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Gail Deutsch

Showing results (11-20 of 52) with videos related to

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Genomics|May 7, 2026
Small partial deletion of a highly GC-rich FOXF1 exon 1 in two deceased siblings with alveolar capillary dysplasiaHiuling Chan Joiner, Shruti A Pande, Przemyslaw Szafranski, et al.
International Journal of Molecular Sciences|May 14, 2022
Hedgehog Signaling Pathway Orchestrates Human Lung Branching MorphogenesisRanda Belgacemi, Soula Danopoulos, Gail Deutsch, et al.
Clinical Epigenetics|October 21, 2023
Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasiaPrzemyslaw Szafranski, Rijutha P Garimella, Haresh Mani, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2023
A Trisomy 21 Lung Cell AtlasSoumyaroop Bhattacharya, Caroline Cherry, Gail Deutsch, et al.
The Journal of Pathology|May 29, 2021
Prenatal histological, cellular, and molecular anomalies in trisomy 21 lungSoula Danopoulos, Soumyaroop Bhattacharya, Gail Deutsch, et al.
Pediatric Pulmonology|November 27, 2025
Childhood Interstitial Lung Disease (chILD) Associated With Toxic Chemical Inhalation Exposures: A State-of-the-Art ReviewWilliam Hadley, Robin Lacagnina, Irfan Rahman, et al.
American Journal of Medical Genetics. Part A|November 18, 2024
The Glu86 Residue in TBX4 Proves Critical for Human Lung DevelopmentPrzemyslaw Szafranski, Tomasz Gambin, Gail Deutsch, et al.
The Journal of Pediatrics|January 24, 2007
Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapyT Andrew Burrow, Mitchell B Cohen, Ronald Bokulic, et al.
Gene|December 11, 2017
In Niemann-Pick C1 mouse models, glial-only expression of the normal gene extends survival much further than do changes in genetic background or treatment with hydroxypropyl-beta-cyclodextrinCraig A Marshall, Dawn E Watkins-Chow, Giampiero Palladino, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 3, 2023
Diminished <i>TMEM</i>100 Expression in a Newborn With Acinar Dysplasia and a Novel <i>TBX4</i> Variant: A Case ReportPrzemyslaw Szafranski, Silvia Patrizi, Tomasz Gambin, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Genomics|May 7, 2026
Small partial deletion of a highly GC-rich FOXF1 exon 1 in two deceased siblings with alveolar capillary dysplasiaHiuling Chan Joiner, Shruti A Pande, Przemyslaw Szafranski, et al.
International Journal of Molecular Sciences|May 14, 2022
Hedgehog Signaling Pathway Orchestrates Human Lung Branching MorphogenesisRanda Belgacemi, Soula Danopoulos, Gail Deutsch, et al.
Clinical Epigenetics|October 21, 2023
Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasiaPrzemyslaw Szafranski, Rijutha P Garimella, Haresh Mani, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2023
A Trisomy 21 Lung Cell AtlasSoumyaroop Bhattacharya, Caroline Cherry, Gail Deutsch, et al.
The Journal of Pathology|May 29, 2021
Prenatal histological, cellular, and molecular anomalies in trisomy 21 lungSoula Danopoulos, Soumyaroop Bhattacharya, Gail Deutsch, et al.
Pediatric Pulmonology|November 27, 2025
Childhood Interstitial Lung Disease (chILD) Associated With Toxic Chemical Inhalation Exposures: A State-of-the-Art ReviewWilliam Hadley, Robin Lacagnina, Irfan Rahman, et al.
American Journal of Medical Genetics. Part A|November 18, 2024
The Glu86 Residue in TBX4 Proves Critical for Human Lung DevelopmentPrzemyslaw Szafranski, Tomasz Gambin, Gail Deutsch, et al.
The Journal of Pediatrics|January 24, 2007
Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapyT Andrew Burrow, Mitchell B Cohen, Ronald Bokulic, et al.
Gene|December 11, 2017
In Niemann-Pick C1 mouse models, glial-only expression of the normal gene extends survival much further than do changes in genetic background or treatment with hydroxypropyl-beta-cyclodextrinCraig A Marshall, Dawn E Watkins-Chow, Giampiero Palladino, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 3, 2023
Diminished <i>TMEM</i>100 Expression in a Newborn With Acinar Dysplasia and a Novel <i>TBX4</i> Variant: A Case ReportPrzemyslaw Szafranski, Silvia Patrizi, Tomasz Gambin, et al.
Pageof 6