K Miyai

Koshien University — Japan

Medicine · Health Sciences

43h-index7.0kcitations346works0.02yr avg
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Research Topics

Thyroid Disorders and Treatments(140), Growth Hormone and Insulin-like Growth Factors(72), Pituitary Gland Disorders and Treatments(26), Monoclonal and Polyclonal Antibodies Research(16), Hypothalamic control of reproductive hormones(14)

Publications346 total

Suppression of Thyroid Function during Ingestion of Seaweed "Kombu" (Laminaria japonoca) in Normal Japanese Adults
Endocrine Journal·2008· 79 citedOpen Access
Congenital Thyrotropin Deficiency-From Discovery to Molecular Biology, Postgenome and Preventive Medicine-
Endocrine Journal·2007· 28 citedOpen Access
Analysis of the Three Dimensional Structure of the CXGXC Motif in the CMGCC and CAGYC Regions of .ALPHA.-and .BETA.-Subunits of Human Chorionic Gonadotropin: Importance of Glycine Residue (G) in the Motif
Endocrine Journal·2006· 3 cited
Further Studies on Episodic Occurrence of Congenital Dysgenetic Hypothyroidism in Osaka, Japan
Endocrine Journal·2005· 22 citedOpen Access
Development of a radiotransporter assay for determination of iodide: preliminary studies
Clinica Chimica Acta·2003
Clinical chemistry, 50 Years of History, Progress into the New Millennium-an Asian Perspective, on a Global Theme-
TRENDS IN THE SCIENCES·2003Open Access
An Improved Method for Measurement of Urinary Iodide Using an Ion Electrode
Medical Entomology and Zoology·2000· 2 cited
Genetic Basis of Congenital Hypothyroidism: Abnormalities in the <i>TSHβ</i> Gene, the <i>PIT1</i> Gene, and the <i>NIS</i> Gene
Clinical Chemistry and Laboratory Medicine (CCLM)·1998· 15 cited
Evaluation of Highly Sensitive Thyrotropin Assay for Detecting Thyroid Diseases in Neonatal Screening: Preliminary Studies.
Endocrine Journal·1998· 5 citedOpen Access
Effect of Site Directed Mutagenesis in the CMGCC Region of the .ALPHA.-Subunit on Immunoreactive Human Thyrotropin.
Endocrine Journal·1998· 5 citedOpen Access
Loss of biological activity due to Glu→Arg mutation at residue 11 of the B subunit of cholera toxin
Microbial Pathogenesis·1997· 2 cited
A novel test for fecal occult blood by the hybridization method with specific human deoxyribonucleic acid in leucocytes: preliminary experiment
Clinica Chimica Acta·1997
Congenital hypothyroidism caused by a mutation in the Na+/l− symporter
Nature Genetics·1997· 161 cited
[Intra-individual and seasonal variations of thyroid function tests in healthy subjects].
PubMed·1996· 2 cited
Loss of biological activity of human chorionic gonadotropin (hCG) by the amino acid substitution on the “CMGCC” region of the α-subunit
Molecular and Cellular Endocrinology·1994· 13 cited
[Molecular genetics of congenital isolated thyrotropin deficiency].
PubMed·1994· 1 cited
Molecular Pathology of Congenital Pituitary Hypothyroidism
Clinical Pediatric Endocrinology·1994Open Access
[Molecular pathology of congenital pituitary hypothyroidism--discovery of new clinical entities].
PubMed·1993· 1 cited
Gestational thyrotoxicosis and hyperemesis gravidarum: possible role of hCG with higher stimulating activity
Clinical Endocrinology·1993· 155 cited
Congenital deficiency of thyrotropin
1993· 2 cited
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Frequent Co-authors

Nobuyuki Amino(33), Y Kumahara(19), Osamu Tanizawa(17), Yoshinori Iwatani(11), Kiyoshi Ichihara(7), Haruo Tamaki(6), H Mori(5), Nobuaki Mitsuda(5), T. Yamamoto(4), M Azukizawa(4), YUKIKO YABU(4), H Tamaki(4), Toshio Onishi(4), Junko Tachi(4), T Kaneda(4), Kaichiro Ishibashi(3), Tokuzo Harada(3), Motoko Kimura(3), Mieko Aozasa(3), Ke-ita Tatsumi(3)