Papers associated with proximal (and clcn5)

Limit to papers also referencing gene:
Show all proximal papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	Diversity of functional alterations of the ClC-5 exchanger in the region of the proton glutamate in patients with Dent disease 1., Sakhi I., Hum Mutat. May 1, 2021; 42 (5): 537-550.
	A single point mutation reveals gating of the human ClC-5 Cl-/H+ antiporter., De Stefano S., J Physiol. December 1, 2013; 591 (23): 5879-93.
	Heterogeneity in the processing of CLCN5 mutants related to Dent disease., Grand T., Hum Mutat. April 1, 2011; 32 (4): 476-83.
	ATP induces conformational changes in the carboxyl-terminal region of ClC-5., Wellhauser L., J Biol Chem. February 25, 2011; 286 (8): 6733-41.
	Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing., Grand T., Kidney Int. November 1, 2009; 76 (9): 999-1005.
	N-glycosylation of the Xenopus laevis ClC-5 protein plays a role in cell surface expression, affecting transport activity at the plasma membrane., Schmieder S., J Cell Physiol. February 1, 2007; 210 (2): 479-88.
	Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease., Tanuma A., Nephron Physiol. January 1, 2007; 107 (4): p87-97.
	Nedd4-2 functionally interacts with ClC-5: involvement in constitutive albumin endocytosis in proximal tubule cells., Hryciw DH., J Biol Chem. December 31, 2004; 279 (53): 54996-5007.
	Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)., Lloyd SE., J Clin Invest. March 1, 1997; 99 (5): 967-74.
	Cloning and functional expression of rat CLC-5, a chloride channel related to kidney disease., Steinmeyer K., J Biol Chem. December 29, 1995; 270 (52): 31172-7.

???pagination.result.page??? 1