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

138 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction.
Chen R, Tsuji T, Ichida F, Bowles KR, Yu X, Watanabe S, Hirono K, Tsubata S, Hamamichi Y, Ohta J, Imai Y, Bowles NE, Miyawaki T, Towbin JA; Noncompaction study collaborators. Chen R, et al. Among authors: bowles kr, bowles ne. Mol Genet Metab. 2002 Dec;77(4):319-25. doi: 10.1016/s1096-7192(02)00195-6. Mol Genet Metab. 2002. PMID: 12468278
Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity.
Xing Y, Ichida F, Matsuoka T, Isobe T, Ikemoto Y, Higaki T, Tsuji T, Haneda N, Kuwabara A, Chen R, Futatani T, Tsubata S, Watanabe S, Watanabe K, Hirono K, Uese K, Miyawaki T, Bowles KR, Bowles NE, Towbin JA. Xing Y, et al. Among authors: bowles kr, bowles ne. Mol Genet Metab. 2006 May;88(1):71-7. doi: 10.1016/j.ymgme.2005.11.009. Epub 2006 Jan 19. Mol Genet Metab. 2006. PMID: 16427346
Gonadal mosaicism of a TAZ (G4.5) mutation in a Japanese family with Barth syndrome and left ventricular noncompaction.
Chang B, Momoi N, Shan L, Mitomo M, Aoyagi Y, Endo K, Takeda I, Chen R, Xing Y, Yu X, Watanabe S, Yoshida T, Kanegane H, Tsubata S, Bowles NE, Ichida F, Miyawaki T; Noncompaction study collaborators. Chang B, et al. Among authors: bowles ne. Mol Genet Metab. 2010 Jun;100(2):198-203. doi: 10.1016/j.ymgme.2010.02.021. Epub 2010 Mar 2. Mol Genet Metab. 2010. PMID: 20303308
Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden death.
Chang B, Nishizawa T, Furutani M, Fujiki A, Tani M, Kawaguchi M, Ibuki K, Hirono K, Taneichi H, Uese K, Onuma Y, Bowles NE, Ichida F, Inoue H, Matsuoka R, Miyawaki T; Noncompaction study collaborators. Chang B, et al. Among authors: bowles ne. Mol Genet Metab. 2011 Feb;102(2):200-6. doi: 10.1016/j.ymgme.2010.09.009. Epub 2010 Sep 29. Mol Genet Metab. 2011. PMID: 20965760
Molecular genetics of left ventricular dysfunction.
Towbin JA, Bowles NE. Towbin JA, et al. Among authors: bowles ne. Curr Mol Med. 2001 Mar;1(1):81-90. doi: 10.2174/1566524013364077. Curr Mol Med. 2001. PMID: 11899244 Review.
Novel mutations in domain I of SCN5A cause Brugada syndrome.
Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA. Vatta M, et al. Among authors: bowles ne. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963
138 results