Makita Y - Search Results

1

Association of TNFRSF4 gene polymorphisms with essential hypertension.

Mashimo Y, Suzuki Y, Hatori K, Tabara Y, Miki T, Tokunaga K, Katsuya T, Ogihara T, Yamada M, Takahashi N, Makita Y, Nakayama T, Soma M, Hirawa N, Umemura S, Ohkubo T, Imai Y, Hata A. Mashimo Y, et al. Among authors: makita y. J Hypertens. 2008 May;26(5):902-13. doi: 10.1097/HJH.0b013e3282f6a65e. J Hypertens. 2008. PMID: 18398332

2

Mutation of the follicle-stimulating hormone receptor gene 5'-untranslated region associated with female hypertension.

Nakayama T, Kuroi N, Sano M, Tabara Y, Katsuya T, Ogihara T, Makita Y, Hata A, Yamada M, Takahashi N, Hirawa N, Umemura S, Miki T, Soma M. Nakayama T, et al. Among authors: makita y. Hypertension. 2006 Sep;48(3):512-8. doi: 10.1161/01.HYP.0000233877.84343.d7. Epub 2006 Jul 24. Hypertension. 2006. PMID: 16864747

3

Association between fatty acid binding protein 3 gene variants and essential hypertension in humans.

Ueno T, Soma M, Tabara Y, Tokunaga K, Tahira K, Fukuda N, Matsumoto K, Nakayama T, Katsuya T, Ogihara T, Makita Y, Hata A, Yamada M, Takahashi N, Hirawa N, Umemura S, Miki T. Ueno T, et al. Among authors: makita y. Am J Hypertens. 2008 Jun;21(6):691-5. doi: 10.1038/ajh.2008.40. Epub 2008 Apr 10. Am J Hypertens. 2008. PMID: 18437121

4

Association of SLC6A9 gene variants with human essential hypertension.

Ueno T, Tabara Y, Fukuda N, Tahira K, Matsumoto T, Kosuge K, Haketa A, Matsumoto K, Sato Y, Nakayama T, Katsuya T, Ogihara T, Makita Y, Hata A, Yamada M, Takahashi N, Hirawa N, Umemura S, Miki T, Soma M. Ueno T, et al. Among authors: makita y. J Atheroscler Thromb. 2009 Jun;16(3):201-6. doi: 10.5551/jat.e125. Epub 2009 Jun 25. J Atheroscler Thromb. 2009. PMID: 19556729 Free article.

5

Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis.

Ohmori H, Makita Y, Funamizu M, Hirooka K, Hosoi T, Orimo H, Suzuki T, Ikari K, Nakajima T, Inoue I, Hata A. Ohmori H, et al. Among authors: makita y. J Hum Genet. 2002;47(8):400-6. doi: 10.1007/s100380200058. J Hum Genet. 2002. PMID: 12181640

6

Haplotype analysis of the human collectin placenta 1 (hCL-P1) gene.

Ohmori H, Makita Y, Funamizu M, Chiba S, Ohtani K, Suzuki Y, Wakamiya N, Hata A. Ohmori H, et al. Among authors: makita y. J Hum Genet. 2003;48(2):82-5. doi: 10.1007/s100380300011. J Hum Genet. 2003. PMID: 12601552

7

The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation.

Hayashi S, Mizuno S, Migita O, Okuyama T, Makita Y, Hata A, Imoto I, Inazawa J. Hayashi S, et al. Among authors: makita y. Am J Med Genet A. 2008 Aug 15;146A(16):2145-51. doi: 10.1002/ajmg.a.32433. Am J Med Genet A. 2008. PMID: 18629876

8

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

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. Uehara DT, et al. Among authors: makita y. J Hum Genet. 2016 Apr;61(4):335-43. doi: 10.1038/jhg.2015.154. Epub 2016 Jan 7. J Hum Genet. 2016. PMID: 26740234

9

Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly.

Hayashi S, Okamoto N, Makita Y, Hata A, Imoto I, Inazawa J. Hayashi S, et al. Among authors: makita y. Am J Med Genet A. 2008 Nov 15;146A(22):2905-10. doi: 10.1002/ajmg.a.32519. Am J Med Genet A. 2008. PMID: 18925664

10

Methylenetetrahydrofolate reductase genotype, vitamin B12, and folate influence plasma homocysteine in hemodialysis patients.

Nakamura T, Saionji K, Hiejima Y, Hirayama H, Tago K, Takano H, Tajiri M, Hayashi K, Kawabata M, Funamizu M, Makita Y, Hata A. Nakamura T, et al. Among authors: makita y. Am J Kidney Dis. 2002 May;39(5):1032-9. doi: 10.1053/ajkd.2002.32779. Am J Kidney Dis. 2002. PMID: 11979347

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