Pages that link to "Q52542895"

The following pages link to Localization of mouse CLC-6 and CLC-7 mRNA and their functional complementation of yeast CLC gene mutant. (Q52542895):

Displaying 14 items.

• Postnatal expression of KLF12 in the inner medullary collecting ducts of kidney and its trans-activation of UT-A1 urea transporter promoter (Q24317484) (← links)
• The Gef1 protein of Saccharomyces cerevisiae is associated with chloride channel activity. (Q27935471) (← links)
• The functioning of mammalian ClC-2 chloride channel in Saccharomyces cerevisiae cells requires an increased level of Kha1p (Q27936789) (← links)
• Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6. (Q30499606) (← links)
• The Princeton Protein Orthology Database (P-POD): a comparative genomics analysis tool for biologists (Q33294829) (← links)
• Inhibition of iron uptake is responsible for differential sensitivity to V-ATPase inhibitors in several cancer cell lines (Q33641308) (← links)
• From stones to bones: the biology of ClC chloride channels (Q34343399) (← links)
• Separate ion pathways in a Cl-/H+ exchanger (Q36493595) (← links)
• Channeling studies in yeast: yeast as a model for channelopathies? (Q36507190) (← links)
• Cell biology and physiology of CLC chloride channels and transporters (Q38110745) (← links)
• ClC Channels and Transporters: Structure, Physiological Functions, and Implications in Human Chloride Channelopathies (Q39225398) (← links)
• A CLC‐type chloride channel gene is required for laccase activity and virulence in Cryptococcus neoformans (Q44658462) (← links)
• Identification and characterization of the three members of the CLC family of anion transport proteins in Trypanosoma brucei (Q47171669) (← links)
• Extra-skeletal manifestations in mice affected by Clcn7-dependent autosomal dominant osteopetrosis type 2 clinical and therapeutic implications (Q92972252) (← links)