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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2002 1
2003 1
2006 1
2007 2
2008 3
2009 3
2010 3
2012 1
2013 2
2015 2
2016 4
2017 8
2018 8
2019 1
2020 3
2021 3
2022 1
2023 2
2024 0

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47 results

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Page 1
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.
Ashraf S, Kudo H, Rao J, Kikuchi A, Widmeier E, Lawson JA, Tan W, Hermle T, Warejko JK, Shril S, Airik M, Jobst-Schwan T, Lovric S, Braun DA, Gee HY, Schapiro D, Majmundar AJ, Sadowski CE, Pabst WL, Daga A, van der Ven AT, Schmidt JM, Low BC, Gupta AB, Tripathi BK, Wong J, Campbell K, Metcalfe K, Schanze D, Niihori T, Kaito H, Nozu K, Tsukaguchi H, Tanaka R, Hamahira K, Kobayashi Y, Takizawa T, Funayama R, Nakayama K, Aoki Y, Kumagai N, Iijima K, Fehrenbach H, Kari JA, El Desoky S, Jalalah S, Bogdanovic R, Stajić N, Zappel H, Rakhmetova A, Wassmer SR, Jungraithmayr T, Strehlau J, Kumar AS, Bagga A, Soliman NA, Mane SM, Kaufman L, Lowy DR, Jairajpuri MA, Lifton RP, Pei Y, Zenker M, Kure S, Hildebrandt F. Ashraf S, et al. Among authors: tsukaguchi h. Nat Commun. 2018 May 17;9(1):1960. doi: 10.1038/s41467-018-04193-w. Nat Commun. 2018. PMID: 29773874 Free PMC article.
Characterization of cytoskeletal and structural effects of INF2 variants causing glomerulopathy and neuropathy.
Ueda H, Tran QTH, Tran LNT, Higasa K, Ikeda Y, Kondo N, Hashiyada M, Sato C, Sato Y, Ashida A, Nishio S, Iwata Y, Iida H, Matsuoka D, Hidaka Y, Fukui K, Itami S, Kawashita N, Sugimoto K, Nozu K, Hattori M, Tsukaguchi H. Ueda H, et al. Among authors: tsukaguchi h. Sci Rep. 2023 Jul 25;13(1):12003. doi: 10.1038/s41598-023-38588-7. Sci Rep. 2023. PMID: 37491439 Free PMC article.
Steroid-resistant nephrotic syndrome.
Kitamura A, Tsukaguchi H, Maruyama K, Shono A, Iijima K, Kagami S, Doi T. Kitamura A, et al. Among authors: tsukaguchi h. Kidney Int. 2008 Nov;74(9):1209-15. doi: 10.1038/ki.2008.297. Epub 2008 Jul 2. Kidney Int. 2008. PMID: 18596732 Free article. No abstract available.
[Molecular basis of hereditary nephrotic syndromes].
Iijima K, Tsukaguchi H. Iijima K, et al. Among authors: tsukaguchi h. Nihon Jinzo Gakkai Shi. 2010;52(7):914-23. Nihon Jinzo Gakkai Shi. 2010. PMID: 21077341 Review. Japanese. No abstract available.
Homozygous splicing mutation in NUP133 causes Galloway-Mowat syndrome.
Fujita A, Tsukaguchi H, Koshimizu E, Nakazato H, Itoh K, Kuraoka S, Komohara Y, Shiina M, Nakamura S, Kitajima M, Tsurusaki Y, Miyatake S, Ogata K, Iijima K, Matsumoto N, Miyake N. Fujita A, et al. Among authors: tsukaguchi h. Ann Neurol. 2018 Dec;84(6):814-828. doi: 10.1002/ana.25370. Ann Neurol. 2018. PMID: 30427554
Biallelic variants/mutations of IL1RAP in patients with steroid-sensitive nephrotic syndrome.
Niitsuma S, Kudo H, Kikuchi A, Hayashi T, Kumakura S, Kobayashi S, Okuyama Y, Kumagai N, Niihori T, Aoki Y, So T, Funayama R, Nakayama K, Shirota M, Kondo S, Kagami S, Tsukaguchi H, Iijima K, Kure S, Ishii N. Niitsuma S, et al. Among authors: tsukaguchi h. Int Immunol. 2020 Apr 12;32(4):283-292. doi: 10.1093/intimm/dxz081. Int Immunol. 2020. PMID: 31954058
A Nationwide Survey on Danon Disease in Japan.
Sugie K, Komaki H, Eura N, Shiota T, Onoue K, Tsukaguchi H, Minami N, Ogawa M, Kiriyama T, Kataoka H, Saito Y, Nonaka I, Nishino I. Sugie K, et al. Among authors: tsukaguchi h. Int J Mol Sci. 2018 Nov 8;19(11):3507. doi: 10.3390/ijms19113507. Int J Mol Sci. 2018. PMID: 30413001 Free PMC article.
47 results