研究業績 Publications


2017年

欧文原著

Kita K, Arai S, Nishiyama A, Taniguchi H, Fukuda K, Wang R, Yamada T, Takeuchi S, Tange S, Tajima A, Nakada M, Yasumoto K, Motoo Y, Murakami T, Yano S.
In vivo imaging xenograft models for the evaluation of anti-brain tumor efficacy of targeted drugs.
Cancer Med 6(12):2972?2983, 2017.

Watanabe H, Goto S, Mori H, Higashi K, Hosomichi K, Aizawa N, Takahashi N, Tsuchida M, Suzuki Y, Yamada T, Horii A, Inoue I, Kurokawa K, Narita I.
Comprehensive microbiome analysis of tonsillar crypts in IgA nephropathy.
Nephrol Dial Transplant 32(12):2072?2079, 2017.

Kawano T, Hosomichi K, Inoue I, Shimono R, Onishi S, Nakame K, Kaji T, Matsufuji H, Ieiri S.
Identification of a novel variant of the RET proto-oncogene in a novel family with Hirschsprung's disease.
Pediatr Surg Int 33(10):1041?1046, 2017.

Kohmoto T, Masuda K, Naruto T, Tange S, Shoda K, Hamada J, Saito M, Ichikawa D, Tajima A, Otsuji E, Imoto I.
Construction of a combinatorial pipeline using two somatic variant calling methods for whole exome sequence data of gastric cancer.
J Med Invest 64(3.4):233-240, 2017.

Ali MAE, Fuse K, Tadokoro Y, Hoshii T, Ueno M, Kobayashi M, Nomura N, Vu HT, Peng H, Hegazy AM, Masuko M, Sone H, Arai F, Tajima A, Hirao A.
Functional dissection of hematopoietic stem cell populations with a stemness-monitoring system based on NS-GFP transgene expression.
Sci Rep 7(1):11442, 2017.

Shinmyo Y, Terashita Y, Dinh Duong TA, Horiike T, Kawasumi M, Hosomichi K, Tajima A, Kawasaki H.
Folding of the cerebral cortex requires Cdk5 in upper-layer neurons in gyrencephalic mammals.
Cell Rep 20(9):2131-2143, 2017.

Higashino T, Takada T, Nakaoka H, Toyoda Y, Stiburkova B, Miyata H, Ikebuchi Y, Nakashima H, Shimizu S, Kawaguchi M, Sakiyama M, Nakayama A, Akashi A, Tanahashi Y, Kawamura Y, Nakamura T, Wakai K, Okada R, Yamamoto K, Hosomichi K, Hosoya T, Ichida K, Ooyama H, Suzuki H, Inoue I, Merriman TR, Shinomiya N, Matsuo H.
Multiple common and rare variants of ABCG2 cause gout.
RMD Open 3(2):e000464, 2017.

Akatsuka H, Kuga S, Masuhara K, Davaadorj O, Okada C, Iida Y, Okada Y, Fukunishi N, Suzuki T, Hosomichi K, Ohtsuka M, Tanaka M, Inoue I, Kimura M, Sato T.
AMBRA1 is involved in T cell receptor-mediated metabolic reprogramming through an ATG7-independent pathway.
Biochem Biophys Res Commun 491(4):1098-1104, 2017.

Oka A, Asano Y, Hasegawa M, Fujimoto M, Ishikawa O, Kuwana M, Kawaguchi Y, Yamamoto T, Takahashi H, Goto D, Endo H, Jinnin M, Mano S, Hosomichi K, Mabuchi T, Ueda MT, Nakagawa S, Beck S, Bahram S, Takehara K, Sato S, Ihn H.
RXRB is a MHC-encoded susceptibility gene associated with anti-topoisomerase I antibody-positive systemic sclerosis.
J Invest Dermatol 137(9):1878-1886, 2017.

Nishi A, Numata S, Tajima A, Zhu X, Ito K, Saito A, Kato Y, Kinoshita M, Shimodera S, Ono S, Ochi S, Imamura A, Kurotaki N, Ueno SI, Iwata N, Fukui K, Imoto I, Kamiya A, Ohmori T.
De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activity.
Sci Rep 7(1):2887, 2017.

Zaimoku Y, Takamatsu H, Hosomichi K, Ozawa T, Nakagawa N, Imi T, Maruyama H, Katagiri T, Kishi H, Tajima A, Muraguchi A, Kashiwase K, Nakao S.
Identification of an HLA class I allele closely involved in the autoantigen presentation in acquired aplastic anemia.
Blood 129(21):2908-2916, 2017.
[Inside Blood Commentary] Blood 129(21):2824-2826, 2017.

Kasuga Y, Hata K, Tajima A, Ochiai D, Saisho Y, Matsumoto T, Arata N, Miyakoshi K, Tanaka M.
Association of common polymorphisms with gestational diabetes mellitus in Japanese women: A case-control study.
Endocr J 64(4):463-475, 2017.

Ahmadloo S, Nakaoka H, Hayano T, Hosomichi K, You H, Utsuno E, Sangai T, Nishimura M, Matsushita K, Hata A, Nomura F, Inoue I.
Rapid and cost-effective high-throughput sequencing for identification of germline mutations of BRCA1 and BRCA2.
J Hum Genet 62(5):561-567, 2017.

Ueda H, Sasaki K, Halder SK, Deguchi Y, Takao K, Miyakawa T, Tajima A.
Prothymosin alpha-deficiency enhances anxiety-like behaviors and impairs learning/memory-functions and neurogenesis.
J Neurochem 141(1):124-136, 2017.

Sato Y, Tajima A, Katsurayama M, 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 independent validation study of three single nucleotide polymorphisms at the sex hormone-binding globulin locus for testosterone levels identified by genome-wide association studies.
Hum Reprod Open 2017(1):hox002, 2017.
[Correction] Hum Reprod Open 2017(1):hox005, 2017.

Kinoshita M, Numata S, Tajima A, Yamamori H, Yasuda Y, Fujimoto M, Watanabe S, Umehara H, Shimodera S, Nakazawa T, Kikuchi M, Nakaya A, Hashimoto H, Imoto I, Hashimoto R, Ohmori T.
Effect of clozapine on DNA methylation in peripheral leukocytes from patients with treatment-resistant schizophrenia.
Int J Mol Sci 18(3):632, 2017.

Yamaguchi T, Hosomichi K, Yano K, Kim YI, Nakaoka H, Kimura R, Otsuka H, Nonaka N, Haga S, Takahashi M, Shirota T, Kikkawa Y, Yamada A, Kamijo R, Park SB, Nakamura M, Maki K, Inoue I.
Comprehensive genetic exploration of selective tooth agenesis of mandibular incisors by exome sequencing.
Hum Genome Var 4:17005, 2017.

Kanzawa-Kiriyama H, Kryukov K, Jinam TA, Hosomichi K, Saso A, Suwa G, Ueda S, Yoneda M, Tajima A, Shinoda KI, Inoue I, Saitou N.
A partial nuclear genome of the Jomons who lived 3000 years ago in Fukushima, Japan.
J Hum Genet 62(2):213-221, 2017.

Mori T, Hosomichi K, Chiga M, Mandai S, Nakaoka H, Sohara E, Okado T, Rai T, Sasaki S, Inoue I, Uchida S.
Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel.
Clin Exp Nephrol 21(1):63-75, 2017.

Takahashi M, Hosomichi K, Yamaguchi T, Yano K, Funatsu T, Adel M, Haga S, Maki K, Tajima A.
Whole-exome sequencing analysis of supernumerary teeth occurrence in Japanese individuals.
Hum Genome Var 4:16044, 2017.

Romero V, Hosomichi K, Nakaoka H, Shibata H, Inoue I.
Structure and evolution of the filaggrin gene repeated region in primates.
BMC Evol Biol 17(1):10, 2017.

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