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Eri Okada

Showing results (21-30 of 35) with videos related to

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Kidney International Reports|January 10, 2022
Last Nucleotide Substitutions of <i>COL4A5</i> Exons Cause Aberrant SplicingYuya Aoto, Tomoko Horinouchi, Tomohiko Yamamura, et al.
Tissue Engineering. Part C, Methods|November 13, 2015
Assessment of the Safety of Chondrocyte Sheet Implantation for Cartilage RegenerationMiyuki Yokoyama, Masato Sato, Akihiro Umezawa, et al.
Internal Medicine (Tokyo, Japan)|June 18, 2025
Initial Suspicion of Autosomal Dominant Polycystic Kidney Disease Resulted in a Diagnosis of Autosomal Dominant Tubulointerstitial Kidney Disease Caused by a UMOD Mutation: A Case ReportToshiaki Usui, Shun Ishibashi, Akihisa Hattori, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 12, 2024
Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndromeRyota Suzuki, Nana Sakakibara, Sae Murakami, et al.
Clinical and Experimental Nephrology|June 15, 2021
X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assayRini Rossanti, Kandai Nozu, Atsushi Fukunaga, et al.
Clinical and Experimental Nephrology|May 30, 2023
All reported non-canonical splice site variants in GLA cause aberrant splicingEri Okada, Tomoko Horinouchi, Tomohiko Yamamura, et al.
Clinical and Experimental Nephrology|September 18, 2021
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypesShinya Ishiko, Naoya Morisada, Atsushi Kondo, et al.
Kidney International Reports|August 13, 2021
Genotype-Phenotype Correlation in <i>WT1</i> Exon 8 to 9 Missense VariantsChina Nagano, Yutaka Takaoka, Koichi Kamei, et al.
Scientific Reports|August 10, 2021
Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databasesAtsushi Kondo, China Nagano, Shinya Ishiko, et al.
Kidney International Reports|October 8, 2021
Systematic Review of Genotype-Phenotype Correlations in Frasier SyndromeYurika Tsuji, Tomohiko Yamamura, China Nagano, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Kidney International Reports|January 10, 2022
Last Nucleotide Substitutions of <i>COL4A5</i> Exons Cause Aberrant SplicingYuya Aoto, Tomoko Horinouchi, Tomohiko Yamamura, et al.
Tissue Engineering. Part C, Methods|November 13, 2015
Assessment of the Safety of Chondrocyte Sheet Implantation for Cartilage RegenerationMiyuki Yokoyama, Masato Sato, Akihiro Umezawa, et al.
Internal Medicine (Tokyo, Japan)|June 18, 2025
Initial Suspicion of Autosomal Dominant Polycystic Kidney Disease Resulted in a Diagnosis of Autosomal Dominant Tubulointerstitial Kidney Disease Caused by a UMOD Mutation: A Case ReportToshiaki Usui, Shun Ishibashi, Akihisa Hattori, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 12, 2024
Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndromeRyota Suzuki, Nana Sakakibara, Sae Murakami, et al.
Clinical and Experimental Nephrology|June 15, 2021
X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assayRini Rossanti, Kandai Nozu, Atsushi Fukunaga, et al.
Clinical and Experimental Nephrology|May 30, 2023
All reported non-canonical splice site variants in GLA cause aberrant splicingEri Okada, Tomoko Horinouchi, Tomohiko Yamamura, et al.
Clinical and Experimental Nephrology|September 18, 2021
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypesShinya Ishiko, Naoya Morisada, Atsushi Kondo, et al.
Kidney International Reports|August 13, 2021
Genotype-Phenotype Correlation in <i>WT1</i> Exon 8 to 9 Missense VariantsChina Nagano, Yutaka Takaoka, Koichi Kamei, et al.
Scientific Reports|August 10, 2021
Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databasesAtsushi Kondo, China Nagano, Shinya Ishiko, et al.
Kidney International Reports|October 8, 2021
Systematic Review of Genotype-Phenotype Correlations in Frasier SyndromeYurika Tsuji, Tomohiko Yamamura, China Nagano, et al.
Pageof 4