K. Takeda

发表

Two Mutations in Thyroid Hormone Receptor Beta Gene (P453A and C36Y) in a Family with Resistance to Thyroid Hormone with Comorbid Myotonic Dystrophy.

R. Sakuta, Y. Hayashi, K. Nemoto, 2019, Thyroid : official journal of the American Thyroid Association.

Regulatory Role of the GTP‐Binding Protein, Go, in the Mechanism of Exocytosis in Adrenal Chromaffin Cells

K. Kameyama, K. Kumakura, K. Takeda, 1992, Journal of neurochemistry.

Free thyroxine concentrations in serum measured by equilibrium dialysis in chronic renal failure.

N. Terao, S. Nakamura, K. Chikamori, 1996, Clinical chemistry.

Recessive inheritance of thyroid hormone resistance caused by complete deletion of the protein-coding region of the thyroid hormone receptor-beta gene.

S. Refetoff, L. Degroot, K. Takeda, 1992, The Journal of clinical endocrinology and metabolism.

Evaluation of Subclinical Hypothyroidism and Subclinical Hyperthyroidism in Medical Checkups during the Ten Year Period

Seiju Sasaki, K. Takeda, K. Masuda, 2017 .

A mutation causing reduced biological activity and stability of thyroxine-binding globulin probably as a result of abnormal glycosylation of the molecule.

G. Bell, Y. Murata, S. Refetoff, 1989, Molecular endocrinology.

Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation.

G. Bell, Y. Hayashi, R. Weiss, 1993, Molecular endocrinology.

Absence of p53 mutation in Japanese patients with malignant thyroid lymphoma

F. Matsuzuka, K. Kuma, K. Takeda, 1994, Journal of endocrinological investigation.

Increased Insulin Sensitivity in Gsα Knockout Mice*

Min Chen, L. Weinstein, K. Takeda, 2001, The Journal of Biological Chemistry.

Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor beta.

S. Seino, G. Bell, K. Ain, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Molecular basis for the properties of the thyroxine-binding globulin-slow variant in American Blacks

S. Refetoff, K. Takeda, T. Pullman, 1990, Journal of endocrinological investigation.

Replacement of Leu227 by Pro in thyroxine-binding globulin (TBG) is associated with complete TBG deficiency in three of eight families with this inherited defect.

S. Refetoff, K. Takeda, M. Charbonneau, 1990, The Journal of clinical endocrinology and metabolism.

Sequence of the variant thyroxine-binding globulin of Australian aborigines. Only one of two amino acid replacements is responsible for its altered properties.

G. Bell, S. Refetoff, K. Takeda, 1989, The Journal of clinical investigation.

Molecular basis of inherited thyroxine-binding globulin defects

R. Weiss, S. Refetoff, K. Takeda, 1992, Trends in Endocrinology & Metabolism.

Sequence of the variant thyroxine-binding globulin (TBG) in a Montreal family with partial TBG deficiency

S. Refetoff, K. Takeda, O. Janssen, 1991, Human Genetics.

Complete thyroxine-binding globulin (TBG) deficiency caused by a single nucleotide deletion in the TBG gene.

S. Refetoff, K. Takeda, O. Janssen, 1991, Metabolism: clinical and experimental.

Screening of nineteen unrelated families with generalized resistance to thyroid hormone for known point mutations in the thyroid hormone receptor beta gene and the detection of a new mutation.

S. Refetoff, L. Degroot, K. Takeda, 1991, The Journal of clinical investigation.

Revised Guidelines for Neonatal Screening Programmes for Primary Congenital Hypothyroidism

R. Fahlbusch, N. Skakkebæk, H. Dörr, 1999, Hormone Research in Paediatrics.

Sequencing of the variant thyroxine-binding globulin (TBG)-Quebec reveals two nucleotide substitutions.

S. Refetoff, K. Takeda, R. Bertenshaw, 1991, American journal of human genetics.

Mutations in Exon 7 of the GTP-Binding Protein Ga s Not a Common Cause of Pseudohypoparathyroidism Aibright's Hereditary Osteodystrophy in Japanese

K. Takeda, Yokoyama, Kozo, 2006 .

Mutations in exon 7 of the GTP-binding protein Gs alpha were not a common cause of pseudohypoparathyroidism with Albright's hereditary osteodystrophy in Japanese.

T. Shimizu, K. Takeda, M. Sasaki, 1997, Endocrine journal.

A 4-base pair deletion mutation of Gsα gene in a Japanese patient with pseudohypoparathyroidism

K. Takeda, T. Okabayashi, K. Hashimoto, 1996 .

Pituitary Adenoma Showing Intermittent Secretion of High Molecular Weight Adrenocorticotropin without Evidence of Cushing’s Disease

K. Hashimoto, K. Takeda, K. Asaba, 1999, Hormone Research in Paediatrics.

Evaluation of a new rapid and fully automated electrochemiluminescence immunoassay for thyrotropin receptor autoantibodies.

A. Miyauchi, S. Morita, N. Amino, 2008, Thyroid : official journal of the American Thyroid Association.

A novel mutation causing complete deficiency of thyroxine binding globulin

I. Hisatome, I. Manabe, S. Taniguchi, 1997, Clinical endocrinology.

Rapid localization of mutations in the thyroid hormone receptor-beta gene by denaturing gradient gel electrophoresis in 18 families with thyroid hormone resistance.

R. Weiss, S. Refetoff, K. Takeda, 1992, The Journal of clinical endocrinology and metabolism.

Free thyroxine concentrationsin serum measured by equilibriumdialysisin chronic renal failure

N. Terao, K. Takeda, M. Kawada, 1996 .

Thieno[3,4-c]pyrrole-incorporated quinoidal terthiophene with dicyanomethylene termini: synthesis, characterization, and redox properties

I. Osaka, K. Takimiya, E. Miyazaki, 2010 .

Effects of pertussis toxin on the affinity of exocytosis for Ca2+ in bovine adrenal chromaffin cells

K. Kumakura, K. Takeda, M. Ohara-Imaizumi, 1990, Neuroscience Letters.

Thyroxine-binding globulin: organization of the gene and variants.

Y. Hayashi, Y. Murata, S. Refetoff, 1996, Hormone research.

Gene screening in Japanese families with complete deficiency of thyroxine‐binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation

S. Refetoff, K. Takeda, Y. Kubo, 1994, Clinical endocrinology.

Increased insulin sensitivity in Gsalpha knockout mice.

L. Weinstein, K. Takeda, A. Castle, 2001, The Journal of biological chemistry.

Evaluated reference intervals for serum free thyroxine and thyrotropin using the conventional outliner rejection test without regard to presence of thyroid antibodies and prevalence of thyroid dysfunction in Japanese subjects.

K. Takeda, S. Hiramatsu, H. Sugiura, 2009, Endocrine journal.

A 4-base pair deletion mutation of Gs alpha gene in a Japanese patient with pseudohypoparathyroidism.

K. Takeda, T. Okabayashi, K. Hashimoto, 1996, Journal of Endocrinological Investigation.

Proposal of a fatigue life prediction method for RC slabs failed under traveling wheel-type load test

Yasuhiko Sato, Kyoko Takeda, Natsuko Hamada, 2018, Journal of Asian Concrete Federation.

[Increased serum soluble Fas ligand in hyperthyroid Graves' disease].

K. Takeda, M. Sasaki, K. Hashimoto, 1999, Rinsho byori. The Japanese journal of clinical pathology.