Atsushi Kimura,1 Kohei Yamaguchi,2,3 Haruka Tohara,3 Yusuke Sato,4 Naoko Sawada,4 Yasuhide Nakagawa,4 Yukako Matsuda,2,5 Motoharu Inoue,2,5 Kazuhiro Tamaki2,4 1College of Risk Management, Nihon University, Setagaya-ku, Tokyo, Japan; 2Dentistry Nanohana Clinic, Medical Corporation Kanjinkai, Nishitama-gun, Tokyo, Japan; 3Department of Gerodontology
Highlight selection of radiochemistry and radiopharmacy developments by editorial board
Abstract Background The Editorial Board of EJNMMI Radiopharmacy and Chemistry releases a biannual highlight commentary to update the readership on trends in the field of radiopharmaceutical development.Main Body This selection of highlights provides commentary on 21 different topics selected by each coauthoring Editorial Board member addressing a v
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.
Fragile X syndrome (FXS) is caused by loss of function mutations in the FMR1 gene.Trinucleotide CGG-repeat expansions, resulting in FMR1 gene silencing, are the most common mutations observed at this locus.Even though the repeat expansion mutation is Course a pied - Femme - Chaussures - Neutre a functional null mutation, few conventional mutations
Nahj al-Balagha; Herald of Health
For downloading the full-text of this article please click here.Imam Ali (AS) is the door to the VR Cases science of Prophet Mohammad (PBUH) and the most outstanding student of his school of revelation.After the Prophet (PBUH), no one is superior to him in terms of virtuosity and perfection.The Messenger of God (Peace be upon him and his household)