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C Alexander Valencia

Showing results (61-70 of 68) with videos related to

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Gastroenterology|March 27, 2021
Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model OrganismsDuc-Hung Pham, Ramesh Kudira, Lingfen Xu, et al.
Molecular Therapy. Methods & Clinical Development|February 3, 2025
The combination of rAAV pseudo-lipid nanoparticle and triamcinolone acetonide enables multi-administration to liverChunmei Gan, Mi Leng, Yu Liu, et al.
Frontiers in Pediatrics|August 19, 2015
Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's ExperienceC Alexander Valencia, Ammar Husami, Jennifer Holle, et al.
Hepatology Communications|May 15, 2023
Clinical spectrum and genetic causes of mitochondrial hepatopathy phenotype in childrenJames E Squires, Alexander G Miethke, C Alexander Valencia, et al.
Science Immunology|March 1, 2020
PAX1 is essential for development and function of the human thymusYasuhiro Yamazaki, Raul Urrutia, Luis M Franco, et al.
Inflammatory Bowel Diseases|August 21, 2018
Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's DiseaseLee A Denson, Ingrid Jurickova, Rebekah Karns, et al.
Human Molecular Genetics|October 18, 2017
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophyYanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.
Emerging Infectious Diseases|January 3, 2023
Sentinel Surveillance System Implementation and Evaluation for SARS-CoV-2 Genomic Data, Washington, USA, 2020-2021Hanna N Oltean, Krisandra J Allen, Lauren Frisbie, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Gastroenterology|March 27, 2021
Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model OrganismsDuc-Hung Pham, Ramesh Kudira, Lingfen Xu, et al.
Molecular Therapy. Methods & Clinical Development|February 3, 2025
The combination of rAAV pseudo-lipid nanoparticle and triamcinolone acetonide enables multi-administration to liverChunmei Gan, Mi Leng, Yu Liu, et al.
Frontiers in Pediatrics|August 19, 2015
Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's ExperienceC Alexander Valencia, Ammar Husami, Jennifer Holle, et al.
Hepatology Communications|May 15, 2023
Clinical spectrum and genetic causes of mitochondrial hepatopathy phenotype in childrenJames E Squires, Alexander G Miethke, C Alexander Valencia, et al.
Science Immunology|March 1, 2020
PAX1 is essential for development and function of the human thymusYasuhiro Yamazaki, Raul Urrutia, Luis M Franco, et al.
Inflammatory Bowel Diseases|August 21, 2018
Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's DiseaseLee A Denson, Ingrid Jurickova, Rebekah Karns, et al.
Human Molecular Genetics|October 18, 2017
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophyYanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.
Emerging Infectious Diseases|January 3, 2023
Sentinel Surveillance System Implementation and Evaluation for SARS-CoV-2 Genomic Data, Washington, USA, 2020-2021Hanna N Oltean, Krisandra J Allen, Lauren Frisbie, et al.
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