C. Aoyama

发表

A Rostrocaudal Muscular Dystrophy Caused by a Defect in Choline Kinase Beta, the First Enzyme in Phosphatidylcholine Biosynthesis*

W. Frankel, D. Vance, P. A. Wood, 2006, Journal of Biological Chemistry.

The heterotrimeric G protein subunits Gαq and Gβ1 have lysophospholipase D activity

M. Satou, H. Sugimoto, Y. Horibata, 2011, The Biochemical journal.

StarD7 Protein Deficiency Adversely Affects the Phosphatidylcholine Composition, Respiratory Activity, and Cristae Structure of Mitochondria*

M. Itoh, K. Reue, H. Sugimoto, 2016, The Journal of Biological Chemistry.

Structure and characterization of the genes for murine choline / ethanolamine kinase isozymes a and b 1

N. Yamazaki, H. Terada, C. Aoyama, 2000 .

Structure and function of choline kinase isoforms in mammalian cells.

C. Aoyama, K. Ishidate, Huanan Liao, 2004, Progress in lipid research.

Structure and characterization of the genes for murine choline/ethanolamine kinase isozymes alpha and beta.

N. Yamazaki, H. Terada, C. Aoyama, 2000, Journal of lipid research.

Expression and characterization of the active molecular forms of choline/ethanolamine kinase-alpha and -beta in mouse tissues, including carbon tetrachloride-induced liver.

C. Aoyama, K. Ishidate, A. Ohtani, 2002, The Biochemical journal.

The phosphatidylcholine transfer protein StarD7 is important for myogenic differentiation in mouse myoblast C2C12 cells and human primary skeletal myoblasts

H. Sugimoto, Y. Horibata, Hiromi Ando, 2020, Scientific Reports.

Transcriptional suppression of CTP:phosphoethanolamine cytidylyltransferase by 25-hydroxycholesterol is mediated by nuclear factor-Y and Yin Yang 1.

M. Itoh, M. Satou, H. Sugimoto, 2015, The Biochemical journal.

Complementary DNA sequence for a 42 kDa rat kidney choline/ethanolamine kinase.

K. Nakashima, C. Aoyama, K. Ishidate, 1998, Biochimica et biophysica acta.

Characterization of glycerophosphodiesterase 4-interacting molecules Gαq/11and Gβ, which mediate cellular lysophospholipase D activity.

H. Sugimoto, Y. Horibata, Hiromi Ando, 2019, The Biochemical journal.

Muscular dystrophy with large mitochondria associated with mutations in the CHKB gene in three British patients: Extending the clinical and pathological phenotype

D. Birchall, K. Bushby, F. Muntoni, 2013, Neuromuscular Disorders.

Early Embryonic Lethality Caused by Disruption of the Gene for Choline Kinase α, the First Enzyme in Phosphatidylcholine Biosynthesis*

S. Young, D. Vance, Gengshu Wu, 2007, Journal of Biological Chemistry.

Purification and characterization of lysophospholipase D from rat brain.

M. Mori, H. Sugimoto, T. Izumi, 2006, Biochimica et biophysica acta.

Choline kinase alpha expression during RA-induced neuronal differentiation: role of C/EBPβ.

C. Banchio, C. Aoyama, P. Domizi, 2014, Biochimica et biophysica acta.

Identification of nuclear localization and nuclear export signals in Ets2, and the transcriptional regulation of Ets2 and CTP:phosphocholine cytidylyltransferase alpha in tetradecanoyl-13-acetate or macrophage-colony stimulating factor stimulated RAW264 cells.

D. Vance, K. Takagishi, H. Sugimoto, 2009, Biochimica et biophysica acta.

A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesis.

I. Nonaka, Y. Hayashi, I. Nishino, 2011, American journal of human genetics.

Side-chain oxysterols suppress the transcription of CTP: Phosphoethanolamine cytidylyltransferase and 3-hydroxy-3-methylglutaryl-CoA reductase by inhibiting the interaction of p300 and NF-Y, and H3K27 acetylation

H. Sugimoto, Y. Horibata, Hiromi Ando, 2019, The Journal of Steroid Biochemistry and Molecular Biology.

The phosphatidylcholine transfer protein StarD7 is important for myogenic differentiation in mouse myoblast C2C12 cells and human primary skeletal myoblasts

H. Sugimoto, Y. Horibata, Hiromi Ando, 2020, Scientific Reports.

Deletion and alanine mutation analyses for the formation of active homo- or hetero-dimer complexes of mouse choline kinase-α and -β

H. Teraoka, C. Aoyama, K. Ishidate, 2006 .

Deletion and alanine mutation analyses for the formation of active homo- or hetero-dimer complexes of mouse choline kinase-alpha and -beta.

H. Teraoka, C. Aoyama, K. Ishidate, 2006, Biochimica et biophysica acta.

Expression and characterization of the active molecular forms of choline/ethanolamine kinase-alpha and -beta in mouse tissues, including carbon tetrachloride-induced liver.

C. Aoyama, K. Ishidate, A. Ohtani, 2002, The Biochemical journal.

Induction of choline kinase alpha by carbon tetrachloride (CCl4) occurs via increased binding of c-jun to an AP-1 element.

D. Vance, H. Sugimoto, C. Aoyama, 2007, Biochimica et biophysica acta.

Molecular cloning of mouse choline kinase and choline/ethanolamine kinase: their sequence comparison to the respective rat homologs.

K. Nakashima, C. Aoyama, K. Ishidate, 1998, Biochimica et biophysica acta.