Detalhe da pesquisa
1.
Down-regulation of the mitochondrial fusion protein Opa1/Mfn2 promotes cardiomyocyte hypertrophy in Su5416/hypoxia-induced pulmonary hypertension rats.
Arch Biochem Biophys
; 747: 109743, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37696382
2.
Artemisia pollen allergy in China: Component-resolved diagnosis reveals allergic asthma patients have significant multiple allergen sensitization.
Allergy
; 74(2): 284-293, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30155917
3.
Antiviral activity of cathelicidin 5, a peptide from Alligator sinensis, against WSSV in caridean shrimp Exopalaemon modestus.
Fish Shellfish Immunol
; 93: 82-89, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31326585
4.
Molecular characterization of allergens and component-resolved diagnosis of IgE-mediated mango fruit allergy.
Allergy
; 78(6): 1699-1703, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36724175
5.
As-Cathelicidin4 enhances the immune response and resistance against Aeromonas hydrophila in caridean shrimp.
J Fish Dis
; 45(5): 743-754, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35100453
6.
Nutritional and health effects of bovine colostrum in neonates.
Nutr Rev
; 2023 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38052234
7.
A neonatal case report of branchiooculofacial syndrome caused by a novel mutation in the TFAP2A gene and literature review.
Medicine (Baltimore)
; 102(44): e34962, 2023 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37932997
8.
Cerebellin-2 promotes endothelial-mesenchymal transition in hypoxic pulmonary hypertension rats by activating NF-κB/HIF-1α/Twist1 pathway.
Life Sci
; 328: 121879, 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37355224
9.
ZPA Regulatory Sequence Variants in Chinese Patients With Preaxial Polydactyly: Genetic and Clinical Characteristics.
Front Pediatr
; 10: 797978, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35652055
10.
Evaluating the therapeutic role of selected active compounds in Plumula Nelumbinis on pulmonary hypertension via network pharmacology and experimental analysis.
Front Pharmacol
; 13: 977921, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36059960
11.
Analysis of Anti-Infective Treatment of 9 Neonates with Raoultella ornithinolytica Sepsis.
Evid Based Complement Alternat Med
; 2022: 2424011, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36185089
12.
Magnolol alleviates hypoxia-induced pulmonary vascular remodeling through inhibition of phenotypic transformation in pulmonary arterial smooth muscle cells.
Biomed Pharmacother
; 150: 113060, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35658230
13.
The Diagnosis and Management of Allergic Reactions Caused by Chinese Materia Medica.
Clin Rev Allergy Immunol
; 62(1): 103-122, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33606192
14.
Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding.
Front Pediatr
; 9: 679279, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34222148
15.
Corrigendum: Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A.
Front Neurosci
; 15: 687435, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33994941
16.
Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A.
Front Neurosci
; 15: 604715, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33679298
17.
Magnolol Attenuates Right Ventricular Hypertrophy and Fibrosis in Hypoxia-Induced Pulmonary Arterial Hypertensive Rats Through Inhibition of the JAK2/STAT3 Signaling Pathway.
Front Pharmacol
; 12: 755077, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34764873
18.
A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly.
Front Pediatr
; 9: 774575, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34912761
19.
GLIS Family Zinc Finger 1 was First Linked With Preaxial Polydactyly I in Humans by Stepwise Genetic Analysis.
Front Cell Dev Biol
; 9: 781388, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35087831
20.
Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis.
Front Pediatr
; 9: 687455, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34408996