緒方 勤 業績リスト 深見 真紀 業績リスト 筒井 和義 業績リスト

 緒方 勤 業績リスト

2015年

原著論文(英文)総数21編
Kagami M, Kurosawa K, Miyazaki O, Ishino F, Matsuoka K and *Ogata T.
Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome).
Eur J Hum Genet, 2015 (in press)

2014年

原著論文(英文)総数26編
Nagata E, Kano H, Kato F, Yamaguchi R, Nakashima S, Takayams S, Kosaki R, Tonoki H, Mizuno S, Watanabe S, Yoshiura K, Kosho T, Hasegawa T, Kimizuka M, Suzuki A, Shimizu K, Ohashi H, Haga N, Numabe H, Horii E, Nagai T, Yoshihashi H, Nishimura G, Toda T, Takada S, Yokoyama S, Asahara H, Sano S, Fukami M, Ikegawa S and *Ogata T.
Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gallop-Wolfgang complex.
Orphanet J Rare Dis, 9, 125, 2014
Kato F, Hamajima T, Hasegawa T, Amano N, Horikawa R, Nishimura G, Nakashima S, Fuke T, Sano S, Fukami M and *Ogata T.
IMAGe syndrome: clinical and genetic implications based on Iinvestigations in three Japanese patients.
Clin Endocrinol, 80, 706-713, 2014

2013年

原著論文(英文)総数17編
Fukami M, Homma K, Hasegawa T and *Ogata T.
Backdoor pathway for dihydrotestosterone biosynthesis: implications for normal and abnormal human sex development.
Dev Dyn, 242, 320-329, 2013

2012年

原著論文(英文)総数21編
Hiura H, Okae H, Miyauchi N, Sato F, Sato A, Van De Pette M, John RM, Kagami M, Nakai K, Soejima H, Ogata T and Arima T.
Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies.
Hum Reprod., 2012 (in press)
Qin X-Y., Kojima Y., Mizuno K., Ueoka K., Massart F., Spinelli C., Zaha H., Okura M., Yoshinaga J., Yonemoto J., Kohri K, Hayashi Y, Ogata T and Sone H.
Association of variants in genes involved in environmental chemical metabolism and risk of cryptorchidism and hypospadias.
J Hum Genet.,57, 434-441, 2012
Ogata T, Fumaki M, Yoshida R, Nagata E, Fujisawa Y, Yoshida A and Yoshimura Y.
Haplotype analysis of ESR2 in Japanese patients with spermatogenic failure.
J Hum Genet, 57, 449-452, 2012
Fumaki M, Tsuchiya T, Takada S, Kanbara A, Asahara H, Igarashi A, Kamiyama Y, Nishimura G and Ogata T.
Complex genomic rearrangements in the SOX9 5' region in a patient with Pierre Robin sequence and hypoplastic left scapula.
Am J Med Genet A, 158A, 1529-1534, 2012
Miyado M, Nakamura M, Miyado K, Morohashi K, Sano S, Nagata E, Fukami M and *Ogata T.
Mamld1 deficiency significantly reduces mRNA expression levels of multiple genes expressed in mouse fetal Leydig cells but permits normal genital and reproductive development.
Endocrinology, 153, 6033-6040, 2012
Qin X-Y, Miyado M, Kojima Y, Zaha H, Akanuma H, Zeng Q, Yoshinaga J, Yonemoto J, Fumaki M, Ogata T and Sone H.
Identification of novel low-dose bisphenol a targets in human foreskin fibroblast cells derived from hypospadias patients.
PLoS ONE, 7, e36711, 2012
Kalfa N, Fumaki M, Philibert P, Audran F, Pienkowski C, Weill G, Pinto C, Manouvrier S, Polak M, Ogata T and C Sultan C.
Screening of MAMLD1 mutations in 70 Children with 46,XY DSD: Identification and functional analysis of two new mutations.
PLoS One, 7, e32505, 2012
Sekii K, Ishikawa T, Ogata T, Itoh H and Iwashima S.
Fetal myocardial tissue Doppler indices before birth physiologically change in proportion to body size adjusted for gestational age in low-risk term pregnancies.
Early Hum Dev., 88, 517-523 2012
Koyama Y, Homma K, Fumaki M, Miwa M, Ikeda K, Ogata T, Hasegawa T and Murata M.
Two-step biochemical differential diagnosis of classical 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants using uUrinary Pregnanetriolone / Tetrahydroxycortisone Ratio and 11β-hydroxyandrosterone by Gas chromatography - mass spectrometry.
Clin Chem., 58, 741-747, 2012
Abe Y, Aoki Y, Kuriyama S, Kawame H, Okamoto N, Kurosawa K, Ohashi H, Mizuno S, Ogata T, Kure S, Niihori T and Matsubara Y.
Prevalence and clinical features of Costello syndrome and cardio-facio-cutaneous syndrome in Japan: Findings from a nationwide epidemiological survey.
Am J Med Genet A., 158A, 1083-1094, 2012
Stoppa-Vaucher S, Ayabe T, Paquette J, Patey N, Francoeur D, Vuissoz J-M, Deladoëy J, Samuels ME, Ogata T and Deal CL.
46, XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicism.
Clin Genet., 82, 505-513, 2012
Fuke-Sato T, Yamazawa K, Nakabayashi K, Matsubara K, Matsuoka K, Hasegawa T, Dobashi K and Ogata T.
Mosaic upd(7)mat in a patient with Silver-Russell syndrome: correlation between phenotype and mosaic ratio in the body and the placenta.
Am J Med Genet A., 158A, 465-468, 2012
Oto Y, Obata K, Matsubara K, Kozu Y, Tsuchiya T, Sakazume S, Yoshino A, Murakami N, Ogata T and Nagai T.
Growth hormone secretion and its effect on height in pediatric patients with different genotypes of Prader-Willi syndrome.
Am J Med Genet A., 158A, 1477-1480, 2012
Kagami M, Kato F, Matsubara K, Sato T, Nishimura G Ogata T.
Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype.
Eur J Hum Genet., 20, 928-932, 2012
Sugihara S, Ogata T, Kawamura T, Urakami T, Takemoto K, Kikuchi N, Takubo N, Tsubouchi K, Horikawa R, Kobayashi K, Kasahara Y, Kikuchi T, Koike A, Mochizuki T, Minamitani K, Takaya R, Mochizuki H, Nishii A, Yokota I, Kizaki Y, Mori T, Shimura N, Mukai T, Matsuura N, Fujisawa T, Ihara K, Kosaka K, Kizu R, Takahashi T, Matsuo S, Hanaki K, Igarashi Y, Sasaki G, Soneda S, Teno S, Kanzaki S, Saji H, Tokunaga K and Amemiya S.
The Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT): Genetic characteristics on HLA-cass II and class I among Japanese type 1A and type 1B diabetic children and their families.
Pediatr Diabetes., 13, 33-44, 2012
Inoue H, Mukai T, Sakamoto Y, Kimura C, Kangawa N, Itakura M, Ogata T, Ito Y and Fujieda K.
Identification of a novel mutation in the exon 2 splice donor site of the POU1F1/PIT-1 gene in Japanese identical twins with mild combined pituitary hormone deficiency.
Clin Endocrinol., 76, 78-87, 2012
総説論文(英文)
Ogata T, Sano S, Nagata E, kato F and Fumaki M.
MAMLD1 and 46,XY disorders of sex development.
Seminars in Reproductive Medicine,30, 410-416, 2012
Fumaki M, Shozu M and Ogata T.
Molecular bases and phenotypic determinants of aromatase excess syndrome.
Int J Endocrinol., 584807, 2012
総説論文(和文)
緒方勤
「性分化疾患」
臨床と研究(特集:小児診療のピットフォールII) 89 (5), 53-58, 2012
緒方勤
「SHOX遺伝子半量不全に起因する低身長:診断・治療アップデート」Pediatric Endocrinology Reviews抄訳シリーズ
ジャパンメディアートパブリッシング No.30, 1-2, 2012
緒方勤
「原発性性線機能低下症」大関武彦、古川漸、横田俊一郎、水口雅、今日の小児治療指針15版
医学書院 244-245, 2012

2011年

Kalfa N, Cassorla F, Audran F, Abdennabi OI, Philibert P, Béroud C, Guys JM, Reynaud R, Alessandrini P, Wagner K, Bréaud J, Valla JS, Morisson Lacombe G, Daures JP, Baskin L, Fumaki M, Ogata T and Sultan C.
Polymorphisms of MAMLD1 gene in hypospadias.
J Pediatr Urol., 7, 585-591, 2011
Ayabe T, Ishizuka B, Maruyama T, Uchida H, Yoshimura Y, Yoshida R, Fumaki M, Nagai T and Ogata T.
Association of primary ovarian insufficiency with a specific HLA haplotype (A*24:02-C*03:03-B*35:01) in Japanese patients.
Sex Dev., 5, 235-240, 2011
Ishizuka B, Okamoto N, Hamada N, Sugishita Y, Saito J, Takahashi N, Ogata T and Itoh MT.
Number of CGG repeats in the FMR1 gene of Japanese patients with primary ovarian insufficiency.
Fertil Steril., 96, 1170-1174, 2011
Soneda S, Yazawa T, Fumaki M, Adachi M, Mizota M, Fujieda K, Miyamoto K and Ogata T.
Proximal promoter of the cytochrome P450 oxidoreductase gene: identification of microdeletions involving the untranslated exon 1 and critical function of the SP1 binding site.
J Clin Endocrinol Metab., 96, E1881-1887, 2011
Inoue H, Sakamoto Y, Kangawa N, Kimura C, Ogata T, Fujieda K, Qian, ZR, SanoT and Itakura M.
Analysis of expression and structure of the rat GH secretagogue/ghrelin receptor (Ghsr) gene: roles of epigenetic modifications in transcriptional regulation.
Mol Cell Endocrinol., 345, 1-15, 2011
Nakabayashi K, Trujillo AM, Tayama C, Camprubi C, Yoshida W, Lapunzina P, Sanchez A, Soejima H, Aburatani H, Nagae G, Ogata T, Hata K and Monk D.
Methylation screening of reciprocal genome-wide UPDs identifies novel human specific imprinted genes.
Hum Mol Genet., 20, 3188-97, 2011
Matsubara K, Murakami N, Nagai T and Ogata T.
Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors.
J Hum Genet., 56, 566-71, 2011
Nakamura M, Fumaki M, Sugawa F, Miyado M, Nonomura K and Ogata T.
Mamld1 knockdown reduces testosterone production and Cyp17a1 expression in mouse Leydig tumor cells.
PLoS ONE, 6, e19123, 2011
Ogata T and Matsubara K.
Steroid 5α-reductase-2 deficiency and fertility.
Fertil Steril., 95, e46, 2011
Fumaki M, Shozu M, Soneda S, Kato F, Inagaki A, Takagi H, Hanaki K, Kanzaki S, Ohyama K, Sano T, Nishigaki T, Yokoya S, Binder G, Horikawa R and Ogata T.
Aromatase excess syndrome: identification of cryptic duplications and deletions leading to gain-of-function of CYP19A1 and assessment of phenotypic determinants.
J Clin Endocrinol Metab., 96, E1035-1043, 2011
Miyazaki O, Nishimura G, Kagami M and Ogata T.
Radiological evaluation of dysmorphic thorax in paternal uniparental disomy for chromosome 14.
Ped Radiol., 41, 1013-1019, 2011
Brandão MP, Costa EM, Fukami M, Gerdulo M, Pereira NP, Domenice S, Ogata T and Mendonca BB.
MAMLD1 (Mastermind-Like Domain Containing 1) Homozygous Gain-of-Function Missense Mutation Causing 46,XX Disorder of Sex Development in a Virilized Female.
Adv Exp Med Biol., 707, 129-31, 2011
Dateki S, Fukami M, Tanaka Y, Sasaki G, Moriuchi H and Ogata T.
Identification of chromosome 15q terminal deletion with telomere sequences and its bearing on genotype-phenotype analysis.
Endocr J., 58, 155-159, 2011
Fukami M, Muroya K, Miyake T, Iso M, Yokoi H, Suzuki Y, Tsubouchi K, Nakagomi Y, Kikuchi N, Horikawa R and Ogata T.
GATA3 abnormalities in six patients with HDR syndrome.
Endocr J., 58, 117-121, 2011
Inoue H, Kangawa N, Kinouchi A, Sakamoto Y, Kimura C, Horikawa R, Shigematsu Y, Itakura M, Ogata T and Fujieda K.
Identification and functional analysis of novel human growth hormone secretagogue receptor (GHSR) gene mutations in Japanese subjects with short stature.
J Clin Endocrinol Metab., 96, E373-378, 2011 (IF=6.202)
Yamazawa K, Nakabayashi K, Matsuoka K, Matsubara K, Hata K, Horikawa R and Ogata T.
Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypes.
J Hum Genet., 56, 91-93, 2011 (IF=2.547)
Inoue H, Kangawa N, Kinouchi A, Sakamoto Y, Kimura C, Horikawa R, Shigematsu Y, Itakura M, Ogata T and Fujieda K.
Identification and functional analysis of novel human growth hormone-releasing hormone receptor (GHRHR) gene mutations in Japanese subjects with short stature.
Clin Endocrinol., 74, 223-233, 2011 (IF=3.201)
総説論文(英文)
Ogata T, Matsubara K, Nagata E, Sano S, Murakami N and Nagai T.
Advanced maternal age and the development of Prader-Willi syndrome resulting from upd(15)mat through non-disjunction at meiosis 1.
J Mamm Ova Res., 28, 96-102, 2011
総説論文(和文)
深見真紀、曽根田瞬、加藤芙弥子、花木啓一、神埼晋、大山建司、佐野友昭、西垣敏紀、稲垣朱実、高木博史、Gerhard Binder、横谷進、堀川玲子、生水真紀夫、緒方勤
「遺伝性女性化乳房症6家系における疾患成立機序と臨床像の解明」
日本内分泌学会雑誌 87(Supple), 94-97, 2011
緒方勤、位田忍、堀川玲子
「性分化疾患の分類と社会的性の決定について臨泌」
臨床泌尿器科 (特集:専門医のための性分化疾患講座) 65(12), 897-902, 2011
緒方勤
「外性器の異常(性分化)」
小児内科 (ちょっと気になる症候のみかた考え方) 43(10), 1795-1799, 2011
深見真紀、緒方勤
「小児内分泌疾患とゲノムコピー数異常」
生体の科学 62(6), 546-551, 2011
緒方勤
「エピジェネティクス・インプリンティングと胎児・胎盤緒方勤成長・発達」
Fetal & Neonatal Medicine 3(3), 101-102, 2011
緒方勤
「ターナー症候群」
井村裕夫、福井次矢、辻省次 (編) 症候群ハンドブック
中山書店 pp682-683, 2011
緒方勤
「クラインフェルター症候群」
井村裕夫、福井次矢、辻省次 (編) 症候群ハンドブック
中山書店 pp684-685, 2011
緒方勤
「性分化疾患」
森崇英、柴原章裕、島田昌之、角田幸雄 (編) 卵子学
京都大学出版会 pp88-100, 2011
緒方勤
「多因子疾患の遺伝的解析:理解へのロードマップ?それとも莫大な資金消費?.Pediatric Endocrinology Reviews抄訳シリーズ.No. 3」
ジャパンメディアートパブリッシング pp2-3, 2011
緒方勤
「減数分裂」
石塚文平、鈴木秋悦 (編) 生殖卵総学:基礎知識と臨床の進展
医歯薬出版株式会社 pp17-25, 2011
緒方勤
「性分化疾患における遺伝カウンセリング」
福嶋義光 (編) 遺伝子医学MOOK別冊 遺伝カウンセリングハンドブック
メディカルドゥ pp130-131, 2011
松原圭子、緒方勤
「高齢出産に伴うPrader-Willi症候群(PWS)病因の変化 PWSの最近のトピックス」
永井敏郎、大野耕策、緒方勤、横谷進 (編) Prader-Willi症候群
診断と治療社 pp133-138, 2011
松原圭子、緒方勤
「Prader-Willi症候群(PWS)と生殖補助医療.PWSの最近のトピックス」
永井敏郎、大野耕策、緒方勤、横谷進 (編) Prader-Willi症候群
診断と治療社 pp139-143, 2011
緒方勤
「多様なヌクレオチド除去修復(NER)とその医学的意義 Pediatric Endocrinology Reviews抄訳シリーズ」
ジャパンメディアートパブリッシングNo.26 pp4-5, 2011
緒方勤
「Lartge ring X chromosomeを有する母娘例:卵巣機能と知能発達の観点から」
新川詔夫、緒方勤 (監) ビジュアル疾患解説:遺伝病とターナー症候群
日本ケミカルリサーチNo.7 pp14-15, 2011
緒方勤
「性線機能低下症」
森昌朋 (編) 内分泌・糖尿病内科学
シュプリンガージャパン pp168-170, 2011
著書
緒方勤
「ヌーナン症候群における成長ホルモン治療 成長障害診療Q & A」
メディカルレビュー社 2011

2010年

Suzumori N, Ogata T, Mizutani E, Hattori Y, Matsubara K, Kagami M, and Suguhara-Ogasawara M.
Prenatal diagnosis of paternal uniparental disomy 14: delineation of further patient.
Am J Med Genet A., 152A, 3189-3192, 2010 (IF=2.404)
Matsubara K, Iwamoto H, Yoshida A and Ogata T.
Semen analysis and successful paternity by intracytoplasmic sperm injection in a man with steroid 5α-reductase-2 deficiency.
Fertil Steril., 94, 2770.e7-2770.e10, 2010 (IF=3.970)
Hiraoka M, Takahashi H, Orimo H, Hiraoka M, Ogata T and Azuma N.
Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity.
Mol Vis., 16, 2572-2577, 2010 (IF=2.541)
Kato H, Yoshida R, Tsukamoto K, Suga H, Eto H, Higashino T, Araki J, Ogata T and Yoshimura K.
Familial cases of atypical clinical features genetically diagnosed as LEOPARD syndrome (multiple lentigines syndrome).
Int J Dermatol., 49, 1146-1151, 2010 (IF=1.177)
Yamazawa K, Nakabayashi K, Kagami M, Sato T, Saitoh S, Horikawa R, Hizuka N and Ogata T.
Parthenogenetic chimaerism/mosaicism with a Silver-Russell Syndrome-like Phenotype.
J Med Genet., 47, 782-785, 2010 (IF=5.751)
Kagami M, O'Sullivan MJ, Green AJ, Watabe Y, Arisaka O, Masawa N, Matsuoka K, Fukami M, Matsubara K, Kato F, Ferguson-Smith AC and Ogata T.
The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers.
PLoS Genet., 6, e1000992, 2010 (IF=9.532)
業績トピックス
Dateki S, Fumaki M, Uematsu A, Kaji M, Iso M, Ono M, Mizota M, Yokoya S, Motomura K, Kinoshita E, Moriuchi H and Ogata T.
Mutation and gene copy number analyses of six pituitary transcription factor genes in 71 patients with combined pituitary hormone deficiency: identification of a single patient with LHX4 deletion.
J Clin Endocrinol Metab., 95, 4043-4047, 2010 (IF=6.202)
Iijima K, Nozu K, Kamei K, Nakayama M, Ito S, Matsuoka K, Ogata T, Kaito H, Nakanishi K and Mastuo M.
Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation.
Pediatr Nephrol., 25, 2165-2170, 2010 (IF=2.425)
Ashkenazi-Hoffnung L, Lebenthal Y, Wyatt AW, Ragge NK, Dateki S, Fumaki M, Ogata T, Phillip M and Gat-Yablonski G.
A novel loss of function mutation in OTX2 is associated with phenotypically variable anophthalmia and isolated growth hormone deficiency.
Hum Genet., 127, 721-729, 2010 (IF=4.523)
Fumaki M, Nagai T, Mochizuki H, Muroya K, Yamada G, Takitani K and Ogata T.
Anorectal and urinary anomalies and aberrant retinoic acid metabolism in cytochrome P450 oxidoreductase deficiency.
Mol Genet Metab., 100, 269-273, 2010 (IF=2.897)
Muroya K, Mochizuki T, Fumaki M, Iso M, Fujita K and Ogata T.
Diabetes mellitus in a Japanese girl with HDR syndrome and GATA3 mutation.
Endocr J., 157, 171-174, 2010 (IF=1.806)
Fumaki M, Maruyama T, Dateki S, Sato N, Yoshimura Y and Ogata T.
Hypothalamic dysfunction in a female with isolated hypogonadotropic hypogonadism and compound heterozygous TACR3 mutations and clinical manifestation in her heterozygous mother.
Horm Res Peadiatr., 73, 477-481, 2010 (IF=1.730)
Dateki S, Kosaka K, Hasegawa K, Tanaka H, Azuma N, Yokoya S, Muroya K, Adachi M, Tajima T, Motomura K, Kinoshita E, Moriuchi H, Sato N, Fumaki M and Ogata T.
Heterozygous OTX2 mutations are associated with variable pituitary phenotype.
J Clin Endocrinol Metab., 95, 756-764, 2010 (IF=6.202)
総説論文(英文)
Yamazawa K., Ogata T. and Ferguson-Smith AC*.
Uniparental disomy and human disease: an overview.
Am J Med Genet C (Seminars in Medical Genetics)., 154C, 329-334, 2010 (IF=2.404)
総説論文(和文)
佐藤直子、緒方勤
「Prokineticin signaling pathwayとKallmann症候群」
医のあゆみ 233 (9)(第5土曜特集:G蛋白質共役受容体研究―疾患解明とシグナル制御の新時代), 934-938, 2010
深見真紀、伊達木澄人、緒方勤
「中枢性性腺機能低下症」
Horm Front Gynecol 17 (2)(目で見る生殖内分泌疾患の診断と治療), 4-8, 2010
勝島由利子、山澤一樹、緒方勤、勝島史夫
「成長ホルモン分泌不全を来し、H19-DMRの低メチル化を認めたSilver-Russell症候群の1例」
ホルモンと臨 91-96, 2010
田中葉子、Paravee K、緒方勤
「良好な成長率を維持している抗GH抗体陰性の成長ホルモン単独欠損症IA型(IGHD IA)の1例」
ホルモンと臨 58(増刊号内分泌クリニカルカンファレンス51), 22-27, 2010
緒方勤
「内分泌撹乱物質:特に性分化・発達にたいする影響について」Pediatric Endocrinology Reviews 抄訳シリーズ
ジャパンメディアートパブリッシング No.3, 2-3, 2010
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 深見 真紀 業績リスト

2015年

Saito K, Miyado M, Kobori Y, Tanaka Y, Ishikawa H, Yoshida A, Katsumi M, Saito H, Kubota T, Okada H, Ogata T and *Fukami M.
Copy-Number Variations in Y Chromosomal Azoospermia Factor Regions Identified by Multiplex Ligation-Dependent Probe Amplification.
J Hum Genet, 60, 127-131, 2015
Kon M, Suzuki E, Dung VC, Hasegawa Y, Mitsui T, Muroya K, Ueoka K, Igarashi N, Nagasaki K, Oto Y, Hamajima T, Yoshino K, Igarashi M, Kato-Fukui Y, Nakabayashi K, Hayashi K, Hata K, Matsubara Y, Moriya K, Ogata T, Nonomura K and *Fukami M.
Molecular basis of non-syndromic hypospadias: Systematic mutation screening and genome-wide copy-number analysis of 62 patients.
Hum Reprod, 30, 499-506, 2015

2014年

*Fukami M, Suzuki J, Nakabayashi K, Tsunasima R, Ogata T, Shozu M and Noguchi S.
Lack of Genomic Rearrangements Involving the Aromatase Gene CYP19A1 in Breast Cancer.
Breast Cancer, 21, 382-385, 2014
Shihara D, Miyado M, Nakabayashi K, Shozu M, Ogata T, Nagasaki K and *Fukami M.
Aromatase excess syndrome in a family with upstream deletion of CYP19A1.
Clin Endocrinol, 81, 314-316, 2014
Suzuki E, Yatsuga S, Igarashi M, Miyado M, Nakabayashi K, Hayashi K, Hata K, Umezawa A, Yamada G, Ogata T and *Fukami M.
De Novo Frameshift Mutation in Fibroblast Growth Factor 8 in a Male Patient with Gonadotropin Deficiency.
Horm Res Paediatr, 81, 139-144, 2014
Izumi Y, Suzuki E, Kanzaki S, Yatsuga S, Kinjo S, Igarashi M, Maruyama T, Sano S, Horikawa R, Sato N, Nakabayashi K, Hata K, Umezawa A, Ogata T, Yoshimura Y and *Fukami M.
Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism.
Fertil Steril, 102, 1130-1136, 2014

2013年

*Fukami M, Iso M, Sato N, Igarashi M, Seo M, Kazukawa I, Kinoshita E, Dateki S and Ogata T.
Submicroscopic deletion involving the fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency.
Endocr J, 60, 1013-1020, 2013
Igarashi M, Dung VC, Suzuki E, Ida S, Nakacho M, Nakabayashi K, Mizuno K, Hayashi Y, Kohri K, Kojima Y, Ogata T and *Fukami M.
Cryptic genomic rearrangements in three patients with 46,XY disorders of sex development.
Plos One, 8, e68194, 2013
*Fukami M, Tsuchiya T, Vollbach H, Brown KA, Abe S, Ohtsu S, Wabitsch M, Burger H, Simpson ER, Umezawa A, Shihara D, Nakabayashi K, Bulun SE, Shozu M and Ogata T.
Genomic Basis of Aromatase Excess Syndrome: Recombination- and Replication-Mediated Rearrangements Leading to CYP19A1 Overexpression.
J Clin Endocrinol Metab, 98, E2013-2021, 2013

2012年

総説論文(和文)
深見真紀
「成長および成長障害のメカニズム」
小児内科, 44(4), 507-511, 2012
深見真紀
「アロマターゼ過剰症候群」
内科, 109(6), 2012(印刷中)
五十嵐麻希、深見真紀
「性分化疾患の新知見:新規男性ホルモン産生経路」
医学のあゆみ, 2012(印刷中)
深見真紀、曽根田瞬、矢澤隆志、宮本薫、緒方勤
「チトクロームP450オキシドレダクターゼ (POR) 異常症の分子基盤:POR遺伝子発現制御機構の解明」
生殖内分泌学会誌, 2012(印刷中)

2011年

原著論文(英文)
*Fukami M, Shozu M, Soneda S, Kato F, Inagaki A, Takagi H, Hanaki K, Kanzaki S, Ohyama K, Sano T, Nishigaki T, Yokoya S, Binder G, Horikawa R and Ogata T.
Aromatase Excess Syndrome: Identification of Cryptic Duplications and Deletions Leading to Gain-of-Function of CYP19A1 and Assessment of Phenotypic Determinants.
J Clin Endocrinol Metab, 96, E1035-1043, 2011
総説論文(和文)
深見真紀
「全ゲノム関連解析と身長」特集:全ゲノム関連解析と内分泌疾患
ホルモンと臨床, 59(1), 79-85, 2011
深見真紀、緒方勤
「小児内分泌疾患とゲノムコピー数異常」
生体の科学, 62(6), 546-551, 2011
深見真紀
「最近話題の遺伝子異常による内分泌および類縁疾患. 性分化疾患」
ホルモンと臨床, 58 (7), 31-36, 2011
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 筒井 和義 業績リスト

2015年

Sasanami T, Izumi S, Sakurai N, Hirata T, Mizushima S, Matsuzaki M, Hiyama G, Yorinaga E, Yoshimura T, Ukena K and *Tsutsui K.
A unique mechanism of successful fertilization in a domestic bird.
Sci Rep, 5, 7700, 2015

2014年

 
原著論文(英文)総数 9 編
Anjum S, Krishna A and *Tsutsui K.
Inhibitory roles of the mammalian GnIH ortholog RFRP-3 in testicular activities in adult mice.
J Endocrinol, 223, 79-91, 2014
Tobari Y, Son YL, Ubuka T, Hasegawa T and *Tsutsui K.
A new pathway mediating social effects on the endocrine system: female presence acting via norepinephrine release stimulates gonadotropin-inhibitory hormone in the paraventricular nucleus and suppresses luteinizing hormone in quail.
J Neurosci, 34, 9803-9811, 2014
Osugi T, Okamura T, Son YL, Ohkubo M, Ubuka T, HenmiY and *Tsutsui K.
Evolutionary origin of GnIH and NPFF in chordates: Insights from novel amphioxus RFamide peptides.
PLoS ONE, 9, e100962, 2014
Son YL, Ubuka T, Narihiro M, Fukuda Y, Hasunuma I, Yamamoto K, Belsham DD and *Tsutsui K.
Molecular basis for the activation of gonadotropin-inhibitory hormone gene transcription by corticosterone.
Endocrinology, 155, 1817-1826, 2014
Ubuka T, Haraguchi S, Tobari Y, Narihiro M, Ishikawa K, Hayashi T, Harada N and Tsutsui K.
Hypothalamic inhibition of socio-sexual behaviour by increasing neuroestrogen synthesis.
Nat. Commun., 5, Article number 3061 doi:10.1038/ncomms4061, 2014
業績トピックス

2013年

原著論文(英文)総数 5 編
Maekawa F, Sakurai M, Yamashita Y, Tanaka K, Haraguchi S, Yamamoto K, Tsutsui K, Yoshioka H, Murakami S, Tadano R, Goto T, Shiraishi J, Tomonari K, Oka T, Ohara K, Maeda T, Bungo T, Tsudzuki M and Ohki-Hamazaki H.
A genetically female brain is required for a regular reproductive cycle in chicken brain chimeras.
Nat. Commun., 4, Article number 1372 doi:10.1038/ncomms2372. 2013
Shima Y, Miyabayashi K, Haraguchi S, Arakawa T, Otake H, Baba T, Matsuzaki S, Shishido Y, Akiyama H, Tachibana T, Tsutsui K and Morohashi K.
Contribution of Leydig and Sertoli cells to testosterone production in mouse fetal testes.
Mol. Endocrinol., 27, 63-73, 2013
総説論文(英文)
Tsutsui K, Ubuka T, Bentley GE and Kriegsfeld L.
Regulatory mechanisms of gonadotropin-inhibitory hormone (GnIH) synthesis and release in photoperiodic animals.
Front. Endocrinol., 2013 (in press)(Review)
Ubuka T, Bentley GE and Tsutsui K.
Neuroendocrine regulation of gonadotropin secretion in seasonally breeding birds.
Front. Endocrinol., 2013 (in press)(Review)
Tsutsui K, Haraguchi S, Fukada Y and Vaudry H.
7α-Hydroxypregnenolone, a new key stimulator of locomotor activity: biosynthesis, mode of action and functional significance.
Front. Neuroendocrinol., 2013 (in press)(Review)
Ukena K, Tachibana T, Tobari Y, Leprince J, Vaudry H and Tsutsui K.
Identification, localization and function of a novel neuropeptide, 26RFa, and its cognate receptor, GPR103 in the avian hypothalamus.
Gen. Comp. Endocrinol., 2013 (in press)(Minireview)
Ubuka T, Son YL, Bentley GE, Millar RP and Tsutsui K.
Gonadotropin-inhibitory hormone (GnIH), GnIH receptor and cell signaling.
Gen. Comp. Endocrinol., 2013 (in press)(Minireview)
Ubuka T, Mizuno T, Fukuda Y, Bentley GE, Wingfield JC and Tsutsui K.
RNA interference of gonadotropin-inhibitory hormone gene induces aggressive and sexual behaviors in birds.
Gen. Comp. Endocrinol., 181, 179-186, 2013 (Review)
Chowdhury VS, Ubuka T and Tsutsui K.
Melatonin stimulates the synthesis and release of gonadotropin-inhibitory hormone in birds.
Gen. Comp. Endocrinol., 181, 175-178, 2013 (Review)
Tsutsui K.
Create new research directions in comparative endocrinology from Asia and Oceania.
Gen. Comp. Endocrinol., 181, 192-196, 2013 (Review)
著書論文(英文)
Tsutsui K.
Neurosteroids and synaptic formation in the cerebellum.
In: Handbook of Cerebellum and Cerebellar Disorders, Manto M, Gruol D, Schmahmann JD, Koibuchi N and Rossi F. (eds)
Springer, 993-1012, 2013
Tsutsui K and Ubuka T.
Gonadotropin-inhibitory hormone (GnIH).
In: The Handbook of Biologically Active Peptides (2nd edition), Kastin AJ. (ed)
Elsevier publisher, 802-811, 2013
Leprince J, Neveu C, Lefrance B, Guilhaudis L, Segalas-Milazzo I, Do Rego JL, Tena-Sempere M, Tsutsui K and Vaudry H.
26RFa.
In: The Handbook of Biologically Active Peptides (2nd edition), Kastin AJ. (ed)
Elsevier publisher, 917-923, 2013
学術著書(英文)
Vaudry H and Tsutsui K.
The E-Book of Neurosteroids: Frontiers Research Topic.
Published by Frontiers in Endocrinology, 2013
http://flashbook.frontiersin.org//clients/Frontiers/Neurosteroids/EBook.html

2012年

原著論文
Haraguchi S, Hara S, Ubuka T, Mita M and Tsutsui K.
Possible role of pineal allopregnanolone in Purkinje cell survival.
Proc. Natl. Acad. Sci. USA, 109, 21110-21115, 2012
MDLinx 4345182 January 9, 2013
Anjum S, Krishna A, Sridaran R and Tsutsui K.
Localization of gonadotropin-releasing hormone (GnRH), gonadotropin-inhibitory hormone (GnIH), kisspeptin and GnRH receptor and their possible roles in testicular activities from birth to senescence in mice.
J. Exp. Zool. Part A., 9999A, 1-15, 2012
Toyoda F, Hasunuma I, Nakada T, Haraguchi S, Tsutsui K and Kikuyama S.
Involvement of a neurosteroid, 7α-hydroxypregnenolone in the courtship behavior performed by the male newt, Cynops pyrrhogaster.
Horm. Behav., 62, 375-380, 2012
Losa-Ward SM, Todd KL, McCaffrey KA, Tsutsui K and Patisaul HB.
Disrupted organization of RFamide pathways in the hypothalamus is associated with advanced puberty in female rats neonatally exposed to bisphenol A.
Biol. Reprod., 87, 1-9, 2012
Oishi H, Klausen C, Bentley GE, Osugi T, Tsutsui K, Gilks CB, Yano T and Leung PCK.
The human gonadotropin-inhibitory hormone ortholog RFamide-related peptide-3 suppresses gonadotropin-induced progesterone production in human granulosa cells.
Endocrinology, 153, 3435-3445, 2012
Daukss D, Gazda K, Kosugi T, Osugi T, Tsutsui K and Sower SA.
Effects of lamprey PQRFamide peptides on brain gonadotropin-releasing hormone concentrations and pituitary gonadotropin-β mRNA expression.
Gen. Comp. Endocrinol., 177, 215-219, 2012
Osugi T, Daukss D, Gazda K, Ubuka T, Kosugi T, Nozaki M, Sower SA and Tsutsui K.
Evolutionary origin of the structure and function of gonadotropin-inhibitory hormone: Insights from lampreys.
Endocrinology, 153, 2362-2374, 2012
Son YL, Ubuka T, Millar RP. and Tsutsui K.
Gonadotropin-inhibitory hormone inhibits GnRH-induced gonadotropin subunit gene transcriptions by inhibiting AC/cAMP/PKA-dependent ERK pathway in LβT2 cells.
Endocrinology, 153, 2332-2343, 2012
Global Medical Discovery: Key Scientific Article June 18, 2012
Chowdhury VS, Tomonaga S, Nishimura S, Tabata S, Cockrem JF, Tsutsui K and Furuse M.
Hypothalamic gonadotropin-inhibitory hormone precursor mRNA is increased during depressed food intake in heat-exposed chicks.
Comp. Biol. Physiol., 162, 227-233, 2012
Treen N, Itoh N, Miura H, Kikuchi I, Ueda T, Takahashi KG, Ubuka T, Yamamoto K, Sharp PJ, Tsutsui K and Osada M.
Mollusc gonadotropin-releasing hormone directly regulates gonadal functions: A primitive endocrine system controlling reproduction.
Gen. Comp. Endocrinol., 176, 167-172, 2012
Morita Y, Wada-Hiraike O, Yano T, Nakagawa S, Shirane A, Hiraike H, Koyama S, Hirano M, Oishi H, Yoshino O, Miyamoto Y, Sone K, Oda K, Tsutsui K and Taketani Y.
Resveratrol promotes expression of SIRT1 and StAR in rat ovarian granulosa cells: an implicative role of SIRT1 in the ovary.
Reprod. Biol. Endocrinol., 10, 14-24, 2012
Iwasa T, Matsuzaki T, Murakami M, Kinouchi R, Osugi T, Gereltsetseg G, Yoshida S, Kuwahara A, Yasui T, Irahara M and Tsutsui K.
Developmental changes in the mammalian gonadotropin-inhibitory hormone (GnIH) ortholog RFamide-related peptide (RFRP) and its cognate receptor GPR147 in the rat hypothalamus.
Int. J. Dev. Neurosci., 30, 31-37, 2012
Ubuka T, Mukai M, Wolfe J, Beverly R, Clegg S, Wang A, Hsia S, Li M, Krause JS, Mizuno T, Fukuda Y, Tsutsui K, Bentley GE and Wingfield JC.
RNA interference of gonadotropin-inhibitory hormone gene induces arousal in songbirds.
PLoS ONE, 7, e30202, 2012
Haraguchi S, Koyama T, Hasunuma I, Okuyama S, Ubuka T, Kikuyama S, Do Rego JL, Vaudry H and Tsutsui K.
Acute stress increases the synthesis of 7α-hydroxypregnenolone, a new key neurosteroid stimulating locomotor activity, through corticosterone action.
Endocrinology, 153, 794-805, 2012
Ubuka T, Inoue K, Ukena K, Kriegsfeld LJ and Tsutsui K.
Identification, expression, and physiological functions of Siberian hamster gonadotropin-inhibitory hormone.
Endocrinology, 153, 373-385, 2012
総説論文(英文)
Vaudry H and Tsutsui K.
Editorial: Research Topic on Neurosteroids.
Front. Endocrinol., 3, article 126, 1, 2012 doi: 10.3389/fendo.2012.00126
Ubuka T, Son YL, Tobari Y and Tsutsui K.
Gonadotropin-inhibitory hormone action in the brain and pituitary.
Front. Endocrinol., 3, article 148, 1-13, 2012 doi: 10.3389/fendo.2012.00148 (Review)
Tsutsui K.
Create new research directions in comparative endocrinology from Asia and Oceania.
Gen. Comp. Endocrinol., 2012 (in press)
Tsutsui K, Ubuka T, Bentley GE and Kriegsfeld LJ.
Gonadotropin-inhibitory hormone (GnIH): Discovery, progress and prospect.
Gen. Comp. Endocrinol., 177, 305-314, 2012 (Review)
Tsutsui K.
Neurosteroid biosynthesis and action during cerebellar development.
Cerebellum, 11, 414-415, 2012 (Review)
Haraguchi S, Sasahara K, Shikimi H, Honda S, Harada N and Tsutsui K.
Estradiol promotes Purkinje dendritic growth, spinogenesis and synaptogenesis during neonatal life by inducing the expression of BDNF.
Cerebellum, 11, 416-417, 2012 (Review)
Tsutsui K, Haraguchi S, Inoue K, Miyabara H, Suzuki S and Ubuka T.
Control of circadian activity of birds by the interaction of melatonin with 7α-hydroxypregnenolone, a newly discovered neurosteroid stimulating locomotion.
J. Ornitol., 153 (Suppl), S235-S243, 2012 (Review)
Tsutsui K, Haraguchi S, Matsunaga M, Koyama T, Do Rego JL and Vaudry H.
7α-Hydroxypregnenolone, a new key regulator of amphibian locomotion: discovery, progress and prospect.
Gen. Comp. Endocrinol., 176, 440-447, 2012 (Review)
Do Rego JL, Seong JY, Burel D, Leprince J, Vaudry D, Luu-The V, Tonon MC, Tsutsui K, Pelletier G and Vaudry H.
Regulation of neurosteroid biosynthesis by neurotransmitters and neuropeptides.
Front. Endocrin., 3, 1-15, 2012 doi: 10.3389/fendo.2012.00004 (Review)
著書論文(英文)
Tsutsui K and Ubuka T.
Gonadotropin-inhibitory hormone (GnIH).
In: The Handbook of Biologically Active Peptides (2nd edition) Brain Peptides Section, Kastin AJ. and Vaudry H. (eds)
Elsevier publisher, 2012 (in press)
J. Leprince, C. Neveu, B. Lefrance, L. Guilhaudis, I. Segalas-Milazzo, J.-C. Do Rego, M. Tena-Sempere, K. Tsutsui and H. Vaudry
RFa.
In: The Handbook of Biologically Active Peptides (2nd edition) Brain Peptides Section, Kastin AJ. and Vaudry H. (eds)
Elsevier publisher, 2012 (in press)
総説論文(和文)
筒井和義
「総説:生殖を制御する新規脳ホルモンの作用機構と発現制御機構 Current Topics 『New Insights of Molecular Genetics on Growth Disorders』」
ファイザー社 Kokua, 7, 13, 2012
筒井和義、大杉知裕、戸張靖子、孫 ユリ、産賀崇由
「総説:生殖を制御する新規脳ホルモンGnIHの起源と分子進化」
比較内分泌学, 38, 76-83, 2012
筒井和義
ニューロペプチド―update「生殖腺刺激ホルモン放出抑制ホルモン」
中外医学社 Clinical Neuroscience, 30(2), 223-225, 2012

2011年

原著論文
Osugi T, Uchida K, Nozaki M and Tsutsui K.
Characterization of novel RFamide peptides in the central nervous system of the brown hagfish: isolation, localization, and functional analysis.
Endocrinology, 152, 4252-4264, 2011
(News and Views: Hagfish, genome duplications, and RFamide neuropeptide evolution. Dores RM. Endocrinology, 152, 4010-4013, 2011)
Singh P, Krishna A, Sridaran R and Tsutsui K.
Immunohistochemical localization of GnRH and RFamide-related peptide-3 during estrous cycle of mouse: Their potential role in the ovarian activity.
J. Mol. Histol., 42, 371-81, 2011
Tobari Y, Iijima N, Tsunekawa K, Osugi T, Ukena K, Okanoya K, Tsutsui K and Ozawa H.
Identification, localization and functional implication of 26RFa ortholog peptide in the brain of zebra finch (Taeniopygia guttata).
J. Neuroendocrinol., 23, 791-803, 2011
Hatori M, Hirota T, Iitsuka M, Kurabayashi N, Haraguchi S, Kokame K, Sato R, Nakai A, Miyata T, Tsutsui K and Fukada Y.
Light-dependent and circadian clock-regulated activation of SREBP, XBP1 and HSF pathways in the pineal gland.
Proc. Natl. Acad. Sci. USA., 108, 4864-4869, 2011
Chowdhury VS, Ubuka T, Osugi T, Shimura T and Tsutsui K.
Identification, localization and expression of LPXRFamide peptides, and melatonin-dependent induction of their precursor mRNA in the newt brain.
J. Endocrinol., 209, 1-12, 2011
Singh P, Krishna A and Tsutsui K.
Effects of gonadotropin-inhibitory hormone on folliculogenesis and steroidogenesis of cyclic mice.
Fertil. Steril., 95, 1397-1404, 2011
Takase M, Haraguchi S, Hasunuma I, Kikuyama S and Tsutsui K.
Expression of cytochrome P450 side-chain cleavage enzyme mRNA and production of pregnenolone in the brain of the red-bellied newt Cynops pyrrhogaster.
Gen. Comp. Endocrinol., 170, 468-474, 2011
Isomura T, Haraguchi S, Miyamoto K, Tsutsui K, Nakamura Y and Nakamura M.
Estrogen biosynthesis in the gonad of the frog Rana rugosa.
Gen. Comp. Endocrinol., 170, 207-212, 2011
Shahjahan M, Ikegami T, Osugi T, Ukena K, Doi H, Hattori A, Tsutsui K and Ando H.
Synchronised expressions of LPXRFamide peptide and its receptor genes: seasonal, diurnal and circadian changes during spawning period in grass puffer.
J. Neuroendocrinol., 23, 39-51, 2011
総説論文(英文)
Vaudry H, Do Rego JL, Burel D, Luu-The V, Pelletier G and Tsutsui K.
Neurosteroid biosynthesis in the brain of amphibians.
Front. Endocrin., 2, 1-9, 2011 (Review)
Tsutsui K, Ukena K, Sakamoto H, Okuyama S and Haraguchi S.
Biosynthesis, mode of action and functional significance of neurosteroids in the Purkinje cell.
Front. Endocrin., 2, 1-9, 2011 (Review)
Tsutsui K.
Neurosteroid biosynthesis and function in the brain of domestic birds.
Front. Endocrin., 2, 1-14, 2011 (Review)
Haraguchi S, Matsunaga M, Vaudry H and Tsutsui K.
Mode of action and functional significance of 7α-hydroxypregnenolone stimulating locomotor activity.
Front. Endocrin., 2, 1-8, 2011 (Review)
Kikuyama S and Tsutsui K.
Historical view of development of comparative endocrinology in Japan.
Gen. Comp. Endocrinol., 171, 117-123, 2011 (Review)
Ukena K, Vaudry H, Leprince J and Tsutsui K.
Molecular evolution and functional characterization of the orexigenic peptide 26RFa and its receptor in vertebrates: Discovery and comparative aspects.
Cell Tissue Res., 343, 475-481, 2011 (Mini-Review)
著書論文(英文)
Tsutsui K.
Neurosteroids and synaptic formation in the cerebellum.
In: Handbook of Cerebellum and Cerebellar Disorders, Manto M., Gruol D., Schmahmann J., Koibuchi N. and Rossi F. (eds)
Springer, 2011 (in press)
総説論文(和文)
筒井和義
トピックス: GnIHの発見とGnIH研究の進展・展望 -鳥類から哺乳類、ヒトへの展開-
比較内分泌学, 37, 21-28 2011
筒井和義
Review: GnIHによる生殖機能調節 「成長 代謝 (Endocrinology and Metabolism Update)」
エルゼビア・ジャパン, 2(3), 1-3, 2011

2010年

原著論文
Sethi S, Tsutsui K and Chaturvedi CM.
Age-dependent variation in the RFRP-3 neurons is inversely correlated with gonadal activity of mice.
Gen. Comp. Endocrinol., 168, 326-332, 2010
Mason AO, Duffy S, Zhao S, Ubuka T, Bentley GE, Tsutsui K, Silver R and Kriegsfeld LJ.
Photoperiod and reproductive condition are associated with changes in RFamide-related peptide (RFRP) expression in Syrian hamsters (Mesocricetus auratus).
J. Biol. Rhythm., 25, 176-85, 2010
Ukena K, Tachibana T, Iwakoshi-Ukena E, Saito Y, Minakata H, Kawaguchi R, Osugi T, Tobari Y, Leprince J, Vaudry H and Tsutsui K.
Identification, localization and function of a novel avian hypothalamic neuropeptide, 26RFa, and its cognate receptor, GPR103.
Endocrinology, 151, 2255-2264, 2010
Haraguchi S, Koyama T, Hasunuma I, Vaudry H and Tsutsui K.
Prolactin increases the synthesis of 7α-hydroxypregnenolone, a key factor for induction of locomotor activity, in breeding male newts.
Endocrinology, 151, 2211-2222, 2010
Tobari Y, Iijima N, Tsunekawa K, Osugi T, Okanoya K, Tsutsui K and Ozawa H.
Identification of gonadotropin-inhibitory hormone in the zebra finch (Taeniopygia guttata): peptide isolation, cDNA cloning and brain distribution.
Peptides, 31, 816-826, 2010
Doi M, Takahashi Y, Komatsu R, Yamazaki F, Yamada H, Haraguchi S, Emoto N, Okuno Y, Tsujimoto G, Kanematsu A, Ogawa O, Todo T, Tsutsui K, van der Horst GT and Okamura H.
Salt-sensitive hypertension in circadian clock-deficient Cry-null mice involves dysregulated adrenal Hsd3b6.
Nature Medicine, 16, 67-74, 2010
Zhao S, Zhu E, Yang C, Bentley GE, Tsutsui K and Kriegsfeld LJ.
RFamide-related peptide (RFRP) and mRNA expression in mammalian testis: Association with the spermatogenic cycle.
Endocrinology, 151, 617-627, 2010
Chowdhury VS, Yamamoto K, Ubuka T, Bentley GE, Hattori A and Tsutsui K.
Melatonin stimulates the release of gonadotropin-inhibitory hormone by the avian hypothalamus.
Endocrinology, 151, 271-280, 2010 (Endocrine news, 34, 7, 2009 Dec.)
Sethi S, Tsutsui K and Chaturvedi CM.
Temporal phase relation of circadian neural oscillations alters RFamide-related peptide-3 (RFRP-3), a mammalian gonadotropin-inhibitory hormone (GnIH) homolog, and testicular function in the mouse (Mus musculus).
Neuroendocrinology, 91, 189-199, 2010
総説論文(英文)
Tsutsui K, Haraguchi S, Matsunaga M, Inoue K and Vaudry H.
7α-Hydroxypregnenolone, a new key regulator of locomotor activity of vertebrates: Identification, mode of action and functional significance.
Front. Endocrin., 1, 1-13, 2010 (Review)
Bentley GE, Tsutsui K and Kriegsfeld LJ.
Recent studies of gonadotropin-inhibitory hormone (GnIH) in the mammalian hypothalamus, pituitary and gonads.
Brain Res., 1364, 62-71, 2010 (Review)
Tsutsui K, Haraguchi S, Matsunaga M, Koyama T, Do Rego JL and Vaudry H.
Identification of 7α-hydroxypregnenolone, a novel bioactive amphibian neurosteroid stimulating locomotor activity, and its physiological roles in the regulation of locomotion.
Gen. Comp. Endocrinol., 168, 275-279, 2010 (Review)
Tsutsui K, Bentley GE, Kriegsfeld LJ, Osugi T, Seong JY, and Vaudry H.
Discovery and evolutionary history of GnIH and Kisspeptin: New key neuropeptides controlling reproduction.
J. Neuroendocrinol., 22, 716-727, 2010 (Review)
Kriegsfeld LJ, Gibson EM, Williams III WP, Zhao S, Mason AO, Bentley GE and Tsutsui K.
The roles of RFamide-related peptide-3 (RFRP-3) in mammalian reproductive function and behaviour.
J. Neuroendocrinol., 22, 692-700, 2010 (Review)
Tsutsui K, Bentley GE, Bedecarrats G, Osugi T, Ubuka T and Kriegsfeld LJ.
Gonadotropin-inhibitory hormone (GnIH) and its control of central and peripheral reproductive function.
Front. Neuroendocrinol., 31, 284-295, 2010 (Review)
Tsutsui K.
Phylogenetic aspects of gonadotropin-inhibitory hormone (GnIH) and its homologs in vertebrates.
Ann. N.Y. Acad. Sci., 1200, 75-84, 2010 (Review)
著書(英文)
Tsutsui K.
Phylogenetic aspects of gonadotropin-inhibitory hormone (GnIH) and its homologs in vertebrates.
In: Phylogenetic Aspects of Neuropeptides: From Invertebrates to Humans, Vaudry H. and Shioda S. (eds)
Blackwell, Boston, Massachusetts, 75-84, 2010
総説論文(和文)
筒井和義、産賀崇由
総説:性周期とニューロペプチド: GnIH 特集「ニューロペプチド」Hormone Frontier in Gynecology
メディカルレビュー社, 17, 25-29, 2010
筒井和義
GnIHによるゴナドトロピン分泌制御 特集/生殖機能調節の新しい視点
産科と婦人科 (Obstet. Gynecol.; 診断と治療社) , 77, 252-258, 2011
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