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XB-ANAT-3335
Papers associated with cell part (and slc12a6)
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The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum., Howard HC., Nat Genet. November 1, 2002; 32 (3): 384-92. |
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Transit defect of potassium-chloride Co-transporter 3 is a major pathogenic mechanism in hereditary motor and sensory neuropathy with agenesis of the corpus callosum., Salin-Cantegrel A., J Biol Chem. August 12, 2011; 286 (32): 28456-65. |
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A trafficking-deficient mutant of KCC3 reveals dominant-negative effects on K-Cl cotransport function., Ding J., PLoS One. January 1, 2013; 8 (4): e61112. |
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Potassium-chloride cotransporter 3 interacts with Vav2 to synchronize the cell volume decrease response with cell protrusion dynamics., Salin-Cantegrel A., PLoS One. May 15, 2013; 8 (5): e65294. |
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SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus., Jin SC., Mol Genet Genomic Med. September 1, 2019; 7 (9): e892. |
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