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Page 1
Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease.
Suzuki R, Sakakibara N, Ichikawa Y, Kitakado H, Ueda C, Tanaka Y, Okada E, Kondo A, Ishiko S, Ishimori S, Nagano C, Yamamura T, Horinouchi T, Okamoto T, Nozu K. Suzuki R, et al. Among authors: ishiko s. Kidney Int Rep. 2023 Jul 4;8(9):1811-1821. doi: 10.1016/j.ekir.2023.06.019. eCollection 2023 Sep. Kidney Int Rep. 2023. PMID: 37705905 Free PMC article.
Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome.
Yamamura T, Horinouchi T, Nagano C, Omori T, Sakakibara N, Aoto Y, Ishiko S, Nakanishi K, Shima Y, Nagase H, Takeda H, Rossanti R, Ye MJ, Nozu Y, Ishimori S, Ninchoji T, Kaito H, Morisada N, Iijima K, Nozu K. Yamamura T, et al. Among authors: ishiko s. Kidney Int. 2020 Dec;98(6):1605-1614. doi: 10.1016/j.kint.2020.06.038. Epub 2020 Jul 24. Kidney Int. 2020. PMID: 32712167 Free article.
Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants.
Nagano C, Takaoka Y, Kamei K, Hamada R, Ichikawa D, Tanaka K, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Okada E, Horinouchi T, Yamamura T, Tsuji Y, Noguchi Y, Ishimori S, Nagase H, Ninchoji T, Iijima K, Nozu K. Nagano C, et al. Among authors: ishiko s. Kidney Int Rep. 2021 May 19;6(8):2114-2121. doi: 10.1016/j.ekir.2021.05.009. eCollection 2021 Aug. Kidney Int Rep. 2021. PMID: 34386660 Free PMC article.
Systematic Review of Genotype-Phenotype Correlations in Frasier Syndrome.
Tsuji Y, Yamamura T, Nagano C, Horinouchi T, Sakakibara N, Ishiko S, Aoto Y, Rossanti R, Okada E, Tanaka E, Tsugawa K, Okamoto T, Sawai T, Araki Y, Shima Y, Nakanishi K, Nagase H, Matsuo M, Iijima K, Nozu K. Tsuji Y, et al. Among authors: ishiko s. Kidney Int Rep. 2021 Jul 16;6(10):2585-2593. doi: 10.1016/j.ekir.2021.07.010. eCollection 2021 Oct. Kidney Int Rep. 2021. PMID: 34622098 Free PMC article.
Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing.
Aoto Y, Horinouchi T, Yamamura T, Kondo A, Nagai S, Ishiko S, Okada E, Rossanti R, Sakakibara N, Nagano C, Awano H, Nagase H, Shima Y, Nakanishi K, Matsuo M, Iijima K, Nozu K. Aoto Y, et al. Among authors: ishiko s. Kidney Int Rep. 2021 Oct 21;7(1):108-116. doi: 10.1016/j.ekir.2021.10.012. eCollection 2022 Jan. Kidney Int Rep. 2021. PMID: 35005319 Free PMC article.
Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease.
Okada E, Morisada N, Horinouchi T, Fujii H, Tsuji T, Miura M, Katori H, Kitagawa M, Morozumi K, Toriyama T, Nakamura Y, Nishikomori R, Nagai S, Kondo A, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Nagano C, Yamamura T, Ishimori S, Usui J, Yamagata K, Iijima K, Imasawa T, Nozu K. Okada E, et al. Among authors: ishiko s. Kidney Int Rep. 2022 Jan 4;7(4):857-866. doi: 10.1016/j.ekir.2021.12.037. eCollection 2022 Apr. Kidney Int Rep. 2022. PMID: 35497811 Free PMC article.
Corrigendum to "Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease"Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866.
Okada E, Morisada N, Horinouchi T, Fujii H, Tsuji T, Miura M, Katori H, Kitagawa M, Morozumi K, Toriyama T, Nakamura Y, Nishikomori R, Nagai S, Kondo A, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Nagano C, Yamamura T, Ishimori S, Usui J, Yamagata K, Iijima K, Imasawa T, Nozu K. Okada E, et al. Among authors: ishiko s. Kidney Int Rep. 2023 Mar 13;8(5):1127-1129. doi: 10.1016/j.ekir.2023.02.1090. eCollection 2023 May. Kidney Int Rep. 2023. PMID: 37180508 Free PMC article.
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.
Yamamura T, Nozu K, Minamikawa S, Horinouchi T, Sakakibara N, Nagano C, Aoto Y, Ishiko S, Nakanishi K, Shima Y, Nagase H, Rossanti R, Ye MJ, Nozu Y, Ishimori S, Morisada N, Kaito H, Iijima K. Yamamura T, et al. Among authors: ishiko s. Mol Genet Genomic Med. 2019 Sep;7(9):e883. doi: 10.1002/mgg3.883. Epub 2019 Jul 30. Mol Genet Genomic Med. 2019. PMID: 31364286 Free PMC article. Clinical Trial.
Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.
Nagano C, Yamamura T, Horinouchi T, Aoto Y, Ishiko S, Sakakibara N, Shima Y, Nakanishi K, Nagase H, Iijima K, Nozu K. Nagano C, et al. Among authors: ishiko s. Sci Rep. 2020 Jan 14;10(1):270. doi: 10.1038/s41598-019-57149-5. Sci Rep. 2020. PMID: 31937884 Free PMC article.
142 results