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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2013 1
2014 25
2015 45
2016 61
2017 59
2018 64
2019 63
2020 101
2021 99
2022 69
2023 71
2024 29

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609 results

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Page 1
α1-Antitrypsin deficiency.
Greene CM, Marciniak SJ, Teckman J, Ferrarotti I, Brantly ML, Lomas DA, Stoller JK, McElvaney NG. Greene CM, et al. Nat Rev Dis Primers. 2016 Jul 28;2:16051. doi: 10.1038/nrdp.2016.51. Nat Rev Dis Primers. 2016. PMID: 27465791 Review.
alpha1-Antitrypsin deficiency (A1ATD) is an inherited disorder caused by mutations in SERPINA1, leading to liver and lung disease. It is not a rare disorder but frequently goes underdiagnosed or misdiagnosed as asthma, chronic obstructive pulmonary disease (COPD) or crypto …
alpha1-Antitrypsin deficiency (A1ATD) is an inherited disorder caused by mutations in SERPINA1, leading to liver and lung disease. It …
Alpha-1 antitrypsin deficiency.
Dasí F. Dasí F. Med Clin (Barc). 2024 Apr 12;162(7):336-342. doi: 10.1016/j.medcli.2023.10.014. Epub 2023 Nov 22. Med Clin (Barc). 2024. PMID: 37993348 Free article. Review. English, Spanish.
Alpha-1 antitrypsin deficiency: outstanding questions and future directions.
Torres-Durán M, Lopez-Campos JL, Barrecheguren M, Miravitlles M, Martinez-Delgado B, Castillo S, Escribano A, Baloira A, Navarro-Garcia MM, Pellicer D, Bañuls L, Magallón M, Casas F, Dasí F. Torres-Durán M, et al. Orphanet J Rare Dis. 2018 Jul 11;13(1):114. doi: 10.1186/s13023-018-0856-9. Orphanet J Rare Dis. 2018. PMID: 29996870 Free PMC article. Review.
Genome-wide Association Study and Meta-analysis on Alcohol-Associated Liver Cirrhosis Identifies Genetic Risk Factors.
Schwantes-An TH, Darlay R, Mathurin P, Masson S, Liangpunsakul S, Mueller S, Aithal GP, Eyer F, Gleeson D, Thompson A, Muellhaupt B, Stickel F, Soyka M, Goldman D, Liang T, Lumeng L, Pirmohamed M, Nalpas B, Jacquet JM, Moirand R, Nahon P, Naveau S, Perney P, Botwin G, Haber PS, Seitz HK, Day CP, Foroud TM, Daly AK, Cordell HJ, Whitfield JB, Morgan TR, Seth D; GenomALC Consortium. Schwantes-An TH, et al. Hepatology. 2021 May;73(5):1920-1931. doi: 10.1002/hep.31535. Hepatology. 2021. PMID: 32853455 Free article.
Meta-analysis (without conditioning) confirmed genome-wide significance for the identified FAF2 locus as well as PNPLA3 and HSD17B13. Two other previously known loci (SERPINA1 and SUGP1/TM6SF2) were also genome-wide significant in the meta-analysis. ...
Meta-analysis (without conditioning) confirmed genome-wide significance for the identified FAF2 locus as well as PNPLA3 and HSD17B13. Two ot …
Bioinformatics reveal macrophages marker genes signature in breast cancer to predict prognosis.
Li Y, Zhao X, Liu Q, Liu Y. Li Y, et al. Ann Med. 2021 Dec;53(1):1019-1031. doi: 10.1080/07853890.2021.1914343. Ann Med. 2021. PMID: 34187256 Free PMC article.
TCGA database was used to construct MMGS model as a training cohort, and GSE96058 dataset was used to validate the MMGS as a validation cohort.Results: Genes included in the MMGS model were: SERPINA1, CD74, STX11, ADAM9, CD24, NFKBIA, PGK1. MMGS risk score stratified by ov …
TCGA database was used to construct MMGS model as a training cohort, and GSE96058 dataset was used to validate the MMGS as a validation coho …
Genetics of vasculitis.
Carmona FD, Martín J, González-Gay MA. Carmona FD, et al. Curr Opin Rheumatol. 2015 Jan;27(1):10-7. doi: 10.1097/BOR.0000000000000124. Curr Opin Rheumatol. 2015. PMID: 25405820 Review.
These associations include ERAP1, CCR1-CCR3, STAT4, KLRC4, GIMAP4, and TNFAIP3 in Behcet's disease; BLK and CD40 in Kawasaki disease; SERPINA1 and SEMA6A in antineutrophil cytoplasmic antibody associated vasculitides; IL12B and FCGR2A/ FCGR2A in Takayasu arteritis; and CEC …
These associations include ERAP1, CCR1-CCR3, STAT4, KLRC4, GIMAP4, and TNFAIP3 in Behcet's disease; BLK and CD40 in Kawasaki disease; SER …
Alpha1-antitrypsin deficiency and asthma.
Pini L, Paoletti G, Heffler E, Tantucci C, Puggioni F; Asthma and Alpha1-Antitrypsin Research Group. Pini L, et al. Curr Opin Allergy Clin Immunol. 2021 Feb 1;21(1):46-51. doi: 10.1097/ACI.0000000000000711. Curr Opin Allergy Clin Immunol. 2021. PMID: 33284159 Review.
Proteome-wide mendelian randomization identifies causal plasma proteins in venous thromboembolism development.
Li H, Zhang Z, Qiu Y, Weng H, Yuan S, Zhang Y, Zhang Y, Xi L, Xu F, Ji X, Hao R, Yang P, Chen G, Zuo X, Zhai Z, Wang C. Li H, et al. J Hum Genet. 2023 Dec;68(12):805-812. doi: 10.1038/s10038-023-01186-6. Epub 2023 Aug 3. J Hum Genet. 2023. PMID: 37537391 Free PMC article.
Of these 13 proteins demonstrated Mendelian randomized correlations. Six proteins (F2, F11, PLEK, SERPINA1, RARRES2, and SERPINE2) had strong support in colocalization analysis. Utilizing multidimensional data, this study suggests PLEK, SERPINA1, and SERPINE2 as com …
Of these 13 proteins demonstrated Mendelian randomized correlations. Six proteins (F2, F11, PLEK, SERPINA1, RARRES2, and SERPINE2) ha …
Plasma exosomal protein PLG and SERPINA1 in colorectal cancer diagnosis and coagulation abnormalities.
Li L, Song X, Chen G, Zhang Z, Zheng B, Zhang Q, Wang S, Xie L. Li L, et al. J Cancer Res Clin Oncol. 2023 Sep;149(11):8507-8519. doi: 10.1007/s00432-023-04776-1. Epub 2023 Apr 24. J Cancer Res Clin Oncol. 2023. PMID: 37093347
RESULTS: The expression levels of serpin peptidase inhibitor clade A member 1 (SERPINA1) and fibrinogen (PLG) in CRC patients were significantly higher than those in healthy groups. ...
RESULTS: The expression levels of serpin peptidase inhibitor clade A member 1 (SERPINA1) and fibrinogen (PLG) in CRC patients were si …
609 results