研究者データベース
名前：堤真紀子(Makiko Tsutsumi)

所属機関/組織 (#1)

所属機関名-1：藤田保健衛生大学

所属部署名(1) 1：総合医科学研究所

所属部署名(2) 1：分子遺伝学研究部門

役職・職名-1：助教

郵便番号-1： 470-1192

住所-1：愛知県豊明市沓掛町田楽ヶ窪1-98

所属学会／研究会 (#1)

所属学会名-1：日本分子生物学会

研究歴／実績 [2006年] (#13)

Papers-13： Tsutsumi M., Imai S., Kyono-Hamaguchi Y., Hamaguchi S., Koga A., Hori H. (2006) Color reversion of the albino medaka fish associated with spontaneous somatic excision of the Tol-1 transposable element from the tyrosinase gene. Pigment Cell Res. 19:243-247.

研究歴／実績 [2007年] (#14)

Papers-14： Tsutsumi M., Itoh M. (2007) Novel transcript nort is a downstream target gene of the Notch signaling pathway in zebrafish. Gene Expr. Patterns 7:227-232.

Yokoi H, Shimada A, Carl M, Takashima S, Kobayashi D, Narita T, Jindo T, Kimura T, Kitagawa T, Kage T, Sawada A, Naruse K, Asakawa S, Shimizu N, Mitani H, Shima A, Tsutsumi M, Hori H, Wittbrodt J, Saga Y, Ishikawa Y, Araki K, Takeda H. (2007) Mutant analyses reveal different functions of fgfr1 in medaka and zebrafish despite conserved ligand-receptor relationships. Dev. Biol. 304:326-337.

研究歴／実績 [2009年] (#16)

Papers-16： Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS. (2009) Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells. Hum. Mol. Genet. 18:3397-3406.

Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T. (2009) Recent advance in our understanding of the molecular nature of chromosomal abnormalities. J. Hum. Genet. 54:253-260.

Bolor H, Mori T, Nishiyama S, Ito Y, Hosoba E, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Kato T, Tong M, Nishizawa H, Pryor-Koishi K, Kitaoka E, Sawada T, Nishiyama Y, Udagawa Y, Kurahashi H. (2009) Mutations of the SYCP3 gene in women with recurrent pregnancy loss. Am. J. Hum. Genet. 84:14-20.

研究歴／実績 [2010年] (#17)

Papers-17： Kurahashi H, Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS. (2010) The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements. Clin Genet. 78: 299-309.

Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H. (2010) Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm. Hum. Mol. Genet. 19:2630-2637.

Kogo H, Kowa-Sugiyama H, Yamada K, Bolor H, Tsutsumi M, Ohye T, Inagaki H, Taniguchi M, Toda T, Kurahashi H. (2010) Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans. J. Hum. Genet. 55:293-299.

Nishizawa H, Kato T, Ota S, Nishiyama S, Pryor-Koishi K, Suzuki M, Tsutsumi M, Inagaki H, Kurahashi H, Udagawa Y. (2010) Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia. Am. J. Reprod. Immunol. 64:68-76.

Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MV, Medne L, Zackai EH, Emanuel BS, Kurahashi H. (2010) Paternal origin of the de novo constitutional t(11;22)(q23;q11). Eur. J. Hum. Genet. 18:783-787.

Tsuda S, Kitagawa T, Takashima S, Asakawa S, Shimizu N, Mitani H, Shima A, Tsutsumi M, Hori H, Naruse K, Ishikawa Y, Takeda H. (2010) FAK-mediated extracellular signals are essential for interkinetic nuclear migration and planar divisions in the neuroepithelium. J. Cell Sci. 123:484-496.

Fri Nov 19 17:44:38 JST 2010

研究者データベース
名前：	堤真紀子(Makiko Tsutsumi)

所属機関/組織 (#1)
所属機関名-1：	藤田保健衛生大学
所属部署名(1) 1：	総合医科学研究所
所属部署名(2) 1：	分子遺伝学研究部門
役職・職名-1：	助教
郵便番号-1：	470-1192
住所-1：	愛知県豊明市沓掛町田楽ヶ窪1-98

所属学会／研究会 (#1)
所属学会名-1：	日本分子生物学会

研究歴／実績 [2006年] (#13)
Papers-13：	Tsutsumi M., Imai S., Kyono-Hamaguchi Y., Hamaguchi S., Koga A., Hori H. (2006) Color reversion of the albino medaka fish associated with spontaneous somatic excision of the Tol-1 transposable element from the tyrosinase gene. Pigment Cell Res. 19:243-247.
研究歴／実績 [2007年] (#14)
Papers-14：	Tsutsumi M., Itoh M. (2007) Novel transcript nort is a downstream target gene of the Notch signaling pathway in zebrafish. Gene Expr. Patterns 7:227-232. Yokoi H, Shimada A, Carl M, Takashima S, Kobayashi D, Narita T, Jindo T, Kimura T, Kitagawa T, Kage T, Sawada A, Naruse K, Asakawa S, Shimizu N, Mitani H, Shima A, Tsutsumi M, Hori H, Wittbrodt J, Saga Y, Ishikawa Y, Araki K, Takeda H. (2007) Mutant analyses reveal different functions of fgfr1 in medaka and zebrafish despite conserved ligand-receptor relationships. Dev. Biol. 304:326-337.
研究歴／実績 [2009年] (#16)
Papers-16：	Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS. (2009) Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells. Hum. Mol. Genet. 18:3397-3406. Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T. (2009) Recent advance in our understanding of the molecular nature of chromosomal abnormalities. J. Hum. Genet. 54:253-260. Bolor H, Mori T, Nishiyama S, Ito Y, Hosoba E, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Kato T, Tong M, Nishizawa H, Pryor-Koishi K, Kitaoka E, Sawada T, Nishiyama Y, Udagawa Y, Kurahashi H. (2009) Mutations of the SYCP3 gene in women with recurrent pregnancy loss. Am. J. Hum. Genet. 84:14-20.
研究歴／実績 [2010年] (#17)
Papers-17：	Kurahashi H, Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS. (2010) The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements. Clin Genet. 78: 299-309. Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H. (2010) Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm. Hum. Mol. Genet. 19:2630-2637. Kogo H, Kowa-Sugiyama H, Yamada K, Bolor H, Tsutsumi M, Ohye T, Inagaki H, Taniguchi M, Toda T, Kurahashi H. (2010) Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans. J. Hum. Genet. 55:293-299. Nishizawa H, Kato T, Ota S, Nishiyama S, Pryor-Koishi K, Suzuki M, Tsutsumi M, Inagaki H, Kurahashi H, Udagawa Y. (2010) Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia. Am. J. Reprod. Immunol. 64:68-76. Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MV, Medne L, Zackai EH, Emanuel BS, Kurahashi H. (2010) Paternal origin of the de novo constitutional t(11;22)(q23;q11). Eur. J. Hum. Genet. 18:783-787. Tsuda S, Kitagawa T, Takashima S, Asakawa S, Shimizu N, Mitani H, Shima A, Tsutsumi M, Hori H, Naruse K, Ishikawa Y, Takeda H. (2010) FAK-mediated extracellular signals are essential for interkinetic nuclear migration and planar divisions in the neuroepithelium. J. Cell Sci. 123:484-496.