Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel
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Identification of a mammalian silicon transporter.Identification of novel tissue-specific genes by analysis of microarray databases: a human and mouse model.Regulation of magnesium balance: lessons learned from human genetic diseaseEffect of diaminopropionic acid (Dap) on the biophysical properties of a modified synthetic channel-forming peptide.Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.
P2860
Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Human FXYD2 G41R mutation resp ...... ward-rectifying cation channel
@ast
Human FXYD2 G41R mutation resp ...... ward-rectifying cation channel
@en
type
label
Human FXYD2 G41R mutation resp ...... ward-rectifying cation channel
@ast
Human FXYD2 G41R mutation resp ...... ward-rectifying cation channel
@en
prefLabel
Human FXYD2 G41R mutation resp ...... ward-rectifying cation channel
@ast
Human FXYD2 G41R mutation resp ...... ward-rectifying cation channel
@en
P2093
P2860
P1476
Human FXYD2 G41R mutation resp ...... ward-rectifying cation channel
@en
P2093
Colin G Nichols
Darian A Wigfall
Lauren C Burcea
Paul H Schlesinger
Robert W Mercer
Wade Pearson
P2860
P356
10.1152/AJPRENAL.00519.2007
P577
2008-04-30T00:00:00Z