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Chung-Hsing Wang

Showing results (41-50 of 93) with videos related to

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Anticancer Research|March 25, 2010
Significant association of XRCC4 single nucleotide polymorphisms with childhood leukemia in TaiwanKang-Hsi Wu, Chung-Hsing Wang, Yung-Li Yang, et al.
Anticancer Research|April 4, 2008
A new single nucleotide polymorphism in XRCC4 gene is associated with breast cancer susceptibility in Taiwanese patientsChang-Fang Chiu, Hwei-Chung Wang, Chung-Hsing Wang, et al.
Anticancer Research|November 1, 2023
Elucidating the Cancer Phenotype in Turner Syndrome: A 20-Year Observational Cohort StudyYu-Nan Huang, Shao-Chia Chen, Jo-Ching Chen, et al.
In Vivo (Athens, Greece)|August 31, 2023
Incidence of Pulmonary and Respiratory Conditions in Gaucher Disease from 2000 to 2020: A Multi-institutional Cohort StudyYu-Nan Huang, Jing-Yang Huang, Wen-Ling Liao, et al.
Pediatrics and Neonatology|April 18, 2013
Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataractYu-Tzu Chang, I-Ching Chou, Chung-Hsing Wang, et al.
Journal of Cellular Biochemistry|November 19, 2016
Nrf2 Activation as a Protective Feedback to Limit Cell Death in High Glucose-Exposed CardiomyocytesCheng-Yen Tsai, Su-Ying Wen, Shi-Yann Cheng, et al.
Human Mutation|February 2, 2017
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib AnomaliesChi-Fan Yang, Chung-Hsing Wang, Weng Siong H'ng, et al.
Diabetes, Obesity & Metabolism|August 22, 2024
Long-term safety and efficacy of glucagon-like peptide-1 receptor agonists in individuals with obesity and without type 2 diabetes: A global retrospective cohort studyYu-Nan Huang, Wen-Ling Liao, Jing-Yang Huang, et al.
Prenatal Diagnosis|August 18, 2006
Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotypeChyi-Chyang Lin, Yao-Yuan Hsieh, Chung-Hsing Wang, 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.
Pageof 10

Showing results (41-50 of 93) with videos related to

Sort By:
Pageof 10
Anticancer Research|March 25, 2010
Significant association of XRCC4 single nucleotide polymorphisms with childhood leukemia in TaiwanKang-Hsi Wu, Chung-Hsing Wang, Yung-Li Yang, et al.
Anticancer Research|April 4, 2008
A new single nucleotide polymorphism in XRCC4 gene is associated with breast cancer susceptibility in Taiwanese patientsChang-Fang Chiu, Hwei-Chung Wang, Chung-Hsing Wang, et al.
Anticancer Research|November 1, 2023
Elucidating the Cancer Phenotype in Turner Syndrome: A 20-Year Observational Cohort StudyYu-Nan Huang, Shao-Chia Chen, Jo-Ching Chen, et al.
In Vivo (Athens, Greece)|August 31, 2023
Incidence of Pulmonary and Respiratory Conditions in Gaucher Disease from 2000 to 2020: A Multi-institutional Cohort StudyYu-Nan Huang, Jing-Yang Huang, Wen-Ling Liao, et al.
Pediatrics and Neonatology|April 18, 2013
Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataractYu-Tzu Chang, I-Ching Chou, Chung-Hsing Wang, et al.
Journal of Cellular Biochemistry|November 19, 2016
Nrf2 Activation as a Protective Feedback to Limit Cell Death in High Glucose-Exposed CardiomyocytesCheng-Yen Tsai, Su-Ying Wen, Shi-Yann Cheng, et al.
Human Mutation|February 2, 2017
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib AnomaliesChi-Fan Yang, Chung-Hsing Wang, Weng Siong H'ng, et al.
Diabetes, Obesity & Metabolism|August 22, 2024
Long-term safety and efficacy of glucagon-like peptide-1 receptor agonists in individuals with obesity and without type 2 diabetes: A global retrospective cohort studyYu-Nan Huang, Wen-Ling Liao, Jing-Yang Huang, et al.
Prenatal Diagnosis|August 18, 2006
Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotypeChyi-Chyang Lin, Yao-Yuan Hsieh, Chung-Hsing Wang, 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.
Pageof 10