نتایج جستجو برای: lpl gene

تعداد نتایج: 1142430  

2017
Yan-yan Li Yan-hong Zhou Ge Gong Hong-yu Geng Xin-xing Yang Xiang-ming Wang Chuan-wei Zhou Jian Xu Yun Qian

BACKGROUND/AIMS Although lipoprotein lipase (LPL) gene Pvu II polymorphism has been associated with an increased risk of hypertriglyceridemia (HT), there is no clear consensus within the scientific community. METHODS A meta-analysis of 1,640 subjects from six individual studies was conducted to better elucidate the potential relationship between the LPL gene Pvu II polymorphism and HT within ...

Journal: :Indian heart journal 2013
Parthasaradhi Reddy Tanguturi Bhoomireddy Pullareddy B S Rama Krishna Dwarkanath K Murthy

INTRODUCTION Studies have reported an association between lipoprotein lipase (LPL) gene and myocardial infarction in some populations. Therefore, the present study aimed to investigate the association of the HindIII polymorphism of the (LPL) gene with myocardial infarction and to explore its potential role in susceptibility in a South Indian population. SUBJECTS AND METHODS We included a tota...

2011
Masayuki Shiseki Akihiro Masuda Norimichi Watanabe Masami Fujii Tomofumi Kimura Kentaro Yoshinaga Naoki Mori Masanao Teramura Toshiko Motoji

Waldenström's macroglobulinemia (WM)/ lymphoplasmacytic lymphoma (LPL) is an indolent mature B-cell neoplasm. In rare cases of WM/LPL, diffuse large B-cell lymphoma (DLBCL) develops as a result of histologic transformation. In this report, we present a case of DLBCL developing in a patient with WM/LPL. Combination chemotherapy for DLBCL was effective and complete remission was eventually achiev...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2009
Xunde Xian Tingting Liu Jia Yu Yuhui Wang Yifei Miao Jianjun Zhang Yan Yu Colin Ross Joanna M Karasinska Michael R Hayden George Liu Dehua Chui

Lipoprotein lipase (LPL) is predominantly expressed in adipose and muscle where it plays a crucial role in the metabolism of triglyceride-rich plasma lipoproteins. LPL is also expressed in the brain with highest levels found in the pyramidal cells of the hippocampus, suggesting a possible role for LPL in the regulation of cognitive function. However, very little is currently known about the spe...

Journal: :Journal of lipid research 2007
Yaomin Hu Yan Ren Robert Z Luo Xiang Mao Xiujun Li Xu Cao Lu Guan Xiang Chen Jianwei Li Yang Long Xiangxun Zhang Haoming Tian

Increased plasma triglyceride and free fatty acid levels are frequently associated with type 2 diabetes mellitus (T2DM). To test the hypothesis that LPL gene mutations contribute to the hypertriglyceridemia observed in members of T2DM pedigrees, we screened the LPL gene in 53 hypertriglyceridemic members of 26 families. Four known and three novel mutations were identified. All three novel mutat...

Journal: :Diabetes 2004
Mark O Goodarzi Xiuqing Guo Kent D Taylor Manuel J Quiñones Mohammad F Saad Huiying Yang Willa A Hsueh Jerome I Rotter

The insulin resistance syndrome is increasingly recognized as a risk factor for cardiovascular disease. Lipoprotein lipase (LPL) is a candidate gene for components of the syndrome. A small number of studies have demonstrated association of single nucleotide polymorphisms within LPL and indirect or surrogate measures of insulin resistance, largely based on glucose and insulin values obtained in ...

2012
Shinji Takasu Michihiro Mutoh Mami Takahashi Hitoshi Nakagama

Epidemiological studies have shown that serum triglyceride (TG) levels are linked with risk of development of cancer, including colorectal and pancreatic cancers, and their precancerous lesions. Thus, it is assumed that serum TG plays an important role in carcinogenesis, and the key enzyme lipoprotein lipase (LPL), which catalyzes the hydrolysis of plasma TG, may therefore be involved. Dysregul...

Journal: :The Journal of clinical investigation 1991
T Gotoda N Yamada M Kawamura K Kozaki N Mori S Ishibashi H Shimano F Takaku Y Yazaki Y Furuichi

The DNA sequences were determined for the lipoprotein lipase (LPL) gene from five unrelated Japanese patients with familial LPL deficiency. The results demonstrated that all five patients are homozygotes for distinct point mutations dispersed throughout the LPL gene. Patient 1 has a G-to-A transition at the first nucleotide of intron 2, which abolishes normal splicing. Patient 2 has a nonsense ...

Journal: :Clinical science 2000
Y Ikeda K Goji A Takagi

We systematically investigated the molecular defects resulting in primary lipoprotein lipase (LPL) deficiency in a Japanese male infant (hereafter called 'the patient') with severe fasting hypertriglyceridaemia (type I hyperlipoproteinaemia). The primary LPL deficiency was diagnosed on the basis of the findings that no LPL activity was detected in post-heparin plasma (PHP) and that the immunore...

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