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Frances V White

Showing results (31-40 of 43) with videos related to

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American Journal of Respiratory Cell and Molecular Biology|July 5, 2016
Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress SyndromeJennifer A Wambach, Ping Yang, Daniel J Wegner, 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.
American Journal of Respiratory Cell and Molecular Biology|December 6, 2003
Progressive lung disease and surfactant dysfunction with a deletion in surfactant protein C geneAaron Hamvas, Lawrence M Nogee, Frances V White, 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.
Annals of the American Thoracic Society|August 21, 2015
Diffuse Lung Disease in Biopsied Children 2 to 18 Years of Age. Application of the chILD Classification SchemeLeland L Fan, Megan K Dishop, Csaba Galambos, et al.
Chest|February 23, 2013
Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1Aaron Hamvas, Robin R Deterding, Susan E Wert, et al.
The American Journal of Surgical Pathology|October 25, 2016
Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter StudyPierre Russo, John C Magee, Robert A Anders, et al.
American Journal of Respiratory Cell and Molecular Biology|December 29, 2023
Homozygous, Intragenic Tandem Duplication of <i>SFTPB</i> Causes Neonatal Respiratory FailureJennifer A Wambach, Daniel J Wegner, Joseph Kitzmiller, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Respiratory Cell and Molecular Biology|July 5, 2016
Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress SyndromeJennifer A Wambach, Ping Yang, Daniel J Wegner, 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.
American Journal of Respiratory Cell and Molecular Biology|December 6, 2003
Progressive lung disease and surfactant dysfunction with a deletion in surfactant protein C geneAaron Hamvas, Lawrence M Nogee, Frances V White, 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.
Annals of the American Thoracic Society|August 21, 2015
Diffuse Lung Disease in Biopsied Children 2 to 18 Years of Age. Application of the chILD Classification SchemeLeland L Fan, Megan K Dishop, Csaba Galambos, et al.
Chest|February 23, 2013
Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1Aaron Hamvas, Robin R Deterding, Susan E Wert, et al.
The American Journal of Surgical Pathology|October 25, 2016
Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter StudyPierre Russo, John C Magee, Robert A Anders, et al.
American Journal of Respiratory Cell and Molecular Biology|December 29, 2023
Homozygous, Intragenic Tandem Duplication of <i>SFTPB</i> Causes Neonatal Respiratory FailureJennifer A Wambach, Daniel J Wegner, Joseph Kitzmiller, et al.
Pageof 5