Genetically modified mouse models of congenital diaphragmatic hernia: opportunities and limitations for studying altered lung development
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: Frontiers in Pediatrics, 10.2022, art. 867307, S. 1-11
- Event
-
Veröffentlichung
- (where)
-
Frankfurt am Main
- (who)
-
Universitätsbibliothek Johann Christian Senckenberg
- (when)
-
2022
- DOI
-
10.3389/fped.2022.867307
- URN
-
urn:nbn:de:hebis:30:3-863952
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:47 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Friedmacher, Florian Michael
- Rolle, Udo
- Puri, Prem
- Universitätsbibliothek Johann Christian Senckenberg
Time of origin
- 2022
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The correlation between defect-size and outcome in congenital diaphragmatic hernia
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Functional analysis of components of the kallikrein-kinin system in genetically altered rat models
The multi-faceted genetically-determined carbohydrate malabsorption in congenital sucrase-isomaltase deficiency and irritable bowel syndrome
Hernia.
Congenital diaphragmatic hernia
Congenital diaphragmatic hernia : 22 tables
Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge
De Novo Duplication of 11p15 Associated With Congenital Diaphragmatic Hernia
The correlation between defect-size and outcome in congenital diaphragmatic hernia
Genetically altered animal models to study tissue actions of angiotensin peptides
The Role of De Novo Variants in Patients with Congenital Diaphragmatic Hernia
From pre- to postnatal and beyond : evolutions in the treatment of congenital diaphragmatic hernia
Vena cava thrombosis after congenital diaphragmatic hernia repair : multivariate analysis of potential risk factors
Functional analysis of components of the kallikrein-kinin system in genetically altered rat models
The multi-faceted genetically-determined carbohydrate malabsorption in congenital sucrase-isomaltase deficiency and irritable bowel syndrome