324
Views
23
CrossRef citations to date
0
Altmetric
Research Article

Deletion of serpina1a, a murine α1-antitrypsin ortholog, results in embryonic lethality

, , , , , & show all
Pages 291-300 | Received 05 Oct 2010, Accepted 14 Dec 2010, Published online: 16 May 2011

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (2)

Monica Yonashiro Marcelino, Natalia Langenfeld Fuoco, Carolina Arruda de Faria, Rodrigo de Las Heras Kozma, Lais Fernanda Marques & João Tadeu Ribeiro-Paes. (2014) Animal models in chronic obstructive pulmonary disease—an overview. Experimental Lung Research 40:6, pages 259-271.
Read now
Shuling Guo, Sheri L Booten, Andrew Watt, Luis Alvarado, Susan M Freier, Jeffery H Teckman, Michael L McCaleb & Brett P Monia. (2014) Using antisense technology to develop a novel therapy for α-1 antitrypsin deficient (AATD) liver disease and to model AATD lung disease. Rare Diseases 2:1.
Read now

Articles from other publishers (21)

Xueguang Zhang, Rui Zheng, Chen Liang, Haotian LiuXiaozhen Zhang, Yongyi MaMohan LiuWei ZhangYang Yang, Man LiuChuan Jiang, Qingjia RenYan Wang, Suren Chen, Yihong Yang & Ying Shen. (2022) Loss-of-function mutations in CEP78 cause male infertility in humans and mice . Science Advances 8:40.
Crossref
Steven P. Grover & Nigel Mackman. (2022) Anticoagulant SERPINs: Endogenous Regulators of Hemostasis and Thrombosis. Frontiers in Cardiovascular Medicine 9.
Crossref
Aneela Nomura & Ichiro Taniuchi. (2021) Is α1-Antitrypsin Important for Murine Thymocyte Development?. Trends in Immunology 42:3, pages 178-180.
Crossref
Rashika Joshi, Mohit Ojha, Jana Lewis, Qiang Fan, Brett Monia, Shuling Guo & Brian M. Varisco. (2019) Sex-specific differences in emphysema using a murine antisense oligonucleotide model of α-1 antitrypsin deficiency. American Journal of Physiology-Lung Cellular and Molecular Physiology 316:6, pages L1165-L1173.
Crossref
Reto Eggenschwiler, Atanas Patronov, Jan Hegermann, Mariane Fráguas-Eggenschwiler, Guangming Wu, Leon Cortnumme, Matthias Ochs, Iris Antes & Tobias Cantz. (2019) A combined in silico and in vitro study on mouse Serpina1a antitrypsin-deficiency mutants. Scientific Reports 9:1.
Crossref
Rashika Joshi, Andrea Heinz, Qiang Fan, Shuling Guo, Brett Monia, Christian E. H. Schmelzer, Anthony S. Weiss, Matthew Batie, Harikrishnan Parameshwaran & Brian M. Varisco. (2018) Role for Cela1 in Postnatal Lung Remodeling and Alpha-1 Antitrypsin–Deficient Emphysema . American Journal of Respiratory Cell and Molecular Biology 59:2, pages 167-178.
Crossref
Karen Jülicher, Annabell Wähner, Kerstin Haase, Karen W. Barbour, Franklin G. Berger, Lutz Wiehlmann, Colin Davenport, Karin Schuster-Gossler, Jörn Stitz, Tobias Cantz & Reto Eggenschwiler. (2018) Functional characterization of the mouse Serpina1 paralog DOM-7. Biological Chemistry 399:6, pages 577-582.
Crossref
Florie Borel, Huaming SunMarina ZiegerAndrew CoxBrynn CardozoWeiying LiGabriella OliveiraAiriel DavisAlisha GruntmanTerence R. FlotteMichael H. Brodsky, Andrew M. HoffmanMai K. ElmallahChristian Mueller. (2018) Editing out five Serpina1 paralogs to create a mouse model of genetic emphysema . Proceedings of the National Academy of Sciences 115:11, pages 2788-2793.
Crossref
Scott M. Gordon & Alan T. Remaley. (2017) High density lipoproteins are modulators of protease activity: Implications in inflammation, complement activation, and atherothrombosis. Atherosclerosis 259, pages 104-113.
Crossref
Dolan SondhiKatie M. StilesBishnu P. DeRonald G. Crystal. (2017) Genetic Modification of the Lung Directed Toward Treatment of Human Disease. Human Gene Therapy 28:1, pages 3-84.
Crossref
Samuel Alam & Ravi Mahadeva. 2017. Alpha-1-antitrypsin Deficiency. Alpha-1-antitrypsin Deficiency 179 195 .
Chi F. Hung & William A. Altemeier. 2017. Acute Lung Injury and Repair. Acute Lung Injury and Repair 25 38 .
Kevin Ni, Karina A. Serban, Chanan Batra & Irina Petrache. (2016) Alpha-1 Antitrypsin Investigations Using Animal Models of Emphysema. Annals of the American Thoracic Society 13:Supplement_4, pages S311-S316.
Crossref
Mayur V. Bakshi, Omid Azimzadeh, Juliane Merl-Pham, Tine Verreet, Stefanie M. Hauck, Mohammed A. Benotmane, Michael J. Atkinson & Soile Tapio. (2016) In-Utero Low-Dose Irradiation Leads to Persistent Alterations in the Mouse Heart Proteome. PLOS ONE 11:6, pages e0156952.
Crossref
Stefanie J. Willmann, Nikola S. Mueller, Silvia Engert, Michael Sterr, Ingo Burtscher, Aurelia Raducanu, Martin Irmler, Johannes Beckers, Steffen Sass, Fabian J. Theis & Heiko Lickert. (2016) The global gene expression profile of the secondary transition during pancreatic development. Mechanisms of Development 139, pages 51-64.
Crossref
Julia G Payne, Ayuko Takahashi, Michelle I Higgins, Emily L Porter, Bela Suki, Alejandro Balazs & Andrew A Wilson. (2016) Multilineage transduction of resident lung cells in vivo by AAV2/8 for α1-antitrypsin gene therapy. Molecular Therapy - Methods & Clinical Development 3, pages 16042.
Crossref
Charaf Benarafa. 2015. The Serpin Family. The Serpin Family 59 76 .
Tiziana P. Cremona, Stefan A. TschanzChristophe von Garnier & Charaf Benarafa. (2013) SerpinB1 deficiency is not associated with increased susceptibility to pulmonary emphysema in mice. American Journal of Physiology-Lung Cellular and Molecular Physiology 305:12, pages L981-L989.
Crossref
Eli C Lewis. (2012) Expanding the Clinical Indications for α1-Antitrypsin Therapy. Molecular Medicine 18:6, pages 957-970.
Crossref
Gillian L. McNab, Timothy R. Dafforn, Alice Wood, Elizabeth Sapey & Robert A. Stockley. (2011) A novel model and molecular therapy for Z alpha-1 antitrypsin deficiency. Mammalian Genome 23:3-4, pages 241-249.
Crossref
Rebecca M. Baron, Alexander J. S. Choi, Caroline A. Owen & Augustine M. K. Choi. (2012) Genetically manipulated mouse models of lung disease: potential and pitfalls. American Journal of Physiology-Lung Cellular and Molecular Physiology 302:6, pages L485-L497.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.