The role of renal chloride channel mutations in kidney stone disease and nephrocalcinosis.
Recent advances in molecular biology have characterised a new class of chloride channels (CLCs) that are referred to as voltage-gated CLCs. To date nine such voltage-gated CLCs (CLC-1 to CLC-7, CLC-Ka and CLC-Kb, which are encoded by the genes CLCN1 to CLCN7, CLC-Ka and CLC-Kb, respectively) have be...
প্রধান লেখক: | Thakker, R |
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বিন্যাস: | Journal article |
ভাষা: | English |
প্রকাশিত: |
1998
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অনুরূপ উপাদানগুলি
অনুরূপ উপাদানগুলি
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Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
অনুযায়ী: Lloyd, SE, অন্যান্য
প্রকাশিত: (1996) -
Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
অনুযায়ী: Lloyd, SE, অন্যান্য
প্রকাশিত: (1997) -
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
অনুযায়ী: Lloyd, SE, অন্যান্য
প্রকাশিত: (1997) -
THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
অনুযায়ী: Thakker, R, অন্যান্য
প্রকাশিত: (1993) -
Chloride channels in renal disease.
অনুযায়ী: Thakker, R
প্রকাশিত: (1999)