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3,295 results
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Bone phenotype in melanocortin 2 receptor-deficient mice.
Sato T, Iwata T, Usui M, Kokabu S, Sugamori Y, Takaku Y, Kobayashi T, Ito K, Matsumoto M, Takeda S, Xu R, Chida D. Sato T, et al. Among authors: takeda s. Bone Rep. 2020 Aug 30;13:100713. doi: 10.1016/j.bonr.2020.100713. eCollection 2020 Dec. Bone Rep. 2020. PMID: 32964075 Free PMC article.
[Recommendations for the diagnosis and treatment of persistent postsurgical symptoms in Hirschsprung disease].
Rocca AM, Nastri M, Takeda S, Neder D, Mortarini A, Paz E, Lavorgna S, Bazo M, Dibenedetto V. Rocca AM, et al. Among authors: takeda s. Arch Argent Pediatr. 2020 Oct;118(5):350-357. doi: 10.5546/aap.2020.350. Arch Argent Pediatr. 2020. PMID: 32924409 Free article. Spanish.
Enhanced Masses on Contrast-Enhanced Breast: Differentiation Using a Combination of Dynamic Contrast-Enhanced MRI and Quantitative Evaluation with Synthetic MRI.
Matsuda M, Tsuda T, Ebihara R, Toshimori W, Takeda S, Okada K, Nakasuka K, Shiraishi Y, Suekuni H, Kamei Y, Kurata M, Kitazawa R, Mochizuki T, Kido T. Matsuda M, et al. Among authors: takeda s. J Magn Reson Imaging. 2020 Sep 11. doi: 10.1002/jmri.27362. Online ahead of print. J Magn Reson Imaging. 2020. PMID: 32914921
Weekend and off-hour effects on the incidence of cerebral palsy: contribution of consolidated perinatal care.
Toyokawa S, Hasegawa J, Ikenoue T, Asano Y, Jojima E, Satoh S, Ikeda T, Ichizuka K, Takeda S, Tamiya N, Nakai A, Fujimori K, Maeda T, Masuzaki H, Suzuki H, Ueda S. Toyokawa S, et al. Among authors: takeda s. Environ Health Prev Med. 2020 Sep 10;25(1):52. doi: 10.1186/s12199-020-00889-y. Environ Health Prev Med. 2020. PMID: 32912144 Free PMC article.
Risk factors for cerebral palsy in neonates due to placental abruption.
Ichizuka K, Toyokawa S, Ikenoue T, Satoh S, Hasegawa J, Ikeda T, Tamiya N, Nakai A, Fujimori K, Maeda T, Kanayama N, Masuzaki H, Iwashita M, Suzuki H, Takeda S. Ichizuka K, et al. Among authors: takeda s. J Obstet Gynaecol Res. 2020 Sep 3. doi: 10.1111/jog.14447. Online ahead of print. J Obstet Gynaecol Res. 2020. PMID: 32885550
Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes.
Kitazawa M, Hayashi S, Imamura M, Takeda S, Oishi Y, Kaneko-Ishino T, Ishino F. Kitazawa M, et al. Among authors: takeda s. Development. 2020 Sep 2;147(21):dev185918. doi: 10.1242/dev.185918. Development. 2020. PMID: 32878913 Free PMC article.
Discovery of small-molecule modulator of heterotrimeric Gi-protein by integrated phenotypic profiling and chemical proteomics.
Kawamura T, Futamura Y, Shang E, Muroi M, Janning P, Ueno M, Wilke J, Takeda S, Kondoh Y, Ziegler S, Watanabe N, Waldmann H, Osada H. Kawamura T, et al. Among authors: takeda s. Biosci Biotechnol Biochem. 2020 Aug 31:1-7. doi: 10.1080/09168451.2020.1812375. Online ahead of print. Biosci Biotechnol Biochem. 2020. PMID: 32867616
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