Liang WC, Nishino I.
State of the art in muscle lipid diseases. Acta Myol.2010 Oct;29(2):351-356.
Mimaki M, Hatakeyama H, Komaki H, Yokoyama M, Arai H, Kirino Y, Suzuki T, Nishino I, Nonaka I, Goto Y.
Reversible infantile respiratory chain deficiency: a clinical and molecular study. Ann Neurol. 2010 Dec;68(6):845-854.
Ishii K, Komaki H,Ohkuma A, Nishino I, Nonaka I, Sasaki M.
Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. Brain Dev. 2010 Sep;32(8):669-672. Epub 2009 Sep 26.
Mitsuhashi H, Hayashi YK, Matsuda C, Noguchi S, Wakatsuki S, Araki T, Nishino I.
Specific phosphorylation of Ser458 of A-type lamins in LMNA-associated myopathy patients. J Cell Sci. 2010 Nov 15;123(Pt 22):3893-3900. Epub 2010 Oct 27.
Mitsui J, Takahashi Y, Goto J, Tomiyama H, Ishikawa S, Yoshino H, Minami N, Smith DI, Lesage S, Aburatani H, Nishino I, Brice A, Hattori N, Tsuji S.
Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines. Am J Hum Genet. 2010 Jul 9;87(1):75-89.
Crotzer V, Glosson N, Zhou D, Nishino I, Blum J.
LAMP-2-deficient human B cells exhibit altered MHC class II presentation of exogenous antigens. Immunology. 2010 Nov;131(3):318-330.
Kim H, Cho A, Lim BC, Kim MJ, Kim KJ, Nishino I, Hwang YS, Chae JH.
A 13-year-old girl with proximal weakness and hypertrophic cardiomyopathy with Danon Disease. Muscle Nerve. 2010 Jun;41(6):879-882.
Iwabu M, Yamauchi T, Okada-Iwabu M, Sato K, Nakagawa T, Funata M, Yamaguchi M, Namiki S, Nakayama R, Tabata M, Ogata H, Kubota N, Takamoto I, Hayashi YK, Yamauchi N, Waki H, Fukayama M, Nishino I, Tokuyama K, Ueki K, Oike Y, Ishii S, Hirose K, Shimizu T, Touhara K, Kadowaki T.
Adiponectin and AdipoR1 regulate PGC-1alpha and mitochondria by Ca2+ and AMPK/SIRT1. Nature. 2010 Apr 29;464(7293):1313-1319. Epub 2010 Mar 31.
Tominaga K, Hayashi YK, Goto K, Minami N, Noguchi S, Nonaka I, Miki T, Nishino I.
Congenital myotonic dystrophy can show congenital fiber type disproportion pathology. Acta Neuropathol. 2010 Apr;119(4):481-486. Epub 2010 Feb 24.
Yamazaki Y,Kamei Y, Sugita S, Akaike F, Kanai S, Miura S, Hirata Y, Troen BR, Kitamura T, Nishino I, Suganami T, Ezaki O, Ogawa Y.
The cathepsin L gene is a direct target of FOXO1 in the skeletal muscle. Biochem J. 2010 Mar 15;427(1):171-178.
Malicdan MC, Noguchi S, Nishino I.
A preclinical trial of sialic acid metabolites on distal myopathy with rimmed vacuoles/hereditary inclusion body myopathy, a sugar-deficient myopathy: a review. Ther Adv Neurol Disord. 2010;3(2):127-135.
Okanishi T, Ishikawa T, Kobayashi S, Ando N, Nishino I, Togari H, Nonaka I.
Bilateral occipital cortical dysplasia and white matter T2 hyperintensity with mild non-specific myopathy: Two sibling cases. Brain Dev. 2010 Apr;32(4):342-346. Epub 2009 Dec 22.