Detalhe da pesquisa
1.
Autoantibodies of IgM and IgG classes show differences in recognition of multiple autoantigens in chronic obstructive pulmonary disease.
Clin Immunol;
183: 344-353, 2017 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28951328
2.
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.
Thorax;
71(6): 501-9, 2016 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26917578
3.
PCR Analysis to Identify AAT Gene Promoters and Splice Variants.
Methods Mol Biol;
2750: 33-39, 2024.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38108965
4.
Matrix metalloproteinase-12 (MMP-12) SNP affects MMP activity, lung macrophage infiltration and protects against emphysema in COPD.
Thorax;
66(11): 970-6, 2011 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21730350
5.
The role of IREB2 and transforming growth factor beta-1 genetic variants in COPD: a replication case-control study.
BMC Med Genet;
12: 24, 2011 Feb 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21320324
6.
A novel monoclonal antibody to characterize pathogenic polymers in liver disease associated with alpha1-antitrypsin deficiency.
Hepatology;
52(3): 1078-88, 2010 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20583215
7.
Deletion of Serpina1a, a murine α1-antitrypsin ortholog, results in embryonic lethality.
Exp Lung Res;
37(5): 291-300, 2011 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21574874
8.
EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity.
Physiol Genomics;
41(1): 71-7, 2010 Mar 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20028935
9.
Association of MMP-2 polymorphisms with severe and very severe COPD: a case control study of MMPs-1, 9 and 12 in a European population.
BMC Med Genet;
11: 7, 2010 Jan 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20078883
10.
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.
Nat Commun;
11(1): 5976, 2020 11 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33239696
11.
A polymorphism of the alpha1-antitrypsin gene represents a risk factor for liver disease.
Hepatology;
47(1): 127-32, 2008 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17972336
12.
The new genetics and chronic obstructive pulmonary disease.
COPD;
5(4): 257-64, 2008 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18671150
13.
SERPINA3 (aka alpha-1-antichymotrypsin).
Front Biosci;
12: 2821-35, 2007 May 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17485262
14.
The hydroxy-methyl-glutaryl CoA reductase promoter polymorphism is associated with Alzheimer's risk and cognitive deterioration.
Neurosci Lett;
416(1): 66-70, 2007 Apr 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17284348
15.
Variants in the fetal genome near FLT1 are associated with risk of preeclampsia.
Nat Genet;
49(8): 1255-1260, 2017 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28628106
16.
Altered transmission of maternal angiotensin II receptor haplotypes in fetal growth restriction.
Hum Mutat;
27(2): 138-44, 2006 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16395664
17.
Cryptic haplotypes of SERPINA1 confer susceptibility to chronic obstructive pulmonary disease.
Hum Mutat;
27(1): 103-9, 2006 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16278826
18.
Association of improved pulmonary phenotype in Irish cystic fibrosis patients with a 3' enhancer polymorphism in alpha-1-antitrypsin.
Pediatr Pulmonol;
41(6): 584-91, 2006 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16617455
19.
Opportunities and challenges in the genetics of COPD 2010: an International COPD Genetics Conference report.
COPD;
8(2): 121-35, 2011 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21495840
20.
A new promoter polymorphism in the alpha-1-antichymotrypsin gene is a disease modifier of Alzheimer's disease.
Neurobiol Aging;
26(4): 449-53, 2005 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15653173