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Endocrine Journal|December 24, 2023
Epigenetic alterations of 11beta-hydroxysteroid dehydrogenase 1 gene in the adipose tissue of patients with primary aldosteronismYoshimichi Takeda, Masashi Demura, Mitsuhiro Kometani, et al.
Genome Integrity|August 4, 2010
Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineeringSatoshi Abe, Hiromi Tanaka, Tomomi Notsu, et al.
Cancer Science|June 19, 2021
MUSASHI-2 confers resistance to third-generation EGFR-tyrosine kinase inhibitor osimertinib in lung adenocarcinomaReheman Yiming, Yasuto Takeuchi, Tatsunori Nishimura, et al.
Scientific Reports|April 21, 2021
Urinary microRNA biomarkers for detecting the presence of esophageal cancerYusuke Okuda, Takaya Shimura, Hiroyasu Iwasaki, et al.
Nature Communications|May 27, 2026
Defective ventral neurogenesis due to midfetal Chd8 mutation drives autistic-like behavior in miceKenta Nitahara, Atsuki Kawamura, Ayumu Tashiro, et al.
International Journal of Hematology|November 1, 2019
Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrateTomoki Togashi, Satomi Nagaya, Masayuki Nagasawa, et al.
Journal of Hypertension|March 3, 2021
Effect of potassium on DNA methylation of aldosterone synthase geneYoshimichi Takeda, Masashi Demura, Fen Wang, et al.
International Journal of Hematology|February 10, 2025
The novel protein C variant p.C101F results in early intracellular degradation that drives type I protein C deficiencyRikuto Yui, Satomi Nagaya, Ibuki Yasuda, et al.
Epigenetics|September 20, 2017
UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neuronsS Jesse Lopez, Keith Dunaway, M Saharul Islam, et al.
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