Citations for
1CABP2, DFNB93
A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment.
Schrauwen I, Helfmann S, Inagaki A, Predoehl F, Tabatabaiefar MA, Picher MM, Sommen M, Seco CZ, Oostrik J, Kremer H, Dheedene A, Claes C, Fransen E, Chaleshtori MH, Coucke P, Lee A, Moser T, Van Camp G.
Am J Hum Genet 91(4):636-45. doi: 10.1016/j.ajhg.2012.08.018. Epub 2012 Sep 13. 2012
2CABP1, CABP2, CABP4, CABP5
Ca2+-binding proteins tune Ca2+-feedback to Cav1.3 channels in mouse auditory hair cells.
Cui G, Meyer AC, Calin-Jageman I, Neef J, Haeseleer F, Moser T, Lee A.
J Physiol 585(Pt 3):791-803. Epub 2007 Oct 18. 2007
3WDHD1, CABP2, CEBPZ, DOCK2, NPFFR2, KLRB1, MMP24, PPM1G, SGCD, SLC4A8
Human-specific subfamilies of HERV-K (HML-2) long terminal repeats: three master genes were active simultaneously during branching of hominoid lineages( small star, filled )
Buzdin A, Ustyugova S, Khodosevich K, Mamedov I, Lebedev Y, Hunsmann G, Sverdlov E.
Genomics 81(2):149-56. 2003
4CABP1, CABP2
Functional roles and efficiencies of the thioredoxin boxes of calcium-binding proteins 1 and 2 in protein folding.
Kramer B, Ferrari DM, Klappa P, Pöhlmann N, Söling HD.
Biochem J 357(Pt 1):83-95. 2001
5CABP1, CABP2, CABP3, CABP4, CABP5
Five members of a novel Ca(2+)-binding protein (CABP) subfamily with similarity to calmodulin.
Haeseleer F, Sokal I, Verlinde CL, Erdjument-Bromage H, Tempst P, Pronin AN, Benovic JL, Fariss RN, Palczewski K.
J Biol Chem 275(2):1247-60. 2000