Detalhe da pesquisa
1.
DKK1 activates the PI3K/AKT pathway via CKAP4 to balance the inhibitory effect on Wnt/ß-catenin signaling and regulates Wnt3a-induced MSC migration.
Stem Cells
; 2024 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38469899
2.
Likelihood of primary cesarean section following induction of labor in singleton cephalic pregnancies at term, compared with expectant management: An Australian population-based, historical cohort study.
Acta Obstet Gynecol Scand
; 103(5): 946-954, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38291953
3.
Operationalizing the Consolidated Framework for Implementation Research to build and support the lived experience workforce in direct health service provision.
Health Expect
; 27(2): e14035, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38567878
4.
Long-Term Effect of Having a Child at Risk of Developmental Delays on Parental Labor Force Participation.
Matern Child Health J
; 2024 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38334864
5.
Alleviatory Role of Panax Notoginseng Saponins in Modulating Inflammation and Pulmonary Vascular Remodeling in Chronic Obstructive Pulmonary Disease: mechanisms and Implications.
COPD
; 21(1): 2329282, 2024 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38622983
6.
Acetylation of FOXO1 activates Bim expression involved in CVB3 induced cardiomyocyte apoptosis.
Apoptosis
; 2023 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38127284
7.
Continuously Flow Photothermal Catalysis Efficiently CO2 Reduction Over S-Scheme 2D/0D Bi5 O7 I-OVs/Cd0.5 Zn0.5 S Heterojunction with Strong Interfacial Electric Field.
Small
; 19(12): e2206225, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36587970
8.
Ethylene response factor MdERF4 and histone deacetylase MdHDA19 suppress apple fruit ripening through histone deacetylation of ripening-related genes.
Plant Physiol
; 188(4): 2166-2181, 2022 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35088866
9.
Tuftelin1 drives experimental pulmonary fibrosis progression by facilitating stress fiber assembly.
Respir Res
; 24(1): 318, 2023 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38105232
10.
Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency.
Thromb J
; 21(1): 3, 2023 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36624481
11.
Brain-targeted nanoreactors prevent the development of organophosphate-induced delayed neurological damage.
J Nanobiotechnology
; 21(1): 256, 2023 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37550745
12.
Han family with essential tremor caused by the P421L variant of the TENM4 gene in China.
Neurol Sci
; 44(6): 2003-2015, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36689009
13.
Unlocking big data to understand health services usage and government funding during pregnancy and early childhood, evidence in Australia.
Birth
; 50(4): 890-915, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37434333
14.
Pan-Cancer Analysis of the Cuproptosis-Related Gene DLD.
Mediators Inflamm
; 2023: 5533444, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38077227
15.
Constitutions in Traditional Chinese Medicine and Factors Influencing Them in Jilin Province of China.
Altern Ther Health Med
; 2023 Aug 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37573585
16.
A Case of Maternal Uniparental Disomy of Chromosome 6 with Intrauterine Growth Restriction.
Altern Ther Health Med
; 29(7): 188-199, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37471662
17.
Long-Term Outcomes After Stenting in Extracranial vs. Intracranial Stenosis.
Altern Ther Health Med
; 29(8): 255-261, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37573598
18.
Intravascular Intervention Combined with Standard Drug Therapy in Patients with Severe Intracranial Atherosclerotic Stenosis and Plaque Enhancement.
Altern Ther Health Med
; 29(6): 143-149, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37295005
19.
VOC emission caps constrained by air quality targets based on response surface model: A case study in the Pearl River Delta Region, China.
J Environ Sci (China)
; 123: 430-445, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36522004
20.
A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.
J Gene Med
; 24(2): e3398, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34786791