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Page 1
The study of copy number variations in the regions of PRKAB2 and PPM1K among congenital heart defects patients.
Dong HQ, Du YX. Dong HQ, et al. Rev Assoc Med Bras (1992). 2019 Jul 22;65(6):786-790. doi: 10.1590/1806-9282.65.6.786. Rev Assoc Med Bras (1992). 2019. PMID: 31340305 Free article.
METHODS: A total of 200 congenital heart disease patients (100 tetralogy of Fallot patients and 100 ventricular septal defect patients) and 100 congenital heart defect-free controls were recruited, and quantitative real-time PCR analysis was used to replicate the as …
METHODS: A total of 200 congenital heart disease patients (100 tetralogy of Fallot patients and 100 ventricular septal defect patient …
AMP-activated protein kinase regulation and biological actions in the heart.
Zaha VG, Young LH. Zaha VG, et al. Circ Res. 2012 Aug 31;111(6):800-14. doi: 10.1161/CIRCRESAHA.111.255505. Circ Res. 2012. PMID: 22935535 Free PMC article. Review.
Activation of the intrinsic AMPK pathway plays an important role in the myocardial response to ischemia, pressure overload, and heart failure. Pharmacological activation of AMPK shows promise as a therapeutic strategy in the treatment of heart disease. The purpose o …
Activation of the intrinsic AMPK pathway plays an important role in the myocardial response to ischemia, pressure overload, and heart …
AMPKβ1 and AMPKβ2 define an isoform-specific gene signature in human pluripotent stem cells, differentially mediating cardiac lineage specification.
Ziegler N, Bader E, Epanchintsev A, Margerie D, Kannt A, Schmoll D. Ziegler N, et al. J Biol Chem. 2020 Dec 18;295(51):17659-17671. doi: 10.1074/jbc.RA120.013990. J Biol Chem. 2020. PMID: 33454005 Free PMC article.
Although the lack of PRKAB1 impacted differentiation into cardiomyocytes only at late stages of cardiac maturation, the availability of PRKAB2 was indispensable for mesoderm specification as shown by gene expression analysis and histochemical staining for cardiac lineage m …
Although the lack of PRKAB1 impacted differentiation into cardiomyocytes only at late stages of cardiac maturation, the availability of P …
Nutrient sensing pathway genes expression dysregulated in patients with T2DM and coronary artery disease.
Rahimi E, Ahmadi A, Boroumand MA, Mohammad Soltani B, Behmanesh M. Rahimi E, et al. Diabetes Res Clin Pract. 2019 May;151:39-45. doi: 10.1016/j.diabres.2019.03.036. Epub 2019 Mar 30. Diabetes Res Clin Pract. 2019. PMID: 30935928
The aim of this study was to investigate the expression levels of nutrient sensing genes including SIRT1, PRKAB1, PRKAB2 and mTOR in CAD(+) versus CAD(-)T2DM patients. METHODS: Sixty-five people with T2DM who referred to Tehran heart center were participated in this …
The aim of this study was to investigate the expression levels of nutrient sensing genes including SIRT1, PRKAB1, PRKAB2 and mTOR in …
Human gene copy number spectra analysis in congenital heart malformations.
Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME. Tomita-Mitchell A, et al. Physiol Genomics. 2012 May 1;44(9):518-41. doi: 10.1152/physiolgenomics.00013.2012. Epub 2012 Feb 7. Physiol Genomics. 2012. PMID: 22318994 Free PMC article.
The clinical significance of copy number variants (CNVs) in congenital heart disease (CHD) continues to be a challenge. Although CNVs including genes can confer disease risk, relationships between gene dosage and phenotype are still being defined. ...Furthermore, CNV gene …
The clinical significance of copy number variants (CNVs) in congenital heart disease (CHD) continues to be a challenge. Although CNVs …
The outcome of renal ischemia-reperfusion injury is unchanged in AMPK-β1 deficient mice.
Mount PF, Gleich K, Tam S, Fraser SA, Choy SW, Dwyer KM, Lu B, Denderen BV, Fingerle-Rowson G, Bucala R, Kemp BE, Power DA. Mount PF, et al. PLoS One. 2012;7(1):e29887. doi: 10.1371/journal.pone.0029887. Epub 2012 Jan 9. PLoS One. 2012. PMID: 22253816 Free PMC article.
AIM: Activation of the master energy-regulator AMP-activated protein kinase (AMPK) in the heart reduces the severity of ischemia-reperfusion injury (IRI) but the role of AMPK in renal IRI is not known. ...In the kidney, however, no difference in AMPK activation by acute is …
AIM: Activation of the master energy-regulator AMP-activated protein kinase (AMPK) in the heart reduces the severity of ischemia-repe …
The regulation of AMPK beta1, TSC2, and PTEN expression by p53: stress, cell and tissue specificity, and the role of these gene products in modulating the IGF-1-AKT-mTOR pathways.
Feng Z, Hu W, de Stanchina E, Teresky AK, Jin S, Lowe S, Levine AJ. Feng Z, et al. Cancer Res. 2007 Apr 1;67(7):3043-53. doi: 10.1158/0008-5472.CAN-06-4149. Cancer Res. 2007. PMID: 17409411
These gene products are shown to be expressed under p53 control in a cell type and tissue-specific fashion with the TSC2 and PTEN proteins being coordinately regulated in those tissues that use insulin-dependent energy metabolism (skeletal muscle, heart, white fat, liver, …
These gene products are shown to be expressed under p53 control in a cell type and tissue-specific fashion with the TSC2 and PTEN proteins b …
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.
Chen CP, Chang SY, Chen YN, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2018 Oct;57(5):739-744. doi: 10.1016/j.tjog.2018.08.024. Taiwan J Obstet Gynecol. 2018. PMID: 30342663 Free article.
CASE REPORT: A 30-year-old, gravida 2, para 1, woman underwent amniocentesis at 22 weeks of gestation because of fetal polydactyly of left foot and echogenic heart foci on prenatal ultrasound. She and her husband and the 2-year-old son were healthy, and there was no family …
CASE REPORT: A 30-year-old, gravida 2, para 1, woman underwent amniocentesis at 22 weeks of gestation because of fetal polydactyly of left f …
11 results