Search details
1.
Aggf1 Specifies Hemangioblasts at the Top of Regulatory Hierarchy via Npas4l and mTOR-S6K-Emp2-ERK Signaling.
Arterioscler Thromb Vasc Biol
; 43(12): 2348-2368, 2023 12.
Article
in English
| MEDLINE | ID: mdl-37881938
2.
Angiogenic factor AGGF1 blocks neointimal formation after vascular injury via interaction with integrin α7 on vascular smooth muscle cells.
J Biol Chem
; 298(4): 101759, 2022 04.
Article
in English
| MEDLINE | ID: mdl-35202649
3.
Identification and characterization of a special type of subnuclear structure: AGGF1-coated paraspeckles.
FASEB J
; 36(6): e22366, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35608889
4.
Hyperlipidemia patients carrying LDLR splicing mutation c.1187-2A>G respond favorably to rosuvastatin and PCSK9 inhibitor evolocumab.
Mol Genet Genomics
; 297(3): 833-841, 2022 May.
Article
in English
| MEDLINE | ID: mdl-35441343
5.
Genetic association analysis between IL9 and coronary artery disease in a Chinese Han population.
Cytokine
; 150: 155761, 2022 02.
Article
in English
| MEDLINE | ID: mdl-34814015
6.
Role of epigenetic m6 A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signaling.
FASEB J
; 35(5): e21465, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33788967
7.
BCAS2 is essential for hematopoietic stem and progenitor cell maintenance during zebrafish embryogenesis.
Blood
; 133(8): 805-815, 2019 02 21.
Article
in English
| MEDLINE | ID: mdl-30482793
8.
Human intracellular ISG15 prevents interferon-α/ß over-amplification and auto-inflammation.
Nature
; 517(7532): 89-93, 2015 Jan 01.
Article
in English
| MEDLINE | ID: mdl-25307056
9.
Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain.
Hum Genet
; 139(4): 545-555, 2020 Apr.
Article
in English
| MEDLINE | ID: mdl-32020363
10.
Losartan protects against myocardial ischemia and reperfusion injury via vascular integrity preservation.
FASEB J
; 33(7): 8555-8564, 2019 07.
Article
in English
| MEDLINE | ID: mdl-30991833
11.
Mutation in NPPA causes atrial fibrillation by activating inflammation and cardiac fibrosis in a knock-in rat model.
FASEB J
; 33(8): 8878-8891, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31034774
12.
Identification of a p.Trp403* nonsense variant in PHEX causing X-linked hypophosphatemia by inhibiting p38 MAPK signaling.
Hum Mutat
; 40(7): 879-885, 2019 07.
Article
in English
| MEDLINE | ID: mdl-30920082
13.
Significant association of rare variant p.Gly8Ser in cardiac sodium channel ß4-subunit SCN4B with atrial fibrillation.
Ann Hum Genet
; 83(4): 239-248, 2019 07.
Article
in English
| MEDLINE | ID: mdl-30821358
14.
Identification of rare variants in cardiac sodium channel ß4-subunit gene SCN4B associated with ventricular tachycardia.
Mol Genet Genomics
; 294(4): 1059-1071, 2019 Aug.
Article
in English
| MEDLINE | ID: mdl-31020414
15.
Genome-Wide Analysis of DNA Methylation and Acute Coronary Syndrome.
Circ Res
; 120(11): 1754-1767, 2017 May 26.
Article
in English
| MEDLINE | ID: mdl-28348007
16.
SUMOylation of Vps34 by SUMO1 promotes phenotypic switching of vascular smooth muscle cells by activating autophagy in pulmonary arterial hypertension.
Pulm Pharmacol Ther
; 55: 38-49, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30703554
17.
Analysis of causal effect of APOA5 variants on premature coronary artery disease.
Ann Hum Genet
; 82(6): 437-447, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30024021
18.
Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1.
Mol Genet Genomics
; 293(3): 699-710, 2018 Jun.
Article
in English
| MEDLINE | ID: mdl-29322253
19.
Significant genetic association of a functional TFPI variant with circulating fibrinogen levels and coronary artery disease.
Mol Genet Genomics
; 293(1): 119-128, 2018 Feb.
Article
in English
| MEDLINE | ID: mdl-28894953
20.
Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation.
PLoS Genet
; 11(8): e1005393, 2015 Aug.
Article
in English
| MEDLINE | ID: mdl-26267381