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European Journal of Drug Metabolism and Pharmacokinetics
|
April 29, 2019
In Vitro Metabolism by Aldehyde Oxidase Leads to Poor Pharmacokinetic Profile in Rats for c-Met Inhibitor MET401
Jiang Wei Zhang, Hai Bing Deng, Chun Ye Zhang, et al.
Cancer Medicine
|
March 19, 2019
Association between polymorphisms in MicroRNA target sites of RAD51D genes and risk of hepatocellular carcinoma
Yan-Ji Jiang, Jian-Hong Zhong, Zi-Han Zhou, et al.
Neuropharmacology
|
March 13, 2016
Pharmacological characterization of EN-9, a novel chimeric peptide of endomorphin-2 and neuropeptide FF that produces potent antinociceptive activity and limited tolerance
Zi-Long Wang, Ning Li, Pei Wang, et al.
BMC Neurology
|
May 15, 2025
Diagnostic journey and genetic analysis of a novel homozygous CYP2U1 mutation causing autosomal recessive spastic paraplegia type 56 (SPG56) in a consanguineous family
Hong-Ping Yu, Jing Zou, Xiang Chen, et al.
Frontiers in Genetics
|
April 3, 2025
Clinical genetic analysis of an adult polyglucosan body disease (APBD) family caused by the compound heterozygous variant of <i>GBE1</i> p.R156C and deletion exon 3-7
Juan Zhu, Hong-Ping Yu, Jing Zou, et al.
Scientific Reports
|
July 9, 2025
Genetic analysis of a novel TSC1 splice mutation causing tuberous sclerosis without neurological phenotypes
Xiu-Juan Yao, Ying Lin, Jing Zou, et al.
Molecular Carcinogenesis
|
February 21, 2013
Genetic variations of mTORC1 genes and risk of gastric cancer in an Eastern Chinese population
Jing He, Meng-Yun Wang, Li-Xin Qiu, et al.
Human Genetics
|
February 29, 2012
Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations
Jing He, Li-Xin Qiu, Meng-Yun Wang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 18, 2024
A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemia
Kai-Ying He, Hong-Ping Yu, Jing Zou, et al.
Annals of Hematology
|
March 21, 2024
Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case report
Jian-Hui Zhang, Hui Chen, Dan-Dan Ruan, et al.
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Search research articles
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Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
European Journal of Drug Metabolism and Pharmacokinetics
|
April 29, 2019
In Vitro Metabolism by Aldehyde Oxidase Leads to Poor Pharmacokinetic Profile in Rats for c-Met Inhibitor MET401
Jiang Wei Zhang, Hai Bing Deng, Chun Ye Zhang, et al.
Cancer Medicine
|
March 19, 2019
Association between polymorphisms in MicroRNA target sites of RAD51D genes and risk of hepatocellular carcinoma
Yan-Ji Jiang, Jian-Hong Zhong, Zi-Han Zhou, et al.
Neuropharmacology
|
March 13, 2016
Pharmacological characterization of EN-9, a novel chimeric peptide of endomorphin-2 and neuropeptide FF that produces potent antinociceptive activity and limited tolerance
Zi-Long Wang, Ning Li, Pei Wang, et al.
BMC Neurology
|
May 15, 2025
Diagnostic journey and genetic analysis of a novel homozygous CYP2U1 mutation causing autosomal recessive spastic paraplegia type 56 (SPG56) in a consanguineous family
Hong-Ping Yu, Jing Zou, Xiang Chen, et al.
Frontiers in Genetics
|
April 3, 2025
Clinical genetic analysis of an adult polyglucosan body disease (APBD) family caused by the compound heterozygous variant of <i>GBE1</i> p.R156C and deletion exon 3-7
Juan Zhu, Hong-Ping Yu, Jing Zou, et al.
Scientific Reports
|
July 9, 2025
Genetic analysis of a novel TSC1 splice mutation causing tuberous sclerosis without neurological phenotypes
Xiu-Juan Yao, Ying Lin, Jing Zou, et al.
Molecular Carcinogenesis
|
February 21, 2013
Genetic variations of mTORC1 genes and risk of gastric cancer in an Eastern Chinese population
Jing He, Meng-Yun Wang, Li-Xin Qiu, et al.
Human Genetics
|
February 29, 2012
Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations
Jing He, Li-Xin Qiu, Meng-Yun Wang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 18, 2024
A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemia
Kai-Ying He, Hong-Ping Yu, Jing Zou, et al.
Annals of Hematology
|
March 21, 2024
Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case report
Jian-Hui Zhang, Hui Chen, Dan-Dan Ruan, et al.
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of 6