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Showing results (581-590 of 2,636,194) with videos related to

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Fertility and Sterility|January 30, 2009
The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyomaYao-Yuan Hsieh, Chi-Chen Chang, Da-Tian Bau, et al.
European Journal of Medical Research|November 7, 2023
Dengue virus serotype did not contribute to clinical severity or mortality in Taiwan's largest dengue outbreak in 2015Jih-Jin Tsai, Ko Chang, Chun-Hong Chen, et al.
Pediatric Research|October 25, 2007
Growth Hormone (GH) receptor C.1319 G>T polymorphism, but not exon 3 retention or deletion is associated with better first-year growth response to GH therapy in patients with GH deficiencyLei Wan, Wei-Cheng Chen, Yuhsin Tsai, et al.
Archives of Osteoporosis|September 8, 2025
Multiple large language models versus clinical guidelines for postmenopausal osteoporosis: a comparative study of ChatGPT-3.5, ChatGPT-4.0, ChatGPT-4o, Google Gemini, Google Gemini Advanced, and Microsoft CopilotChun-Ru Lin, Yi-Jun Chen, Po-An Tsai, et al.
Investigative Ophthalmology & Visual Science|July 31, 2010
Association of interleukin-1beta (IL1B) polymorphisms with Graves' ophthalmopathy in Taiwan Chinese patientsYu-Huei Liu, Rong-Hsing Chen, Hsin-Hung Wu, et al.
Frontiers in Neurology|March 30, 2018
Risk of Microangiopathy in Patients with Epilepsy under Long-term Antiepileptic Drug TherapyNai-Ching Chen, Chih-Hsin Chen, Tsu-Kung Lin, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndromeChing-Fen Chang, Ling-Hui Li, Chung-Hsing Wang, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|August 13, 2003
Association of interleukin 1beta and receptor antagonist gene polymorphisms with primary open-angle glaucomaHui-Ju Lin, San-Chang Tsai, Fuu-Jen Tsai, et al.
Technology and Health Care : Official Journal of the European Society for Engineering and Medicine|May 16, 2022
Applying the task-technology fit model to construct the prototype of a medical staff scheduling systemGary Yu-Hsin Chen, Ping-Shun Chen, Tzu-Tao Tsai
Molecular Vision|August 28, 2009
Sclera-related gene polymorphisms in high myopiaHui-Ju Lin, Lei Wan, Yuhsin Tsai, et al.
Pageof 263,620

Showing results (581-590 of 2,636,194) with videos related to

Sort By:
Pageof 263,620
Fertility and Sterility|January 30, 2009
The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyomaYao-Yuan Hsieh, Chi-Chen Chang, Da-Tian Bau, et al.
European Journal of Medical Research|November 7, 2023
Dengue virus serotype did not contribute to clinical severity or mortality in Taiwan's largest dengue outbreak in 2015Jih-Jin Tsai, Ko Chang, Chun-Hong Chen, et al.
Pediatric Research|October 25, 2007
Growth Hormone (GH) receptor C.1319 G>T polymorphism, but not exon 3 retention or deletion is associated with better first-year growth response to GH therapy in patients with GH deficiencyLei Wan, Wei-Cheng Chen, Yuhsin Tsai, et al.
Archives of Osteoporosis|September 8, 2025
Multiple large language models versus clinical guidelines for postmenopausal osteoporosis: a comparative study of ChatGPT-3.5, ChatGPT-4.0, ChatGPT-4o, Google Gemini, Google Gemini Advanced, and Microsoft CopilotChun-Ru Lin, Yi-Jun Chen, Po-An Tsai, et al.
Investigative Ophthalmology & Visual Science|July 31, 2010
Association of interleukin-1beta (IL1B) polymorphisms with Graves' ophthalmopathy in Taiwan Chinese patientsYu-Huei Liu, Rong-Hsing Chen, Hsin-Hung Wu, et al.
Frontiers in Neurology|March 30, 2018
Risk of Microangiopathy in Patients with Epilepsy under Long-term Antiepileptic Drug TherapyNai-Ching Chen, Chih-Hsin Chen, Tsu-Kung Lin, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndromeChing-Fen Chang, Ling-Hui Li, Chung-Hsing Wang, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|August 13, 2003
Association of interleukin 1beta and receptor antagonist gene polymorphisms with primary open-angle glaucomaHui-Ju Lin, San-Chang Tsai, Fuu-Jen Tsai, et al.
Technology and Health Care : Official Journal of the European Society for Engineering and Medicine|May 16, 2022
Applying the task-technology fit model to construct the prototype of a medical staff scheduling systemGary Yu-Hsin Chen, Ping-Shun Chen, Tzu-Tao Tsai
Molecular Vision|August 28, 2009
Sclera-related gene polymorphisms in high myopiaHui-Ju Lin, Lei Wan, Yuhsin Tsai, et al.
Pageof 263,620