References
- 장부변증논치 김완희;최달영
- 대한한의학회지 v.8 no.1 신기능에 대한 동서의학적 고찰 류도곤;이호섭;강순수;정우열
- 경희대학교논문집 v.11 수기병에 관한 문헌적 연구 성현제
- 醫林撮要 金世坤
- 동의방제와 처방해설 윤용갑
- 한방재활의학회지 v.8 no.1 태권도 선수의 체중감량시 신체조성 및 혈청지질 성분변화에 補中治濕湯이 미치는 영향 김범철;금동호;이명종
- 경희대학교 대학원 석사학위논문 補中治濕湯이 간 및 腎臟의 손상에 미치는 영향 조창섭
- 동의생리병리학회지 v.15 no.2 補中治濕湯의 백서 신장 기능에 미치는 영향 김종균;김유겸;유장현;이호섭
- Anal Biochem v.72 A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Bradford, M. M. https://doi.org/10.1016/0003-2697(76)90527-3
- 腎臟學 서울대학교 의과대학
- 生理學 김종규
- 人體生理學 김광진;김창주;김형진;박사훈
- 전정판 腎臟學 서울대학교 의과대학
-
Pflugers Arch.
v.329
The localization of the
$Na^{+}-K^{+}$ -ATPase in the cells of rat kidney cortex. A study on isolated plasma membranes. Kinne, R.;Schmitz, J. E.;Kinne, S. E. https://doi.org/10.1007/BF00586614 -
Curr. Probl. Clin. Biochem.
v.3
$Na^{+},K^{+}$ -ATPase in the rat nephron related to sodium transport: results with quantitative histochemistry. Schmidt, U.;Dubach, U. C. - J Biol Chem v.269 Na,K-ATPase. Lingrel, J. B.;Kuntzweiler, T.
- J. Biol. Chem. v.263 Tissue-specific and developmental regulation of rat Na,K-ATPase catalytic alpha iso form and beta subunit mRNAs. Orlowski, J;Lingrel, J. B.
- Kidney Int. v.57 no.4 Diminished adenylate cyclase activity and aquaporin 2 expression in acute renal failure rats. Kim, S. W.;Jeon, Y. S.;Lee, J. U.;Kang, D. G.;Kook, H.;Ahn, K. Y., Kim, S. Z., Cho, K. W.;Kim, N. H.; Han, J. S;Choi, K.C. https://doi.org/10.1046/j.1523-1755.2000.00008.x
- J. Clin. Invest. v.99 no.7 Upregulation of aquaporin-2 water channel expression in chronic heart failure rat. Xu, D. L.;Martin, P. Y.;Ohara, M.;St John, J.;Pattison, T.;Meng, X.;Morris, K.;Kim, J. K.;Schrier. R. W. https://doi.org/10.1172/JCI119312
- Kidney Int. v.53 Impaired auaporin and urea transporter expression in rats with adriamicine-induced nephrotic syndrome. Fernadez-llama, P.;Andrews, P.;Nielsen, S.;Ecelbarger, C. A.;Knepper, M. A. https://doi.org/10.1046/j.1523-1755.1998.00878.x
- J. Clin. Invest. v.102 no.1 An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex. Mulders, S. M.;Bichet, D. G.;Rijss, J. P.;Kamsteeg, E. J.;Arthus, M. F.;Lonergan, M.;Fujiwara, M.;Morgan, K.;Leijendekker, R.;van der Sluijs, P.;van Os, C. H.;Deen, P. M. https://doi.org/10.1172/JCI2605
- Am. J. Physiol. v.277 no.3 Reduced abundance of aquaporins in rats with bilateral ischemia-induced acute renal failure: prevention by alpha-MSH. Kwon, T. H.;Frokiaer, J.;Fernandez-Llama, P.;Knepper, M.A.;Nielsen, S.
- Clin. Exp. Hypertens. v.22 no.5 Increased expression and shuttling of aquaporin-2 water channels in the kidney in DOCA-salt hypertensive rats. Lee, J. U.;Kang, D. G.;Kim, Y. J. https://doi.org/10.1081/CEH-100100089
- Kidney Int. v.45 no.4 Location of an inducible nitric oxide synthase mRNA in the normal kidney. Morrissey, J. J.;McCracken, R.;Kaneto, H.;Vehaskari, M.;Montani, D.;Klahr, S. https://doi.org/10.1038/ki.1994.135
- Am. J. Physiol. v.275 no.3 Neuronal nitric oxide synthase is expressed in principal cell of collecting duct. Wang, X.;Lu, M.;Gao, Y.;Papapetropoulos, A;Sessa, W. C.;Wang, W.
- Hypertension v.21 no.6 Genomic analysis and expression patterns reveal distinct genes for endothelial and brain nitric oxide synthase. Sessa, W. C.;Harrison, J. K.;Luthin, D. R.;Pollock, J. S.;Lynch, K. R. https://doi.org/10.1161/01.HYP.21.6.934
- Am. J. Physiol. v.261 no.6 Effects of NG-nitro-L-arginine methyl ester on renal function and blood pressure. Lahera, V.;Salom, M. G.;Miranda-Guardiola, F.;Moncada, S.;Romero, J. C.
- Hypertension v.23 no.6 Nitric oxide regulates renal hemodynamics and urinary sodium excretion in dogs. Manning, R. D.;Hu, J. L. https://doi.org/10.1161/01.HYP.23.5.619
- Kidney Int. v.46 Endogenous nitric oxide synthesis determines sensitivity to the pressor effect of salt. Tolins, J. P.;Shultz, P. J. https://doi.org/10.1038/ki.1994.264
- Hypertension v.25 no.4 Relation between pressure natriuresis and urinary excretion of nitrate/nitrite in anesthetized dogs. Majid, D. S. A.;Godfrey, M.;Grisham, M. B.;Navar, L. G. https://doi.org/10.1161/01.HYP.25.4.860
- Circulation v.91 no.4 Direct measure- ments of endothelium-derived nitric oxide release by stimulation of endothelin receptors in rat kidney and its alteration in salt-induced hypertension. Hirata, Y.;Hayakawa, H.;Suzuki, E.;Kimura, K.;Kikuchi, K.;Nagano, T.;Hirobe, M.;Omata, M., https://doi.org/10.1161/01.CIR.91.4.1229
- Hypertension v.10 no.7 Deficient production of nitric oxide induces volume-dependent hypertension. Lahera, V.;Salazar, J.;Salom, M. G.;Romero, J. C. https://doi.org/10.1097/00004872-199212007-00018
- Am. J. Physiol. v.274 no.5 Dietary sodium affects systemic and renal hemodynamic response to NO inhibition in healthy humans. Bech, J. N.;Nielsen, C. B.;Ivarsen, P.;Jensen, K. T.;Pedersen, E. B.
- Biochem. Biophys. Res. Commun. v.196 no.3 Differential expression of iNOS and cNOS mRNA in human vascular smooth muscle cells and endothelial cells under normal and inflammatory conditions. MacNaul, K. L.;Hutchinson, N. I. https://doi.org/10.1006/bbrc.1993.2398
- J. Clin. Invest. v.100 no.2 Inhibition of constitutive nitric oxide synthase (NOS) by nitric oxide generated by inducible NOS after lipopolysaccharide administration provokes renal dysfunction in rats. Schwartz, D.;Mendonca, M.;Schwartz, I.;Xia, Y.;Satriano, J.;Wilson, C. B.;Blantz, R. C. https://doi.org/10.1172/JCI119551