Hattori H - Search Results

1

Identification of recurrent and novel mutations in the LDL receptor gene in Japanese familial hypercholesterolemia. Mutation in brief no. 248. Online.

Hattori H, Nagano M, Iwata F, Homma Y, Egashira T, Okada T. Hattori H, et al. Hum Mutat. 1999;14(1):87. doi: 10.1002/(SICI)1098-1004(1999)14:1<87::AID-HUMU14>3.0.CO;2-N. Hum Mutat. 1999. PMID: 10447263

2

Eight novel mutations and functional impairments of the LDL receptor in familial hypercholesterolemia in the north of Japan.

Hattori H, Hirayama T, Nobe Y, Nagano M, Kujiraoka T, Egashira T, Ishii J, Tsuji M, Emi M. Hattori H, et al. J Hum Genet. 2002;47(2):80-7. doi: 10.1007/s100380200005. J Hum Genet. 2002. PMID: 11916007

3

A novel missense mutation Ile193Val in cholesteryl ester transfer protein gene.

Nagano M, Ito M, Sagehashi Y, Hattori H, Egashira T. Nagano M, et al. Among authors: hattori h. Hum Mutat. 1999 Sep 19;14(3):271. Hum Mutat. 1999. PMID: 10477490 No abstract available.

4

A novel missense mutation Thr316Ala in lysosomal acid lipase gene in Japanese population.

Nagano M, Iwasaki T, Hattori H, Egashira T. Nagano M, et al. Among authors: hattori h. Hum Mutat. 1999 Sep 19;14(3):271. Hum Mutat. 1999. PMID: 10477491 No abstract available.

5

Two novel missense mutations in the CETP gene in Japanese hyperalphalipoproteinemic subjects: high-throughput assay by Invader assay.

Nagano M, Yamashita S, Hirano K, Ito M, Maruyama T, Ishihara M, Sagehashi Y, Oka T, Kujiraoka T, Hattori H, Nakajima N, Egashira T, Kondo M, Sakai N, Matsuzawa Y. Nagano M, et al. Among authors: hattori h. J Lipid Res. 2002 Jul;43(7):1011-8. doi: 10.1194/jlr.m200024-jlr200. J Lipid Res. 2002. PMID: 12091484 Free article.

6

Point mutation (-69 G-->A) in the promoter region of cholesteryl ester transfer protein gene in Japanese hyperalphalipoproteinemic subjects.

Nagano M, Yamashita S, Hirano K, Kujiraoka T, Ito M, Sagehashi Y, Hattori H, Nakajima N, Maruyama T, Sakai N, Egashira T, Matsuzawa Y. Nagano M, et al. Among authors: hattori h. Arterioscler Thromb Vasc Biol. 2001 Jun;21(6):985-90. doi: 10.1161/01.atv.21.6.985. Arterioscler Thromb Vasc Biol. 2001. PMID: 11397708

7

Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis.

Ishii J, Nagano M, Kujiraoka T, Ishihara M, Egashira T, Takada D, Tsuji M, Hattori H, Emi M. Ishii J, et al. Among authors: hattori h. J Hum Genet. 2002;47(7):366-9. doi: 10.1007/s100380200051. J Hum Genet. 2002. PMID: 12111371

8

Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients.

Ishihara M, Iwasaki T, Nagano M, Ishii J, Takano M, Kujiraoka T, Tsuji M, Hattori H, Emi M. Ishihara M, et al. Among authors: hattori h. J Hum Genet. 2004;49(6):302-307. doi: 10.1007/s10038-004-0151-6. Epub 2004 May 18. J Hum Genet. 2004. PMID: 15148590

9

Molecular mechanisms of cholesteryl ester transfer protein deficiency in Japanese.

Nagano M, Yamashita S, Hirano K, Takano M, Maruyama T, Ishihara M, Sagehashi Y, Kujiraoka T, Tanaka K, Hattori H, Sakai N, Nakajima N, Egashira T, Matsuzawa Y. Nagano M, et al. Among authors: hattori h. J Atheroscler Thromb. 2004;11(3):110-21. doi: 10.5551/jat.11.110. J Atheroscler Thromb. 2004. PMID: 15256762 Free article. Review.

10

Measurement of human plasma phospholipid transfer protein by sandwich ELISA.

Oka T, Kujiraoka T, Ito M, Nagano M, Ishihara M, Iwasaki T, Egashira T, Miller NE, Hattori H. Oka T, et al. Among authors: hattori h. Clin Chem. 2000 Sep;46(9):1357-64. Clin Chem. 2000. PMID: 10973866

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

1,179 results

Search Page

Filters