I. Iuchi

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.

Characterization of Hb Ube-4: alpha 116 (GH4) Glu yield Ala.

T. Miyaji, Y. Ohba, I. Iuchi, 1978, Hemoglobin.

Characterization of a red minor component of abnormal hemoglobin found in Hb M Hyde Park disease.

S. Shibata, I. Iuchi, 1977, Hemoglobin.

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

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

An improved diacetylmonoxime method for the determination of urea in blood and urine.

I. Iuchi, M. Kitamura, 1959, Clinica chimica acta; international journal of clinical chemistry.

A new method for the examination of melituria: separation and identification of urinary sugars by means of paper electrophoresis at high potential gradient.

S. Shibata, I. Iuchi, 1960, Clinica chimica acta; international journal of clinical chemistry.

Diffuse palmoplantar keratoderma with deafness.

A. Hatamochi, H. Ueki, S. Nakagawa, 1982, Archives of Dermatology.

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 YUSA (β21 (B3) Asp → Tyr), A New Abnormal Hemoglobin Found in Japan

S. Shibata, S. Ueda, K. Harano, 1981 .

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

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

Haemoglobin Hiroshima and the mechanism of the alkaline Bohr effect.

M. Perutz, J. Kilmartin, L. T. Eyck, 1971, Nature: New biology.

Hemoglobin Tochigi (β56-59 Deleted) A New Unstable Hemoglobin Discovered in a Japanese Family

Kaneo Yamada, N. Shinkai, S. Shibata, 1970 .

Hemoglobin Hiroshima (beta-143 histidine--aspartic acid): a newly identified fast moving beta chain variant associated with increased oxygen affinity and compensatory erythremia.

S. Shibata, T. Miyaji, H. Hamilton, 1969, The Journal of clinical investigation.

Hemoglobin Hijiyama: A New Fast-Moving Hemoglobin in a Japanese Family

S. Shibata, T. Miyaji, H. Hamilton, 1968, Science.

Japanese Haemoglobin Variant

S. Shibata, T. Miyaji, Y. Ohba, 1968, Nature.

A New Type of Hereditary Nigremia Discovered in Akita-Hemoglobin M Hyde Park Disease

S. Shibata, T. Miyaji, Y. Ohba, 1967 .

Hemoglobin hikari (α2Aβ261AspNH2: A fast-moving hemoglobin found in two unrelated japanese families

S. Shibata, T. Miyaji, S. Ueda, 1964 .

The First Instance of Hemoglobin E in a Japanese Family

S. Shibata, H. Hamilton, I. Iuchi, 1964 .

Characterization of alpha23GluNH2 in hemoglobin Memphis. Hemoglobin Memphis/S, a new variant of molecular disease.

A. Kraus, T. Miyaji, L. Kraus, 1966, Biochemistry.

A Consanguineous Kindred of Serum Pseudocholinesterase Anomaly found in Japan

S. Shibata, I. Iuchi, Y. Hashimoto, 1967 .

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.

HEMOLYTIC DISEASE ASSOCIATED WITH THE PRODUCTION OF ABNORMAL HEMOGLOBIN AND INTRAERYTHROCYTIC HEINZ BODIES.

S. Shibata, T. Miyaji, S. Ueda, 1963, Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society.

Benzidine-positive Pigments in Serum of Patients with Sickle Cell Anemia During Painful Crises

L. W. Diggs, I. Iuchi, J. Upshaw, 1964 .

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

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

Hemoglobin M1: Demonstration of a New Abnormal Hemoglobin in Hereditary Nigremia.

S. Shibata, A. Tamura, I. Iuchi, 1960 .

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.

Amino acid substitution of hemoglobin Ube 2 (alpha-2 68asp beta-2): an example of successful application of partial hydrolysis of peptide with 5 per cent acetic acid.

S. Shibata, T. Miyaji, Y. Ohba, 1967, Clinica chimica acta; international journal of clinical chemistry.

EFFECT OF ERYTHROPOIETIN UPON HEMOGLOBIN BIOSYNTHESIS *

L. Kraus, I. Iuchi, Brother Thomas Kraus, 1968, Annals of the New York Academy of Sciences.

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 .

Occurrence of Hemoglobin G Cousha in Japan

T. Miyaji, Y. Ohba, I. Iuchi, 1978 .

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 .