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Browse Low density lipoproteins topic

Genetic aspects subtopic

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1-50 out of 50 article(s)
Title Author Type Date Words
Effect of Statin Therapy in Tpe-Interval and Tpe/Qtc Ratio in Patients with Familial Hypercholesterolemia. Kucukosmanoglu, Mehmet; Kilic, Salih; Saracoglu, Erhan; Cekici, Yusuf; Vuruskan, Ertan; Kayikcioglu, Sep 1, 2020 4742
Study the Association of Tumor Necrosis Factor Promoter Polymorphism with Type 2 Diabetic Nephropathy. Emara, Mahmoud; Edel, Rawhia El; Fathy, Waleed M.; Aboelkhair, Noran T.; Watany, Mona M.; Abou-Elela Jul 31, 2020 5499
The CC Genotype of Insulin-Induced Gene 2 rs7566605 Is a Protective Factor of Hypercholesteremia Susceptible to Mild Cognitive Impairment, Especially to the Executive Function of Patients with Type 2 Diabetes Mellitus. Zhang, Haoqiang; Huang, Rong; Tian, Sai; An, Ke; Zhu, Wenwen; Shi, Jijing; Cao, Wuyou; Wang, Shaohua Jun 30, 2020 5692
Cutaneous Xanthoma--A Clue to Familial Hypercholesterolemia. Philip, Shilpa Accamma; Sri, Swarna; Jeshtadi, Anunayi Jun 22, 2020 1473
The Association between Adiponectin Single Nucleotide Polymorphisms and Side Effects of Isotretinoin in Acne Patients. Garba, Munir; Khabour, Omar F.; Alzoubi, Karem H.; Abu-Siniyeh, Ahmed; Al-Qarqaz, Firas May 31, 2020 5464
A Study of the Relationship between the Polymorphism and Mutation of rs682429 and rs3781590 in the LRP5 Gene and Bone Metabolism in Postmenopausal Type 2 Diabetic Women in Xinjiang. Li, Jun; Li, SiYuan; Zhao, HuiRong; Li, JiaJia; Wang, Shuang; Shi, YanQiu May 31, 2020 3092
Apolipoprotein E Gene Polymorphism, Glycated Hemoglobin, and Peripheral Arterial Disease Risk in Chinese Type 2 Diabetic Patients. Hu, Yujing; Ling, Tinghuan; Yu, Min; Bai, Yang; Feng, Tongbao; Zhang, Ping; Wang, Yan Mar 31, 2020 5079
The APOB rs693 polymorphism impacts the lipid profile of Brazilian older adults. Alves, E.S.; Henriques, A.D.; Tonet-Furioso, A.C.; Paula, R.S.; Gomes, L.O.; Moraes, C.F.; Nobrega, Mar 1, 2020 5343
Lipoprotein(a) Should Be Measured in All Individuals Suspected of Having Familial Hypercholesterolemia. Langsted, Anne; Nordestgaard, Borge G. Oct 1, 2019 2240
Analysis of the oxidized low density lipoprotein receptor 1 gene as a potential marker for carcass quality traits in Qinchuan cattle. Gui, Lin-sheng; Raza, Sayed Haidar Abbas; Jia, jianlei Report Jan 1, 2019 3468
Characterization of Atherosclerosis Formation in a Murine Model of Type IIa Human Familial Hypercholesterolemia. Miyajima, Chiharu; Iwaki, Takayuki; Umemura, Kazuo; Ploplis, Victoria A.; Castellino, Francis J. Jan 1, 2018 8988
APOE Gene polymorphism among Jordanian Alzheimer's patients with relation to lipid profile. Shafagoj, Yanal A.; Naffa, Randa G.; Khateeb, Mohammed S. El-; Abdulla, Yazeed L.; Qaddoumi, Aseem A Jan 1, 2018 4433
A Gene's eye view of health as buying time. Nov 1, 2014 1002
Dietary blueberry and bifidobacteria attenuate nonalcoholic fatty liver disease in rats by affecting SIRT1-mediated signaling pathway. Ren, Tingting; Huang, Chao; Cheng, Mingliang Report Jan 1, 2014 7925
Investigation of serum oxidized low-density lipoprotein IgG levels in patients with angiographically defined coronary artery disease. Moohebati, Mohsen; Kabirirad, Vahid; Ghayour-Mobarhan, Majid; Esmaily, Habibollah; Tavallaie, Shima; Report Jan 1, 2014 5140
Proatherogenic oxidized low-density lipoprotein/[beta]2- glycoprotein I complexes in arterial and venous disease. Berger, Jeffrey S.; Rockman, Caron B.; Guyer, Kirk E.; Lopez, Luis R. Report Jan 1, 2014 2860
Gene linked to high cholesterol in blood found. Sep 16, 2010 378
Effect of naked neck gene on immune competence, serum biochemical and carcass traits in chickens under a tropical climate. Rajkumar, U.; Reddy, B.L.N.; Rajaravindra, K.S.; Niranjan, M.; Bhattacharya, T.K.; Chatterjee, R.N.; Report Jul 1, 2010 4598
HIV, atherosclerosis and inflammation: implications for treatment. Chan, William; Sviridov, Dmitri; Dart, Anthony M. Report Nov 1, 2009 6415
Genzyme and Isis Obtain Apolipoprotein B (apoB) Expression Antisense Modulation Patent. Jul 1, 2008 1108
Association between the UGT1A1 TA-repeat polymorphism and bilirubin concentration in patients with intermittent claudication: results from the CAVASIC study. Rantner, Barbara; Kollerits, Barbara; Anderwald-Stadler, Marietta; Klein-Weigel, Peter; Gruber, Ingr Clinical report May 1, 2008 4784
Factors associated with paraoxonase genotypes and activity in a diverse, young, healthy population: the Coronary Artery Risk Development in Young Adults (CARDIA) study. Thyagarajan, Bharat; Jacobs, David R., Jr.; Carr, J. Jeffery; Alozie, Ogechika; Steffes, Michael W.; Apr 1, 2008 6351
An unusual case of severe hypertriglyceridemia and splenomegaly. Rahalkar, Amit R.; Wang, Jian; Sirrs, Sandra; Dimmick, James; Holmes, Daniel; Urquhart, Nadine; Hege Mar 1, 2008 3263
Association of circulating lactoferrin concentration and 2 nonsynonymous LTF gene polymorphisms with dyslipidemia in men depends on glucose-tolerance status. Moreno-Navarrete, Jose Maria; Ortega, Francisco Jose; Bassols, Judit; Castro, Antoni; Ricart, Wifred Feb 1, 2008 5562
Target obesity in kids with genetic syndromes: reserve medications for those with genetic conditions such as familial hypercholesterolemia. Bates, Betsy Jan 15, 2008 699
Serum proprotein convertase subtilisin kexin type 9 is correlated directly with serum LDL cholesterol. Alborn, William E.; Cao, Guoqing; Careskey, Holly E.; Qian, Yue-Wei; Subramaniam, Danise R.; Davies, Oct 1, 2007 3531
Vitamin C deficiency and scurvy are not only a dietary problem but are codetermined by the haptoglobin polymorphism. Delanghe, Joris R.; Langlois, Michel R.; De Buyzere, Marc L.; Torck, Mathieu A. Aug 1, 2007 2263
Increased serum lipoprotein(a) concentrations and low molecular weight phenotypes of apolipoprotein(a) are associated with symptomatic peripheral arterial disease. Dieplinger, Benjamin; Lingenhel, Arno; Baumgartner, Nadja; Poelz, Werner; Dieplinger, Hans; Haltmaye Jul 1, 2007 6282
Homocysteine, 5, 10-methylenetetrahydrofolate reductase 677C>T polymorphism, nutrient intake, and incident cardiovascular disease in 24 968 initially healthy women. Zee, Robert Y.L.; Mora, Samia; Cheng, Suzanne; Erlich, Henry A.; Lindpaintner, Klaus; Rifai, Nader; Clinical report May 1, 2007 5941
Protease inhibitor-associated dyslipidemia in HIV-infected patients is strongly influenced by the APOA5-1131T [right arrow] C gene variation. Guardiola, Montse; Ferre, Raimon; Salazar, Juliana; Alonso-Villaverde, Carlos; Coll, Blai; Parra, Sa Oct 1, 2006 3598
Model system for phenotypic characterization of sequence variations in the LDL receptor gene. Ranheim, Trine; Kulseth, Mari Ann; Berge, Knut Erik; Leren, Trond Paul Aug 1, 2006 6847
Reliable low-density DNA array based on allele-specific probes for detection of 118 mutations causing familial hypercholesterolemia. Tejedor, Diego; Castillo, Sergio; Mozas, Pilar; Jimenez, Elisa; Lopez, Monica; Tejedor, M. Teresa; A Clinical report Jul 1, 2005 5875
Platelet-activating factor acetylhydrolase is not associated with carotid intima-media thickness in hypercholesterolemic Sicilian individuals. Campo, Salvatore; Sardo, Maria A.; Bitto, Alessandra; Bonaiuto, Antonio; Trimarchi, Giuseppe; Bonaiu Nov 1, 2004 4280
Lipid disorders and mutations in the APOB gene. Whitfield, Amanda J.; Barrett, P. Hugh R.; van Bockxmeer, Frank M.; Burnett, John R. Oct 1, 2004 5633
Biochemical and genetic markers of iron status and the risk of coronary artery disease: an angiography-based study. Bozzini, Claudia; Girelli, Domenico; Tinazzi, Elisa; Olivieri, Oliviero; Stranieri, Chiara; Bassi, A Clinical report Apr 1, 2002 4937
Genotyping of the apolipoprotein B R3500Q mutation using immobilized locked nucleic acid capture probes. Jacobsen, Nana; Fenger, Mogens; Bentzen, Joan; Rasmussen, Soren Lind; Jakobsen, Mogens Havsteen; Fen Apr 1, 2002 2793
Instability of lipoprotein(a) in plasma stored at -70[degrees]C: effects of concentration, apolipoprotein(a) genotype, and donor cardiovascular disease. Simo, Josep M.; Camps, Jordi; Vilella, Elisabet; Gomez, Federico; Paul, Antonio; Joven, Jorge Sep 1, 2001 4581
Compound heterozygous familial hypercholesterolemia and familial defective apolipoprotein B-100 produce exaggerated hypercholesterolemia. Tai, E. Shyong; Koay, Evelyn S.C.; Chan, Edmund; Seng, Tzer Ding; Loh, Lih Ming; Sethi, Sunil K.; Ta Mar 1, 2001 4071
Identification of two LDL-receptor mutations causing familial hypercholesterolemia in Indian subjects by a simplified rapid PCR-heteroduplex method. Ashavaid, Tester F.; Kondkar, Altaf A.; Nair, Kappiareth G. Aug 1, 2000 1702
Flow cytometric assessment of LDL ligand function for detection of heterozygous familial defective apolipoprotein B-100. Raungaard, Bent; Heath, Finn; Hansen, Peter Steen; Brorholt-Petersen, Jens Uffe; Jensen, Henrik Kjae Feb 1, 2000 6896
Long-distance PCR-based screening for large rearrangements of the LDL receptor gene in Korean patients with familial hypercholesterolemia. Kim, Sung Han; Bae, Ji Hyun; Chae, Jae Jin; Kim, Un Kyung; Choe, Seong-Joon; Namkoong, Yong; Kim, Hy Sep 1, 1999 4168
Estrogen replacement therapy, serum lipids, and polymorphism of the apolipoprotein E gene. Garry, Philip J.; Baumgartner, Richard N.; Brodie, Steven G.; Montoya, George D.; Liang, Hwa Chi; Li Aug 1, 1999 7258
Type 2 diabetes: an overview. Lebovitz, Harold E. Clinical report Aug 1, 1999 5026
Mutations in the apolipoprotein (apo) B-100 receptor-binding region: detection of apo B-100 ([Arg.sup.3500] [right arrow] Trp) associated with two new haplotypes and evidence that apo B-100 ([Glu.sup.3405] [right arrow] Gln) diminishes receptor-mediated uptake of LDL. Fisher, Eva; Scharnagl, Hubert; Hoffmann, Michael M.; Kusterer, Klaus; Wittmann, Daniela; Wieland, H Clinical report Jul 1, 1999 9254
High-speed apolipoprotein E genotyping and apolipoprotein B3500 mutation detection using real-time fluorescence PCR and melting curves. Aslanidis, Charalampos; Schmitz, Gerd Jul 1, 1999 2629
Correlations between cholesterol, vitamin E, and vitamin [K.sub.1] in serum: paradoxical relationships to established epidemiological risk factors for cardiovascular disease. Cham, Bill E.; Smith, Jeffery L.; Colquhoun, David M. Aug 1, 1998 1929
Flow cytometry with a monoclonal antibody to the low density lipoprotein receptor compared with gene mutation detection in diagnosis of heterozygous familial hypercholesterolemia. Raungaard, Bent; Heath, Finn; Brorholt-Petersen, Jens Uffe; Jensen, Henrik Kjaerulf; Faergeman, Ole May 1, 1998 4261
Oligonucleotide ligation assay for detection of apolipoprotein E polymorphisms. Baron, Heike; Fung, Steven; Aydin, Atakan; Bahring, Sylvia; Jeschke, Eva; Luft, Friedrich C.; Schust Oct 1, 1997 2288
Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: two cases of [arginine.sub.3500] [right arrow] tryptophan mutation associated with a unique haplotype. Choong, Meng-Ling; Koay, Evelyn S.C.; Khoo, Kah-lin; Khaw, Min-Cheh; Sethi, Sunil K. Jun 1, 1997 6232
Single-strand conformation polymorphism analysis with high throughput modifications, and its use in mutation detection in familial hypercholesterolemia. Humphries, Steve E.; Gudnason, Vilmundur; Whittall, Ros; Day, Ian N.M. Mar 1, 1997 6854

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