Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Kesami Minemura"'
Publikováno v:
Endocrine Journal. 66:193-198
There is a great deal of research interest regarding the underlying causes of slightly elevated TSH values in patients with subclinical hypothyroidism (SH) without abnormal findings on ultrasonography or anti-thyroid antibodies. Twelve infertile wome
Publikováno v:
Pathology International. 66:102-107
A 63-year-old male with a previous infection was admitted to our hospital because of acute pancreatitis. Although he had no history of diabetes mellitus, laboratory examinations revealed marked hyperglycemia on admission, and intensive insulin treatm
Publikováno v:
Endocrine. 23:45-50
Multiple endocrine neoplasia type 1 (MEN1) is an hereditary tumor syndrome that involves specific endocrine organs such as parathyroids, anterior pituitary gland, and endocrine pancreas. The responsible gene for this syndrome, MEN1, has been isolated
Autor:
Kunihide Hiramatsu, Mieko Kumagai, Kesami Minemura, Yasuto Ikeo, Kiyoshi Hashizume, Takeshi Inagaki, Wataru Yumita, Satoru Suzuki, Tpru Aizawa
Publikováno v:
Endocrine Journal. 48:363-367
We report a case of an ectopic ACTH-producing carcinoid in the lung. Typical Cushingoid appearance, elevated plasma ACTH and serum cortisol, bilateral enlargement of the adrenal glands, absence of pituitary adenoma and negativity in petrosus sinus ve
Autor:
Keiko Minemura, Rosario Leopardi, Leslie J. DeGroot, Takeshi Nagasawa, Teiji Takeda, Rusheng Zhang, Kesami Minemura
Publikováno v:
Endocrinology. 141:1814-1822
Herpes simplex virus thymidine kinase (HSVtk) gene transfer followed by ganciclovir administration is a common strategy for experimental cancer therapy. To evaluate the feasibility of using the human calcitonin promoter to target medullary thyroid ca
Publikováno v:
Endocrinology. 139:601-608
We have evaluated the feasibility of gene transduction using replication-defective adenovirus vector as a novel therapy for medullary thyroid carcinoma (MTC), a thyroid C cell neoplasm. Replication-defective adenoviruses were constructed to express m
Novel 14 Base-Pair Deletion of the MEN1 Gene in a Patient with Recurrent Primary Hyperparathyroidism
Autor:
Kiyoshi Hashizume, Miyuki Katai, Yoshimitsu Fukushima, Kesami Minemura, Akihiro Sakurai, Shinya Uchino
Publikováno v:
Japanese Journal of Clinical Oncology. 36:395-397
MEN1 is the causative gene for multiple endocrine neoplasia type 1 (MEN1), a hereditary syndrome characterized by hyperplastic and neoplastic disorder of endocrine organs such as parathyroid, anterior pituitary and gastroenteropancreatic endocrine ti
Autor:
Hidehumi Inaba, Takahide Miyamoto, Kazuo Ichikawa, Leslie J. DeGroot, Yosuke Imai, Satoru Suzuki, Teiji Takeda, Tomoko Kakizawa, Kiyoshi Hashizume, Masanori Yamazaki, Jun-ichirou Mori, Kesami Minemura
Publikováno v:
Cancer gene therapy. 9(10)
Recombinant adenoviruses, carrying herpes simplex virus thymidine kinase (HSVtk) genes, were developed to evaluate the possibility of tissue-specific gene therapy for thyroid carcinomas. The HSVtk gene was driven by a minimal thyroglobulin (TG) promo
Autor:
Satoru Suzuki, Akihiro Sakurai, Kiyoshi Hashizume, Kesami Minemura, Koh Yamashita, Yasuto Ikeo, Wataru Yumita, Yumiko Uehara
Publikováno v:
Endocrine journal. 48(4)
We report the kindred with familial isolated hyperparathyroidism with parathyroid cancer. The proband was diagnosed as having primary hyperparathyroidism at age 43. The same disorder was also found in his daughter who had low bone mass. His son was f
Autor:
Naomi Suzuki, Satoshi Shigematsu, Nobuo Itoh, Masahiro Hara, Kesami Minemura, Kazuo Ichikawa, Kunihide Hiramatsu, Hiroaki Kobayashi, Kiyoshi Hashizume
Publikováno v:
Internal medicine (Tokyo, Japan). 40(9)
A 45-year-old male was admitted because of chest pain, lumbago, and bilateral ankle pain. Examination disclosed hypophosphatemic osteomalacia, acquired Fanconi syndrome, and abnormalities in distal nephron such as distal renal tubular acidosis and re