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Plos One|December 17, 2014
Negative association between serum parathyroid hormone levels and urinary perchlorate, nitrate, and thiocyanate concentrations in U.S. adults: the National Health and Nutrition Examination Survey 2005-2006Wen-Ching Ko, Chien-Liang Liu, Jie-Jen Lee, et al.Laryngoscope Investigative Otolaryngology|April 18, 2022
Comparison of SNOT-25 and ENS6Q in evaluating patients with empty nose syndromeChien-Chia Huang, Pei-Wen Wu, Cheng-Chi Lee, et al.Anticancer Research|July 3, 2019
Cetrimonium Bromide Inhibits Cell Migration and Invasion of Human Hepatic SK-HEP-1 Cells Through Modulating the Canonical and Non-canonical TGF-β Signaling PathwaysTsai-Kun Wu, Chung-Hung Chen, Ying-Ru Pan, et al.International Journal of Molecular Sciences|July 16, 2020
Mice Lacking Connective Tissue Growth Factor in the Forebrain Exhibit Delayed Seizure Response, Reduced C-Fos Expression and Different Microglial Phenotype Following Acute PTZ InjectionPei-Fen Siow, Chih-Yu Tsao, Ho-Ching Chang, et al.Molecular Therapy. Nucleic Acids|May 14, 2020
Transcriptional Suppression of miR-7 by MTA2 Induces Sp1-Mediated KLK10 Expression and Metastasis of Cervical CancerChia-Liang Lin, Tsung-Ho Ying, Shun-Fa Yang, et al.The Laryngoscope|March 23, 2024
Morphology, Not Only Volume: A Study on Empty Nose Syndrome and Inferior TurbinatesChia-Hsiang Fu, Chien-Cheng Chen, Chi-Che Huang, et al.Frontiers in Endocrinology|March 15, 2024
Identification and characterization of a novel CASR mutation causing familial hypocalciuric hypercalcemiaChien-Ming Lin, Yi-Xuan Ding, Shih-Ming Huang, et al.Pesticide Biochemistry and Physiology|April 6, 2024
Biophysical mechanisms underlying tefluthrin-induced modulation of gating changes and resurgent current generation in the human Nav1.4 channelHsing-Jung Lai, Ming-Jen Lee, Hsin-Wei Yu, et al.Journal of Alzheimer'S Disease : JAD|February 22, 2011
Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's diseaseYa-Ying Wu, Irene Han-Juo Cheng, Chin-Cheng Lee, et al.Archives of Neurology|October 13, 2004
Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathyLong-Sun Ro, Guey-Jen Lee-Chen, Tzu-Ching Lin, et al.Pageof 92