Detalhe da pesquisa
1.
Everolimus Rescues the Phenotype of Elastin Insufficiency in Patient Induced Pluripotent Stem Cell-Derived Vascular Smooth Muscle Cells.
Arterioscler Thromb Vasc Biol
; 40(5): 1325-1339, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32212852
2.
Targeted next generation sequencing reveals genetic defects underlying inherited retinal disease in Iranian families.
Mol Vis
; 25: 106-117, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30820146
3.
Loss of PPARγ in endothelial cells leads to impaired angiogenesis.
J Cell Sci
; 129(4): 693-705, 2016 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26743080
4.
Transcription factor GATA4 associates with mesenchymal-like gene expression in human hepatoblastoma cells.
Tumour Biol
; 40(7): 1010428318785498, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30074440
5.
Germline copy number variation analysis in Finnish families with hereditary prostate cancer.
Prostate
; 76(3): 316-24, 2016 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26552734
6.
Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.
Eur Heart J
; 36(34): 2327-37, 2015 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26084686
7.
Late dumping syndrome preceded by Coxsackievirus B4 infection and cholecystectomy.
J Surg Case Rep
; 2023(4): rjad205, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37124576
8.
Age and Sex Differences in the Genetics of Cardiomyopathy.
J Cardiovasc Transl Res
; 16(6): 1287-1302, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37477868
9.
Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy.
NPJ Genom Med
; 7(1): 18, 2022 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35288587
10.
Evolving Up-regulation of Biliary Fibrosis-Related Extracellular Matrix Molecules After Successful Portoenterostomy.
Hepatol Commun
; 5(6): 1036-1050, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34141988
11.
Quality of whole genome sequencing from blood versus saliva derived DNA in cardiac patients.
BMC Med Genomics
; 13(1): 11, 2020 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31996208
12.
Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy.
Sci Rep
; 10(1): 17264, 2020 Oct 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33037269
13.
Machine Learning Identifies Clinical and Genetic Factors Associated With Anthracycline Cardiotoxicity in Pediatric Cancer Survivors.
JACC CardioOncol
; 2(5): 690-706, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34396283
14.
Return of genetic and genomic research findings: experience of a pediatric biorepository.
BMC Med Genomics
; 12(1): 173, 2019 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31775751
15.
Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy.
Sci Rep
; 9(1): 4093, 2019 03 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30858397
16.
GATA4 Regulates Blood-Testis Barrier Function and Lactate Metabolism in Mouse Sertoli Cells.
Endocrinology
; 157(6): 2416-31, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26974005
17.
Prevalence of Titin Truncating Variants in General Population.
PLoS One
; 10(12): e0145284, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26701604
18.
GATA4 is a key regulator of steroidogenesis and glycolysis in mouse Leydig cells.
Endocrinology
; 156(5): 1860-72, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25668067
19.
copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.
PLoS One
; 8(8): e71802, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23967248