Journal of Animal and Veterinary Advances

Year: 2012
Volume: 11
Issue: 12
Page No. 2054 - 2058

Development of Hydronephrosis Inbred Strain Mouse, ICR/Mlac-Hydro

Authors : Kanchana Kengkoom, Khin Maeung Zaw, Rapee Inpunkaew, Wannee Angkhasirisap, Pravate Thongsiri and Sumate Ampawong

References

Astarabadi, T. and E.T. Bell, 1962. Spontaneous hydronephrosis in albino rats. Nature, 195: 392-393.
CrossRef  |  

Beulter, E., C. West, H.A. Britton, J. Harris and L. Forman, 1997. GlucosePhosphate Isomerase (GPI) deficiency mutations associated with Hereditary Nonspherocytic Hemolytic Anemia (HNSHA). Blood Cells Mol. Dis., 23: 402-409.
CrossRef  |  

Cohen, B.J., De R.W. Bruin and W.J. Kort, 1970. Heritable hydronephrosis in a mutant strain of Brown Norway rats. Lab. Anim. Care., 20: 489-493.
PubMed  |  

Collins, G.R., C.R. Goodheart and D. Henson, 1972. Spontaneous heritable hydronephrosis in inbred mice. 1. Description, incidence and distribution of lesions. Lab. Anim. Sci., 22: 333-338.
PubMed  |  

Favor, J., R. Sandulache, A. Neuhauser-Klaus, W. Pretsch, B. Chatterjee and E. Senft, 1996. The mouse Pax2 (1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye and kidney. Proc. Natl. Acad. Sci. USA., 93: 13870-13875.
Direct Link  |  

Goto, N., Y. Nakajima, T. Onodera and K. Imamura, 1984. Inheritance of hydronephrosis in the mouse strain DDD. Lab. Anim., 18: 22-25.
PubMed  |  

Hoffman, H.A., 1984. Qualitative Characters in Genetic Monitoring. In: ICLAS Manual for Genetic Monitoring of Inbred Mice, Nomura, T., K. Esaki and T. Tomita (Eds.). University of Tokyo Press, Tokyo, Japan, pp: 26-113.

Horton Jr., C.E., M.T. Davisson, J.B. Jacobs, G.T. Bernstein and A.B. Retik, 1988. Congenital progressive hydronephrosis in mice: A new recessive mutation. J. Urol., 140: 1310-1315.
PubMed  |  

Kume, T., K. Deng and B.L. Hogan, 2000. Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract. Development, 127: 1387-1395.
PubMed  |  

Lamont, G.W., 1991. Hereditary hydronephrosis in C57BUKsJ mice. Lab. Anim. Sci., 41: 312-312.

Lozzio, B.B., E. Buonocure and D. Kentera, 1972. Radiologic and functional studies in rats with hereditary hydronephrosis. Invest. Urol., 10: 84-87.
PubMed  |  

McDill, B.W., S.Z. Li, P.A. Kovach, L. Ding and F. Chen, 2006. Congenital pregressive hydronephrosis (cph) is caused by an S256L mutation in AQP-2 that affects its phosphorylation and apical membrane accumulation. Proc. Natl. Acad. Sci. USA., 103: 6952-6957.
CrossRef  |  

Miyazaki, Y., K. Oshima, A. Fogo, B.L. Hogan and I. Ichikawa, 2000. Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter. J. Clin. Invest., 105: 863-873.
PubMed  |  

Nakajima, Y., K. Emamura, T. Onodera and N. Goto, 1983. Hydronephrosis in the inbred mouse strain ODD. Lab. Anim., 17: 143-147.
CrossRef  |  

Percy, D.H. and S.W. Barthold, 2001. The Mouse. In: Pathology of Laboratory Rodents and Rabbits, Percy, D.H. and S.W. Barthold (Eds.). Iowa State University Press, USA., pp: 3-106.

Peter, C.A., 2001. Animal models of fatal renal disease. Prenat. Diagn., 21: 917-923.
PubMed  |  

Repiso, A., R. Andres, F. Climent and J.M. Urena, 2008. Expression patterns in mouse embryos of neuroleukin/glucose-6-phosphate isomerase and autocrine motility factor receptor. Anat. Histol. Embryol., 37: 380-382.
PubMed  |  

Schuchardt, A., V. D'Agati , V. Pachnis and F. Costantini, 1996. Renal agenesis and hypodysplasia in ret-k-mutant mice result from defects in ureteric bud development. Development, 122: 1919-1929.
PubMed  |  

Sellers, A.L., S. Rosenfeld and N.B. Friedman, 1960. Spontaneous hydronephrosis in the rat. Proc. Soc. Exp. Biol. Med., 104: 512-515.

Silverstein, E., L. Sokotoff, O. Mickelsen and G.E. Jay, 1961. Primary polydipsia and hydronephrosis in an inbred strain of mice. Am. J. Pathol., 38: 143-159.
PubMed  |  

Susic, D., J.C. Sparks and D. Kentera, 1975. The renin-angiotensin system in rats with hereditary hydronephrosis. Pflugers Arch., 358: 265-274.
PubMed  |  

Takano, K., A. Ogura, O. Suzuki, Y. Noguchi, Y. Yamamoto and T. Asano, 1973. Heredity hydronephrosis in C57UMsNrs mice. Lab. Anim., 42: 107-109.

Tauchi, K. and H. Kanehara, 1996. Hypertension and the renin-angiotensin system in the congenital hydronephrosis rat with non-obstructive pelviureteric junction abnormalities. Exp. Nephrol., 4: 60-64.

Wallace, M.E. and S.G. Spickett, 1967. Hydronephrosis in mouse, rat and man. J. Med. Genet., 4: 73-82.
PubMed  |  

Warner, N.L., 1971. Spontaneous hydronephrosis in the inbred mouse strain NZC. Aust. J. Exp. Biol. Med. Sci., 49: 477-486.
CrossRef  |  

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