Výsledky vyhledávání - Shiro Ikegawa
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Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers Autor Atsushi Watanabe, Tatsuki Karasugi, Hideaki Sawai, Banyar Than Naing, Shiro Ikegawa, Hideo Orimo, Takashi Shimada
Vydáno 2010Artigo -
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Identification of DNA methylation changes associated with disease progression in subchondral bone with site-matched cartilage in knee osteoarthritis Autor Yanfei Zhang, Naoshi Fukui, M. Yahata, Yozo Katsuragawa, Toshiyuki Tashiro, Shiro Ikegawa, Ming Ta Michael Lee
Vydáno 2016Artigo -
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Replication of the association of the aspartic acid repeat polymorphism in the asporin gene with knee-osteoarthritis susceptibility in Han Chinese Autor Qing Jiang, Dongquan Shi, Long Yi, Shiro Ikegawa, Yong Wang, Takahiro Nakamura, Di Qiao, Cheng Liu, Jin Dai
Vydáno 2006Artigo -
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PLAP-1/Asporin, a Novel Negative Regulator of Periodontal Ligament Mineralization Autor Satoru Yamada, Miki Tomoeda, Yasuhiro Ozawa, Shinya Yoneda, Yoshimitsu Terashima, Kazuhiko Ikezawa, Shiro Ikegawa, Masahiro Saito, Satoru Toyosawa, Shinya Murakami
Vydáno 2007Artigo -
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Meta-analysis of association between the ASPN D-repeat and osteoarthritis Autor Takahiro Nakamura, Dongquan Shi, Maria Tzetis, Julio A. Rodriguez‐Lopez, Yoshinari Miyamoto, Aspasia Tsezou, Antonio González, Qing Jiang, Naoyuki Kamatani, John Loughlin, Shiro Ikegawa
Vydáno 2007Revisão -
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TRPV1 alleviates osteoarthritis by inhibiting M1 macrophage polarization via Ca2+/CaMKII/Nrf2 signaling pathway Autor Zhongyang Lv, Xingquan Xu, Ziying Sun, Yannick Xiaofan Yang, Hu Guo, Jiawei Li, Kuoyang Sun, Rui Wu, Jia Xu, Qing Jiang, Shiro Ikegawa, Dongquan Shi
Vydáno 2021Artigo -
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Association of the D repeat polymorphism in the ASPNgene with developmental dysplasia of the hip: a case-control study in Han Chinese Autor Dongquan Shi, Jin Dai, Pengsheng Zhu, Jianghui Qin, Lunqing Zhu, Hongtao Zhu, Baocheng Zhao, Xusheng Qiu, Zhihong Xu, Dongyang Chen, Long Yi, Shiro Ikegawa, Qing Jiang
Vydáno 2011Artigo -
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Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction Autor Nobuaki Ishii, Kouichi Ozaki, Hiroshi Sato, Hiroya Mizuno, Susumu Saito, Atsushi Takahashi, Yoshinari Miyamoto, Shiro Ikegawa, Naoyuki Kamatani, Masatsugu Hori, Satoshi Saito, Yusuke Nakamura, Toshihiro Tanaka
Vydáno 2006Artigo -
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Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases Autor Masahiro Kanai, Masato Akiyama, Atsushi Takahashi, Nana Matoba, Yukihide Momozawa, Masashi Ikeda, Nakao Iwata, Shiro Ikegawa, Makoto Hirata, Koichi Matsuda, Michiaki Kubo, Yukinori Okada, Yoichiro Kamatani
Vydáno 2018Artigo -
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SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese Autor Yanhui Fan, You‐Qiang Song, Danny Chan, Yohei Takahashi, Shiro Ikegawa, Morio Matsumoto, Ikuyo Kou, Kathryn S.E. Cheah, Pak C. Sham, Kmc Cheung, K.D.K. Luk
Vydáno 2012Artigo -
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Functional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis De... Autor Long Guo, Hiroshi Yamashita, Ikuyo Kou, Aki Takimoto, Makiko Meguro‐Horike, Shin‐ichi Horike, Tetsushi Sakuma, Shigenori Miura, Taiji ADACHI, Takashi Yamamoto, Shiro Ikegawa, Yuji Hiraki, Chisa Shukunami
Vydáno 2016Artigo -
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Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases Autor Tatsuya Furuichi, Hülya Kayserili, Shûichi Hiraoka, Gen Nishimura, Hirofumi Ohashi, Yasemin Alanay, JUAN LERENA, Ayça Dilruba Aslanger, Haruhiko Koseki, Daniel H. Cohn, Andrea Superti‐Furga, Sheila Unger, Shiro Ikegawa
Vydáno 2009Carta
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Genotype
Pathology
Single-nucleotide polymorphism
Phenotype
Alternative medicine
Anatomy
Internal medicine
Osteoarthritis
Genetic association
Allele
Mutation
Cell biology
Genome-wide association study
Genome
Bioinformatics
Biochemistry
Cartilage
Scoliosis
Chemistry
Computational biology
Exome sequencing
Molecular biology
Odds ratio
SNP
Dysplasia
Endocrinology