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Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica
|
June 20, 2015
[Cassae-type diterpenes from seeds of Caesalpinia minax]
Zhong-hao Sun, Guo-xu Ma, Yu Tian, et al.
Experimental Parasitology
|
March 25, 2014
Molecular characterization and functional analysis of serine/threonine protein phosphatase of Toxocara canis
Guang Xu Ma, Rong Qiong Zhou, Shi Jun Hu, et al.
Current Eye Research
|
July 6, 2010
A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese family
Xiaobo Gao, Jie Cheng, Cailing Lu, et al.
Endocrine
|
October 22, 2010
Interleukin 1 beta (IL-1β) promoter C [-511] T polymorphism but not C [+3953] T polymorphism is associated with polycystic ovary syndrome
Yuan Mu, Jingjing Liu, Binbin Wang, et al.
Human Reproduction (Oxford, England)
|
February 8, 2011
Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women
Binbin Wang, Peisu Suo, Beili Chen, et al.
Molecular Vision
|
May 2, 2008
Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts
Fei-feng Li, Si-quan Zhu, Shu-zhen Wang, et al.
Chemical Biology & Drug Design
|
January 3, 2013
Synthesis and biological evaluation of [1,2,4]triazolo[3,4-a]phthalazine and tetrazolo[5,1-a]phthalazine derivatives bearing substituted benzylpiperazine moieties as positive inotropic agents
Yan Wu, Liang-Peng Sun, Long-Xu Ma, et al.
Plos One
|
April 5, 2013
Identification and functional analysis of GJA8 mutation in a Chinese family with autosomal dominant perinuclear cataracts
Dongmei Su, Zhenfei Yang, Qian Li, et al.
Molecular Vision
|
December 19, 2009
A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family
Kaijie Wang, Binbin Wang, Jing Wang, et al.
Oncotarget
|
February 14, 2018
Genetic and functional analysis of two missense <i>DUOX2</i> mutations in congenital hypothyroidism and goiter
Shiguo Liu, Wenhui Zhang, Liqin Zhang, et al.
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Showing results (511-520 of 1,039) with videos related to
Sort By:
Page
of 104
Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica
|
June 20, 2015
[Cassae-type diterpenes from seeds of Caesalpinia minax]
Zhong-hao Sun, Guo-xu Ma, Yu Tian, et al.
Experimental Parasitology
|
March 25, 2014
Molecular characterization and functional analysis of serine/threonine protein phosphatase of Toxocara canis
Guang Xu Ma, Rong Qiong Zhou, Shi Jun Hu, et al.
Current Eye Research
|
July 6, 2010
A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese family
Xiaobo Gao, Jie Cheng, Cailing Lu, et al.
Endocrine
|
October 22, 2010
Interleukin 1 beta (IL-1β) promoter C [-511] T polymorphism but not C [+3953] T polymorphism is associated with polycystic ovary syndrome
Yuan Mu, Jingjing Liu, Binbin Wang, et al.
Human Reproduction (Oxford, England)
|
February 8, 2011
Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women
Binbin Wang, Peisu Suo, Beili Chen, et al.
Molecular Vision
|
May 2, 2008
Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts
Fei-feng Li, Si-quan Zhu, Shu-zhen Wang, et al.
Chemical Biology & Drug Design
|
January 3, 2013
Synthesis and biological evaluation of [1,2,4]triazolo[3,4-a]phthalazine and tetrazolo[5,1-a]phthalazine derivatives bearing substituted benzylpiperazine moieties as positive inotropic agents
Yan Wu, Liang-Peng Sun, Long-Xu Ma, et al.
Plos One
|
April 5, 2013
Identification and functional analysis of GJA8 mutation in a Chinese family with autosomal dominant perinuclear cataracts
Dongmei Su, Zhenfei Yang, Qian Li, et al.
Molecular Vision
|
December 19, 2009
A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family
Kaijie Wang, Binbin Wang, Jing Wang, et al.
Oncotarget
|
February 14, 2018
Genetic and functional analysis of two missense <i>DUOX2</i> mutations in congenital hypothyroidism and goiter
Shiguo Liu, Wenhui Zhang, Liqin Zhang, et al.
Page
of 104