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J Wegner

Showing results (121-130 of 154) with videos related to

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The Journal of Nutritional Biochemistry|February 15, 2017
Astaxanthin inhibits inflammation and fibrosis in the liver and adipose tissue of mouse models of diet-induced obesity and nonalcoholic steatohepatitisBohkyung Kim, Callie Farruggia, Chai Siah Ku, et al.
The Journal of Pediatrics|December 5, 2017
Infants with Atypical Presentations of Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins Who Underwent Bilateral Lung TransplantationChristopher T Towe, Frances V White, R Mark Grady, et al.
Pediatric Research|March 5, 2008
Population and disease-based prevalence of the common mutations associated with surfactant deficiencyTami H Garmany, Jennifer A Wambach, Hillary B Heins, et al.
American Journal of Respiratory Cell and Molecular Biology|May 6, 2026
Lentiviral-mediated gene complementation to rescue pathogenic ABCA3 variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
Biorxiv : the Preprint Server for Biology|September 5, 2025
Lentiviral-mediated gene complementation rescues pathogenic <i>ABCA3</i> variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
American Journal of Medical Genetics. Part A|May 1, 2021
Biallelic ASCC1 variants including a novel intronic variant result in expanded phenotypic spectrum of spinal muscular atrophy with congenital bone fractures 2 (SMABF2)Kristen K Rosano, Daniel J Wegner, Marwan Shinawi, et al.
Nature Methods|March 3, 2009
Quantification of rare allelic variants from pooled genomic DNATodd E Druley, Francesco L M Vallania, Daniel J Wegner, et al.
The Journal of Pediatrics|August 4, 2009
Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genesAaron Hamvas, Lawrence M Nogee, Daniel J Wegner, et al.
Pediatric Pulmonology|April 3, 2008
Recombination as a mechanism for sporadic mutation in the surfactant protein-C geneAmy D McBee, Daniel J Wegner, Christopher S Carlson, et al.
Pediatric Research|July 4, 2018
Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizuresJennifer A Wambach, Daniel J Wegner, Ping Yang, et al.
Pageof 16

Showing results (121-130 of 154) with videos related to

Sort By:
Pageof 16
The Journal of Nutritional Biochemistry|February 15, 2017
Astaxanthin inhibits inflammation and fibrosis in the liver and adipose tissue of mouse models of diet-induced obesity and nonalcoholic steatohepatitisBohkyung Kim, Callie Farruggia, Chai Siah Ku, et al.
The Journal of Pediatrics|December 5, 2017
Infants with Atypical Presentations of Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins Who Underwent Bilateral Lung TransplantationChristopher T Towe, Frances V White, R Mark Grady, et al.
Pediatric Research|March 5, 2008
Population and disease-based prevalence of the common mutations associated with surfactant deficiencyTami H Garmany, Jennifer A Wambach, Hillary B Heins, et al.
American Journal of Respiratory Cell and Molecular Biology|May 6, 2026
Lentiviral-mediated gene complementation to rescue pathogenic ABCA3 variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
Biorxiv : the Preprint Server for Biology|September 5, 2025
Lentiviral-mediated gene complementation rescues pathogenic <i>ABCA3</i> variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
American Journal of Medical Genetics. Part A|May 1, 2021
Biallelic ASCC1 variants including a novel intronic variant result in expanded phenotypic spectrum of spinal muscular atrophy with congenital bone fractures 2 (SMABF2)Kristen K Rosano, Daniel J Wegner, Marwan Shinawi, et al.
Nature Methods|March 3, 2009
Quantification of rare allelic variants from pooled genomic DNATodd E Druley, Francesco L M Vallania, Daniel J Wegner, et al.
The Journal of Pediatrics|August 4, 2009
Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genesAaron Hamvas, Lawrence M Nogee, Daniel J Wegner, et al.
Pediatric Pulmonology|April 3, 2008
Recombination as a mechanism for sporadic mutation in the surfactant protein-C geneAmy D McBee, Daniel J Wegner, Christopher S Carlson, et al.
Pediatric Research|July 4, 2018
Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizuresJennifer A Wambach, Daniel J Wegner, Ping Yang, et al.
Pageof 16