Detalhe da pesquisa
1.
Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy.
J Med Genet;
59(2): 147-154, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33323469
2.
STARD3NL inhibits the osteogenic differentiation by inactivating the Wnt/ß-catenin pathway via binding to Annexin A2 in osteoporosis.
J Cell Mol Med;
26(5): 1643-1655, 2022 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35098646
3.
Downregulation of MEG3 and upregulation of EZH2 cooperatively promote neuroblastoma progression.
J Cell Mol Med;
26(8): 2377-2391, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35257481
4.
PARD3 gene variation as candidate cause of nonsyndromic cleft palate only.
J Cell Mol Med;
26(15): 4292-4304, 2022 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35789100
5.
A novel adiponectin receptor agonist (AdipoAI) ameliorates type 2 diabetes-associated periodontitis by enhancing autophagy in osteoclasts.
J Periodontal Res;
57(2): 381-391, 2022 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34984683
6.
Advances in the Genetics of Congenital Ptosis.
Ophthalmic Res;
65(2): 131-139, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34969027
7.
ARID1B/SUB1-activated lncRNA HOXA-AS2 drives the malignant behaviour of hepatoblastoma through regulation of HOXA3.
J Cell Mol Med;
25(7): 3524-3536, 2021 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33683826
8.
Morphine promotes tumorigenesis and cetuximab resistance via EGFR signaling activation in human colorectal cancer.
J Cell Physiol;
236(6): 4445-4454, 2021 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33184860
9.
Recent advances in the epigenetics of bone metabolism.
J Bone Miner Metab;
39(6): 914-924, 2021 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34250565
10.
Diagnostic and clinical utility of genetic testing in children with kidney failure.
Pediatr Nephrol;
36(11): 3653-3662, 2021 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34031707
11.
The roles of SMYD4 in epigenetic regulation of cardiac development in zebrafish.
PLoS Genet;
14(8): e1007578, 2018 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30110327
12.
Hypermethylation-mediated down-regulation of lncRNA TBX5-AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression.
J Cell Mol Med;
24(11): 6472-6484, 2020 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32368852
13.
[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (1) - Procedures prior to genetic testing].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
37(3): 334-338, 2020 Mar 10.
Artigo
em Zh
| MEDLINE
| ID: mdl-32128754
14.
[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (4) - Report interpretation and genetic counseling].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
37(3): 352-357, 2020 Mar 10.
Artigo
em Zh
| MEDLINE
| ID: mdl-32128757
15.
Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.
J Cell Mol Med;
23(6): 4454-4463, 2019 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31016877
16.
Deregulated lncRNA expression profile in the mouse lung adenocarcinomas with KRAS-G12D mutation and P53 knockout.
J Cell Mol Med;
23(10): 6978-6988, 2019 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31410985
17.
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.
Hum Mol Genet;
26(2): 383-394, 2017 01 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28013291
18.
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss.
Clin Genet;
96(4): 300-308, 2019 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31231791
19.
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
Clin Genet;
96(5): 402-410, 2019 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31328266
20.
A brief measure of predeath grief in dementia caregivers: the Caregiver Grief Questionnaire.
Int Psychogeriatr;
31(8): 1099-1107, 2019 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31030690