Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Cardiovascular Diseases and LDLR[original query] |
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Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia. BMC medical genetics 2011 12 (1): 40. Al-Khateeb Alyaa, Zahri Mohd K, Mohamed Mohd S, Sasongko Teguh H, Ibrahim Suhairi, Yusof Zurkurnai, Zilfalil Bin |
A variant in LDLR is associated with abdominal aortic aneurysm.
Circulation. Cardiovascular genetics 2013 Oct 6 (5): 498-504. Bradley Declan T, Hughes Anne E, Badger Stephen A, Jones Gregory T, Harrison Seamus C, Wright Benjamin J, Bumpstead Suzannah, Baas Annette F, Grétarsdóttir Sólveig, Burnand Kevin, Child Anne H, Clough Rachel E, Cockerill Gillian, Hafez Hany, Scott D Julian A, Ariëns Robert A S, Johnson Anne, Sohrabi Soroush, Smith Alberto, Thompson Matthew M, van Bockxmeer Frank M, Waltham Matthew, Matthíasson Stefán E, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Blankensteijn Jan D, Teijink Joep A W, Wijmenga Cisca, de Graaf Jacqueline, Kiemeney Lambertus A, Wild John B, Edkins Sarah, Gwilliam Rhian, Hunt Sarah E, Potter Simon, Lindholt Jes S, Golledge Jonathan, Norman Paul E, van Rij Andre, Powell Janet T, Eriksson Per, Stefánsson Kári, Thompson John R, Humphries Steve E, Sayers Robert D, Deloukas Panos, Samani Nilesh J, Bown Matthew |
Genetic polymorphisms in LDLR, APOB, PCSK9 and other lipid related genes associated with familial hypercholesterolemia in Malaysia. PloS one 2013 8 (4): e60729. Lye Say-Hean, Chahil Jagdish Kaur, Bagali Pramod, Alex Livy, Vadivelu Jamunarani, Ahmad Wan Azman Wan, Chan Siew-Pheng, Thong Meow-Keong, Zain Shamsul Mohd, Mohamed Rosmawa |
Genetic polymorphism of LDLR (rs688) is associated with primary intracerebral hemorrhage. Current neurovascular research 2013 Dec . Lee JD, Hsiao KM, Lee TH, Kuo YW, Huang YC, Hsu HL, Lin YH, Wu CY, Huang YC, Lee M, Yang HT, Hsu CY, Pan YT |
Single step PCR for the identification of Low Density Lipoprotein Receptor (LDL-R) gene mutations. Pakistan journal of medical sciences 2014 Jul 30 (4): 830-3. Khan Samia Perwaiz, Ghani Rubina, Yaqub Z |
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.
Circulation research 2017 Jan 120 (2): 341-353. Jones Gregory T, Tromp Gerard, Kuivaniemi Helena, Gretarsdottir Solveig, Baas Annette F, Giusti Betti, Strauss Ewa, Van't Hof Femke N G, Webb Thomas R, Erdman Robert, Ritchie Marylyn D, Elmore James R, Verma Anurag, Pendergrass Sarah, Kullo Iftikhar J, Ye Zi, Peissig Peggy L, Gottesman Omri, Verma Shefali S, Malinowski Jennifer, Rasmussen-Torvik Laura J, Borthwick Kenneth M, Smelser Diane T, Crosslin David R, de Andrade Mariza, Ryer Evan J, McCarty Catherine A, Böttinger Erwin P, Pacheco Jennifer A, Crawford Dana C, Carrell David S, Gerhard Glenn S, Franklin David P, Carey David J, Phillips Victoria L, Williams Michael J A, Wei Wenhua, Blair Ross, Hill Andrew A, Vasudevan Thodor M, Lewis David R, Thomson Ian A, Krysa Jo, Hill Geraldine B, Roake Justin, Merriman Tony R, Oszkinis Grzegorz, Galora Silvia, Saracini Claudia, Abbate Rosanna, Pulli Raffaele, Pratesi Carlo, Saratzis Athanasios, Verissimo Ana R, Bumpstead Suzannah, Badger Stephen A, Clough Rachel E, Cockerill Gillian, Hafez Hany, Scott D Julian A, Futers T Simon, Romaine Simon P R, Bridge Katherine, Griffin Kathryn J, Bailey Marc A, Smith Alberto, Thompson Matthew M, van Bockxmeer Frank M, Matthiasson Stefan E, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Blankensteijn Jan D, Teijink Joep A W, Wijmenga Cisca, de Graaf Jacqueline, Kiemeney Lambertus A, Lindholt Jes S, Hughes Anne, Bradley Declan T, Stirrups Kathleen, Golledge Jonathan, Norman Paul E, Powell Janet T, Humphries Steve E, Hamby Stephen E, Goodall Alison H, Nelson Christopher P, Sakalihasan Natzi, Courtois Audrey, Ferrell Robert E, Eriksson Per, Folkersen Lasse, Franco-Cereceda Anders, Eicher John D, Johnson Andrew D, Betsholtz Christer, Ruusalepp Arno, Franzén Oscar, Schadt Eric E, Björkegren Johan L M, Lipovich Leonard, Drolet Anne M, Verhoeven Eric L, Zeebregts Clark J, Geelkerken Robert H, van Sambeek Marc R, van Sterkenburg Steven M, de Vries Jean-Paul, Stefansson Kari, Thompson John R, de Bakker Paul I W, Deloukas Panos, Sayers Robert D, Harrison Seamus C, van Rij Andre M, Samani Nilesh J, Bown Matthew |
LDLR C1725T Gene Polymorphism Frequency in Type 2 Diabetes Mellitus Patients With Dyslipidemia. Journal of clinical medicine research 2016 Nov 8 (11): 793-796. Eroglu Zuhal, Harman Ece, Vardarli Egemen, Kayikcioglu Meral, Vardarli Asli Tet |
A randomized trial and novel SPR technique identifies altered lipoprotein-LDL receptor binding as a mechanism underlying elevated LDL-cholesterol in APOE4s. Scientific reports 2017 Mar 7 44119. Calabuig-Navarro M V, Jackson K G, Kemp C F, Leake D S, Walden C M, Lovegrove J A, Minihane A |
Genetic spectrum of low density lipoprotein receptor gene variations in South Indian population. Clinica chimica acta; international journal of clinical chemistry 2017 Dec 478 28-36. ArulJothi K N, Suruthi Abirami B, Devi Arikke |
Characterization of LDLR rs5925 and PCSK9 rs505151 genetic variants frequencies in healthy subjects from northern Chile: Influence on plasma lipid levels. Journal of clinical laboratory analysis 2019 Aug e23001. Rojas Claudio, Ramírez Hugo, Salazar Luis A, Kalergis Alexis M, Gálvez Anita S, Escobar-Vera Jor |
LDLR Gene Polymorphisms (rs5925 and rs1529729) Are Associated with Susceptibility to Coronary Artery Disease in a South Indian Population. Medical sciences (Basel, Switzerland) 2019 Jul 7 (7): . K Jha Chandan, Mir Rashid, Elfaki Imadeldin, Banu Shaheena, Chahal S M |
Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations. PloS one 2020 15 (2): e0229098. Hayat Mahtaab, Kerr Robyn, Bentley Amy R, Rotimi Charles N, Raal Frederick J, Ramsay Michè |
Cascade screening and genetic diagnosis of familial hypercholesterolemia in clusters of the Southeastern region from Brazil. Molecular biology reports 2020 11 47 (12): 9279-9288. de Paiva Silvino Júnea Paolucci, Jannes Cinthia Elim, Tada Mauricio Teruo, Lima Isabella Ramos, Silva Iêda de Fátima Oliveira, Pereira Alexandre Costa, Gomes Karina Bra |
Multiplex Protein Biomarker Profiling in Patients with Familial Hypercholesterolemia. Genes 2021 10 12 (10): . Dlouha Dana, Blaha Milan, Rohlova Eva, Hubacek Jaroslav A, Lanska Vera, Visek Jakub, Blaha Vladim |
Identification of genetic variants related to metabolic syndrome by next-generation sequencing. Diabetology & metabolic syndrome 2022 Aug 14 (1): 119. Lee Sanghoo, Kim Seol-A, Hong Jeonghoon, Kim Yejin, Hong Gayeon, Baik SaeYun, Choi Kyeonghwan, Lee Mi-Kyeong, Lee Kyoung-Ry |
Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/Cas9 constructs. Gene 2023 9 147821. Augusto Akira Mori, Vanessa Barbosa Malaquias, Kennedy Bonjour, Glaucio Monteiro Ferreira, Raul Hernandes Bortolin, Jéssica Bassani Borges, Victor Fernandes de Oliveira, Rodrigo Marques Gonçalves, Andre Arpad Faludi, Gisele Monteiro Bastos, Helena Thurow, Marcelo Ferraz Sampaio, Rozana Mesquita Ciconelli, Adriano Namo Cury, Cristina Moreno Fajardo, Rosario Dominguez Crespo Hirata, Mário Hiroyuki Hira |
Genetically instrumented LDL-cholesterol lowering and multiple disease outcomes: a Mendelian randomisation phenome-wide association study in the UK Biobank. British journal of clinical pharmacology 2023 5 . Kitty Pham, Anwar Mulugeta, Amanda Lumsden, Elina Hypp?n |
Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning. Vavilovskii zhurnal genetiki i selektsii 2023 10 27 (5): 522-529. D E Ivanoshchuk, A B Kolker, O V Timoshchenko, S E Semaev, E V Shakhtshneid |
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- Page last updated:Apr 29, 2024
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