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Rini Rossanti

Showing results (11-20 of 36) with videos related to

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Clinical and Experimental Nephrology|March 15, 2021
Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1Tomohiko Inoue, China Nagano, Masafumi Matsuo, et al.
Kidney International Reports|February 24, 2025
<i>COL4A5</i> Intronic Variants at Third to Fifth Nucleotides Cause Alport SyndromeHideaki Kitakado, Tomoko Horinouchi, Shuhei Aoyama, et al.
CEN Case Reports|June 29, 2026
Nephrin-IgG co-localization expression in pediatric steroid-resistant nephrotic syndrome: a case series from IndonesiaRini Rossanti, Ahmedz Widiasta, Nana Sakakibara, et al.
Journal of Human Genetics|March 24, 2020
Clinical and genetic variability of PAX2-related disorder in the Japanese populationRini Rossanti, Naoya Morisada, Kandai Nozu, et al.
Children (Basel, Switzerland)|December 30, 2025
Anemia as a Part of the Triple Burden Among Children Under-Five with Stunting and Tuberculosis in Bandung, IndonesiaSusi Susanah, Delita Prihatni, Rini Rossanti, et al.
Kidney International Reports|June 9, 2025
Comprehensive Splice Pattern Analysis for Previously Reported <i>OCRL</i> Splicing Variants and Their Phenotypic ContributionsRini Rossanti, Eri Okada, Nana Sakakibara, et al.
Journal of Human Genetics|February 10, 2022
Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese populationNana Sakakibara, Kandai Nozu, Tomohiko Yamamura, et al.
Scientific Reports|September 5, 2019
Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assayTomoko Horinouchi, Kandai Nozu, Tomohiko Yamamura, et al.
Kidney International Reports|January 10, 2022
Last Nucleotide Substitutions of <i>COL4A5</i> Exons Cause Aberrant SplicingYuya Aoto, Tomoko Horinouchi, Tomohiko Yamamura, et al.
Journal of Human Genetics|April 25, 2019
Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndromeRini Rossanti, Akemi Shono, Kenichiro Miura, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Clinical and Experimental Nephrology|March 15, 2021
Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1Tomohiko Inoue, China Nagano, Masafumi Matsuo, et al.
Kidney International Reports|February 24, 2025
<i>COL4A5</i> Intronic Variants at Third to Fifth Nucleotides Cause Alport SyndromeHideaki Kitakado, Tomoko Horinouchi, Shuhei Aoyama, et al.
CEN Case Reports|June 29, 2026
Nephrin-IgG co-localization expression in pediatric steroid-resistant nephrotic syndrome: a case series from IndonesiaRini Rossanti, Ahmedz Widiasta, Nana Sakakibara, et al.
Journal of Human Genetics|March 24, 2020
Clinical and genetic variability of PAX2-related disorder in the Japanese populationRini Rossanti, Naoya Morisada, Kandai Nozu, et al.
Children (Basel, Switzerland)|December 30, 2025
Anemia as a Part of the Triple Burden Among Children Under-Five with Stunting and Tuberculosis in Bandung, IndonesiaSusi Susanah, Delita Prihatni, Rini Rossanti, et al.
Kidney International Reports|June 9, 2025
Comprehensive Splice Pattern Analysis for Previously Reported <i>OCRL</i> Splicing Variants and Their Phenotypic ContributionsRini Rossanti, Eri Okada, Nana Sakakibara, et al.
Journal of Human Genetics|February 10, 2022
Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese populationNana Sakakibara, Kandai Nozu, Tomohiko Yamamura, et al.
Scientific Reports|September 5, 2019
Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assayTomoko Horinouchi, Kandai Nozu, Tomohiko Yamamura, et al.
Kidney International Reports|January 10, 2022
Last Nucleotide Substitutions of <i>COL4A5</i> Exons Cause Aberrant SplicingYuya Aoto, Tomoko Horinouchi, Tomohiko Yamamura, et al.
Journal of Human Genetics|April 25, 2019
Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndromeRini Rossanti, Akemi Shono, Kenichiro Miura, et al.
Pageof 4