متابعة
Aritoshi Iida
Aritoshi Iida
Medical Genome Center, NCNP, Tokyo
بريد إلكتروني تم التحقق منه على ncnp.go.jp
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis
A Suzuki, R Yamada, X Chang, S Tokuhiro, T Sawada, M Suzuki, ...
Nature genetics 34 (4), 395-402, 2003
14412003
Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction
K Ozaki, Y Ohnishi, A Iida, A Sekine, R Yamada, T Tsunoda, H Sato, ...
Nature genetics 32 (4), 650-654, 2002
12992002
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease
K Yamazaki, D McGovern, J Ragoussis, M Paolucci, H Butler, D Jewell, ...
Human molecular genetics 14 (22), 3499-3506, 2005
6052005
An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis
H Kizawa, I Kou, A Iida, A Sudo, Y Miyamoto, A Fukuda, A Mabuchi, ...
Nature genetics 37 (2), 138-144, 2005
5472005
Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-α secretion in vitro
K Ozaki, K Inoue, H Sato, A Iida, Y Ohnishi, A Sekine, H Sato, K Odashiro, ...
Nature 429 (6987), 72-75, 2004
3112004
Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
K Yamazaki, M Takazoe, T Tanaka, T Ichimori, S Saito, A Iida, Y Onouchi, ...
Journal of human genetics 49 (12), 664-668, 2004
1602004
Catalog of 605 single-nucleotide polymorphisms (snps) among 13 genes encoding human atp-binding cassette transporters: abca4, abca7, abca8, abcd1, abcd3, abcd4, abce1, abcf1 …
A Iida, S Saito, A Sekine, C Mishima, Y Kitamura, K Kondo, S Harigae, ...
Journal of human genetics 47 (6), 285-310, 2002
1592002
A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese
H Mototani, A Mabuchi, S Saito, M Fujioka, A Iida, Y Takatori, A Kotani, ...
Human molecular genetics 14 (8), 1009-1017, 2005
1552005
Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR)
S Saito, A Iida, A Sekine, Y Miura, C Ogawa, S Kawauchi, S Higuchi, ...
Journal of human genetics 47 (4), 147-171, 2002
1472002
A functional SNP in BNC2 is associated with adolescent idiopathic scoliosis
Y Ogura, I Kou, S Miura, A Takahashi, L Xu, K Takeda, Y Takahashi, ...
The American Journal of Human Genetics 97 (2), 337-342, 2015
1442015
Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disorders
M Nakajima, S Mizumoto, N Miyake, R Kogawa, A Iida, H Ito, H Kitoh, ...
The American Journal of Human Genetics 92 (6), 927-934, 2013
1442013
A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population
K Ozaki, H Sato, A Iida, H Mizuno, T Nakamura, Y Miyamoto, A Takahashi, ...
Nature genetics 38 (8), 921-925, 2006
1312006
Expansion of GGC repeat in GIPC1 is associated with oculopharyngodistal myopathy
J Deng, J Yu, P Li, X Luan, L Cao, J Zhao, M Yu, W Zhang, H Lv, Z Xie, ...
The American Journal of Human Genetics 106 (6), 793-804, 2020
1292020
Citrullination of RGG motifs in FET proteins by PAD4 regulates protein aggregation and ALS susceptibility
C Tanikawa, K Ueda, A Suzuki, A Iida, R Nakamura, N Atsuta, G Tohnai, ...
Cell reports 22 (6), 1473-1483, 2018
126*2018
Molecular Strategy for Detecting Metastatic Cancers with Use of Multiple Tumor-specific MAGE-A Genes
I Miyashiro, C Kuo, K Huynh, A Iida, D Morton, A Bilchik, A Giuliano, ...
Clinical Chemistry 47 (3), 505-512, 2001
1262001
Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association …
N Kamatani, A Sekine, T Kitamoto, A Iida, S Saito, A Kogame, E Inoue, ...
The American Journal of Human Genetics 75 (2), 190-203, 2004
1102004
Single nucleotide polymorphisms in the gene encoding Krüppel-like factor 7 are associated with type 2 diabetes
A Kanazawa, Y Kawamura, A Sekine, A Iida, T Tsunoda, A Kashiwagi, ...
Diabetologia 48, 1315-1322, 2005
1082005
Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes
A Iida, A Sekine, S Saito, Y Kitamura, T Kitamoto, S Osawa, C Mishima, ...
Journal of human genetics 46 (4), 225-240, 2001
1052001
Three hundred twenty-six genetic variations in genes encoding nine members of ATP-binding cassette, subfamily B (ABCB/MDR/TAP), in the Japanese population
S Saito, A Iida, A Sekine, Y Miura, C Ogawa, S Kawauchi, S Higuchi, ...
Journal of human genetics 47 (1), 38-50, 2002
1042002
CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations
M Ogasawara, A Iida, T Kumutpongpanich, A Ozaki, Y Oya, H Konishi, ...
Acta Neuropathologica Communications 8, 1-8, 2020
1002020
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مقالات 1–20