HuGE Literature Finder
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Records 1-22
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Clinical and biochemical features of different molecular etiologies of familial chylomicronemia.
Journal of clinical lipidology 2018 Apr . Hegele Robert A, Berberich Amanda J, Ban Matthew R, Wang Jian, Digenio Andres, Alexander Veronica J, D'Erasmo Laura, Arca Marcello, Jones Alan, Bruckert Eric, Stroes Erik S, Bergeron Jean, Civeira Fernando, Witztum Joseph L, Gaudet Dani |
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Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): A reappraisal by using a resequencing approach.
Atherosclerosis 2015 Oct 242 (2): 618-24. Minicocci Ilenia, Prisco Cristina, Montali Anna, Di Costanzo Alessia, Ceci Fabrizio, Pigna Giovanni, Arca Marcel |
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Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia.
Atherosclerosis 2015 Jul 241 (1): 79-86. Rabacchi Claudio, Pisciotta Livia, Cefalù Angelo B, Noto Davide, Fresa Raffaele, Tarugi Patrizia, Averna Maurizio, Bertolini Stefano, Calandra Sebastia |
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Angptl3 deficiency is associated with increased insulin sensitivity, lipoprotein lipase activity, and decreased serum free fatty acids.
Arteriosclerosis, thrombosis, and vascular biology 2013 Jul 33 (7): 1706-13. Robciuc Marius R, Maranghi Marianna, Lahikainen Anna, Rader Daniel, Bensadoun Andre, Öörni Katariina, Oörni Katariina, Metso Jari, Minicocci Ilenia, Ciociola Ester, Ceci Fabrizio, Montali Anna, Arca Marcello, Ehnholm Christian, Jauhiainen Mat |
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
Journal of medical genetics 2013 May 50 (5): 298-308. Weissglas-Volkov Daphna, Aguilar-Salinas Carlos A, Nikkola Elina, Deere Kerry A, Cruz-Bautista Ivette, Arellano-Campos Olimpia, Muñoz-Hernandez Linda Liliana, Gomez-Munguia Lizeth, Ordoñez-Sánchez Maria Luisa, Reddy Prasad M V Linga, Lusis Aldons J, Matikainen Niina, Taskinen Marja-Riitta, Riba Laura, Cantor Rita M, Sinsheimer Janet S, Tusie-Luna Teresa, Pajukanta Päi |
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Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia.
Atherosclerosis 2010 Nov . Evans D, Arzer J, Aberle J, Beil FU |
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The expression of type III hyperlipoproteinemia: involvement of lipolysis genes.
European journal of human genetics : EJHG 2009 May 17 (5): 620-8. Henneman Peter, van der Sman-de Beer Femke, Moghaddam Payman Hanifi, Huijts Petra, Stalenhoef Anton F H, Kastelein John J P, van Duijn Cornelia M, Havekes Louis M, Frants Rune R, van Dijk Ko Willems, Smelt Augustinus H |
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Sex-associated effect of CETP and LPL polymorphisms on postprandial lipids in familial hypercholesterolaemia.
Lipids in health and disease 2009 8 (1): 24. Anagnostopoulou Katherine K, Kolovou Genovefa D, Kostakou Peggy M, Mihas Constantinos, Hatzigeorgiou Georgios, Marvaki Christina, Degiannis Dimitrios, Mikhailidis Dimitri P, Cokkinos Dennis |
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Small and dense LDL in familial combined hyperlipidemia and N291S polymorphism of the lipoprotein lipase gene.
Lipids in health and disease 2009 8 12. López-Ruiz Antonio, Jarabo María M, Martínez-Triguero María L, Morales-Suárez-Varela Maria, Solá Eva, Bañuls Celia, Casado Marta, Hernández-Mijares Anton |
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High frequency of a retinoid X receptor gamma gene variant in familial combined hyperlipidemia that associates with atherogenic dyslipidemia.
Arteriosclerosis, thrombosis, and vascular biology 2007 Apr 27 (4): 923-8. Nohara Atsushi, Kawashiri Masa-aki, Claudel Thierry, Mizuno Mihoko, Tsuchida Masayuki, Takata Mutsuko, Katsuda Shoji, Miwa Kenji, Inazu Akihiro, Kuipers Folkert, Kobayashi Junji, Koizumi Junji, Yamagishi Masakazu, Mabuchi Hiros |
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The D9N, N291S and S447X variants in the lipoprotein lipase (LPL) gene are not associated with Type III hyperlipidemia.
BMC medical genetics 2007 8 (1): 56. Evans David, Beil Frank |
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Polymorphisms associated with apolipoprotein B levels in Greek patients with familial hypercholesterolemia.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2006 44 (7): 799-806. Choumerianou Despoina M, Maumus Sandy, Skoumas John, Pitsavos Christos, Stefanadis Christodoulos, Visvikis-Siest Sophie, Dedoussis George V |
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The lipoprotein lipase gene in combined hyperlipidemia: evidence of a protective allele depletion.
Lipids in health and disease 2006 5 (): 19. Wung Shu-Fen, Kulkarni Medha V, Pullinger Clive R, Malloy Mary J, Kane John P, Aouizerat Bradley |
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Genetic determinants of plasma HDL-cholesterol levels in familial hypercholesterolemia.
European journal of human genetics : EJHG 2005 Oct 13 (10): 1137-42. van Aalst-Cohen Emily S, Jansen Angelique C M, Boekholdt S Matthijs, Tanck Michael W T, Fontecha Marcel R, Cheng Suzanne, Li Jia, Defesche Joep C, Kuivenhoven Jan Albert, Kastelein John J |
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Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes.
Atherosclerosis 2005 Sep 182 (1): 153-9. Pisciotta L, Calabresi L, Lupattelli G, Siepi D, Mannarino MR, Moleri E, Bellocchio A, Cantafora A, Tarugi P, Calandra S, Bertolini S |
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Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia.
Atherosclerosis 2004 May 174 (1): 57-65. Bertolini Stefano, Pisciotta Livia, Di Scala Lilla, Langheim Silvia, Bellocchio Antonella, Masturzo Paola, Cantafora Alfredo, Martini Scipione, Averna Maurizio, Pes Gianni, Stefanutti Claudio, Calandra Sebastia |
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[Study on lipoprotein lipase gene Hind III polymorphism in Chinese type IIb hyperlipoproteinemia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2003 Dec 20 (6): 539-41. Zhang Rong, Liu Yu, Yang Lu-chuan, Bai Huai, Liu Bing-w |
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Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes.
Human mutation 2003 Apr 21 (4): 453. Yang Tao, Pang Chi-Pui, Tsang Man-Wo, Lam Ching-Wan, Poon Priscilla M K, Chan Lisa Y S, Wu Xiang-Qian, Tomlinson Brian, Baum Lar |
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Lipoprotein lipase activity and common gene variants in severely hypertriglyceridemic patients with and without diabetes.
Hormone research 2003 60 (2): 61-7. Chadarevian Rita, Foubert Luc, Beucler Isabel, Kottler Marie-Laure, Raisonnier Alain, Ajlouni Ali, Giral Philippe, Turpin Gérard, Bruckert Er |
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Characterization of LDL particle size among carriers of a defective or a null mutation in the lipoprotein lipase gene: the Québec LIPD Study.
Arteriosclerosis, thrombosis, and vascular biology 2002 Jul 22 (7): 1181-6. Ruel Isabelle L, Gaudet Daniel, Perron Patrice, Bergeron Jean, Julien Pierre, Lamarche Beno |
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Apolipoprotein E and lipoprotein lipase gene polymorphisms interaction on the atherogenic combined expression of hypertriglyceridemia and hyperapobetalipoproteinemia phenotypes.
Journal of endocrinological investigation 0 30 (7): 551-7. Perron P, Brisson D, Santuré M, Blackburn P, Bergeron J, Vohl M C, Després J P, Gaudet |
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Pathogenic classification of LPL gene variants reported to be associated with LPL deficiency.
Journal of clinical lipidology 0 10 (2): 394-409. Rodrigues Rute, Artieda Marta, Tejedor Diego, Martínez Antonio, Konstantinova Pavlina, Petry Harald, Meyer Christian, Corzo Deyanira, Sundgreen Claus, Klor Hans U, Gouni-Berthold Ioanna, Westphal Sabine, Steinhagen-Thiessen Elisabeth, Julius Ulrich, Winkler Karl, Stroes Erik, Vogt Anja, Hardt Phillip, Prophet Heinrich, Otte Britta, Nordestgaard Borge G, Deeb Samir S, Brunzell John |
- Page last reviewed:Jul 30, 2019
- Page last updated:Dec 5, 2019
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