年単位の研究成果
Fingerprint Takema Katoが取り組む研究トピックをご確認ください。これらのトピックラベルは、この人物の研究に基づいています。これらを共に使用することで、固有の認識が可能になります。
- 12 同様のプロファイル
Pre-Eclampsia
Medicine & Life Sciences
Genes
Medicine & Life Sciences
Genetic Translocation
Medicine & Life Sciences
Spermatozoa
Medicine & Life Sciences
Genomic Instability
Medicine & Life Sciences
DNA
Medicine & Life Sciences
Mothers
Medicine & Life Sciences
Alleles
Medicine & Life Sciences
ネットワーク
最近の共同研究。丸をクリックして詳細を確認しましょう。
研究成果 2006 2019
A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysis
Tsuchiya, H., Akiyama, T., Kuhara, T., Nakajima, Y., Ohse, M., Kurahashi, H., Kato, T., Maeda, Y., Yoshinaga, H. & Kobayashi, K., 01-03-2019, ： : Brain and Development. 41, 3, p. 280-284 5 p.研究成果: Article
Metabolome
Urine
Mutation
Fluorouracil
Metabolomics
2
引用
(Scopus)
DNA methylation accumulation in gastric mucosa adjacent to cancer after Helicobacter pylori eradication
Tahara, S., Tahara, T., Horiguchi, N., Kato, T., Shinkai, Y., Yamashita, H., Yamada, H., Kawamura, T., Terada, T., Okubo, M., Nagasaka, M., Nakagawa, Y., Shibata, T., Yamada, S., Urano, M., Tsukamoto, T., Kurahashi, H., Kuroda, M. & Omiya, N., 01-01-2019, ： : International Journal of Cancer. 144, 1, p. 80-88 9 p.研究成果: Article
DNA Methylation
Gastric Mucosa
Helicobacter pylori
Methylation
Stomach
1
引用
(Scopus)
Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders
Terasawa, S., Kato, A., Nishizawa, H., Kato, T., Yoshizawa, H., Noda, Y., Miyazaki, J., Ito, M., Sekiya, T., Fujii, T. & Kurahashi, H., 01-01-2019, ： : Congenital anomalies. 59, 1, p. 4-10 7 p.研究成果: Article
Thanatophoric Dysplasia
Achondroplasia
Multiplex Polymerase Chain Reaction
Prenatal Diagnosis
Mutation
Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures
Inagaki, H., Ota, S., Nishizawa, H., Miyamura, H., Nakahira, K., Suzuki, M., Nishiyama, S., Kato, T., Yanagihara, I. & Kurahashi, H., 01-05-2019, ： : Journal of Human Genetics. 64, 5, p. 459-466 8 p.研究成果: Article
G-Quadruplexes
Annexin A5
Obstetrics
Gene Expression
DNA
FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency
Boda, H., Miyata, M., Inagaki, H., Shinkai, Y., Kato, T., Yoshikawa, T. & Kurahashi, H., 01-01-2018, (Accepted/In press) ： : European Journal of Medical Genetics.研究成果: Article
Pituitary Hormones
Missense Mutation
Intestinal Atresia
Imperforate Anus
Haploinsufficiency