Inagaki N - Search Results

1

Shared decision making between patients with Fabry disease and physicians in Japan: An online survey.

Inagaki N, Tsuchiya M, Otani K, Nakayama T. Inagaki N, et al. Mol Genet Metab Rep. 2022 Aug 10;32:100899. doi: 10.1016/j.ymgmr.2022.100899. eCollection 2022 Sep. Mol Genet Metab Rep. 2022. PMID: 36046392 Free PMC article.

2

Clinical and genetic backgrounds of hypertrophic cardiomyopathy with mid-ventricular obstruction.

Inagaki N, Hayashi T, Takei Y, Tanimoto K, Chikamori T, Kimura A. Inagaki N, et al. J Hum Genet. 2018 Dec;63(12):1273-1276. doi: 10.1038/s10038-018-0509-9. Epub 2018 Sep 11. J Hum Genet. 2018. PMID: 30206291 Clinical Trial.

3

A family case of X-linked Alport syndrome patients with a novel variant in COL4A5.

Kashiwagi Y, Suzuki S, Agata K, Morishima Y, Inagaki N, Numabe H, Kawashima H. Kashiwagi Y, et al. Among authors: inagaki n. CEN Case Rep. 2019 May;8(2):75-78. doi: 10.1007/s13730-018-0368-4. Epub 2018 Oct 6. CEN Case Rep. 2019. PMID: 30293132 Free PMC article.

4

A Case of Primary Ciliary Dyskinesia Caused by a Mutation in OFD1, Which Was Diagnosed Owing to Clostridium difficile Infection.

Hasegawa R, Suzuki S, Nishimata S, Kashiwagi Y, Inagaki N, Kawashima H. Hasegawa R, et al. Among authors: inagaki n. Pediatr Rep. 2021 May 10;13(2):241-244. doi: 10.3390/pediatric13020033. Pediatr Rep. 2021. PMID: 34068458 Free PMC article.

5

Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia.

Ueda K, Nakamura K, Hayashi T, Inagaki N, Takahashi M, Arimura T, Morita H, Higashiuesato Y, Hirano Y, Yasunami M, Takishita S, Yamashina A, Ohe T, Sunamori M, Hiraoka M, Kimura A. Ueda K, et al. Among authors: inagaki n. J Biol Chem. 2004 Jun 25;279(26):27194-8. doi: 10.1074/jbc.M311953200. Epub 2004 Apr 30. J Biol Chem. 2004. PMID: 15123648 Free article.

6

Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking defect.

Aizawa Y, Ueda K, Wu LM, Inagaki N, Hayashi T, Takahashi M, Ohta M, Kawano S, Hirano Y, Yasunami M, Aizawa Y, Kimura A, Hiraoka M. Aizawa Y, et al. Among authors: inagaki n. FEBS Lett. 2004 Sep 10;574(1-3):145-50. doi: 10.1016/j.febslet.2004.08.018. FEBS Lett. 2004. PMID: 15358555 Free article.

7

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy.

Hayashi T, Arimura T, Itoh-Satoh M, Ueda K, Hohda S, Inagaki N, Takahashi M, Hori H, Yasunami M, Nishi H, Koga Y, Nakamura H, Matsuzaki M, Choi BY, Bae SW, You CW, Han KH, Park JE, Knöll R, Hoshijima M, Chien KR, Kimura A. Hayashi T, et al. Among authors: inagaki n. J Am Coll Cardiol. 2004 Dec 7;44(11):2192-201. doi: 10.1016/j.jacc.2004.08.058. J Am Coll Cardiol. 2004. PMID: 15582318 Free article.

8

Functional analysis of titin/connectin N2-B mutations found in cardiomyopathy.

Matsumoto Y, Hayashi T, Inagaki N, Takahashi M, Hiroi S, Nakamura T, Arimura T, Nakamura K, Ashizawa N, Yasunami M, Ohe T, Yano K, Kimura A. Matsumoto Y, et al. Among authors: inagaki n. J Muscle Res Cell Motil. 2005;26(6-8):367-74. doi: 10.1007/s10974-005-9018-5. J Muscle Res Cell Motil. 2005. PMID: 16465475

9

Alpha B-crystallin mutation in dilated cardiomyopathy.

Inagaki N, Hayashi T, Arimura T, Koga Y, Takahashi M, Shibata H, Teraoka K, Chikamori T, Yamashina A, Kimura A. Inagaki N, et al. Biochem Biophys Res Commun. 2006 Apr 7;342(2):379-86. doi: 10.1016/j.bbrc.2006.01.154. Epub 2006 Feb 8. Biochem Biophys Res Commun. 2006. PMID: 16483541

10

Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy.

Arimura T, Hayashi T, Matsumoto Y, Shibata H, Hiroi S, Nakamura T, Inagaki N, Hinohara K, Takahashi M, Manatsu SI, Sasaoka T, Izumi T, Bonne G, Schwartz K, Kimura A. Arimura T, et al. Among authors: inagaki n. Biochem Biophys Res Commun. 2007 May 25;357(1):162-7. doi: 10.1016/j.bbrc.2007.03.128. Epub 2007 Mar 30. Biochem Biophys Res Commun. 2007. PMID: 17416352

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