نتایج جستجو برای: pparg

تعداد نتایج: 1029  

Journal: :nephro-urology monthly 0
lakkakula vks bhaskar department of biomedical sciences, sri ramachandra university, sow~miohmnnii-600116, india. tel: +91-4424768027, fax: +91-4424767008 ; department of biomedical sciences, sri ramachandra university, sow~miohmnnii-600116, india. tel: +91-4424768027, fax: +91-4424767008 sultana mahin department of biomedical sciences, sri ramachandra university, sow~miohmnnii-600116, india. tel: +91-4424768027, fax: +91-4424767008 raju thankabai ginila department of biomedical sciences, sri ramachandra university, sow~miohmnnii-600116, india. tel: +91-4424768027, fax: +91-4424767008 periyasamy soundararajan department of nephrology, sri ramachandra medical college and hospital, sri ramachandra university, chennai, india

conclusions in conclusion, the ace and pparg genes do not have a key role in conferring risk for diabetic nephropathy. results ace id genotypes followed hardy-weinberg equilibrium in both cases and controls. but p12a genotypes deviated from hardy-weinberg equilibrium in diabetic controls. chi2 test was applied for the analysis of genotypic distributions in genotypic and dominant models. odds ra...

2015
Shin-Jen Lin Dong-Rong Yang Nancy Wang Ming Jiang Hiroshi Miyamoto Gonghui Li Chawnshang Chang

A recent report indicated that the TR4 nuclear receptor might suppress the prostate cancer (PCa) initiation via modulating the DNA damage/repair system. Knocking-out peroxisome proliferator-activated receptor gamma (PPARG), a nuclear receptor that shares similar ligands/activators with TR4, promoted PCa initiation. Here we found 9% of PCa patients have one allele of PPARG deletion. Results from...

2012
Sebastian Pott Nima K. Kamrani Guillaume Bourque Sven Pettersson Edison T. Liu

BACKGROUND Genome-wide comparisons of transcription factor binding sites in different species can be used to evaluate evolutionary constraints that shape gene regulatory circuits and to understand how the interaction between transcription factors shapes their binding landscapes over evolution. RESULTS We have compared the PPARG binding landscapes in macrophages to investigate the evolutionary...

2016
XIAO CONG ZENG LANG LI HONG WEN QI BI

The aim of the present study was to investigate the effects of microRNA (miR)-128 inhibition on the targeted activation of peroxisome proliferator-activated receptor gamma (PPARG) and on cardiomyocyte apoptosis induced by myocardial ischemia/reperfusion (I/R) injury. In vitro, the expression of PPARG was detected by reverse transcription-quantitative polymerase chain reaction and western blotti...

2016
Kai Wu Yang Yang Donglei Liu Yu Qi Chunyang Zhang Jia Zhao Song Zhao

Although substantial studies on peroxisome proliferator-activated receptor g (PPARg) have focused on the mechanisms by which PPARg regulates glucose and lipid metabolism, recent reports have suggested that PPARg shows tumorigenic or antitumorigenic effects. The roles and mechanisms of PPARg activation in esophageal cancer remain unclarified. EC109 and TE10 esophageal cancer cells were treated w...

2014
M. Aprile M. R. Ambrosio V. D'Esposito F. Beguinot P. Formisano V. Costa A. Ciccodicola

The nuclear receptor PPAR γ is a key regulator of adipogenesis, and alterations of its function are associated with different pathological processes related to metabolic syndrome. We recently identified two PPARG transcripts encoding dominant negative PPAR γ isoforms. The existence of different PPARG variants suggests that alternative splicing is crucial to modulate PPAR γ function, underlying ...

2010
Avani A. Pendse Lance A. Johnson Yau-Sheng Tsai Nobuyo Maeda

OBJECTIVE The dominant-negative P467L mutation in peroxisome proliferator activated receptor-γ (PPARγ) was identified in insulin-resistant patients with hyperglycemia and lipodystrophy. In contrast, mice carrying the corresponding Pparg-P465L mutation have normal insulin sensitivity, with mild hyperinsulinemia. We hypothesized that murine Pparg-P465L mutation leads to covert insulin resistance,...

1999
Amr K. El-Jack Jonathan K. Hamm Paul F. Pilch Stephen R. Farmer

Adipocyte differentiation is regulated by at least two major transcription factors, CCAAT/enhancer-binding protein a (C/EBPa) and peroxisome proliferator-activated receptor g (PPARg). Expression of PPARg in fibroblasts converts them to fat-laden cells with an adipocyte-like morphology. Here, we investigate the ability of PPARg to confer insulin-sensitive glucose transport to a variety of murine...

2010
Massimo Pancione Lina Sabatino Alessandra Fucci Vincenzo Carafa Angela Nebbioso Nicola Forte Antonio Febbraro Domenico Parente Concetta Ambrosino Nicola Normanno Lucia Altucci Vittorio Colantuoni

The relationship between peroxisome proliferator-activated receptor γ (PPARG) expression and epigenetic changes occurring in colorectal-cancer pathogenesis is largely unknown. We investigated whether PPARG is epigenetically regulated in colorectal cancer (CRC) progression. PPARG expression was assessed in CRC tissues and paired normal mucosa by western blot and immunohistochemistry and related ...

2015
Marzena Wójcik Katarzyna Mac-Marcjanek Iwona Nadel Lucyna Woźniak Katarzyna Cypryk

INTRODUCTION Peroxisome proliferator-activated receptor γ (PPARγ) is a ligand-activated transcription factor of the nuclear receptor superfamily that is involved in lipid and carbohydrate metabolism as well as inflammation; thereby it participates in metabolic diseases including diabetes. Although PPARγ expression has been observed in different tissues of diabetic patients, its level in leukocy...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید