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Cited by in F6Publishing
For: Matamala N, Gomez-Mariano G, Perez JA, Baladrón B, Torres-Durán M, Michel FJ, Saez R, Hernández-Pérez JM, Belmonte I, Rodriguez-Frias F, Blanco I, Strnad P, Janciauskiene S, Martinez-Delgado B. New cis-Acting Variants in PI*S Background Produce Null Phenotypes Causing Alpha-1 Antitrypsin Deficiency. Am J Respir Cell Mol Biol 2020;63:444-51. [PMID: 32515985 DOI: 10.1165/rcmb.2020-0021OC] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Hernández-Pérez JM, Ramos-Díaz R, Vaquerizo-Pollino C, Pérez JA. Frequency of alleles and genotypes associated with alpha-1 antitrypsin deficiency in clinical and general populations: Revelations about underdiagnosis. Pulmonology 2022:S2531-0437(22)00030-7. [PMID: 35346640 DOI: 10.1016/j.pulmoe.2022.01.017] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Seixas S, Marques PI. Known Mutations at the Cause of Alpha-1 Antitrypsin Deficiency an Updated Overview of SERPINA1 Variation Spectrum. Appl Clin Genet 2021;14:173-94. [PMID: 33790624 DOI: 10.2147/TACG.S257511] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Ghosh AJ, Hobbs BD. Recent advancements in understanding the genetic involvement of alpha-1 antitrypsin deficiency associated lung disease: a look at future precision medicine approaches. Expert Rev Respir Med 2022;:1-10. [PMID: 35025710 DOI: 10.1080/17476348.2022.2027755] [Reference Citation Analysis]
4 Chapman KR. Bench to Bedside and Back: The Evolving Story of Alpha-1 Antitrypsin Deficiency. Am J Respir Cell Mol Biol 2020;63:403-4. [PMID: 32716630 DOI: 10.1165/rcmb.2020-0243ED] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]