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Inatomi, J
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Citation: T. Takemura et al., Identification of two novel mutations in the CLCN5 gene in Japanese patients with familial idiopathic low molecular weight proteinuria (Japanese Dent's disease), AM J KIDNEY, 37(1), 2001, pp. 138-143
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Citation: T. Usui et al., Molecular basis of ocular abnormalities associated with proximal renal tubular acidosis, J CLIN INV, 108(1), 2001, pp. 107-115
Authors:
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Citation: O. Yanagida et al., Human L-type amino acid transporter 1 (LAT1): characterization of functionand expression in tumor cell lines, BBA-BIOMEMB, 1514(2), 2001, pp. 291-302
Authors:
Kim, JY
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Citation: Jy. Kim et al., Human cystine/glutamate transporter: cDNA cloning and upregulation by oxidative stress in glioma cells, BBA-BIOMEMB, 1512(2), 2001, pp. 335-344
Authors:
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Citation: H. Matsuo et al., Expression of a system L neutral amino acid transporter at the blood-brainbarrier, NEUROREPORT, 11(16), 2000, pp. 3507-3511
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Kim, DK
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Saito, I
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Kanai, Y
Citation: J. Nakauchi et al., Cloning and characterization of a human brain Na+-independent transporter for small neutral amino acids that transports D-serine with high affinity, NEUROSCI L, 287(3), 2000, pp. 231-235
Authors:
Igarashi, T
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Citation: T. Igarashi et al., Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease, KIDNEY INT, 58(2), 2000, pp. 520-527
Authors:
Hara, C
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Citation: C. Hara et al., Intracellular pH regulatory mechanism in a human renal proximal cell line (HKC8): evidence for Na+/M+ exchanger, Cl-MCO3- exchanger and Na+-HCO3- cotransporter, PFLUG ARCH, 440(5), 2000, pp. 713-720
Authors:
Igarashi, T
Inatomi, J
Sekine, T
Cha, SH
Kanai, Y
Kunimi, M
Tsukamoto, K
Satoh, H
Shimadzu, M
Tozawa, F
Mori, T
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Seki, G
Endou, H
Citation: T. Igarashi et al., Mutations in SLC4A4 cause permanent isolated proximal renal tubular acidosis with ocular abnormalities, NAT GENET, 23(3), 1999, pp. 264-266
Authors:
Igarashi, T
Inatomi, J
Wake, A
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Katayama, H
Iwata, T
Citation: T. Igarashi et al., Failure of pre-diarrheal antibiotics to prevent hemolytic uremic syndrome in serologically proven Escherichia coli O157 : H7 gastrointestinal infection, J PEDIAT, 135(6), 1999, pp. 768-769