C. Sakai

发表

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

S. Tsuji, H. Shimazaki, Y. Fukuda, 2012, Journal of Medical Genetics.

Mitochondrial fumarate reductase as a target of chemotherapy: from parasites to cancer cells.

H. Esumi, C. Sakai, K. Kita, 2012, Biochimica et biophysica acta.

Inhibition of cancer cell growth by GRP78 siRNA lipoplex via activation of unfolded protein response.

S. Kawakami, M. Hashida, F. Yamashita, 2014, Biological & pharmaceutical bulletin.

Type II Fp of human mitochondrial respiratory complex II and its role in adaptation to hypoxia and nutrition-deprived conditions.

M. Miyagishi, C. Sakai, K. Kita, 2013, Mitochondrion.

Mitochondrial Complex III Deficiency Caused by a Homozygous UQCRC2 Mutation Presenting with Neonatal‐Onset Recurrent Metabolic Decompensation

N. Matsumoto, M. Shiina, K. Ogata, 2013, Human mutation.

Selective Cytotoxicity of Dihydroorotate Dehydrogenase Inhibitors to Human Cancer Cells Under Hypoxia and Nutrient-Deprived Conditions

H. Saimoto, C. Sakai, A. Moore, 2018, Front. Pharmacol..

Homoplasmy of a mitochondrial 3697G>A mutation causes Leigh syndrome

S. Saitoh, C. Sakai, E. Takeshita, 2014, Journal of Human Genetics.

ECHS1 Mutations Cause Combined Respiratory Chain Deficiency Resulting in Leigh Syndrome

Yuichi Matsushima, Masayuki Sasaki, Seiji Yamaguchi, 2015, Human mutation.

NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathy

Y. Goto, I. Nishino, C. Sakai, 2018, Clinical genetics.

IBA57 mutations abrogate iron-sulfur cluster assembly leading to cavitating leukoencephalopathy

Y. Goto, I. Nonaka, Y. Hayashi, 2017, Neurology: Genetics.