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World Journal of Clinical Cases
|
December 11, 2025
Correlation between concentrations of NAMPT and NMNAT1 and the risk of upper respiratory infections in the island reef
Guo-Feng Gao, Jiao Yu, Sui-Yi Liu
World Journal of Gastroenterology
|
July 14, 2025
Rate of abnormal renal function index and related risk factors in patients with chronic hepatitis B
Guo-Feng Gao, Xiao-Yu Wang, Jiao Yu
World Journal of Gastroenterology
|
August 14, 2025
Predictive value of core-fucosylated low-molecular-weight kininogen levels in patients with liver fibrosis: A prospective study
Guo-Feng Gao, Jiao Yu, Lin Tong, et al.
World Journal of Gastroenterology
|
December 8, 2025
Influence of an internet-based proactive follow-up management model on the prognosis of nonalcoholic fatty liver disease
Sui-Yi Liu, Guo-Feng Gao, Xiao-Yu Wang, et al.
Molecular Medicine Reports
|
December 12, 2012
Amino acid substitutions in the pore affect the anomalous mole fraction effect of CaV1.2 channels
Zhe Li, He Huang, Bo Yang, et al.
Biochemical and Biophysical Research Communications
|
April 6, 2012
Heteroplasmy levels of mtDNA1555A>G mutation is positively associated with diverse phenotypes and mutation transmission in a Chinese family
Shan-Shan Shen, Chang Liu, Zhi-Yong Xu, et al.
Forensic Science International. Genetics
|
December 17, 2008
Analysis of mitochondrial DNA polymorphisms in Guangdong Han Chinese
Feng Chen, Sha-Yan Wang, Ruan-Zhang Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 8, 2009
[GJB2 gene mutation in deaf patients]
Zhi-yong Xu, Guo-feng Gao, Chang Liu, et al.
Forensic Science International. Genetics
|
May 25, 2010
Mitochondrial DNA polymorphisms in Gelao ethnic group residing in Southwest China
Chang Liu, Sha-Yan Wang, Mian Zhao, et al.
Molecular and Cellular Endocrinology
|
April 23, 2003
A complex heterozygous mutation of His373Leu and Asp487-Ser488-Phe489 deletion in human cytochrome P450c17 causes 17alpha-hydroxylase/17,20-lyase deficiency in three Chinese sisters
Jie Qiao, Ren-Ming Hu, Yong-De Peng, et al.
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Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
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World Journal of Clinical Cases
|
December 11, 2025
Correlation between concentrations of NAMPT and NMNAT1 and the risk of upper respiratory infections in the island reef
Guo-Feng Gao, Jiao Yu, Sui-Yi Liu
World Journal of Gastroenterology
|
July 14, 2025
Rate of abnormal renal function index and related risk factors in patients with chronic hepatitis B
Guo-Feng Gao, Xiao-Yu Wang, Jiao Yu
World Journal of Gastroenterology
|
August 14, 2025
Predictive value of core-fucosylated low-molecular-weight kininogen levels in patients with liver fibrosis: A prospective study
Guo-Feng Gao, Jiao Yu, Lin Tong, et al.
World Journal of Gastroenterology
|
December 8, 2025
Influence of an internet-based proactive follow-up management model on the prognosis of nonalcoholic fatty liver disease
Sui-Yi Liu, Guo-Feng Gao, Xiao-Yu Wang, et al.
Molecular Medicine Reports
|
December 12, 2012
Amino acid substitutions in the pore affect the anomalous mole fraction effect of CaV1.2 channels
Zhe Li, He Huang, Bo Yang, et al.
Biochemical and Biophysical Research Communications
|
April 6, 2012
Heteroplasmy levels of mtDNA1555A>G mutation is positively associated with diverse phenotypes and mutation transmission in a Chinese family
Shan-Shan Shen, Chang Liu, Zhi-Yong Xu, et al.
Forensic Science International. Genetics
|
December 17, 2008
Analysis of mitochondrial DNA polymorphisms in Guangdong Han Chinese
Feng Chen, Sha-Yan Wang, Ruan-Zhang Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 8, 2009
[GJB2 gene mutation in deaf patients]
Zhi-yong Xu, Guo-feng Gao, Chang Liu, et al.
Forensic Science International. Genetics
|
May 25, 2010
Mitochondrial DNA polymorphisms in Gelao ethnic group residing in Southwest China
Chang Liu, Sha-Yan Wang, Mian Zhao, et al.
Molecular and Cellular Endocrinology
|
April 23, 2003
A complex heterozygous mutation of His373Leu and Asp487-Ser488-Phe489 deletion in human cytochrome P450c17 causes 17alpha-hydroxylase/17,20-lyase deficiency in three Chinese sisters
Jie Qiao, Ren-Ming Hu, Yong-De Peng, et al.
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of 2