Publications by authors named "Xue Jun Fu"

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Off-axis eight-pass neodymium glass laser amplifier with high efficiency and excellent energy stability.
Ke Yao, Song Gao, Jun Tang, Xudong Xie, Chen Fan, XueJun Fu

Appl Opt· October 2018

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Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome.
Tomohiko Yamamura, Kandai Nozu, Xue Jun Fu, Yoshimi Nozu, Ming Juan Ye

Kidney Int Rep· September 2017

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Early RAAS Blockade Exerts Renoprotective Effects in Autosomal Recessive Alport Syndrome.
Nao Uchida, Naonori Kumagai, Kandai Nozu, Xue Jun Fu, Kazumoto Iijima

Tohoku J Exp Med· November 2016

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X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 gene.
Xue Jun Fu, Kandai Nozu, Aya Eguchi, Yoshimi Nozu, Naoya Morisada

Clin Exp Nephrol· October 2016

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Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.
Naohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu, Naoya Morisada, Yoshimi Nozu, Aya Imafuku

Clin J Am Soc Nephrol· August 2016

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Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome.
Xue Jun Fu, Kandai Nozu, Hiroshi Kaito, Takeshi Ninchoji, Naoya Morisada

Eur J Hum Genet· March 2016

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Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics.
Natsuki Matsunoshita, Kandai Nozu, Akemi Shono, Yoshimi Nozu, Xue Jun Fu

Genet Med· February 2016

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Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing.
Takeshi Kato, Naoya Morisada, Hiroaki Nagase, Masahiro Nishiyama, Daisaku Toyoshima, Xue Jun Fu

Brain Dev· October 2015

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X-linked Alport syndrome caused by splicing mutations in COL4A5.
Kandai Nozu, Igor Vorechovsky, Hiroshi Kaito, Xue Jun Fu, Koichi Nakanishi, Fusako Hashimoto

Clin J Am Soc Nephrol· November 2014

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Natural history of genetically proven autosomal recessive Alport syndrome.
Masafumi Oka, Kandai Nozu, Hiroshi Kaito, Xue Jun Fu, Koichi Nakanishi, Masafumi Matsuo

Pediatr Nephrol· September 2014

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Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY.
Kandai Nozu, Kazumoto Iijima, Yasufumi Ohtsuka, Xue Jun Fu, Hiroshi Kaito

Mol Genet Genomic Med· September 2014

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Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain.
Yuya Hashimura, Kandai Nozu, Hiroshi Kaito, Koichi Nakanishi, Xue Jun Fu, Fusako Hashimoto, Masafumi Oka

Kidney Int· May 2014

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[Analysis of the changes of microbial community structure on bio-carrier of recirculating aquaculture systems (RAS)].
Hai-Geng Zhang, Shao-Sai Ma, Qiu-Fen Li, Xue-Jun Fu, Yan Zhang

Huan Jing Ke Xue· January 2011

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A deep intronic mutation in the SLC12A3 gene leads to Gitelman syndrome.
Kandai Nozu, Kazumoto Iijima, Yoshimi Nozu, Ei Ikegami, Takehide Imai, Xue Jun Fu, Masafumi Matsuo

Pediatr Res· November 2009

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In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.
Kandai Nozu, Kazumoto Iijima, Kazuo Kawai, Yoshimi Nozu, Atsushi Nishida, Xue Jun Fu, Masafumi Matsuo

Hum Genet· October 2009

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Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.
Hajime Yamazaki, Kandai Nozu, Ichiei Narita, Michio Nagata, Yoshimi Nozu, Xue Jun Fu, Masafumi Matsuo, Fumitake Gejyo

Pediatr Nephrol· February 2009

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Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.
Rafal Przybyslaw Krol, Kandai Nozu, Koichi Nakanishi, Kazumoto Iijima, Yasuhiro Takeshima, Xue Jun Fu, Masafumi Matsuo

Nephrol Dial Transplant· August 2008

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Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR.
Kandai Nozu, Xue Jun Fu, Koichi Nakanishi, Norishige Yoshikawa, Hiroshi Kaito, Masafumi Matsuo

Pediatr Res· September 2007

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A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism.
Kandai Nozu, Xue Jun Fu, Hiroshi Kaito, Kyoko Kanda, Naoki Yokoyama, Masafumi Matsuo

Pediatr Nephrol· August 2007

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OCRL1 mutations in patients with Dent disease phenotype in Japan.
Takashi Sekine, Kandai Nozu, Rashmi Iyengar, Xue Jun Fu, Masafumi Matsuo

Pediatr Nephrol· July 2007

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Enamel-renal syndrome associated with hypokalaemic metabolic alkalosis and impaired renal concentration: a novel syndrome?
Xue Jun Fu, Kandai Nozu, Katsumi Goji, Kazushige Ikeda, Ichiro Kamioka, Teruo Fujita, Masafumi Matsuo

Nephrol Dial Transplant· October 2006

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Role of p38 MAP kinase pathway in a toxin-induced model of hemolytic uremic syndrome.
Xue Jun Fu, Kazumoto Iijima, Kandai Nozu, Kiyoshi Hamahira, Ryojiro Tanaka, Masafumi Matsuo

Pediatr Nephrol· August 2004

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