Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

677 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Genetic and Functional Analyses of Patients with Marked Hypo-High-Density Lipoprotein Cholesterolemia.
Furuta Y, Osaki Y, Nakagawa Y, Han SI, Araki M, Shikama A, Ohuchi N, Yamazaki D, Matsuda E, Nohara S, Mizunoe Y, Kainoh K, Suehara Y, Ohno H, Takeuchi Y, Miyamoto T, Murayama Y, Sugano Y, Iwasaki H, Hirano KI, Koseki M, Nakano S, Tokiwa H, Sekiya M, Yahagi N, Matsuzaka T, Nakamagoe K, Tomidokoro Y, Mitsui J, Tsuji S, Suzuki H, Shimano H. Furuta Y, et al. J Atheroscler Thromb. 2024 Sep 1;31(9):1304-1318. doi: 10.5551/jat.64579. Epub 2024 Mar 28. J Atheroscler Thromb. 2024. PMID: 38538338 Free PMC article.
A case of NASH with genetic predisposition successfully treated with an SGLT2 inhibitor: a possible involvement of mitochondrial dysfunction.
Nakajima R, Sekiya M, Furuta Y, Miyamoto T, Sato M, Fukuda K, Hattori K, Suehara Y, Sakata-Yanagimoto M, Chiba S, Okajima Y, Matsuzaka T, Takase S, Takanashi M, Okazaki H, Takashima Y, Yuhara M, Mitani Y, Matsumoto N, Murayama Y, Ohyama Osawa M, Ohuchi N, Yamazaki D, Mori S, Sugano Y, Osaki Y, Iwasaki H, Suzuki H, Shimano H. Nakajima R, et al. Among authors: furuta y. Endocrinol Diabetes Metab Case Rep. 2022 Dec 1;2022:22-0368. doi: 10.1530/EDM-22-0368. Online ahead of print. Endocrinol Diabetes Metab Case Rep. 2022. PMID: 36571472 Free PMC article.
Common protein-altering variant in GFAP is associated with white matter lesions in the older Japanese population.
Furuta Y, Akiyama M, Hirabayashi N, Honda T, Shibata M, Ohara T, Hata J, Terao C, Momozawa Y, Tatewaki Y, Taki Y, Nakaji S, Maeda T, Ono K, Mimura M, Nakashima K, Iga JI, Takebayashi M, Ninomiya T; Japan Prospective Studies for Aging and Dementia (JPSC-AD) Study Group. Furuta Y, et al. NPJ Genom Med. 2024 Nov 13;9(1):59. doi: 10.1038/s41525-024-00431-x. NPJ Genom Med. 2024. PMID: 39537646 Free PMC article.
The Clinical Spectrum of Mosaic Genetic Disease.
Geiger H, Furuta Y, van Wyk S, Phillips JA 3rd, Tinker RJ. Geiger H, et al. Among authors: furuta y. Genes (Basel). 2024 Sep 24;15(10):1240. doi: 10.3390/genes15101240. Genes (Basel). 2024. PMID: 39457364 Free PMC article. Review.
Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal recessive condition.
Ezell KM, Furuta Y, Oglesbee D, Pivnick EK, Rinker D, Sheehan JH, Tinker RJ, Hamid R, Cogan JD, Rives L, Neumann S, Corner B, Koziura M, Phillips JA 3rd; Undiagnosed Diseases Network. Ezell KM, et al. Among authors: furuta y. Mol Genet Metab Rep. 2024 Oct 5;41:101145. doi: 10.1016/j.ymgmr.2024.101145. eCollection 2024 Dec. Mol Genet Metab Rep. 2024. PMID: 39435313 Free PMC article.
677 results