欧文原著(2016)Ⅰ

2016年1月12日

欧文原著 

2016 

 

 

Umehara H, Numata S, Tajima A, Nishi A, Nakataki M, Imoto I, Sumitani S, Ohmori T.

Calcium signaling pathway is associated with the long-term clinical response to selective serotonin reuptake inhibitors (SSRI) and SSRI with antipsychotics in patients with obsessive-compulsive disorder.

PLoS One. 2016 Jun 9;11(6):e0157232. doi: 10.1371/journal.pone.0157232. 

 

 

 Inoshita M, Numata S, Tajima A, Kinoshita M, Umehara H, Nakataki M, Ikeda M, Maruyama S, Yamamori H, Kanazawa T, Shimodera S, Hashimoto R, Imoto I, Yoneda H, Iwata N, Ohmori T.

A significant causal association between C-reactive protein levels and schizophrenia.

Sci Rep. 2016;6:26105. doi: 10.1038/srep26105.

 

 

 Watanabe M, Hayabuchi Y, Ono A, Naruto T, Horikawa H,Kohmoto T, Masuda K, Nakagawa R, Hiromichi Ito H, Kagami S, Imoto I*.

Detection of 1p36 deletion by clinical exome-first diagnostic approach.

Hum Genome Var.2016:3:16006. ​doi:10.1038/hgv.2016.6.

 

 

 Hamada J, Shoda K, Masuda K, Fujita Y, Naruto T, Kohmoto T, Miyakami Y, Watanabe M, Kudo Y, Fujiwara H, Ichikawa D, Otsuji E, Imoto I*.

Tumor-promoting function and prognostic significance of the RNA-binding protein T-cell intracellular antigen-1 in esophageal squamous cell carcinoma.

Oncotarget.2016;7:17111-28. doi: 10.18632/oncotarget.7937.

 

 

Nishimoto S, Fukuda D, Higashikuni Y, Tanaka K, Hirata Y, Murata C, Kim-Kaneyama J, Sato F, Bando M, Yagi S, Soeki T, Hayashi T, Imoto I, Sakaue H, Shimabukuro M, Sata M.

Obesity-induced DNA release from adipocytes provokes chronic adipose tissue inflammation and insulin resistance.

2016;2(3):e1501332. doi: 10.1126/sciadv.1501332.

 

 

Kohmoto T, Shono M, Naruto T, Watanabe M, Suga K, Nakagawa R, Kagami S, Masuda K, Imoto I*.

A novel frameshift mutation of CHD7 in a Japanese patient with CHARGE syndrome.

Hum Genome Variation.2016;3:16004. doi: 10.1038/hgv.2016.4.

 

 

 Kohmoto T, Tsuji A, Morita K, Naruto T, Masuda K, Kashimada K, Enomoto K, Morio T, Harada H, Imoto I*.

A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndrome.

Hum Genome Variation .2016;3:16003. doi: 10.1038/hgv.2016.3.

 

 

 Obayashi M, Yoshida M, Tsunematsu T, Ogawa I, Sasahira T, Kuniyasu H, Imoto I, Abiko Y, Xu D, Fukunaga S, Tahara H, Kudo Y, Nagao T, Takata T.

microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer.

Oncotarget. 2016 Jan 22. doi: 10.18632/oncotarget.6972.

 

 

 Shoda K, Ichikawa D, Fujita Y, Masuda K, Hiramoto H, Hamada J, Arita T, Konishi H, Komatsu S, Shinozaki A, Kakihara N, Okamoto K, Taniguchi H, Imoto I*, Otsuji E.

Monitoring the HER2 copy number status in circulating tumor DNA by droplet digital PCR in patients with gastric cancer.

Gastric Cancer 2016 Feb 13. [Epub ahead of print]doi. 10.1007/s10120-016-0599-z.

 

 

 Murata C, Sawaya H, Nakata K, Yamada F, Imoto I, Kuroiwa A.

The cryptic Y-autosome translocation in the small Indian mongoose, Herpestes auropunctatus, revealed by molecular cytogenetic approaches.

Chromosoma. 2016 Jan 7. [Epub ahead of print]

 

 

 Kawarai T, Tajima A, Kuroda Y, Saji N, Orlacchio A, Terasawa H, Shimizu, Kita Y, Izumi Y, Mitsui T, Imoto I*, Kaji R.

A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability.

J Neurol Neurosurg Psychiatry. 2015 Jul 8. [Epub ahead of print] doi:10.1136/jnnp-2014-309828.

 

 

 Uehara DT, Hayashi S, Okamoto N, Mizuno S, Chinen Y, Kosaki R, Kosho T, Kurosawa K, Matsumoto H, Mitsubuchi H, Numabe H, Saitoh S, Makita Y, Hata A, Imoto I, Inazawa J.

SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements.

J Hum Genet. 2016 Jan 7. doi: 10.1038/jhg.2015.154. Epub 2016 Jan 7

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