Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

16 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus.
Saito R, Koebis M, Nagai T, Shimizu K, Liao J, Wulaer B, Sugaya Y, Nagahama K, Uesaka N, Kushima I, Mori D, Maruyama K, Nakao K, Kurihara H, Yamada K, Kano M, Fukada Y, Ozaki N, Aiba A. Saito R, et al. Among authors: koebis m. Transl Psychiatry. 2020 Feb 5;10(1):35. doi: 10.1038/s41398-020-0723-z. Transl Psychiatry. 2020. PMID: 32066675 Free PMC article.
[Myotonic dystrophy].
Ishiura S, Oana K, Koebis M. Ishiura S, et al. Among authors: koebis m. Rinsho Shinkeigaku. 2013;53(11):1109-11. doi: 10.5692/clinicalneurol.53.1109. Rinsho Shinkeigaku. 2013. PMID: 24291894 Review. Japanese.
Splicing of human chloride channel 1.
Nakamura T, Ohsawa-Yoshida N, Zhao Y, Koebis M, Oana K, Mitsuhashi H, Ishiura S. Nakamura T, et al. Among authors: koebis m. Biochem Biophys Rep. 2015 Nov 11;5:63-69. doi: 10.1016/j.bbrep.2015.11.006. eCollection 2016 Mar. Biochem Biophys Rep. 2015. PMID: 28955807 Free PMC article.
16 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page