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Lulin Huang

Showing results (71-80 of 81) with videos related to

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Plos Genetics|October 15, 2019
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleftLulin Huang, Zhonglin Jia, Yi Shi, et al.
Nature Genetics|August 11, 2014
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3Shengping Hou, Liping Du, Bo Lei, et al.
Ebiomedicine|July 12, 2020
Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesisFei Zhao, Dake Zhang, Qingyi Zhou, et al.
Science China. Life Sciences|April 10, 2020
Detection of serum IgM and IgG for COVID-19 diagnosisLing Zhong, Junlan Chuan, Bo Gong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2019
Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axisBo Gong, Houbin Zhang, Lulin Huang, et al.
Nature Genetics|April 19, 2016
A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathyLulin Huang, Houbin Zhang, Ching-Yu Cheng, et al.
Nature Communications|January 29, 2015
New loci and coding variants confer risk for age-related macular degeneration in East AsiansChing-Yu Cheng, Kenji Yamashiro, Li Jia Chen, et al.
Nature Communications|March 31, 2015
Corrigendum: New loci and coding variants confer risk for age-related macular degeneration in East AsiansChing-Yu Cheng, Kenji Yamashiro, Li Jia Chen, et al.
Nature Genetics|May 29, 2015
Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Nature Genetics|February 24, 2015
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
Plos Genetics|October 15, 2019
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleftLulin Huang, Zhonglin Jia, Yi Shi, et al.
Nature Genetics|August 11, 2014
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3Shengping Hou, Liping Du, Bo Lei, et al.
Ebiomedicine|July 12, 2020
Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesisFei Zhao, Dake Zhang, Qingyi Zhou, et al.
Science China. Life Sciences|April 10, 2020
Detection of serum IgM and IgG for COVID-19 diagnosisLing Zhong, Junlan Chuan, Bo Gong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2019
Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axisBo Gong, Houbin Zhang, Lulin Huang, et al.
Nature Genetics|April 19, 2016
A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathyLulin Huang, Houbin Zhang, Ching-Yu Cheng, et al.
Nature Communications|January 29, 2015
New loci and coding variants confer risk for age-related macular degeneration in East AsiansChing-Yu Cheng, Kenji Yamashiro, Li Jia Chen, et al.
Nature Communications|March 31, 2015
Corrigendum: New loci and coding variants confer risk for age-related macular degeneration in East AsiansChing-Yu Cheng, Kenji Yamashiro, Li Jia Chen, et al.
Nature Genetics|May 29, 2015
Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Nature Genetics|February 24, 2015
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Pageof 9