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H-Y Lo

Showing results (51-60 of 89) with videos related to

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Zhonghua Yi Xue Za Zhi|September 25, 2004
[A de nono I462S mutation in the KRT6A gene is associated with pachyonychia congenita type I]Xiao-jing Kang, Miao Sun, Wei Yang, et al.
Journal of Human Genetics|May 23, 2009
A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese familyDan Lv, Yang Luo, Wei Yang, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|December 9, 2003
Rare pulmonary complications after transarterial chemoembolisation for hepatocellular carcinoma: two case reportsP C H Kwok, T W Lam, C L Lam, et al.
Journal of Virology|December 1, 1996
E5 proteins of human papillomavirus types 11 and 16 transactivate the c-fos promoter through the NF1 binding elementS L Chen, Y K Lin, L Y Li, et al.
Science (New York, N.Y.)|December 20, 2014
Quantum optics. Quantum harmonic oscillator state synthesis by reservoir engineeringD Kienzler, H-Y Lo, B Keitch, et al.
Fertility and Sterility|February 26, 2000
The expression of DAZL1 in the ovary of the human female fetusM Y Tsai, S Y Chang, H Y Lo, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|April 6, 2016
Does enhanced diabetes management reduce the risk and improve the outcome of tuberculosis?H-Y Lo, S-L Yang, H-H Lin, et al.
Andrology|June 7, 2014
Evaluation of candidate spermatogonial markers ID4 and GPR125 in testes of adult human cadaveric organ donorsC Sachs, B D Robinson, L Andres Martin, et al.
The Journal of Investigative Dermatology|April 23, 2004
Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditariaQing Liu, Wenli Liu, Li Jiang, et al.
Journal of Human Genetics|February 20, 2008
Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangismWei Yang, Lihua Cao, Wenli Liu, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Zhonghua Yi Xue Za Zhi|September 25, 2004
[A de nono I462S mutation in the KRT6A gene is associated with pachyonychia congenita type I]Xiao-jing Kang, Miao Sun, Wei Yang, et al.
Journal of Human Genetics|May 23, 2009
A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese familyDan Lv, Yang Luo, Wei Yang, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|December 9, 2003
Rare pulmonary complications after transarterial chemoembolisation for hepatocellular carcinoma: two case reportsP C H Kwok, T W Lam, C L Lam, et al.
Journal of Virology|December 1, 1996
E5 proteins of human papillomavirus types 11 and 16 transactivate the c-fos promoter through the NF1 binding elementS L Chen, Y K Lin, L Y Li, et al.
Science (New York, N.Y.)|December 20, 2014
Quantum optics. Quantum harmonic oscillator state synthesis by reservoir engineeringD Kienzler, H-Y Lo, B Keitch, et al.
Fertility and Sterility|February 26, 2000
The expression of DAZL1 in the ovary of the human female fetusM Y Tsai, S Y Chang, H Y Lo, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|April 6, 2016
Does enhanced diabetes management reduce the risk and improve the outcome of tuberculosis?H-Y Lo, S-L Yang, H-H Lin, et al.
Andrology|June 7, 2014
Evaluation of candidate spermatogonial markers ID4 and GPR125 in testes of adult human cadaveric organ donorsC Sachs, B D Robinson, L Andres Martin, et al.
The Journal of Investigative Dermatology|April 23, 2004
Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditariaQing Liu, Wenli Liu, Li Jiang, et al.
Journal of Human Genetics|February 20, 2008
Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangismWei Yang, Lihua Cao, Wenli Liu, et al.
Pageof 9