Nakagawa M - Search Results

1

YY1 binds to α-synuclein 3'-flanking region SNP and stimulates antisense noncoding RNA expression.

Mizuta I, Takafuji K, Ando Y, Satake W, Kanagawa M, Kobayashi K, Nagamori S, Shinohara T, Ito C, Yamamoto M, Hattori N, Murata M, Kanai Y, Murayama S, Nakagawa M, Toda T. Mizuta I, et al. Among authors: nakagawa m. J Hum Genet. 2013 Nov;58(11):711-9. doi: 10.1038/jhg.2013.90. Epub 2013 Sep 12. J Hum Genet. 2013. PMID: 24026176

2

The functional alteration of mutant GFAP depends on the location of the domain: morphological and functional studies using astrocytoma-derived cells.

Yoshida T, Tomozawa Y, Arisato T, Okamoto Y, Hirano H, Nakagawa M. Yoshida T, et al. Among authors: nakagawa m. J Hum Genet. 2007;52(4):362-369. doi: 10.1007/s10038-007-0124-7. Epub 2007 Feb 22. J Hum Genet. 2007. PMID: 17318298

3

Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity.

Maeda K, Kaji R, Yasuno K, Jambaldorj J, Nodera H, Takashima H, Nakagawa M, Makino S, Tamiya G. Maeda K, et al. Among authors: nakagawa m. J Hum Genet. 2007;52(11):907-914. doi: 10.1007/s10038-007-0193-7. Epub 2007 Oct 2. J Hum Genet. 2007. PMID: 17906970

4

Serial MRI changes in a patient with infantile Alexander disease and prolonged survival.

Shiihara T, Yoneda T, Mizuta I, Yoshida T, Nakagawa M, Shimizu N. Shiihara T, et al. Among authors: nakagawa m. Brain Dev. 2011 Aug;33(7):604-7. doi: 10.1016/j.braindev.2010.10.007. Epub 2010 Oct 30. Brain Dev. 2011. PMID: 21041050

5

A commentary on Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan.

Nakagawa M. Nakagawa M. J Hum Genet. 2011 May;56(5):341-2. doi: 10.1038/jhg.2011.32. Epub 2011 Mar 31. J Hum Genet. 2011. PMID: 21451531 No abstract available.

6

A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth disease.

Shiga K, Noto Y, Mizuta I, Hashiguchi A, Takashima H, Nakagawa M. Shiga K, et al. Among authors: nakagawa m. J Peripher Nerv Syst. 2012 Jun;17(2):206-9. doi: 10.1111/j.1529-8027.2012.00403.x. J Peripher Nerv Syst. 2012. PMID: 22734907

7

The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement.

Ishiura H, Sako W, Yoshida M, Kawarai T, Tanabe O, Goto J, Takahashi Y, Date H, Mitsui J, Ahsan B, Ichikawa Y, Iwata A, Yoshino H, Izumi Y, Fujita K, Maeda K, Goto S, Koizumi H, Morigaki R, Ikemura M, Yamauchi N, Murayama S, Nicholson GA, Ito H, Sobue G, Nakagawa M, Kaji R, Tsuji S. Ishiura H, et al. Among authors: nakagawa m. Am J Hum Genet. 2012 Aug 10;91(2):320-9. doi: 10.1016/j.ajhg.2012.07.014. Am J Hum Genet. 2012. PMID: 22883144 Free PMC article.

8

Effects of a polymorphism in the GFAP promoter on the age of onset and ambulatory disability in late-onset Alexander disease.

Yoshida T, Mizuta I, Saito K, Ohara R, Kurisaki H, Ohnari K, Riku Y, Hayashi Y, Suzuki H, Shii H, Fujiwara Y, Yonezu T, Nagaishi A, Nakagawa M. Yoshida T, et al. Among authors: nakagawa m. J Hum Genet. 2013 Sep;58(9):635-8. doi: 10.1038/jhg.2013.83. Epub 2013 Aug 1. J Hum Genet. 2013. PMID: 23903069

9

ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.

Takahashi Y, Fukuda Y, Yoshimura J, Toyoda A, Kurppa K, Moritoyo H, Belzil VV, Dion PA, Higasa K, Doi K, Ishiura H, Mitsui J, Date H, Ahsan B, Matsukawa T, Ichikawa Y, Moritoyo T, Ikoma M, Hashimoto T, Kimura F, Murayama S, Onodera O, Nishizawa M, Yoshida M, Atsuta N, Sobue G; JaCALS; Fifita JA, Williams KL, Blair IP, Nicholson GA, Gonzalez-Perez P, Brown RH Jr, Nomoto M, Elenius K, Rouleau GA, Fujiyama A, Morishita S, Goto J, Tsuji S. Takahashi Y, et al. Am J Hum Genet. 2013 Nov 7;93(5):900-5. doi: 10.1016/j.ajhg.2013.09.008. Epub 2013 Oct 10. Am J Hum Genet. 2013. PMID: 24119685 Free PMC article.

10

Definite familial multiple system atrophy with unknown genetics.

Itoh K, Kasai T, Tsuji Y, Saito K, Mizuta I, Harada Y, Sudoh S, Mizuno T, Nakagawa M, Fushiki S. Itoh K, et al. Among authors: nakagawa m. Neuropathology. 2014 Jun;34(3):309-13. doi: 10.1111/neup.12092. Epub 2014 Jan 7. Neuropathology. 2014. PMID: 24397755

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