Gdf2-KO 基因敲除小鼠

1. Topiwala, Karan K, Patel, Smit D, Nouh, Amre M, Alberts, Mark J. 2020. Novel GDF2 Gene Mutation Associated with Pulmonary Arteriovenous Malformation. In Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 29, 105301. doi:10.1016/j.jstrokecerebrovasdis.2020.105301. https://pubmed.ncbi.nlm.nih.gov/32992168/

2. Gräf, Stefan, Haimel, Matthias, Bleda, Marta, Trembath, Richard C, Morrell, Nicholas W. 2018. Identification of rare sequence variation underlying heritable pulmonary arterial hypertension. In Nature communications, 9, 1416. doi:10.1038/s41467-018-03672-4. https://pubmed.ncbi.nlm.nih.gov/29650961/

3. Shovlin, Claire L, Simeoni, Ilenia, Downes, Kate, Jovine, Luca, Turro, Ernest. . Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasia. In Blood, 136, 1907-1918. doi:10.1182/blood.2019004560. https://pubmed.ncbi.nlm.nih.gov/32573726/

4. Parrot, A, Barral, M, Amiot, X, Dupuis-Girod, S, Cadranel, J. 2023. [Hereditary hemorrhagic telangiectasia]. In Revue des maladies respiratoires, 40, 391-405. doi:10.1016/j.rmr.2023.02.007. https://pubmed.ncbi.nlm.nih.gov/37062633/

5. Welch, Carrie L, Aldred, Micheala A, Balachandar, Srimmitha, Tenorio-Castano, Jair, Chung, Wendy K. 2023. Defining the clinical validity of genes reported to cause pulmonary arterial hypertension. In Genetics in medicine : official journal of the American College of Medical Genetics, 25, 100925. doi:10.1016/j.gim.2023.100925. https://pubmed.ncbi.nlm.nih.gov/37422716/