Detalhe da pesquisa
1.
Astrocyte Responses to Complement Peptide C3a are Highly Context-Dependent.
Neurochem Res
; 48(4): 1233-1241, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36097103
2.
Intestinal gluconeogenesis is downregulated in pediatric patients with celiac disease.
BMC Med
; 20(1): 440, 2022 11 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36369023
3.
A family-based genome-wide association study of recurrent aphthous stomatitis.
Oral Dis
; 26(8): 1696-1705, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32558109
4.
Haplotypes of the inducible nitric oxide synthase gene are strongly associated with exhaled nitric oxide levels in adults: a population-based study.
J Med Genet
; 51(7): 449-54, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24729625
5.
Heredity of nasal polyps.
Rhinology
; 53(1): 25-8, 2015 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25756074
6.
Proteome profiling of home-sampled dried blood spots reveals proteins of SARS-CoV-2 infections.
Commun Med (Lond)
; 4(1): 55, 2024 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38565620
7.
Transcriptomics unravels molecular changes associated with cilia and COVID-19 in chronic rhinosinusitis with nasal polyps.
Sci Rep
; 13(1): 6592, 2023 04 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37085563
8.
Complement C3a treatment accelerates recovery after stroke via modulation of astrocyte reactivity and cortical connectivity.
J Clin Invest
; 133(10)2023 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36995772
9.
The influence of heredity versus environment on coeliac disease.
Gut
; 65(11): 1779-1780, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27449660
10.
The associations between ADHD, pain, inflammation, and quality of life in children and adolescents-a clinical study protocol.
PLoS One
; 17(9): e0273653, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36083951
11.
Loss of Y in leukocytes as a risk factor for critical COVID-19 in men.
Genome Med
; 14(1): 139, 2022 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36514076
12.
Altered peripheral amino acid profile indicate a systemic impact of active celiac disease and a possible role of amino acids in disease pathogenesis.
PLoS One
; 13(3): e0193764, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29538446
13.
A family-based genome-wide association study of chronic rhinosinusitis with nasal polyps implicates several genes in the disease pathogenesis.
PLoS One
; 12(12): e0185244, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29253858
14.
Shared Genetic Factors Involved in Celiac Disease, Type 2 Diabetes and Anorexia Nervosa Suggest Common Molecular Pathways for Chronic Diseases.
PLoS One
; 11(8): e0159593, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27483138
15.
Single Nucleotide Polymorphisms in the FADS Gene Cluster but not the ELOVL2 Gene are Associated with Serum Polyunsaturated Fatty Acid Composition and Development of Allergy (in a Swedish Birth Cohort).
Nutrients
; 7(12): 10100-15, 2015 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26633493
16.
A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
PLoS One
; 8(8): e70174, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23936387
17.
[Early research investment is generating long-term commitment]. / Tidig forskningssatsning ger långsiktigt engagemang.
Lakartidningen
; 1142017 03 21.
Artigo
em Sueco
| MEDLINE | ID: mdl-28323308