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Brain & Development|March 2, 2005
Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphismsTakayuki Fukuda, Yushiro Yamashita, Shinichiro Nagamitsu, et al.
Epilepsia|November 19, 2011
Acute encephalopathy in children with Dravet syndromeAkihisa Okumura, Mitsugu Uematsu, George Imataka, et al.
Brachytherapy|February 14, 2009
High-dose-rate interstitial brachytherapy for previously untreated cervical carcinomaFumiaki Isohashi, Yasuo Yoshioka, Masahiko Koizumi, et al.
Arthritis and Rheumatism|April 13, 2004
Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosisMauro Silingardi, Carlo Salvarani, Luigi Boiardi, et al.
Annals of Hematology|July 7, 2011
Functional analysis and gene expression profile of umbilical cord blood regulatory T cellsGiovanni Fernando Torelli, Roberta Maggio, Nadia Peragine, et al.
Nature Communications|June 14, 2019
Non-coding cis-element of Period2 is essential for maintaining organismal circadian behaviour and body temperature rhythmicityMasao Doi, Hiroyuki Shimatani, Yuta Atobe, et al.
Journal of the American Chemical Society|November 10, 2015
Post-Synthesis Incorporation of ⁶⁴Cu in CuS Nanocrystals to Radiolabel Photothermal Probes: A Feasible Approach for ClinicsAndreas Riedinger, Tommaso Avellini, Alberto Curcio, et al.
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