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XB--481400
Papers associated with aqp2 (and Disease Ontology)
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Molecular characterization of an aquaporin-2 mutation causing a severe form of nephrogenic diabetes insipidus., Saglar Ozer E, Moeller HB, Karaduman T, Fenton RA, Mergen H., Cell Mol Life Sci. March 1, 2020; 77 (5): 953-962. |
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Functional Recovery of AQP2 Recessive Mutations Through Hetero-Oligomerization with Wild-Type Counterpart., El Tarazi A, Lussier Y, Da Cal S, Bissonnette P, Bichet DG., Sci Rep. September 19, 2016; 6 33298.  |
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ROMK expression remains unaltered in a mouse model of familial hyperkalemic hypertension caused by the CUL3Δ403-459 mutation., Murthy M, Kurz T, O'Shaughnessy KM., Physiol Rep. July 1, 2016; 4 (13):  |
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Novel treatment for lithium-induced nephrogenic diabetes insipidus rat model using the Sendai-virus vector carrying aquaporin 2 gene., Suga H, Nagasaki H, Kondo TA, Okajima Y, Suzuki C, Ozaki N, Arima H, Yamamoto T, Ozaki N, Akai M, Sato A, Uozumi N, Inoue M, Hasegawa M, Oiso Y., Endocrinology. November 1, 2008; 149 (11): 5803-10. |
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Evidence for stabilization of aquaporin-2 folding mutants by N-linked glycosylation in endoplasmic reticulum., Buck TM, Eledge J, Skach WR., Am J Physiol Cell Physiol. November 1, 2004; 287 (5): C1292-9. |
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Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus., Kamsteeg EJ, Bichet DG, Konings IB, Nivet H, Lonergan M, Arthus MF, van Os CH, Deen PM., J Cell Biol. December 8, 2003; 163 (5): 1099-109.  |
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Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families., Lin SH, Bichet DG, Sasaki S, Kuwahara M, Arthus MF, Lonergan M, Lin YF., J Clin Endocrinol Metab. June 1, 2002; 87 (6): 2694-700. |
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