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Desheng Liang

Showing results (1-10 of 171) with videos related to

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Drug Delivery and Translational Research|December 1, 2023
Aqueous remote loading of model cationic peptides in uncapped poly(lactide-co-glycolide) microspheres for long-term controlled releaseDesheng Liang, Simon Frank, Steven P Schwendeman
Human Gene Therapy|January 26, 2018
Gene Therapy for Hemophilia and Duchenne Muscular Dystrophy in ChinaXionghao Liu, Mujun Liu, Lingqian Wu, et al.
Frontiers in Genetics|October 11, 2021
Prenatal Diagnosis in a Fetus With X-Linked Recessive Chondrodysplasia Punctata: Identification and Functional Study of a Novel Missense Mutation in <i>ARSE</i>Li Zhang, Haoran Hu, Desheng Liang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 19, 2021
Novel variants in OSGEP leading to Galloway-Mowat syndrome by altering its subcellular localizationHua Teng, Chen Liang, Desheng Liang, et al.
Journal of Clinical Laboratory Analysis|September 27, 2019
Development and validation of a haplotype-free technique for non-invasive prenatal diagnosis of spinal muscular atrophyXianda Wei, Weigang Lv, Hu Tan, et al.
Gene|December 3, 2014
Two novel NIPBL gene mutations in Chinese patients with Cornelia de Lange syndromeLibin Mei, Desheng Liang, Yanru Huang, et al.
Genetic Testing and Molecular Biomarkers|August 4, 2012
Mutation analysis in Chinese patients with Cornelia de Lange syndromeQiulian Zhong, Desheng Liang, Jing Liu, et al.
Molecular Vision|March 23, 2011
A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmusJunjie Hu, Desheng Liang, Jinjie Xue, et al.
Journal of Molecular Modeling|August 29, 2013
Computational insight into novel molecular recognition mechanism of different bioactive GAs and the Arabidopsis receptor GID1AHongxia Duan, Dongling Li, Hongchen Liu, et al.
Frontiers in Genetics|September 27, 2021
Simultaneous Identification of Both <i>MFSD8</i> and <i>RDH12</i> Pathogenic Variants in a Chinese Family Affected With Retinitis PigmentosaYihui Wang, Yanling Teng, Desheng Liang, et al.
Pageof 18

Showing results (1-10 of 171) with videos related to

Sort By:
Pageof 18
Drug Delivery and Translational Research|December 1, 2023
Aqueous remote loading of model cationic peptides in uncapped poly(lactide-co-glycolide) microspheres for long-term controlled releaseDesheng Liang, Simon Frank, Steven P Schwendeman
Human Gene Therapy|January 26, 2018
Gene Therapy for Hemophilia and Duchenne Muscular Dystrophy in ChinaXionghao Liu, Mujun Liu, Lingqian Wu, et al.
Frontiers in Genetics|October 11, 2021
Prenatal Diagnosis in a Fetus With X-Linked Recessive Chondrodysplasia Punctata: Identification and Functional Study of a Novel Missense Mutation in <i>ARSE</i>Li Zhang, Haoran Hu, Desheng Liang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 19, 2021
Novel variants in OSGEP leading to Galloway-Mowat syndrome by altering its subcellular localizationHua Teng, Chen Liang, Desheng Liang, et al.
Journal of Clinical Laboratory Analysis|September 27, 2019
Development and validation of a haplotype-free technique for non-invasive prenatal diagnosis of spinal muscular atrophyXianda Wei, Weigang Lv, Hu Tan, et al.
Gene|December 3, 2014
Two novel NIPBL gene mutations in Chinese patients with Cornelia de Lange syndromeLibin Mei, Desheng Liang, Yanru Huang, et al.
Genetic Testing and Molecular Biomarkers|August 4, 2012
Mutation analysis in Chinese patients with Cornelia de Lange syndromeQiulian Zhong, Desheng Liang, Jing Liu, et al.
Molecular Vision|March 23, 2011
A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmusJunjie Hu, Desheng Liang, Jinjie Xue, et al.
Journal of Molecular Modeling|August 29, 2013
Computational insight into novel molecular recognition mechanism of different bioactive GAs and the Arabidopsis receptor GID1AHongxia Duan, Dongling Li, Hongchen Liu, et al.
Frontiers in Genetics|September 27, 2021
Simultaneous Identification of Both <i>MFSD8</i> and <i>RDH12</i> Pathogenic Variants in a Chinese Family Affected With Retinitis PigmentosaYihui Wang, Yanling Teng, Desheng Liang, et al.
Pageof 18