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Scientific Reports
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January 25, 2025
Pseudogenization of the Slc23a4 gene is necessary for the survival of Xdh-deficient mice
Kazuki Terada, Tamaki Watanabe, Nobuhiro Yasuno, et al.
Journal of the American Society of Nephrology : JASN
|
December 25, 2003
Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion
Kimiyoshi Ichida, Makoto Hosoyamada, Ichiro Hisatome, et al.
Journal of Child Neurology
|
February 3, 2011
Prenatal brain disruption in molybdenum cofactor deficiency
Nirit Carmi-Nawi, Gustavo Malinger, Hanna Mandel, et al.
Amino Acids
|
August 1, 2018
Diet-induced hyperhomocysteinemia impairs vasodilation in 5/6-nephrectomized rats
Lei Li, Hiroshi Hasegawa, Niro Inaba, et al.
Internal Medicine (Tokyo, Japan)
|
January 16, 2010
Effect of fenofibrate on uric acid metabolism and urate transporter 1
Daijiro Uetake, Iwao Ohno, Kimiyoshi Ichida, et al.
Kidney International
|
December 11, 2002
Urate transport via human PAH transporter hOAT1 and its gene structure
Kimiyoshi Ichida, Makoto Hosoyamada, Hiroaki Kimura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
April 21, 2007
Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure
Yasufumi Ohtsuka, Masafumi Zaitsu, Kimiyoshi Ichida, et al.
The Journal of Biological Chemistry
|
August 25, 2023
Allopurinol and oxypurinol differ in their strength and mechanisms of inhibition of xanthine oxidoreductase
Mai Sekine, Ken Okamoto, Emil F Pai, et al.
Fluids and Barriers of the CNS
|
October 26, 2013
Ependymal cells of the mouse brain express urate transporter 1 (URAT1)
Naoko H Tomioka, Makiko Nakamura, Masaru Doshi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 6, 2012
Molybdenum cofactor deficiency: review of 12 cases (MoCD and review)
Erhan Bayram, Yasemin Topcu, Pakize Karakaya, et al.
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Search research articles
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Showing results (61-70 of 154) with videos related to
Sort By:
Page
of 16
Scientific Reports
|
January 25, 2025
Pseudogenization of the Slc23a4 gene is necessary for the survival of Xdh-deficient mice
Kazuki Terada, Tamaki Watanabe, Nobuhiro Yasuno, et al.
Journal of the American Society of Nephrology : JASN
|
December 25, 2003
Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion
Kimiyoshi Ichida, Makoto Hosoyamada, Ichiro Hisatome, et al.
Journal of Child Neurology
|
February 3, 2011
Prenatal brain disruption in molybdenum cofactor deficiency
Nirit Carmi-Nawi, Gustavo Malinger, Hanna Mandel, et al.
Amino Acids
|
August 1, 2018
Diet-induced hyperhomocysteinemia impairs vasodilation in 5/6-nephrectomized rats
Lei Li, Hiroshi Hasegawa, Niro Inaba, et al.
Internal Medicine (Tokyo, Japan)
|
January 16, 2010
Effect of fenofibrate on uric acid metabolism and urate transporter 1
Daijiro Uetake, Iwao Ohno, Kimiyoshi Ichida, et al.
Kidney International
|
December 11, 2002
Urate transport via human PAH transporter hOAT1 and its gene structure
Kimiyoshi Ichida, Makoto Hosoyamada, Hiroaki Kimura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
April 21, 2007
Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure
Yasufumi Ohtsuka, Masafumi Zaitsu, Kimiyoshi Ichida, et al.
The Journal of Biological Chemistry
|
August 25, 2023
Allopurinol and oxypurinol differ in their strength and mechanisms of inhibition of xanthine oxidoreductase
Mai Sekine, Ken Okamoto, Emil F Pai, et al.
Fluids and Barriers of the CNS
|
October 26, 2013
Ependymal cells of the mouse brain express urate transporter 1 (URAT1)
Naoko H Tomioka, Makiko Nakamura, Masaru Doshi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 6, 2012
Molybdenum cofactor deficiency: review of 12 cases (MoCD and review)
Erhan Bayram, Yasemin Topcu, Pakize Karakaya, et al.
Page
of 16