Matsumori M - Search Results

1

Five novel SLC7A7 variants and y+L gene-expression pattern in cultured lymphoblasts from Japanese patients with lysinuric protein intolerance.

Shoji Y, Noguchi A, Shoji Y, Matsumori M, Takasago Y, Takayanagi M, Yoshida Y, Ihara K, Hara T, Yamaguchi S, Yoshino M, Kaji M, Yamamoto S, Nakai A, Koizumi A, Hokezu Y, Nagamatsu K, Mikami H, Kitajima I, Takada G. Shoji Y, et al. Among authors: matsumori m. Hum Mutat. 2002 Nov;20(5):375-81. doi: 10.1002/humu.10140. Hum Mutat. 2002. PMID: 12402335

2

SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families.

Noguchi A, Shoji Y, Koizumi A, Takahashi T, Matsumori M, Kayo T, Ohata T, Wada Y, Yoshimura I, Maisawa S, Konishi M, Takasago Y, Takada G. Noguchi A, et al. Among authors: matsumori m. Hum Mutat. 2000;15(4):367-72. doi: 10.1002/(SICI)1098-1004(200004)15:4<367::AID-HUMU9>3.0.CO;2-C. Hum Mutat. 2000. PMID: 10737982

3

Stroke-like episode involving a cerebral artery in a patient with MELAS.

Noguchi A, Shoji Y, Matsumori M, Komatsu K, Takada G. Noguchi A, et al. Among authors: matsumori m. Pediatr Neurol. 2005 Jul;33(1):70-1. doi: 10.1016/j.pediatrneurol.2005.01.013. Epub 2005 Apr 13. Pediatr Neurol. 2005. PMID: 15993323

4

A molecular lesion in a Japanese patient with severe phenotype of 3-methylglutaconic aciduria type I.

Matsumori M, Shoji Y, Takahashi T, Shoji Y, Takada G. Matsumori M, et al. Pediatr Int. 2005 Dec;47(6):684-6. doi: 10.1111/j.1442-200x.2005.02130.x. Pediatr Int. 2005. PMID: 16354225 No abstract available.

5

Novel mutation of methylmalonyl-CoA mutase gene causing the mut0 form of methylmalonic acidemia in a Japanese girl.

Oyama C, Takahashi T, Matsumori M, Shoji Y, Tajima G, Sakura N, Hasegawa Y, Yamaguchi S, Kakinuma H, Takada G. Oyama C, et al. Among authors: matsumori m. Pediatr Int. 2007 Apr;49(2):232-4. doi: 10.1111/j.1442-200X.2007.02325.x. Pediatr Int. 2007. PMID: 17445044 No abstract available.

6

3-Methylglutaconic aciduria type I: clinical heterogeneity as a neurometabolic disease.

Shoji Y, Takahashi T, Sawaishi Y, Ishida A, Matsumori M, Shoji Y, Enoki M, Watanabe H, Takada G. Shoji Y, et al. Among authors: matsumori m. J Inherit Metab Dis. 1999 Feb;22(1):1-8. doi: 10.1023/a:1005421111554. J Inherit Metab Dis. 1999. PMID: 10070612

7

Characterization of the 105-kDa molecular chaperone. Identification, biochemical properties, and localization.

Matsumori M, Itoh H, Toyoshima I, Komatsuda A, Sawada K, Fukuda J, Tanaka T, Okubo A, Kinouchi H, Mizoi K, Hama T, Suzuki A, Hamada F, Otaka M, Shoji Y, Takada G. Matsumori M, et al. Eur J Biochem. 2002 Nov;269(22):5632-41. doi: 10.1046/j.1432-1033.2002.03272.x. Eur J Biochem. 2002. PMID: 12423363 Free article.

8

Influence of right ventricular volume and pressure overloads on assessment of left ventricular volume using two-dimensional echocardiography in infants and children with congenital heart diseases.

Matsumori M, Ito T, Toyono M, Harada K, Takada G. Matsumori M, et al. Am J Cardiol. 1997 Oct 1;80(7):965-8. doi: 10.1016/s0002-9149(97)00559-6. Am J Cardiol. 1997. PMID: 9382021

9

Molecular cloning of a novel gene involved in serotonin receptor-mediated signal transduction in rat stomach.

Ohya S, Takii T, Yamazaki HF, Matsumori M, Onozaki K, Watanabe M, Imaizumi Y. Ohya S, et al. Among authors: matsumori m. FEBS Lett. 1997 Jan 20;401(2-3):252-8. doi: 10.1016/s0014-5793(96)01485-8. FEBS Lett. 1997. PMID: 9013898 Free article.

10

Effects of citrin deficiency in the perinatal period: feasibility of newborn mass screening for citrin deficiency.

Tamamori A, Fujimoto A, Okano Y, Kobayashi K, Saheki T, Tagami Y, Takei H, Shigematsu Y, Hata I, Ozaki H, Tokuhara D, Nishimura Y, Yorifuji T, Igarashi N, Ohura T, Shimizu T, Inui K, Sakai N, Abukawa D, Miyakawa T, Matsumori M, Ban K, Kaneko H, Yamano T. Tamamori A, et al. Among authors: matsumori m. Pediatr Res. 2004 Oct;56(4):608-14. doi: 10.1203/01.PDR.0000139713.64264.BC. Epub 2004 Aug 4. Pediatr Res. 2004. PMID: 15295082

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