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[Publications] Muller J,Gondos B,Kosugi S,Mori T,Shenker A: "Severe testotoxicosis phenotype associated with a strongly activating mutation of the lutropin receptor." J Med Genet. 35. 340-341 (1998)
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[Publications] Kosugi S,Mori T,Shenker A: "An anionic residue at position 564 is important for maintaining the inactive conformation of the human lutropin/choriogonadotropin receptor." Mol Pharmacol. 53. 894-901 (1998)
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[Publications] Kosugi S,Inoue O,Matsuda A,Jhiang SM.: "Novel,missense and loss-of-function mutations in the sodium/iodide symporter gene causing iodide transport defect in three Japanese patients." J Clin Endocrinol Metab. 83. 3373-3376 (1998)
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[Publications] Kosugi S,Sato Y,Matsuda A,Chyama Y,Fujieda K,Inomata H,Kameya T,Isozaki O,Jhiang SM: "High prevalence of T354P sodium/iodide symporter gene mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures." J Clin Endocrinol Metab. 83. 4123-4129 (1998)
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[Publications] Yoshida A,Sasaki N,Mori A,Taniguchi S,Ueta Y,Hattori K,Tanaka Y,Igawa O,Tuboi M,Sugawa H,Sato R,Hisatome I,Shigemasa C,Grollman EF,Kosugi S.: "Differences in the electrophysiological response to I^- and the inhibotory anions SCN^- and ClO_4^- studies in FRTL-5 cells." Biochim Biophys Acta. 1414. 231-237 (1998)
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[Publications] Miyauchi A,Futami H,Hai N,Yokozawa T,Kuma K,Aoki N,Kosugi S,Sugano K,Yamaguchi K.: "Two germline missense mutations at codons 804 and 806 of the RET protooncogene in the same allele in a patient with multiple neoplasia type 2B without codon 918 mutation." Jpn J Cancer Res. 90. 1-5 (1999)
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[Publications] Sugawa H,Ueda Y,Ueda M,Kosugi S,Ichiyama S,Mori T: "Immunization with the “immunogenic peptide"of TSH receptor induces oligoclonal antibodies with various biological activities." Peptides. 19. 1303-1307 (1998)
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[Publications] Sugawa H,Ueda M,Matsuda A,Hai A,Yoshida A,Kosugi S: "Lack of measurable maximal capacity of inorganic iodide pool in non-thyroid cell." International Journal Thyroidology Clinical and Experimental.(in press). (1998)
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[Publications] Hai N,Aoki N,Matsuda A,Mori T,Kosugi S.: "Germline mutations in the MEN1 gene in 30 Japanese patients with multiple endocrine neoplasia type 1(MEN1):clinical features of MEN1 phenocopy." J Clin Endocrinol Metab.(in press). (1999)
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[Publications] Sawada H,Inoue S,Sugimoto T,Nagamachi S,Kosugi S.: "Sisters with iodide transport defect caused by a mutation of NIS gene not found by the neonatal mass screening for cretinism." J Pediatric Endocrinol. (in press). (1999)
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[Publications] 小杉眞司: "ヨード濃縮障害におけるヨードトランスポータ遺伝子変異。" Molecular Medicine. 35. 96-102 (1998)
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[Publications] 小杉眞司: "甲状腺のヨード摂取機構。" 遺伝子医学. 2. 63-67 (1998)
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[Publications] 小杉眞司: "TSH受容体遺伝子変異による疾患。" 日本臨床(受容体研究の進歩と臨床、ReceptorとSignal Transduction,V_o受容体異常症、シグナル伝達異常症の臨床分子遺伝学). 56. 210-214 (1998)
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[Publications] 小杉眞司: "甲状腺機能に対する喫煙産物の影響-チオサイアネートのナトリウム・ヨードシンポーターに対する影響-" 平成9年度喫煙科学研究財団研究年報. 578-583 (1998)
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[Publications] 小杉眞司: "Na/lシンポータの発見:構造と機能。特集:分子甲状腺学の進歩。" ホルモンと臨床. (印刷中). (1999)
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[Publications] 小杉眞司: "遺伝医学的診断法:分子医学的診断法。" 臨床総合月刊誌「臨床医」. 25(印刷中). (1999)
