Emi M - Search Results

1

A single nucleotide polymorphism in the CCL1 gene predicts acute exacerbations in chronic obstructive pulmonary disease.

Takabatake N, Shibata Y, Abe S, Wada T, Machiya J, Igarashi A, Tokairin Y, Ji G, Sato H, Sata M, Takeishi Y, Emi M, Muramatsu M, Kubota I. Takabatake N, et al. Among authors: emi m. Am J Respir Crit Care Med. 2006 Oct 15;174(8):875-85. doi: 10.1164/rccm.200603-443OC. Epub 2006 Jul 24. Am J Respir Crit Care Med. 2006. PMID: 16864713

2

Association of CC chemokine ligand 5 genotype with urinary albumin excretion in the non-diabetic Japanese general population: the Takahata study.

Konta T, Emi M, Toriyama S, Ariumi H, Ishii M, Takasaki S, Ikeda A, Ichikawa K, Shibata Y, Takabatake N, Takeishi Y, Kato T, Kawata S, Kubota I. Konta T, et al. Among authors: emi m. J Hum Genet. 2008;53(3):267. doi: 10.1007/s10038-008-0246-6. Epub 2008 Jan 24. J Hum Genet. 2008. PMID: 18217191

3

Salt consumption-dependent association of the GNB3 gene polymorphism with type 2 DM.

Daimon M, Sato H, Sasaki S, Toriyama S, Emi M, Muramatsu M, Hunt SC, Hopkins PN, Karasawa S, Wada K, Jimbu Y, Kameda W, Susa S, Oizumi T, Fukao A, Kubota I, Kawata S, Kato T. Daimon M, et al. Among authors: emi m. Biochem Biophys Res Commun. 2008 Sep 26;374(3):576-80. doi: 10.1016/j.bbrc.2008.07.065. Epub 2008 Jul 24. Biochem Biophys Res Commun. 2008. PMID: 18656447

4

Genetic polymorphisms of paraoxonase-1 are associated with chronic kidney disease in Japanese women.

Ichikawa K, Konta T, Emi M, Toriyama S, Takasaki S, Ikeda A, Shibata Y, Takabatake N, Takeishi Y, Kato T, Kawata S, Kubota I. Ichikawa K, et al. Among authors: emi m. Kidney Int. 2009 Jul;76(2):183-9. doi: 10.1038/ki.2009.97. Epub 2009 Apr 8. Kidney Int. 2009. PMID: 19357718 Free article.

5

Linkage disequilibrium analyses of natriuretic peptide precursor B locus reveal risk haplotype conferring high plasma BNP levels.

Takeishi Y, Toriyama S, Takabatake N, Shibata Y, Konta T, Emi M, Kato T, Kawata S, Kubota I. Takeishi Y, et al. Among authors: emi m. Biochem Biophys Res Commun. 2007 Oct 19;362(2):480-4. doi: 10.1016/j.bbrc.2007.08.028. Epub 2007 Aug 13. Biochem Biophys Res Commun. 2007. PMID: 17719005

6

A nonfunctioning single nucleotide polymorphism in olfactory receptor gene family is associated with the forced expiratory volume in the first second/the forced vital capacity values of pulmonary function test in a Japanese population.

Takabatake N, Toriyama S, Takeishi Y, Shibata Y, Konta T, Inoue S, Abe S, Igarashi A, Tokairin Y, Ishii M, Koyano S, Emi M, Kato T, Kawata S, Kubota I. Takabatake N, et al. Among authors: emi m. Biochem Biophys Res Commun. 2007 Dec 21;364(3):662-7. doi: 10.1016/j.bbrc.2007.10.068. Epub 2007 Oct 22. Biochem Biophys Res Commun. 2007. PMID: 17964544

7

A functional polymorphism of the TNF-alpha gene that is associated with type 2 DM.

Susa S, Daimon M, Sakabe J, Sato H, Oizumi T, Karasawa S, Wada K, Jimbu Y, Kameda W, Emi M, Muramatsu M, Kato T. Susa S, et al. Among authors: emi m. Biochem Biophys Res Commun. 2008 May 9;369(3):943-7. doi: 10.1016/j.bbrc.2008.02.121. Epub 2008 Mar 6. Biochem Biophys Res Commun. 2008. PMID: 18328809

8

The novel and independent association between single-point SNP of NPHP4 gene and renal function in non-diabetic Japanese population: the Takahata study.

Konta T, Takasaki S, Ichikawa K, Emi M, Toriyama S, Satoh H, Ikeda A, Suzuki K, Mashima Y, Shibata Y, Watanabe T, Kato T, Kawata S, Kubota I. Konta T, et al. Among authors: emi m. J Hum Genet. 2010 Dec;55(12):791-5. doi: 10.1038/jhg.2010.113. Epub 2010 Sep 16. J Hum Genet. 2010. PMID: 20844548

9

Association of the PIK3C2G gene polymorphisms with type 2 DM in a Japanese population.

Daimon M, Sato H, Oizumi T, Toriyama S, Saito T, Karasawa S, Jimbu Y, Wada K, Kameda W, Susa S, Yamaguchi H, Emi M, Muramatsu M, Kubota I, Kawata S, Kato T. Daimon M, et al. Among authors: emi m. Biochem Biophys Res Commun. 2008 Jan 18;365(3):466-71. doi: 10.1016/j.bbrc.2007.10.180. Epub 2007 Nov 6. Biochem Biophys Res Commun. 2008. PMID: 17991425

10

Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populations.

Iijima H, Emi M, Wada M, Daimon M, Toriyama S, Koyano S, Sato H, Hopkins PN, Hunt SC, Kubota I, Kawata S, Kato T. Iijima H, et al. Among authors: emi m. J Hum Genet. 2008;53(3):193-200. doi: 10.1007/s10038-007-0236-0. Epub 2007 Dec 27. J Hum Genet. 2008. PMID: 18160998

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

441 results

Search Page

Filters