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Showing results (801-810 of 951) with videos related to

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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.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
Discovery of small molecule guanylyl cyclase A receptor positive allosteric modulatorsS Jeson Sangaralingham, Kanupriya Whig, Satyamaheshwar Peddibhotla, 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.
ACS Pharmacology & Translational Science|July 13, 2022
Allosteric Binders of ACE2 Are Promising Anti-SARS-CoV-2 AgentsJoshua E Hochuli, Sankalp Jain, Cleber Melo-Filho, et al.
International Journal for Parasitology|December 21, 2017
A reference genome and methylome for the Plasmodium knowlesi A1-H.1 lineErnest Diez Benavente, Paola Florez de Sessions, Robert W Moon, et al.
Emerging Microbes & Infections|June 16, 2020
Emergence of multidrug-resistant <i>Mycobacterium tuberculosis</i> of the Beijing lineage in Portugal and Guinea-Bissau: a snapshot of moving clones by whole-genome sequencingJoão Perdigão, Carla Silva, Fernando Maltez, et al.
British Journal of Cancer|October 5, 2023
ACAA2 is a novel molecular indicator for cancers with neuroendocrine phenotypeMichelle Shen, Shiqin Liu, Angus Toland, 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.
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 96

Showing results (801-810 of 951) with videos related to

Sort By:
Pageof 96
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.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
Discovery of small molecule guanylyl cyclase A receptor positive allosteric modulatorsS Jeson Sangaralingham, Kanupriya Whig, Satyamaheshwar Peddibhotla, 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.
ACS Pharmacology & Translational Science|July 13, 2022
Allosteric Binders of ACE2 Are Promising Anti-SARS-CoV-2 AgentsJoshua E Hochuli, Sankalp Jain, Cleber Melo-Filho, et al.
International Journal for Parasitology|December 21, 2017
A reference genome and methylome for the Plasmodium knowlesi A1-H.1 lineErnest Diez Benavente, Paola Florez de Sessions, Robert W Moon, et al.
Emerging Microbes & Infections|June 16, 2020
Emergence of multidrug-resistant <i>Mycobacterium tuberculosis</i> of the Beijing lineage in Portugal and Guinea-Bissau: a snapshot of moving clones by whole-genome sequencingJoão Perdigão, Carla Silva, Fernando Maltez, et al.
British Journal of Cancer|October 5, 2023
ACAA2 is a novel molecular indicator for cancers with neuroendocrine phenotypeMichelle Shen, Shiqin Liu, Angus Toland, 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.
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 96