Citations for
1CMTDIF, GNB4
Exome Sequencing Identifies GNB4 Mutations as a Cause of Dominant Intermediate Charcot-Marie-Tooth Disease.
Soong BW, Huang YH, Tsai PC, Huang CC, Pan HC, Lu YC, Chien HJ, Liu TT, Chang MH, Lin KP, Tu PH, Kao LS, Lee YC.
Am J Hum Genet 92(3):422-30. doi: 10.1016/j.ajhg.2013.01.014. Epub 2013 Feb 21. 2013
2GNB2, GNB4
Gβ2 and Gβ4 participate in the opioid and adrenergic receptor-mediated Ca2+ channel modulation in rat sympathetic neurons.
Mahmoud S, Yun JK, Ruiz-Velasco V.
J Physiol 590(Pt 19):4673-89. doi: 10.1113/jphysiol.2012.237644. Epub 2012 Jun 18. 2012
3GNB4
Characterization of intron-1 haplotypes of the G protein beta 4 subunit gene--association with survival and progression in patients with urothelial bladder carcinoma.
Riemann K, Struwe H, Eisenhardt A, Obermaier B, Schmid KW, Siffert W.
Pharmacogenet Genomics 18(11):999-1008. doi: 10.1097/FPC.0b013e3283117d79. 2008
4CLIC3, GNB4, ITSN1
Isolation and characterization ofthree human chromosome 21 (HC21) genes.
Guipponi M, Mittaz L, guidi S, Chen H, Barras C, Sail-Duriaux G, Schebesta A, Rossier C, Neerman-Arbez M, Blouin JL, Scott HS, Antonarakis SE.
Cytogenet Cell Genet 86:16 1999
5GNB1, GNB2, GNB3, GNB4, GNB5, RACK1
Folding a WD repeat propeller. Role of highly conserved aspartic acid residues in the G protein beta subunit and Sec13.
Garcia-Higuera I, Gaitatzes C, Smith TF, Neer EJ.
J Biol Chem 273(15):9041-9. 1998