Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (4)
Literature for OMIM 241200: BARTTER SYNDROME, TYPE 2, ANTENATAL; BARTS2


Xenbase Articles:
( Denotes literature images)
Organization of the pronephric kidney revealed by large-scale gene expression mapping., Raciti D,Reggiani L,Geffers L,Jiang Q,Bacchion F,Clements D,Tindal C,Davidson DR,Kaissling B,Brändli AW,Subrizi AE, Genome Biol. January 1, 2008; 9(5):1474-760X.
Functional and structural characterization of PKA-mediated pHi gating of ROMK1 channels., Lee CH,Lee CH,Lee CH,Huang PT,Lou KL,Liou HH, J Mol Graph Model. October 1, 2008; 27(3):1873-4243.
Identification of compound heterozygous KCNJ1 mutations (encoding ROMK) in a kindred with Bartter's syndrome and a functional analysis of their pathogenicity., Srivastava S,Edwards N,Hynes AM,Wood K,Al-Hamed M,Reaich D,Moochhala SH,Welling PA,Sayer JA,Li D,Wroe AC, Physiol Rep. November 1, 2013; 1(6):2051-817X.
State-dependent network connectivity determines gating in a K+ channel., Bollepalli MK,Fowler PW,Rapedius M,Shang L,Sansom MS,Tucker SJ,Baukrowitz T, Structure. July 8, 2014; 22(7):1878-4186.