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Shinichi Uchida

Showing results (171-180 of 288) with videos related to

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Clinical Case Reports|March 9, 2019
<i>PKD1</i> mutation may epistatically ameliorate nephronophthisis progression in patients with <i>NPHP1</i> deletionSaki Watanabe, Jun Ino, Takuya Fujimaru, et al.
In Vitro Cellular & Developmental Biology. Animal|February 15, 2022
Generation of NPHP1 knockout human pluripotent stem cells by a practical biallelic gene deletion strategy using CRISPR/Cas9 and ssODNYuta Nakano, Koichiro Susa, Tomoki Yanagi, et al.
Biochemical and Biophysical Research Communications|August 1, 2012
Phosphorylation of Na-Cl cotransporter by OSR1 and SPAK kinases regulates its ubiquitinationMuhammad Zakir Hossain Khan, Eisei Sohara, Akihito Ohta, et al.
Journal of Neuroscience Research|August 1, 2012
Accumulation of autofluorescent storage material in brain is accelerated by ischemia in chloride channel 3 gene-deficient miceHirokazu Ohtaki, Kenji Ohara, Dandan Song, et al.
Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|August 16, 2016
Removal Dynamics of Immunoglobulin and Fibrinogen by Conventional Plasma Exchange, Selective Plasma Exchange, and a Combination of the TwoSatoko Miyamoto, Atsushi Ohkubo, Hiroshi Seshima, et al.
Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|August 16, 2016
Removal Characteristics of Immunoadsorption With the Immusorba TR-350 Column Using Conventional and Selective Plasma SeparatorsAtsushi Ohkubo, Tomokazu Okado, Satoko Miyamoto, et al.
CEN Case Reports|June 8, 2020
Bartter syndrome representing digenic-based salt-losing tubulopathies presumably accelerated by renal insufficiencyRyusuke Umene, Mineaki Kitamura, Hideyuki Arai, et al.
Plos One|July 1, 2020
Sodium-calcium exchanger 1 is the key molecule for urinary potassium excretion against acute hyperkalemiaWakana Shoda, Naohiro Nomura, Fumiaki Ando, et al.
Human Mutation|December 21, 2020
Phenotypic differences of mutation-negative cases in Gitelman syndrome clinically diagnosed in adulthoodTakayasu Mori, Motoko Chiga, Takuya Fujimaru, et al.
Internal Medicine (Tokyo, Japan)|April 7, 2017
The Resection of Thyroid Cancer Was Associated with the Resolution of Hyporesponsiveness to an Erythropoiesis-stimulating Agent in a Hemodialysis Patient with AceruloplasminemiaSoichiro Nagata, Naoki Ikegaya, Shuhei Ogino, et al.
Pageof 29

Showing results (171-180 of 288) with videos related to

Sort By:
Pageof 29
Clinical Case Reports|March 9, 2019
<i>PKD1</i> mutation may epistatically ameliorate nephronophthisis progression in patients with <i>NPHP1</i> deletionSaki Watanabe, Jun Ino, Takuya Fujimaru, et al.
In Vitro Cellular & Developmental Biology. Animal|February 15, 2022
Generation of NPHP1 knockout human pluripotent stem cells by a practical biallelic gene deletion strategy using CRISPR/Cas9 and ssODNYuta Nakano, Koichiro Susa, Tomoki Yanagi, et al.
Biochemical and Biophysical Research Communications|August 1, 2012
Phosphorylation of Na-Cl cotransporter by OSR1 and SPAK kinases regulates its ubiquitinationMuhammad Zakir Hossain Khan, Eisei Sohara, Akihito Ohta, et al.
Journal of Neuroscience Research|August 1, 2012
Accumulation of autofluorescent storage material in brain is accelerated by ischemia in chloride channel 3 gene-deficient miceHirokazu Ohtaki, Kenji Ohara, Dandan Song, et al.
Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|August 16, 2016
Removal Dynamics of Immunoglobulin and Fibrinogen by Conventional Plasma Exchange, Selective Plasma Exchange, and a Combination of the TwoSatoko Miyamoto, Atsushi Ohkubo, Hiroshi Seshima, et al.
Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|August 16, 2016
Removal Characteristics of Immunoadsorption With the Immusorba TR-350 Column Using Conventional and Selective Plasma SeparatorsAtsushi Ohkubo, Tomokazu Okado, Satoko Miyamoto, et al.
CEN Case Reports|June 8, 2020
Bartter syndrome representing digenic-based salt-losing tubulopathies presumably accelerated by renal insufficiencyRyusuke Umene, Mineaki Kitamura, Hideyuki Arai, et al.
Plos One|July 1, 2020
Sodium-calcium exchanger 1 is the key molecule for urinary potassium excretion against acute hyperkalemiaWakana Shoda, Naohiro Nomura, Fumiaki Ando, et al.
Human Mutation|December 21, 2020
Phenotypic differences of mutation-negative cases in Gitelman syndrome clinically diagnosed in adulthoodTakayasu Mori, Motoko Chiga, Takuya Fujimaru, et al.
Internal Medicine (Tokyo, Japan)|April 7, 2017
The Resection of Thyroid Cancer Was Associated with the Resolution of Hyporesponsiveness to an Erythropoiesis-stimulating Agent in a Hemodialysis Patient with AceruloplasminemiaSoichiro Nagata, Naoki Ikegaya, Shuhei Ogino, et al.
Pageof 29