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Yoshimi Nozu

Showing results (11-20 of 23) with videos related to

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Nephron|November 14, 2017
Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin DepositsYurika Tsuji, Kandai Nozu, Tadashi Sofue, et al.
Kidney International Reports|January 1, 2019
Clinical and Genetic Characteristics in Patients With Gitelman SyndromeJunya Fujimura, Kandai Nozu, Tomohiko Yamamura, et al.
Kidney International Reports|December 23, 2017
Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport SyndromeTomohiko Yamamura, Kandai Nozu, Xue Jun Fu, et al.
Journal of Human Genetics|October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndromeKandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.
Clinical Journal of the American Society of Nephrology : CJASN|June 10, 2016
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport SyndromeNaohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu, et al.
Journal of Human Genetics|November 8, 2018
Clinical spectrum of male patients with OFD1 mutationsNana Sakakibara, Naoya Morisada, Kandai Nozu, et al.
Molecular Genetics & Genomic Medicine|August 1, 2019
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndromeTomohiko Yamamura, Kandai Nozu, Shogo Minamikawa, et al.
Clinical and Experimental Nephrology|November 1, 2016
Female X-linked Alport syndrome with somatic mosaicismKana Yokota, Kandai Nozu, Shogo Minamikawa, et al.
Journal of Human Genetics|February 21, 2018
Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent diseaseShogo Minamikawa, Kandai Nozu, Yoshimi Nozu, et al.
Kidney International|July 27, 2020
Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndromeTomohiko Yamamura, Tomoko Horinouchi, China Nagano, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Nephron|November 14, 2017
Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin DepositsYurika Tsuji, Kandai Nozu, Tadashi Sofue, et al.
Kidney International Reports|January 1, 2019
Clinical and Genetic Characteristics in Patients With Gitelman SyndromeJunya Fujimura, Kandai Nozu, Tomohiko Yamamura, et al.
Kidney International Reports|December 23, 2017
Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport SyndromeTomohiko Yamamura, Kandai Nozu, Xue Jun Fu, et al.
Journal of Human Genetics|October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndromeKandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.
Clinical Journal of the American Society of Nephrology : CJASN|June 10, 2016
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport SyndromeNaohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu, et al.
Journal of Human Genetics|November 8, 2018
Clinical spectrum of male patients with OFD1 mutationsNana Sakakibara, Naoya Morisada, Kandai Nozu, et al.
Molecular Genetics & Genomic Medicine|August 1, 2019
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndromeTomohiko Yamamura, Kandai Nozu, Shogo Minamikawa, et al.
Clinical and Experimental Nephrology|November 1, 2016
Female X-linked Alport syndrome with somatic mosaicismKana Yokota, Kandai Nozu, Shogo Minamikawa, et al.
Journal of Human Genetics|February 21, 2018
Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent diseaseShogo Minamikawa, Kandai Nozu, Yoshimi Nozu, et al.
Kidney International|July 27, 2020
Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndromeTomohiko Yamamura, Tomoko Horinouchi, China Nagano, et al.
Pageof 3