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Human Molecular Genetics
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March 20, 2018
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
Yanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.
Haematologica
|
February 22, 2020
Factor IX alteration p.Arg338Gln (FIX Shanghai) potentiates FIX clotting activity and causes thrombosis
Wenman Wu, Lin Xiao, Xi Wu, et al.
Frontiers in Pharmacology
|
June 20, 2022
Centenarians Alleviate Inflammaging by Changing the Ratio and Secretory Phenotypes of T Helper 17 and Regulatory T Cells
Lixing Zhou, Meiling Ge, Yan Zhang, et al.
Pediatric Blood & Cancer
|
January 29, 2014
The 253-kb inversion and deep intronic mutations in UNC13D are present in North American patients with familial hemophagocytic lymphohistiocytosis 3
Yaping Qian, Judith A Johnson, Jessica A Connor, et al.
Journal of Medical Virology
|
March 6, 2024
A superior heterologous prime-boost vaccination strategy against COVID-19: A bivalent vaccine based on yeast-derived RBD proteins followed by a heterologous vaccine
Yu Liu, Miao Li, Tingting Cui, et al.
Journal of Clinical Microbiology
|
October 9, 2004
Large-scale comparative genomics meta-analysis of Campylobacter jejuni isolates reveals low level of genome plasticity
Eduardo N Taboada, Rey R Acedillo, Catherine D Carrillo, et al.
Molecular Biomedicine
|
January 5, 2022
Optimization of miR-22 expression cassette for rAAV delivery on diabetes
Li Yang, Wenya Du, Zhaoyue Zheng, et al.
Plos One
|
August 3, 2016
Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism
C Alexander Valencia, Xinjian Wang, Jin Wang, et al.
Human Gene Therapy
|
February 26, 2026
An Engineered Adeno-Associated Virus Variant Enables Efficient Gene Editing in Human T Cells
Mi Leng, Chunmei Gan, Zhaoyue Zheng, et al.
Journal of Inherited Metabolic Disease
|
March 9, 2026
Signal Peptide Engineering and Codon Optimization to Enhance α-Gal A Activity for rAAV Gene Therapy of Fabry Disease
Siwu He, Li Yang, Ke Wan, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 68) with videos related to
Sort By:
Page
of 7
Human Molecular Genetics
|
March 20, 2018
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
Yanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.
Haematologica
|
February 22, 2020
Factor IX alteration p.Arg338Gln (FIX Shanghai) potentiates FIX clotting activity and causes thrombosis
Wenman Wu, Lin Xiao, Xi Wu, et al.
Frontiers in Pharmacology
|
June 20, 2022
Centenarians Alleviate Inflammaging by Changing the Ratio and Secretory Phenotypes of T Helper 17 and Regulatory T Cells
Lixing Zhou, Meiling Ge, Yan Zhang, et al.
Pediatric Blood & Cancer
|
January 29, 2014
The 253-kb inversion and deep intronic mutations in UNC13D are present in North American patients with familial hemophagocytic lymphohistiocytosis 3
Yaping Qian, Judith A Johnson, Jessica A Connor, et al.
Journal of Medical Virology
|
March 6, 2024
A superior heterologous prime-boost vaccination strategy against COVID-19: A bivalent vaccine based on yeast-derived RBD proteins followed by a heterologous vaccine
Yu Liu, Miao Li, Tingting Cui, et al.
Journal of Clinical Microbiology
|
October 9, 2004
Large-scale comparative genomics meta-analysis of Campylobacter jejuni isolates reveals low level of genome plasticity
Eduardo N Taboada, Rey R Acedillo, Catherine D Carrillo, et al.
Molecular Biomedicine
|
January 5, 2022
Optimization of miR-22 expression cassette for rAAV delivery on diabetes
Li Yang, Wenya Du, Zhaoyue Zheng, et al.
Plos One
|
August 3, 2016
Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism
C Alexander Valencia, Xinjian Wang, Jin Wang, et al.
Human Gene Therapy
|
February 26, 2026
An Engineered Adeno-Associated Virus Variant Enables Efficient Gene Editing in Human T Cells
Mi Leng, Chunmei Gan, Zhaoyue Zheng, et al.
Journal of Inherited Metabolic Disease
|
March 9, 2026
Signal Peptide Engineering and Codon Optimization to Enhance α-Gal A Activity for rAAV Gene Therapy of Fabry Disease
Siwu He, Li Yang, Ke Wan, et al.
Page
of 7