Detalhe da pesquisa
1.
The sputum microbiome, airway inflammation, and mortality in chronic obstructive pulmonary disease.
J Allergy Clin Immunol
; 147(1): 158-167, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32353489
2.
Neutrophil extracellular traps are associated with disease severity and microbiota diversity in patients with chronic obstructive pulmonary disease.
J Allergy Clin Immunol
; 141(1): 117-127, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28506850
3.
Genetic mannose binding lectin deficiency is associated with airway microbiota diversity and reduced exacerbation frequency in COPD.
Thorax
; 73(6): 510-518, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29101284
4.
Novel TGM5 mutations in acral peeling skin syndrome.
Exp Dermatol
; 24(4): 285-9, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25644735
5.
The sputum microbiome and clinical outcomes in patients with bronchiectasis: a prospective observational study.
Lancet Respir Med
; 9(8): 885-896, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33961805
6.
Exome Sequencing Reveals Common and Rare Variants in F5 Associated With ACE Inhibitor and Angiotensin Receptor Blocker-Induced Angioedema.
Clin Pharmacol Ther
; 108(6): 1195-1202, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32496628
7.
The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases.
Hum Mutat
; 29(3): 351-60, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18033728
8.
Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis.
J Invest Dermatol
; 126(8): 1770-5, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16810297
9.
Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus
Med. oral patol. oral cir. bucal (Internet)
; 23(2): e144-e150, mar. 2018. ilus, tab
Artigo
em Inglês
| IBECS (Espanha) | ID: ibc-171394
10.
Gauging NOTCH1 Activation in Cancer Using Immunohistochemistry.
PLoS One
; 8(6): e67306, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23825651
11.
Insights into genotype-phenotype correlation in pachyonychia congenita from the human intermediate filament mutation database.
J Investig Dermatol Symp Proc
; 10(1): 31-6, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16250207
12.
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome.
Am J Hum Genet
; 77(6): 909-17, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16380904
13.
The genetic basis of pachyonychia congenita.
J Investig Dermatol Symp Proc
; 10(1): 21-30, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16250206