K. Toyota

发表

Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia☆

Takeo Kato, M. Mori, Hiroaki Haga, 2014, Molecular genetics and metabolism reports.

A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy

G. Tamiya, K. Hayasaka, Hiroshi Sato, 2013, Journal of Human Genetics.

The double-stranded break-forming activity of plant SPO11s and a novel rice SPO11 revealed by a Drosophila bioassay

Tsutomu Mikawa, T. Shibata, K. Wakasa, 2012, BMC Molecular Biology.

Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding

G. Tamiya, K. Hayasaka, Hiroko Sato, 2012, Journal of Human Genetics.

Careful Clinical Surveillance Is Important for the Identification of Parechovirus Type A3-Associated Myalgia/Myositis: a Sporadic Case Found in a Season with a Low Level of Its Activity in Yamagata, Japan in 2017.

K. Mizuta, K. Komabayashi, Masayuki Furuyama, 2019, Japanese journal of infectious diseases.

Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis

G. Tamiya, M. Hattori, K. Hayasaka, 2015, Journal of Human Genetics.

Expression profiling of starch metabolism-related plastidic translocator genes in rice

Yasunori Nakamura, Takashi Ohdan, M. Tamura, 2005, Planta.

Sweetness Sensor with Lipid/Polymer Membranes : Response to Various Sugars

Kentaro Abe, Kiyoshi Toko, Hidekazu Ikezaki, 2011 .

Sweetness Sensor with Lipid/Polymer Membranes : Sweet-Responsive Substances

Kentaro Abe, Kiyoshi Toko, Hidekazu Ikezaki, 2011 .

Transcriptional activation of phosphoenolpyruvate carboxylase by phosphorus deficiency in tobacco.

F. Sato, N. Koizumi, K. Toyota, 2003, Journal of experimental botany.

Transcriptional activation of phospho enol pyruvate carboxylase by phosphorus de ® ciency in tobacco

F. Sato, N. Koizumi, K. Toyota, 2022 .

Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms

G. Tamiya, K. Hayasaka, Hiroko Sato, 2014, Journal of Human Genetics.

A second pediatric patient with lipoprotein glomerulopathy carrying a heterozygous APOE-Sendai mutation

K. Hayasaka, D. Ogino, A. Matsunaga, 2011 .

Aftertaste evaluation of sake using a taste sensor

H. Ikezaki, Akira Totsuka, K. Toyota, 2016 .

INF2 mutations in Charcot‐Marie‐Tooth disease complicated with focal segmental glomerulosclerosis

Kayoko Saito, H. Tsukaguchi, K. Hayasaka, 2013, Journal of the peripheral nervous system : JPNS.

Tight regulation of transgene expression by tetracycline‐dependent activator and repressor in brain

S. Kida, S. Masushige, T. Ishii, 2005, Genes, brain, and behavior.

Treatment with lactose (galactose)-restricted and medium-chain triglyceride-supplemented formula for neonatal intrahepatic cholestasis caused by citrin deficiency.

K. Hayasaka, T. Kimura, C. Numakura, 2012, JIMD Reports.

An elderly Japanese patient with adult-onset type II citrullinemia with a novel D493G mutation in the SLC25A13 gene.

Hiroaki Haga, T. Kawanami, K. Hayasaka, 2012, Internal medicine.