欧文原著(2015)

2015年1月23日

欧文原著

2015

 

Murata C, Kuroki Y, Imoto I, Tsukahara M, Ikejiri N, Kuroiwa A.

Initiation of recombination suppression and PAR formation during the early stages of neo-sex chromosome differentiation in the Okinawa spiny rat, Tokudaia muenninki.

BMC Evolutionary Biology 2015, 15:234  doi:10.1186/s12862-015-0514-y.

 

 

 

Kohmoto T, Naruto T, Kobayashi H, Watanabe M, Okamoto N, Masuda K, Imoto I*, Okamoto N.

A novel COL11A1 mutation affecting splicing in a patient with Stickler syndrome.

Hum Genome Variation.2015215043​doi:10.1038/hgv.2015.43.

 

 
Morita K, Naruto T, Tanimoto K, Yasukawa C, Oikawa Y, Masuda K, Imoto I, Inazawa J, Omura K, Harada H.

Simultaneous detection of both single nucleotide variations and copy number alterations by next-generation sequencing in Gorlin syndrome.

PLoS One.2015;10(11):e0140480.doi: 10.1371/journal.pone.0140480.

 

 
Nishijima H, Kitano S, Miyachi H, Morimoto J, Kawano H, Hirota F, Morita R, Mouri Y, Masuda K, Imoto I, Ikuta K, Matsumoto M.

Ectopic Aire expression in 1 the thymic cortex reveals inherent properties of Aire as a tolerogenic factor within the medulla.

J Immunol.2015;195(10):4641-9. doi: 10.4049/jimmunol.1501026.

 

 
Shoda K, Masuda K, Ichikawa D, Arita T, Miyagami Y, Watanabe M, Konishi H, Imoto I*, Otsuji E.

HER2 amplification detected in the circulating DNA of patients with gastric cancer: a retrospective pilot study.

Gastric Cancer 2015;18(4):698-710. doi: 10.1007/s10120-014-0432-5.

 

 
Morine M, Kohmoto T, Masuda K, Inagaki H, Watanabe M, Naruto T, Kurahashi H, Maeda K, Imoto I*.

A unique TBX5 microdeletion with microinsertion detected in patient with Holt–Oram syndrome.

Am J Med Genet A2015 Sep 4. doi: 10.1002/ajmg.a.37359. [Epub ahead of print].

 


Numata S, Kinoshita M, Tajima A, Nishi A, Imoto I, Ohmori T. 

Evaluation of an association between plasma total homocysteine and schizophrenia by a Mendelian randomization analysis.

2015;167(12):3192-6. doi: 10.1002/ajmg.a.37359.

 

 

 

Honda S, Loher P, Shigematsu M, Palazzo JP, Suzuki R, Imoto I, Rigoutsos I, Kirino Y.

Sex hormone-dependent tRNA halves enhance cell proliferation in breast and prostate cancers.

Proc Natl Acad Sci USA.2015; 112(29):E3816-25. doi: 10.1073/pnas.1510077112.

 

 

 

Inoshita M, Numata S, Tajima A, Kinoshita M, Umehara H, Yamamori H, Hashimoto R, Imoto I, Ohmori T.

Sex differences of leukocytes DNA methylation adjusted for estimated cellular proportions.

Biology of Sex Differences (in press)

 

 

 

Naruto T, Okamoto N, Masuda K, Endo T, Hatsukawa Y, Kohmoto T, Imoto I*.

Deep intronic GPR143 mutation in a Japanese family with ocular albinism.

Scientific Reports 2015 Jun 10;5:11334. doi: 10.1038/srep11334.

 

 

Umehara H, Numata S, Tajima A, Kinoshita M, Nakaaki S, Imoto I, Sumitani S, Ohmori T.

No association between the COMT Val158Met polymorphism and the long-term clinical response in obsessive-compulsive disorder in the Japanese population.

Hum Psychopharmacol.2015;30(5):372-6. doi: 10.1002/hup.2485.

 

 
Sato Y, Tajima A Tsunematsu K, Nozawa S, Yoshiike M, Koh E, Kanaya J, Namiki M, Matsumiya K, Tsujimura A, Komatsu K,Itoh N, Eguchi J, Imoto I, Yamauchi A, Iwamoto T.

An association study of four candidate loci for human male fertility traits with male infertility.

Hum Reprod 2015 Jun;30(6):1510-4. doi: 10.1093/humrep/dev088.

 

 
Sato Y, Tajima A Tsunematsu K, Nozawa S, Yoshiike M, Koh E, Kanaya J, Namiki M, Matsumiya K, Tsujimura A, Komatsu K,Itoh N, Eguchi J, Imoto I, Yamauchi A, Iwamoto T.

Lack of replication of four candidate SNPs implicated in human male fertility traits: a large-scale population-based study.

Hum Reprod 2015 Jun;30(6):1505-9. doi: 10.1093/humrep/dev081.

 

 

 

Yanagisawa S, Sakurada Y, Miki A, Matsumiya W, Imoto I, Honda S.

The association of elastin gene variants with two angiographic subtypes of polypoidal choroidal vasculopathy.

PLoS One 2015;10(3):e0120643. doi: 10.1371/journal.pone.0120643

 

 

 

Numata S, Ishii K, Tajima A, Iga JI, Kinoshita M, Watanabe S, Umehara H, Fuchikami M, Okada S, Boku S, Hishimoto A,Shimodera S, Imoto I, Morinobu S, Ohmori T.

Blood diagnostic biomarkers for major depressive disorder using multiplex DNA methylation profiles: discovery and validation.

Epigenetics 2015;10(2):135-41. doi: 10.1080/15592294.2014.1003743.

 

 

 

Yoshioka M, Shirayama Y, Imoto I, Hinode D, Yanagisawa S, Takeuchi Y.

Current status of collaborative relationships between dialysis facilities and dental facilities in Japan: results of a nationwide survey.

BMC Nephrology 2015;16:17 doi:10.1186/s12882-015-0001-0

 

 
Gao W, Higaki T, Eguchi-Ishimae M, Iwabuki H, Wu Z, Yamamoto E, Takata H, Ohta M, Imoto I, Ishii E, Eguchi M.

DGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defects.

Hum Genome Variation 2015;2:15004_1-7 doi:10.1038/hgv.2015.4

 


Kohmoto T, Okamoto N, Satomura S, Naruto T, Komori T, Hashimoto T, Imoto I*.

A FRMD7 variant in a Japanese family causes congenital nystagmus.

Hum Genome Variation 2015;2:15002_1-4 doi:10.1038/hgv.2015.2

 

 
Komatsu S, Ichikawa D, Hirajima S, Nagata H, Nishimura Y, Kawaguchi T, Miyamae M, Okajima W, Ohashi T, Konishi H,Shiozaki A, Fujiwara H, Okamoto K, Tsuda H, Imoto I, Inazawa J, Otsuji E.

Overexpression of SMYD2 contributes to malignant outcome in gastric cancer.

Br J Cancer. 2015;112(2):357-64. doi: 10.1038/bjc.2014.543.

 

 
Inoue A, Okamoto K, Fujino Y, Nakagawa T, Muguruma N, Sannomiya K, Mitsui Y, Takaoka T, Kitamura S, Miyamoto H,Okahisa T, Fujimori T, Imoto I, Takayama T.

B-RAF mutation and accumulated gene methylation in aberrant crypt foci (ACF), sessile serrated adenoma/polyp (SSA/P)and cancer in SSA/P.

Br J Cancer. 2015;112(2):403-12. doi: 10.1038/bjc.2014.545.

 

 

 

Maeda K, Imoto I, Kaji T, Yoshida Y, Nakayama S, Irahara M.

A case of non-mosaic trisomy 20 in amniotic fluid cultures without anomalies in the fetus: cytogenetic discrepancy betweenamniocytes and fetal blood.

J Obstet Gynecol Res 2015;41(1):141-4. doi: 10.1111/jog.12488.

 

 
Hosoda F, Arai Y, Okada N, Shimizu H, Miyamoto M, Kitagawa N, Katai H, Taniguchi H, Yanagihara K, Imoto I, Inazawa J,Ohki M, Shibata T.

Integrated genomic and functional analyses reveal glyoxalase I as a novel metabolic oncogene in human gastric cancer.

Oncogene 2015;34(9):1196-206. doi: 10.1038/onc.2014.57.

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