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Jacob J Hagen

Showing results (1-10 of 7) with videos related to

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BMC Cell Biology|March 13, 2014
Tissue specific expression of myosin IC isoformsNeil L Sielski, Ivanna Ihnatovych, Jacob J Hagen, et al.
Human Mutation|March 11, 2015
Novel, compound heterozygous, single-nucleotide variants in MARS2 associated with developmental delay, poor growth, and sensorineural hearing lossBryn D Webb, Patricia G Wheeler, Jacob J Hagen, et al.
Autophagy|February 20, 2018
HEPES activates a MiT/TFE-dependent lysosomal-autophagic gene network in cultured cells: A call for cautionMarc J Tol, Martijn J C van der Lienden, Tanit L Gabriel, et al.
HGG Advances|May 6, 2022
Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulasGuojie Zhong, Priyanka Ahimaz, Nicole A Edwards, et al.
HGG Advances|July 8, 2022
Erratum: Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulasGuojie Zhong, Priyanka Ahimaz, Nicole A Edwards, et al.
Genome Medicine|May 11, 2021
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAHNa Zhu, Emilia M Swietlik, Carrie L Welch, et al.
Genome Medicine|June 23, 2021
Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAHNa Zhu, Emilia M Swietlik, Carrie L Welch, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
BMC Cell Biology|March 13, 2014
Tissue specific expression of myosin IC isoformsNeil L Sielski, Ivanna Ihnatovych, Jacob J Hagen, et al.
Human Mutation|March 11, 2015
Novel, compound heterozygous, single-nucleotide variants in MARS2 associated with developmental delay, poor growth, and sensorineural hearing lossBryn D Webb, Patricia G Wheeler, Jacob J Hagen, et al.
Autophagy|February 20, 2018
HEPES activates a MiT/TFE-dependent lysosomal-autophagic gene network in cultured cells: A call for cautionMarc J Tol, Martijn J C van der Lienden, Tanit L Gabriel, et al.
HGG Advances|May 6, 2022
Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulasGuojie Zhong, Priyanka Ahimaz, Nicole A Edwards, et al.
HGG Advances|July 8, 2022
Erratum: Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulasGuojie Zhong, Priyanka Ahimaz, Nicole A Edwards, et al.
Genome Medicine|May 11, 2021
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAHNa Zhu, Emilia M Swietlik, Carrie L Welch, et al.
Genome Medicine|June 23, 2021
Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAHNa Zhu, Emilia M Swietlik, Carrie L Welch, et al.
Pageof 1