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C Alexander Valencia

Showing results (31-40 of 68) with videos related to

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Human Pathology|January 31, 2016
Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubulesNancy Leslie, Xinjian Wang, Yanyan Peng, et al.
Frontiers in Pharmacology|May 15, 2023
Enhanced sensitivity of neutralizing antibody detection for different AAV serotypes using HeLa cells with overexpressed AAVRZhaoyue Zheng, Jingya Ye, Mi Leng, et al.
The Journal of Molecular Diagnostics : JMD|March 20, 2012
Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophyC Alexander Valencia, Devin Rhodenizer, Shruti Bhide, et al.
Pancreas|May 13, 2016
Genophenotypic Analysis of Pediatric Patients With Acute Recurrent and Chronic PancreatitisJoseph J Palermo, Tom K Lin, Lindsey Hornung, et al.
Blood|July 26, 2014
Misleading results from saliva samples of patients post-BMT in exome analysesC Alexander Valencia, Subba Rao Indugula, Abhinav Mathur, et al.
Hepatology (Baltimore, Md.)|November 2, 2017
Zebrafish abcb11b mutant reveals strategies to restore bile excretion impaired by bile salt export pump deficiencyJillian L Ellis, Kevin E Bove, Erin G Schuetz, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|May 16, 2019
Genetic variants in acute, acute recurrent and chronic pancreatitis affect the progression of disease in childrenMaisam Abu-El-Haija, C Alexander Valencia, Lindsey Hornung, et al.
BMC Biotechnology|July 27, 2025
Production of SARS-CoV-2 virus-like particles as a vaccine candidate in stable cell lines through inducible E and M protein expressionYu Liu, Zhian Chen, Li Yang, et al.
Plos One|January 18, 2013
Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panelC Alexander Valencia, Arunkanth Ankala, Devin Rhodenizer, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2020
Low-Pass Genome Sequencing: Validation and Diagnostic Utility from 409 Clinical Cases of Low-Pass Genome Sequencing for the Detection of Copy Number Variants to Replace Constitutional MicroarrayAlka Chaubey, Suresh Shenoy, Abhinav Mathur, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
Human Pathology|January 31, 2016
Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubulesNancy Leslie, Xinjian Wang, Yanyan Peng, et al.
Frontiers in Pharmacology|May 15, 2023
Enhanced sensitivity of neutralizing antibody detection for different AAV serotypes using HeLa cells with overexpressed AAVRZhaoyue Zheng, Jingya Ye, Mi Leng, et al.
The Journal of Molecular Diagnostics : JMD|March 20, 2012
Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophyC Alexander Valencia, Devin Rhodenizer, Shruti Bhide, et al.
Pancreas|May 13, 2016
Genophenotypic Analysis of Pediatric Patients With Acute Recurrent and Chronic PancreatitisJoseph J Palermo, Tom K Lin, Lindsey Hornung, et al.
Blood|July 26, 2014
Misleading results from saliva samples of patients post-BMT in exome analysesC Alexander Valencia, Subba Rao Indugula, Abhinav Mathur, et al.
Hepatology (Baltimore, Md.)|November 2, 2017
Zebrafish abcb11b mutant reveals strategies to restore bile excretion impaired by bile salt export pump deficiencyJillian L Ellis, Kevin E Bove, Erin G Schuetz, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|May 16, 2019
Genetic variants in acute, acute recurrent and chronic pancreatitis affect the progression of disease in childrenMaisam Abu-El-Haija, C Alexander Valencia, Lindsey Hornung, et al.
BMC Biotechnology|July 27, 2025
Production of SARS-CoV-2 virus-like particles as a vaccine candidate in stable cell lines through inducible E and M protein expressionYu Liu, Zhian Chen, Li Yang, et al.
Plos One|January 18, 2013
Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panelC Alexander Valencia, Arunkanth Ankala, Devin Rhodenizer, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2020
Low-Pass Genome Sequencing: Validation and Diagnostic Utility from 409 Clinical Cases of Low-Pass Genome Sequencing for the Detection of Copy Number Variants to Replace Constitutional MicroarrayAlka Chaubey, Suresh Shenoy, Abhinav Mathur, et al.
Pageof 7