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American Journal of Respiratory Cell and Molecular Biology
|
September 16, 2003
Surfactant protein B in type II pneumocytes and intra-alveolar surfactant forms of human lungs
Frank Brasch, Georg Johnen, Alexandra Winn-Brasch, et al.
American Journal of Respiratory Cell and Molecular Biology
|
May 30, 2002
Involvement of cathepsin H in the processing of the hydrophobic surfactant-associated protein C in type II pneumocytes
Frank Brasch, Anja Ten Brinke, Georg Johnen, et al.
Cell Death & Disease
|
July 19, 2024
Human papillomavirus-associated head and neck squamous cell carcinoma cells lose viability during triggered myocyte lineage differentiation
Sarah Gendreizig, Laura Martínez-Ruiz, Alba López-Rodríguez, et al.
British Journal of Cancer
|
January 8, 2026
Diagnostic accuracy of combinatorial mRNA biomarkers for non-invasive detection and therapy monitoring of oral and oropharyngeal SCC
Leonie Hose, Alina Celine Tekin, Bart Verwaaijen, et al.
The Journal of Biological Chemistry
|
September 18, 2003
Involvement of napsin A in the C- and N-terminal processing of surfactant protein B in type-II pneumocytes of the human lung
Frank Brasch, Matthias Ochs, Thilo Kahne, et al.
Pediatric Pulmonology
|
May 14, 2016
Tools to explore ABCA3 mutations causing interstitial lung disease
Thomas Wittmann, Ulrike Schindlbeck, Stefanie Höppner, et al.
Orphanet Journal of Rare Diseases
|
March 28, 2018
Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood
Meike Hengst, Lutz Naehrlich, Poornima Mahavadi, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 27, 2006
Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency
Frank Brasch, Sven Schimanski, Christian Mühlfeld, et al.
BMC Pediatrics
|
August 19, 2011
Long-term follow-up and treatment of congenital alveolar proteinosis
Matthias Griese, Jan Ripper, Anke Sibbersen, et al.
Orphanet Journal of Rare Diseases
|
September 27, 2015
Categorizing diffuse parenchymal lung disease in children
Matthias Griese, Armin Irnstetter, Meike Hengst, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
American Journal of Respiratory Cell and Molecular Biology
|
September 16, 2003
Surfactant protein B in type II pneumocytes and intra-alveolar surfactant forms of human lungs
Frank Brasch, Georg Johnen, Alexandra Winn-Brasch, et al.
American Journal of Respiratory Cell and Molecular Biology
|
May 30, 2002
Involvement of cathepsin H in the processing of the hydrophobic surfactant-associated protein C in type II pneumocytes
Frank Brasch, Anja Ten Brinke, Georg Johnen, et al.
Cell Death & Disease
|
July 19, 2024
Human papillomavirus-associated head and neck squamous cell carcinoma cells lose viability during triggered myocyte lineage differentiation
Sarah Gendreizig, Laura Martínez-Ruiz, Alba López-Rodríguez, et al.
British Journal of Cancer
|
January 8, 2026
Diagnostic accuracy of combinatorial mRNA biomarkers for non-invasive detection and therapy monitoring of oral and oropharyngeal SCC
Leonie Hose, Alina Celine Tekin, Bart Verwaaijen, et al.
The Journal of Biological Chemistry
|
September 18, 2003
Involvement of napsin A in the C- and N-terminal processing of surfactant protein B in type-II pneumocytes of the human lung
Frank Brasch, Matthias Ochs, Thilo Kahne, et al.
Pediatric Pulmonology
|
May 14, 2016
Tools to explore ABCA3 mutations causing interstitial lung disease
Thomas Wittmann, Ulrike Schindlbeck, Stefanie Höppner, et al.
Orphanet Journal of Rare Diseases
|
March 28, 2018
Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood
Meike Hengst, Lutz Naehrlich, Poornima Mahavadi, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 27, 2006
Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency
Frank Brasch, Sven Schimanski, Christian Mühlfeld, et al.
BMC Pediatrics
|
August 19, 2011
Long-term follow-up and treatment of congenital alveolar proteinosis
Matthias Griese, Jan Ripper, Anke Sibbersen, et al.
Orphanet Journal of Rare Diseases
|
September 27, 2015
Categorizing diffuse parenchymal lung disease in children
Matthias Griese, Armin Irnstetter, Meike Hengst, et al.
Page
of 4