Publications by authors named "Motoko Chiga"

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Progressive Renal Dysfunction in Autosomal-dominant Alport Syndrome Co-occurring with C1q Nephropathy.
Kasumi Konishi, Takuya Fujimaru, Michio Nagata, Nozomi Kadota, Yugo Ito, Motoko Chiga

Intern Med· December 2025

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Importance of family history and health checkup for school-aged children for type IV collagen-associated nephropathy in hereditary kidney disease.
Ryosuke Kawamoto, Takayasu Mori, Motoko Chiga, Takuya Fujimaru, Azuma Nanamatsu

J Nephrol· September 2025

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CFAP47 is Implicated in X-Linked Polycystic Kidney Disease.
Takayasu Mori, Takuya Fujimaru, Chunyu Liu, Karynne Patterson, Kouhei Yamamoto, Motoko Chiga

Kidney Int Rep· December 2024

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ULK1-regulated AMP sensing by AMPK and its application for the treatment of chronic kidney disease.
Tomoki Yanagi, Hiroaki Kikuchi, Koh Takeuchi, Koichiro Susa, Takayasu Mori, Motoko Chiga

Kidney Int· November 2024

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Importance of in Patients with Polycystic Kidney Disease Without a Family History.
Takuya Fujimaru, Takayasu Mori, Akinari Sekine, Motoko Chiga, Shintaro Mandai

Kidney Int Rep· September 2024

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is a novel causative gene implicated in X-linked polycystic kidney disease.
Takayasu Mori, Takuya Fujimaru, Chunyu Liu, Karynne Patterson, Kohei Yamamoto, Motoko Chiga

medRxiv· April 2024

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Genetic Diagnosis of Adult Hemodialysis Patients With Unknown Etiology.
Takuya Fujimaru, Takayasu Mori, Motoko Chiga, Shintaro Mandai, Hiroaki Kikuchi

Kidney Int Rep· April 2024

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Circulating Extracellular Vesicle-Propagated microRNA Signature as a Vascular Calcification Factor in Chronic Kidney Disease.
Takaaki Koide, Shintaro Mandai, Reo Kitaoka, Hisazumi Matsuki, Motoko Chiga

Circ Res· February 2023

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Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus.
Kenichiro Iio, Takayasu Mori, Saki Bessho, Yosuke Imai, Masaki Hatanaka, Motoko Chiga

CEN Case Rep· May 2022

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Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney Disease.
Ryohei Miyamoto, Akinari Sekine, Takuya Fujimaru, Tatsuya Suwabe, Hiroki Mizuno, Motoko Chiga

Kidney Dis (Basel)· May 2022

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Genetics May Predict Effectiveness of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease.
Akinari Sekine, Junichi Hoshino, Takuya Fujimaru, Tatsuya Suwabe, Hiroki Mizuno, Motoko Chiga

Am J Nephrol· July 2021

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Genetic Background and Clinicopathologic Features of Adult-onset Nephronophthisis.
Takuya Fujimaru, Kunio Kawanishi, Takayasu Mori, Eikan Mishima, Akinari Sekine, Motoko Chiga

Kidney Int Rep· May 2021

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Phenotypic differences of mutation-negative cases in Gitelman syndrome clinically diagnosed in adulthood.
Takayasu Mori, Motoko Chiga, Takuya Fujimaru, Ryosuke Kawamoto, Shintaro Mandai

Hum Mutat· March 2021

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Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene.
Kiyoshi Nakano, Yasuo Kubota, Takayuki Mori, Motoko Chiga, Takayasu Mori

Nephrology (Carlton)· November 2020

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Genotype-Clinical Correlations in Polycystic Kidney Disease with No Apparent Family History.
Akinari Sekine, Takuya Fujimaru, Junichi Hoshino, Tatsuya Suwabe, Masahiko Oguro, Motoko Chiga

Am J Nephrol· May 2020

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Renal histology and MRI findings in a 37-year-old Japanese patient with autosomal recessive polycystic kidney disease
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Yusuke Ito, Akinari Sekine, Daisuke Takada, Junko Yabuuchi, Yuta Kogure, Motoko Chiga

Clin Nephrol· November 2017

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The proteasome inhibitor bortezomib attenuates renal fibrosis in mice via the suppression of TGF-β1.
Moko Zeniya, Takayasu Mori, Naofumi Yui, Naohiro Nomura, Shintaro Mandai, Motoko Chiga

Sci Rep· October 2017

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Post-infectious Proliferative Glomerulonephritis with Monoclonal Immunoglobulin G Deposits Associated with Complement Factor H Mutation.
Eriko Takehara, Shintaro Mandai, Satomi Shikuma, Wataru Akita, Motoko Chiga

Intern Med· June 2017

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WNK4 is an Adipogenic Factor and Its Deletion Reduces Diet-Induced Obesity in Mice.
Daiei Takahashi, Takayasu Mori, Eisei Sohara, Miyako Tanaka, Motoko Chiga

EBioMedicine· April 2017

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Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel.
Takayasu Mori, Kazuyoshi Hosomichi, Motoko Chiga, Shintaro Mandai, Hirofumi Nakaoka

Clin Exp Nephrol· February 2017

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Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous Mutation.
Takeshi Kusuda, Tadashi Hosoya, Takayasu Mori, Katsuhito Ihara, Hidenori Nishida, Motoko Chiga

Intern Med· January 2017

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A patient with pseudohypoaldosteronism type II complicated by congenital hypopituitarism carrying a mutation.
Marie Mitani, Munehiro Furuichi, Satoshi Narumi, Tomonobu Hasegawa, Motoko Chiga

Clin Pediatr Endocrinol· October 2016

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Impaired degradation of WNK by Akt and PKA phosphorylation of KLHL3.
Yuki Yoshizaki, Yutaro Mori, Yoshihito Tsuzaki, Takayasu Mori, Naohiro Nomura, Motoko Chiga

Biochem Biophys Res Commun· November 2015

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Aberrant glycosylation and localization of polycystin-1 cause polycystic kidney in an AQP11 knockout model.
Yuichi Inoue, Eisei Sohara, Katsuki Kobayashi, Motoko Chiga, Tatemitsu Rai

J Am Soc Nephrol· December 2014

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Impaired degradation of WNK1 and WNK4 kinases causes PHAII in mutant KLHL3 knock-in mice.
Koichiro Susa, Eisei Sohara, Tatemitsu Rai, Moko Zeniya, Yutaro Mori, Motoko Chiga

Hum Mol Genet· October 2014

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