業績 of 藤田保健衛生大学・総合医科学研究所・分子遺伝学研究部門

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藤田保健衛生大学 総合医科学研究所 分子遺伝学研究部門
Division of Molecular Genetics. Institute for Comprehensive Medical Science. Fujita Health University.



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染色体構造異常プロジェクト

Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations.
Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
Nat Commun. 2013;4:1592. doi: 10.1038/ncomms2595.
中日新聞3月13日朝刊, 朝日新聞3月13日朝刊, 時事通信

Chromosomal translocations and palindromic AT-rich repeats.
Kato T, Kurahashi H, Emanuel BS.
LinkIconCurr Opin Genet Dev. 2012 Mar 6.

Mechanism of complex gross chromosomal rearrangements: a commentary on concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation.
Kurahashi H, Ohye T, Inagaki H, Kogo H, Tsutsumi M.
LinkIconJ Hum Genet. 2012 Feb;57(2):81-3. doi: 10.1038/jhg.2011.143. Epub 2011 Dec 15. No abstract available.

DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation.
Kato T, Inagaki H, Tong M, Kogo H, Ohye T, Yamada K, Tsutsumi M, Emanuel BS, Kurahashi H.
LinkIconMol Cytogenet. 2011 Sep 8;4(1):18.

A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli G, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, Kurahashi H, Zackai EH, Emanuel BS.
LinkIconAm J Hum Genet. 2010 Aug 13;87(2):209-18. Epub 2010 Jul 30.

The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.
Kurahashi H, Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS.
LinkIconClin Genet. 2010 Oct;78(4):299-309

Paternal origin of the de novo constitutional t(11;22)(q23;q11).
Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MV, Medne L, Zackai EH, Emanuel BS, Kurahashi H.
LinkIconEur J Hum Genet. 2010 Jul;18(7):783-7. Epub 2010 Feb 24.

Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.
Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H.
LinkIconHum Mol Genet. 2010 Jul 1;19(13):2630-7. Epub 2010 Apr 13.

Impaired DNA replication prompts deletion within palindromic sequences, but does not induce translocations in human cells.
Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS
LinkIconHum Mol Genet. 2009 Sep; 18(18):3397-406.

Chromosomal instability mediated by non-B DNA: Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.
Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H
LinkIconGenome Res. 2009 Feb; 19(2):191-8.

Two different forms of palindrome resolution in the human genome: deletion or translocation.
Kato T, Inagaki H, Kogo H, Ohye T, Yamada K, Emanuel BS, Kurahashi H
LinkIconHum Mol Genet. 2008 Apr 15; 17(8):1184-91.

Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm.
Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Emanuel BS, Kurahashi H
LinkIconFertil Steril. 2007 Nov; 88(5):1446-8.

Molecular cloning of a translocation hotspot in 22q11.
Kurahashi H, Inagaki H, Hosoba E, Kato T, Ohye T, Kogo H, Emanuel BS
LinkIconGenome Res. 2007 Apr; 17(4):461-9.

Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.
Kogo H, Inagaki H, Ohye T, Kato T, Emanuel BS, Kurahashi H
LinkIconNucleic Acids Res. 2007 Jan 30; 35(4):1198-208.

Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22).
Ashley T, Gaeth AP, Inagaki H, Seftel A, Cohen MM, Anderson L, Kurahashi H, Emanuel BS
LinkIconAm J Hum Genet. 2006 Sep; 79(3):524-38.

Palindrome-mediated chromosomal translocations in humans.
Kurahashi H, Inagaki H, Kogo H, Ohye T, Kato T, Emanuel BS
LinkIconDNA Repair. 2006 Sep 8; 5(9-10):1136-1145.

Genetic variation affects de novo translocation frequency.
Kato T, Inagaki H, Yamada K, Kogo H, Ohye T, Kowa H, Nagaoka K, Taniguchi M, Emanuel BS, Kurahashi H
LinkIconScience. 2006 Feb 17; 311(5763):971. (Free full text)

Chromosomal translocations mediated by palindromic DNA.
Kurahashi H, Inagaki H, Kogo H, Ohye T, Kato T, Emanuel BS
LinkIconCell Cycle. 2006 Jun 15; 5(12):1297-303.

Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved among primates.
Inagaki H, Ohye T, Kogo H, Yamada K, Kowa H, Shaikh TH, Emanuel BS, Kurahashi H
LinkIconHum Mutat. 2005 Oct; 26(4):332-42.

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.
Kurahashi H, Inagaki H, Yamada K, Ohye T, Taniguchi M, Emanuel BS, Toda T
LinkIconJ Biol Chem. 2004 Aug; 279(34):35377-83.

染色体異数性(不妊・不育)プロジェクト

HORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activity.
Kogo H, Tsutsumi M, Inagaki H, Ohye T, Kiyonari H, Kurahashi H.
LinkIconGenes Cells. 2012 Nov;17(11):897-912. doi: 10.1111/gtc.12005. Epub 2012 Oct 8.

Failure of homologous synapsis and sex-specific reproduction problems.
Kurahashi H, Kogo H, Tsutsumi M, Inagaki H, Ohye T.
LinkIconFront Genet. 2012;3:112. doi: 10.3389/fgene.2012.00112. Epub 2012 Jun 18.

HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes.
Kogo H, Tsutsumi M, Ohye T, Inagaki H, Abe T, Kurahashi H.
LinkIconGenes Cells. 2012 Jun;17(6):439-54.

Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytes.
Tsutsumi M, Kowa-Sugiyama H, Bolor H, Kogo H, Inagaki H, Ohye T, Yamada K, Taniguchi-Ikeda M, Toda T, Kurahashi H.
LinkIconJ Hum Genet. 2012 May 31.

Molecular basis of maternal age-related increase in oocyte aneuploidy.
Kurahashi H, Tsutsumi M, Nishiyama S, Kogo H, Inagaki H, Ohye T.
LinkIconCongenit Anom (Kyoto). 2012 Mar;52(1):8-15

Characterization of a novel mouse gene encoding an SYCP3-like protein that relocalizes from the XY body to the nucleolus during prophase of male meiosis I.
Tsutsumi M, Kogo H, Kowa-Sugiyama H, Inagaki H, Ohye T, Kurahashi H.
LinkIconBiol Reprod. 2011 Jul;85(1):165-71. Epub 2011 Mar 30.

Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans.
Kogo H, Kowa-Sugiyama H, Yamada K, Bolor H, Tsutsumi M, Ohye T, Inagaki H, Taniguchi M, Toda T, Kurahashi H.
LinkIconJ Hum Genet. 2010 May;55(5):293-9. Epub 2010 Mar 26.

Recent advance in our understanding of the molecular nature of chromosomal abnormalities.
Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T
LinkIconJ Hum Genet. 2009; 54(5):253-60.

Mutations of the SYCP3 gene in women with recurrent pregnancy loss.
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
LinkIconAm J Hum Genet. 2009 Jan; 84(1):14-20.

CDH1 is a specific marker for undifferentiated spermatogonia in mouse testes.
Tokuda M, Kadokawa Y, Kurahashi H, Marunouchi T
LinkIconBiol Reprod. 2007 Jan; 76(1):130-41

Candidate genes for male factor infertility-validation.
Mori T, Kurahashi H, Shinka T, Nakahori Y, Taniguchi M, Toda T, Iwamoto T
LinkIconFertil Steril. 2006 Nov; 86(5):1553-4

Expression analysis of a mouse orthologue of HSFY, a candidate for the azoospermic factor on the human Y chromosome.
Kinoshita K, Shinka T, Sato Y, Kurahashi H, Kowa H, Chen G, Umeno M, Toida K, Kiyokage E, Nakano T, Ito S, Nakahori Y
LinkIconJ Med Invest. 2006 Feb; 53 (1-2):117-22.

周産期遺伝学プロジェクト

Contribution of fetal ANXA5 gene promoter polymorphisms to the onset of pre-eclampsia.
Ota S, Miyamura H, Nishizawa H, Inagaki H, Inagaki A, Inuzuka H, Suzuki M, Miyazaki J, Sekiya T, Udagawa Y, Kurahashi H.
LinkIconPlacenta. 2013 Dec;34(12):1202-10. doi: 10.1016/j.placenta.2013.09.010. Epub 2013 Oct 7.

Decreased expression of apelin in placentas from severe pre-eclampsia patients.
Inuzuka H, Nishizawa H, Inagaki A, Suzuki M, Ota S, Miyamura H, Miyazaki J, Sekiya T, Kurahashi H, Udagawa Y.
LinkIconHypertens Pregnancy. 2013 Nov;32(4):410-21.

MTA3 regulates CGB5 and Snail genes in trophoblast.
Chen Y, Miyazaki J, Nishizawa H, Kurahashi H, Leach R, Wang K.
LinkIconBiochem Biophys Res Commun. 2013 Apr 19;433(4):379-84.

Upregulation of HtrA4 in the placentas of patients with severe pre-eclampsia.
Inagaki A, Nishizawa H, Ota S, Suzuki M, Inuzuka H, Miyamura H, Sekiya T, Kurahashi H, Udagawa Y.
LinkIconPlacenta. 2012 Nov;33(11):919-26. doi: 10.1016/j.placenta.2012.08.003. Epub 2012 Sep 8.

Impact of indoleamine 2,3-dioxygenase on the antioxidant system in the placentas of severely pre-eclamptic patients.
Nishizawa H, Suzuki M, Pryor-Koishi K, Sekiya T, Tada S, Kurahashi H, Udagawa Y.
LinkIconSyst Biol Reprod Med. 2011 Aug.;57(4):174-178. Epub 2011 Jul 1.

Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction.
Nishizawa H, Ota S, Suzuki M, Kato T, Sekiya T, Kurahashi H, Udagawa Y.
LinkIconReprod Biol Endocrinol. 2011 Aug 2;9:107.

Polymorphism in annexin A5 gene promoter in Japanese women with recurrent pregnancy loss.
Miyamura H, Nishizawa H, Ota S,SuzukiM, Inagaki A, Egusa H, Nishiyama S, Kato T,Pryor-Koishi K,NakanishiI, FujitaT, ImayoshiY,Markoff A, Yanagihara I, Udagawa Y, Kurahashi H.
LinkIconMol Hum Reprod, 2011 Feb 2.

A rare synaptonemal complex protein 3 gene variant in unexplained female infertility.
Nishiyama S, Kishi T, Kato T, Suzuki M, Bolor H, Nishizawa H, Iwata N, Udagawa Y, Kurahashi H.
LinkIconMol Hum Reprod. 2010 Dec 15.

Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia.
Nishizawa H, Kato T, Ota S, Nishiyama S, Pryor-Koishi K, Suzuki M, Tsutsumi M, Inagaki H, Kurahashi H, Udagawa Y.
LinkIconAm J Reprod Immunol. 2010 Jul 1;64(1):68-76. Epub 2010 Feb 28.

CD9 Gene Variations Are Not Associated with Female Infertility in Humans
.
Nishiyama S, Kishi T, Kato T, Suzuki M, Nishizawa H, Pryor-Koishi K, Sawada T, Nishiyama Y, Iwata N, Udagawa Y, Kurahashi H
LinkIconGynecol Obstet Invest. 2010; 69(2): 116-21.

Analysis of nitric oxide metabolism as a placental or maternal factor underlying the etiology of pre-eclampsia.
Nishizawa H, Pryor-Koishi K, Suzuki M, Kato T, Sekiya T, Tada S, Kurahashi H, Udagawa Y
LinkIconGynecol Obstet Invest. 2009; 68(4): 239-47.

Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patients.
Nishizawa H, Pryor-Koishi K, Suzuki M, Kato T, Kogo H, Sekiya T, Kurahashi H, Udagawa Y
LinkIconMol Hum Reprod. 2008 Oct; 14(10): 595-602.

Mouse model for allogeneic fetal rejection recapitulates human pre-eclampsia.
Nishizawa H, Hasegawa K, Suzuki M, Achiwa Y, Kato T, Saito K, Kurahashi H, Udagawa Y
LinkIconJ Obstet Gynaecol Res. 2008 Feb; 34(1): 1-6.

Overproduction of the follistatin-related gene protein in the placenta and maternal serum of women with pre-eclampsia.
Pryor-Koishi K, Nishizawa H, Kato T, Kogo H, Murakami T, Tsuchida K, Kurahashi H, Udagawa Y
LinkIconBJOG. 2007 Sep; 114(19): 1128-37.

The etiological role of allogeneic fetal rejection in pre-eclampsia.
Nishizawa H, Hasegawa K, Suzuki M, Achiwa Y, Kato T, Saito K, Kurahashi H, Udagawa Y
LinkIconAm J Reprod Immunol. 2007 Jul; 58(1): 11- 20.

Microarray analysis of differentially expressed fetal genes in placental tissue derived from early and late onset severe pre-eclampsia.
Nishizawa H, Pryor-Koishi K, Kato T, Kowa H, Kurahashi H, Udagawa Y
LinkIconPlacenta. 2007 May-Jun; 28(5-6): 487-97.

学内共同研究プロジェクト

A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis.
Hibi Y, Ohye T, Ogawa K, Shimizu Y, Shibata M, Kagawa C, Mizuno Y, Kurahashi H, Iwase K.
LinkIconEndocr J. 2013 Oct 22. [Epub ahead of print]

Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient.
Tsuge I, Ito K, Ohye T, Kando N, Kondo Y, Nakajima Y, Inuo C, Kurahashi H, Urisu A.
LinkIconPediatr Pulmonol. 2013 Sep 18. doi: 10.1002/ppul.22814. [Epub ahead of print]

Global Gene Expression Profiling in PPAR-γ Agonist-Treated Kidneys in an Orthologous Rat Model of Human Autosomal Recessive Polycystic Kidney Disease.
Yoshihara D, Kugita M, Yamaguchi T, Aukema HM, Kurahashi H, Morita M, Hiki Y, Calvet JP, Wallace DP, Toyohara T, Abe T, Nagao S.
LinkIconPPAR Res. 2012;2012:695898. doi: 10.1155/2012/695898. Epub 2012 May 13.

A functional variation in the hypocretin neuropeptide precursor gene may be associated with obstructive sleep apnea syndrome in Japan.
Ahmed WA, Tsutsumi M, Nakata S, Mori T, Nishimura Y, Fujisawa T, Kato I, Nakashima M, Kurahashi H, Suzuki K.
LinkIconLaryngoscope. 2012 Apr;122(4):925-9. doi: 10.1002/lary.23179. Epub 2012 Feb 2.

Serum neutrophil gelatinase associated lipocalin during the early postoperative period predicts the recovery of graft function after kidney transplantation from donors after cardiac death.
Kusaka M, Iwamatsu F, Kuroyanagi Y, Nakaya M, Ichino M, Marubashi S, Nagano H, Shiroki R, Kurahashi H, Hoshinaga K.
LinkIconJ Urol. 2012 Jun;187(6):2261-7. Epub 2012 Apr 13.

You have full text access to this contentLack of association between orexin receptor gene polymorphisms and obstructive sleep apnea syndrome in Japanese (pages 73–77)
Wael A AHMED, Terumi MORI, Yoichi NISHIMURA, Seiichi NAKATA, Takema KATO, Wam ABDELHAMID, Hiroki KURAHASHI and Kenji SUZUKI
LinkIcon Sleep Biol Rhythms 9. 73-77 (2011),Article first published online: 22 FEB 2011

PPAR-gamma agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease.
Yoshihara D, Kurahashi H, Morita M, Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S.
LinkIconAm J Physiol Renal Physiol. 2011 Feb;300(2):F465-74. Epub 2010 Dec 8.

Polycystic kidney disease in Han:SPRD Cy rats is associated with elevated expression and mislocalization of SamCystin.
Nagao S, Morita M, Kugita M, Yoshihara D, Yamaguchi T, Kurahashi H, Calvet JP, Wallace DP.
LinkIconAm J Physiol Renal Physiol. 2010 Nov;299(5)

Global gene expression profiling in early-stage polycystic kidney disease in the Han:SPRD Cy rat identifies a role for RXR signaling.
Kugita M, Nishii K, Morita M, Yoshihara D, Kowa-Sugiyama H, Yamada K, Yamaguchi T, Wallace DP, Calvet JP, Kurahashi H, Nagao S.
LinkIconAm J Physiol Renal Physiol. 2010 Oct 6

Serum tissue inhibitor of metalloproteinases 1 (TIMP-1) predicts organ recovery from delayed graft function after kidney transplantation from donors after cardiac death.
Kusaka M, Kuroyanagi Y, Ichino M, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Sugitani A, Kurahashi H, Hoshinaga K.
LinkIconCell Transplant. 2010 Jun 3

Urinary neutrophil gelatinase-associated lipocalin is a potential non-invasive marker for renal scarring in patients with vesicoureteral reflux
Ichino M, Kusaka M, Kuroyanagi Y, Mori T, Morooka M, Sasaki H, Shiroki R, Shishido S, Kurahashi H, Hoshinaga K
LinkIconJ Urol. 2010 May;183(5):2001-7. Epub 2010 Mar 19.

Angiotensin converting enzyme 2 gene expression increased compensatory for left ventricular remodeling in patients with end-stage heart failure.
Ohtsuki M, Morimoto SI, Izawa H, Ismail TF, Ishibashi-Ueda H, Kato Y, Horii T, Isomura T, Suma H, Nomura M, Hishida H, Kurahashi H, Ozaki Y
LinkIconInt J Cardiol. 2010 Jan 6.

Global expression profiles in one hour biopsy of human kidney transplantation from donors after cardiac death
Kusaka M, Kuroyanagi Y, Mori T, Nagaoka K, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Kurahashi H, Hoshinaga K
LinkIconCell Transplant. 2009 Nov 5-6; 18(10): 647-56.

Correlation of axillary osmidrosis to a SNP in the ABCC11 gene determined by the smart-amplification process (SMAP).
Inoue Y, Mori T, Sakurai A, Mitani Y, Toyoda Y, Ishikawa T, Hayashizaki Y, Yoshimura Y, Kurahashi H, Sakai Y
LinkIconJ Plast Reconstr Aesthet Surg. 2009 Jul 20.

Increased urinary neutrophil gelatinase-associated lipocalin levels in a rat model of upper urinary tract infection.
Ichino M, Kuroyanagi Y, Kusaka M, Mori T, Ishikawa K, Shiroki R, Kurahashi H, Hoshinaga K
LinkIconJ Urol. 2009 May; 181(5): 2326-31.

Up-regulated cytokine inducible SH2-containing protein expression in allergen-stimulated T cells from hen’s egg-allergic patients.
Nakajima Y, Tsuge I, Kondo Y, Komatsubara R, Hirata N, Kakami M, Kato M, Kurahashi H, Urisu A, Asano Y
LinkIconClin Exp Allergy. 2008 Sep; 38(9): 1499-506.

Global gene expression profiling on renal scarring in rat model of pyelonephritis
Ichino M, Mori T, Kusaka M, Kuroyanagi Y, Ishikawa K, Shiroki R, Kowa H, Kurahashi H, Hoshinaga K
LinkIconPediatr Nephrol. 2008 Jul; 23(7): 1059-71.

Serum neutrophil gelatinase-associated lipocalin as a predictor of organ recovery from delayed graft function after kidney transplantation applying donation after cardiac death
Kusaka M, Kuroyanagi Y, Mori T, Nagaoka K, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Kurahashi H, Hoshinaga K
LinkIconCell Transplant. 2008; 17(1-2): 129-34.

Calcium channel inhibition with verapamil accelerates polycystic kidney disease progression in the Cy/+ rat
Nagao S, Nishii K, Yoshihara D, Kurahashi H, Nagaoka K, Yamashita T, Takahashi H, Yamaguchi T, Calvet JP, Wallace DP
LinkIconKidney Int. 2008 Feb; 73(3): 269-77.

Genomewide expression profiles of rat model renal isografts from brain dead donors
Kusaka M, Kuroyanagi Y, Kowa H, Nagaoka K, Mori T, Yamada K, Shiroki R, Kurahashi H, Hoshinaga K
LinkIconTransplantation. 2007 Jan 15; 83(1): 62-70.

Up-regulation of osteopontin, chemokines, adhesion molecule, and heat shock proteins in 1-hour biopsy from cardiac death donor kidneys.
Kusaka M, Kuroyanagi Y, Mori T, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Kurahashi H, Hoshinaga K
LinkIconTransplant Proc. 2006 Dec; 38(10): 3347-50.

Increased water intake decreases progression of polycystic kidney disease in the PCK rat
Nagao S, Nishii K, Katsuyama M, Kurahashi H, Marunouchi T, Takahashi H, Wallace DP
LinkIconJ Am Soc Nephrol. 2006 Aug; 17(8): 2220-7.

Androgen receptor pathway in rats with autosomal dominant polycystic kidney disease.
Nagao S, Kusaka M, Nishii K, Marunouchi T, Kurahashi H, Takahashi H, Grantham J
LinkIconJ Am Soc Nephrol. 2005 Jul; 16(7): 2052-62.

Gene expression profile in rat renal isografts from brain death donors.
Kusaka M, Yamada K, Kuroyanagi Y, Terauchi A, Kowa H, Kurahashi H, Hoshinaga K
LinkIconTransplant Proc. 2005 Jan-Feb; 37(1): 364-6.

学外共同研究プロジェクト


Definition and refinement of the 7q36.3 duplication region associated with schizophrenia.
Aleksic B, Kushima I, Ohye T, Ikeda M, Kunimoto S, Nakamura Y, Yoshimi A, Koide T, Iritani S, Kurahashi H, Iwata N, Ozaki N.
LinkIconSci Rep. 2013;3:2587. doi: 10.1038/srep02587.

Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy.
Taniguchi-Ikeda M, Kobayashi K, Kanagawa M, Yu CC, Mori K, Oda T, Kuga A, Kurahashi H, Akman HO, DiMauro S, Kaji R, Yokota T, Takeda S, Toda T.
LinkIconNature. 2011 Oct 5;478(7367):127-31.

Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype
Kano H, Kurahashi H, Toda T
LinkIconProc Natl Acad Sci U S A. 2007 Nov 27; 104(48): 19034-9.

Analysis of gene expression profiles by oligonucleotide microarray in children with influenza.
Kawada J, Kimura H, Kamachi Y, Nishikawa K, Taniguchi M, Nagaoka K, Kurahashi H, Kojima S, Morishima T
LinkIconJ Gen Virol. 2006 Jun; 87(Pt 6): 1677-83.

Differential expression of caveolin-3 in mouse smooth muscle cells in vivo.
Kogo H, Ito S, Moritoki Y, Kurahashi H, Fujimoto T
LinkIconCell Tissue Res. 324(2): 291-300. 2006.

Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-α2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T
LinkIconBiochem Biophys Res Commun. 2006 Apr 7; 342(2): 489-502.

Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in α-dystroglycanopathies
Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, Tsukahara T, Tajima Y, Ozono K, Nishino I, Nonaka I, Toda T
LinkIconHum Mol Genet. 2006 Apr 15;15(8): 1279-89.

Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation (SHFM)
Kano H, Kurosawa K, Horii E, Ikegawa S, Yoshikawa H, Kurahashi H, Toda T
LinkIconHum Genet. 2005 Dec; 118(3-4): 477-83.

Basement membrane fragility underlies embryonic lethality in fukutin-null mice
Kurahashi H, Taniguchi M, Meno C, Taniguchi Y, Takeda S, Horie M, Otani H, Toda T
LinkIconNeurobiol Dis. 2005 Jun-Jul; 19(1-2): 208-217.

Fukutin and α-dystroglycanopahties
Toda T, Chiyonobu T, Xiong H, Tachikawa M, Kobayashi K, Manya H, Takeda S, Taniguchi M, Kurahashi H, Endo T
LinkIconActa Myol. 2005 Oct;24(2):60-3.

Human herpesvirus 6 (HHV-6) is transmitted from parent to child in an integrated form and characterization of cases with chromosomally integrated HHV-6 DNA.
Tanaka-Taya K, Sashihara J, Kurahashi H, Amo K, Miyagawa H, Kondo K, Okada S, Yamanishi K.
LinkIconJ Med Virol. 2004 Jul; 73(3): 465-73.


Ras/MEK pathway is required for NGF-induced expression of tyrosine hydroxylase gene
Suzuki T, Kurahashi H, Ichinose H
LinkIconBiochem Biophys Res Commun. 2004 Mar 5;315(2):389-96.




2014/01/25