2+ handling in intracellular stores.
Yazawa M, Ferrante C, Feng J, Mio K, Ogura T, Zhang M, Lin PH, Pan Z, Komazaki S, Kato K, Nishi M, Zhao X, Weisleder N, Sato C, Ma J, Takeshima H.
Nature 448(7149):78-82. 2007