Detalhe da pesquisa
1.
Placental DNA methylation of peroxisome-proliferator-activated receptor-γ co-activator-1α promoter is associated with maternal gestational glucose level.
Clin Sci (Lond)
; 129(4): 385-94, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25875376
2.
IUGR with infantile overnutrition programs an insulin-resistant phenotype through DNA methylation of peroxisome proliferator-activated receptor-γ coactivator-1α in rats.
Pediatr Res
; 77(5): 625-32, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25675425
3.
Challenges of PICC placement via the popliteal vein under ultrasound guidance in a patient with severe burns: A case report.
J Vasc Access
; : 11297298241245066, 2024 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38581270
4.
Predominance of A2063G mutant strains in the Mycoplasma pneumoniae epidemic in children: A clinical and epidemiological study in 2023 in Wuhan, China.
Int J Infect Dis
; 145: 107074, 2024 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38734057
5.
Effects of SOCS 1/3 gene silencing on the expression of C/EBPα and PPARγ during differentiation and maturation of rat preadipocytes.
Pediatr Res
; 73(3): 263-7, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23222907
6.
Structural characterization and anti-lipotoxicity effects of a pectin from okra (Abelmoschus esculentus (L.) Moench).
Int J Biol Macromol
; 238: 124111, 2023 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36948330
7.
Downregulating SOCS3 with siRNA ameliorates insulin signaling and glucose metabolism in hepatocytes of IUGR rats with catch-up growth.
Pediatr Res
; 72(6): 550-9, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23007031
8.
Isosilybin regulates lipogenesis and fatty acid oxidation via the AMPK/SREBP-1c/PPARα pathway.
Chem Biol Interact
; 368: 110250, 2022 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36347319
9.
The influence of down-regulation of suppressor of cellular signaling proteins by RNAi on glucose transport of intrauterine growth retardation rats.
Pediatr Res
; 69(6): 497-503, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21364493
10.
[Effect of recombinant adenovirus Ad-mir-22 on glucose uptake in HepG2 cells].
Sheng Wu Gong Cheng Xue Bao
; 36(4): 763-771, 2020 Apr 25.
Artigo
em Zh
| MEDLINE | ID: mdl-32347070
11.
Association of Low Birth Weight and Premature Birth With the Risk of Metabolic Syndrome: A Meta-Analysis.
Front Pediatr
; 8: 405, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32850529
12.
Effects of EPHX1 rs2260863 polymorphisms on warfarin maintenance dose in very elderly, frail Han-Chinese population.
Pharmacogenomics
; 21(12): 863-870, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32559398
13.
Diagnosis of intellectual disability/global developmental delay via genetic analysis in a central region of China.
Chin Med J (Engl)
; 132(13): 1533-1540, 2019 Jul 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31205075
14.
Low IGF-I Bioavailability Impairs Growth and Glucose Metabolism in a Mouse Model of Human PAPPA2 p.Ala1033Val Mutation.
Endocrinology
; 160(6): 1363-1376, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30977789
15.
PAPPA2 as a Therapeutic Modulator of IGF-I Bioavailability: in Vivo and in Vitro Evidence.
J Endocr Soc
; 2(7): 646-656, 2018 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29942928
16.
Two Siblings with a Mutation in CCDC8 Presenting with Mild Short Stature: A Case of 3-M Syndrome.
Horm Res Paediatr
; 88(5): 364-370, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28675896
17.
Protective effects of activated protein C on neurovascular unit in a rat model of intrauterine infection-induced neonatal white matter injury.
J Huazhong Univ Sci Technolog Med Sci
; 35(6): 904-909, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26670444
18.
Neuroprotective effects of activated protein C on intrauterine inflammation-induced neonatal white matter injury are associated with the downregulation of fibrinogen-like protein 2/fibroleukin prothrombinase and the inhibition of pro-inflammatory cytokine expression.
Int J Mol Med
; 35(5): 1199-212, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25777531
19.
[Analysis of a case with typical Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes and review of literature].
Zhonghua Er Ke Za Zhi
; 52(2): 112-6, 2014 Feb.
Artigo
em Zh
| MEDLINE | ID: mdl-24739722
20.
A novel COMP mutation in a Chinese patient with pseudoachondroplasia.
Gene
; 522(1): 102-6, 2013 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23562786