K. Hidaka

发表

Gene analysis of genomic DNA from stored serum by polymerase chain reaction: identification of three missense mutations in patients with cholinesterasemia and ABO genotyping.

M. Tomita, Y. Watanabe, N. Ueda, 2001, Clinica chimica acta; international journal of clinical chemistry.

HB Ube-2 (α68[E-17]ASN→ASP): The Second Instance in Japan

S. Shimasaki, S. Shibata, S. Ueda, 1981 .

Hemoglobin Takamatsu (β120 (GH 3) Lys → Gln): A New Abnormal Hemoglobin Detected in Three Unrelated Families in the Takamatsu Area of Shikoku

S. Shimasaki, T. Uchida, S. Shibata, 1980 .

Identification of a point mutation associated with a silent phenotype of human serum butyrylcholinesterase--a case of familial cholinesterasemia.

M. Maeda, N. Sakamoto, K. Hidaka, 1998, Clinica chimica acta; international journal of clinical chemistry.

Abnormal hemoglobins in the Takamatsu district with emphasis on epidemiological characteristics.

S. Shimasaki, S. Shibata, S. Ueda, 1982, Hemoglobin.

Genetic analysis of a Japanese patient with butyrylcholinesterase deficiency

K. Iwasaki, M. Tomita, Y. Watanabe, 1997, Annals of human genetics.

Hemoglobin Hoshida (343 (CD-2) Glu → Gln), a New Hemoglobin Variant Discovered in Japan

S. Shibata, S. Ueda, K. Hidaka, 1978 .

Hemoglobin G Taichung (alpha 74 aspartic acid replaced by histidine) heterozygotes found in two Japanese families.

S. Shibata, S. Ueda, K. Hidaka, 1978, Hemoglobin.

Nonsense mutation in exon 2 of the butyrylcholinesterase gene: a case of familial cholinesterasemia.

N. Ueda, K. Hidaka, I. Iuchi, 1997, Clinica chimica acta; international journal of clinical chemistry.

Hb Fukutomi [alpha 126(H9)Asp----Val]: a new hemoglobin variant with high oxygen affinity.

K. Yaguchi, T. Kobayashi, K. Hidaka, 1990, Hemoglobin.

First case of missense mutation (LDH-H:R171P) in exon 4 of the lactate dehydrogenase gene detected in a Japanese patient

Yoko Watanabe, N. Ueda, K. Hidaka, 1999, Journal of Human Genetics.

Hemoglobin J Bangkok (β56 [D7]Gly → Asp) : A Hemoglobin Variant Discovered by the Hemoglobinopathy Survey in Takamatsu District

S. Shimasaki, S. Shibata, S. Ueda, 1981 .

The Survey of Abnormal Hemoglobins in the Kobe District: HB G-Coushatta [β22(B4)GLU→ALA], HB Ankara [β10(A7)ALA→ASP], HB Handa [α90(FG2)LYS→MET], and HB J-HABANA [α71(E20)ALA→GLU]

S. Shimasaki, A. Tohdoh, M. Matsuo, 1986 .

Identification of missense mutation (G365R) of the butyrylcholinesterase (BCHE) gene in a Japanese patient with familial cholinesterasemia.

Y. Watanabe, K. Sakaguchi, T. Maeda, 2001, The Kobe journal of medical sciences.

HB Fukuyama [β77(EF1)HIS→TYR]: A New Abnormal Hemoglobin Discovered in a Japanese

H. Nakahara, K. Miyake, K. Hidaka, 1988 .

Hb Ube-4 (alpha 116 Glu leads to Ala): a second independent instance found in a Korean family of Japan.

S. Shibata, S. Ueda, K. Hidaka, 1978, Hemoglobin.

Kobe University Repository : Kernel タイトル Tit le Ident ificat ion of missense mutat ion ( G 365 R ) of the Butyrylcholinesterase ( BChE ) gene in a Japanese pat ient with familial cholinesterasemia 著者

K. Sakaguchi, T. Maeda, T. Fujisawa, 2019 .