Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Efficiency and LDLR[original query] |
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[Distribution of HLA DQA1, LDLR, GYPA, HBGG, D7S8, and GC locus alleles in the population of Russia]. Sudebno-meditsinskaia ekspertiza 0 45 (3): 20-3. Kornienko I V, Afanas'eva G V, Shcherbakova E V, Ivanov P |
Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia. Clinical chemistry and laboratory medicine : CCLM / FESCC 2002 May 40 (5): 441-5. Salazar Luis A, Hirata Mario H, Hirata Rosario D |
[Population study of HLA DQA1, LDLR, GYPA, HBGG, D7S8, and GC loci in Caucasians living in the Ural region of Russia]. Sudebno-meditsinskaia ekspertiza 0 45 (2): 28-32. Pushkarev V P, Novikov P |
Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome. Journal of medical genetics 2004 Aug 41 (8): 577-84. Witsch-Baumgartner M, Gruber M, Kraft H G, Rossi M, Clayton P, Giros M, Haas D, Kelley R I, Krajewska-Walasek M, Utermann |
Increased intestinal cholesterol absorption in autosomal dominant hypercholesterolemia and no mutations in the low-density lipoprotein receptor or apolipoprotein B genes. The Journal of clinical endocrinology and metabolism 2007 Sep 92 (9): 3667-73. García-Otín A L, Cofán M, Junyent M, Recalde D, Cenarro A, Pocoví M, Ros E, Civeira |
A common polymorphism decreases low-density lipoprotein receptor exon 12 splicing efficiency and associates with increased cholesterol. Human molecular genetics 2007 Jul 16 (14): 1765-72. Zhu Haiyan, Tucker H Michael, Grear Karrie E, Simpson James F, Manning Alisa K, Cupples L Adrienne, Estus Stev |
Sex-dependent association of a common low-density lipoprotein receptor polymorphism with RNA splicing efficiency in the brain and Alzheimer's disease. Human molecular genetics 2008 Apr 17 (7): 929-35. Zou Fanggeng, Gopalraj Rangaraj K, Lok Johann, Zhu Haiyan, Ling I-Fang, Simpson James F, Tucker H Michael, Kelly Jeremiah F, Younkin Samuel G, Dickson Dennis W, Petersen Ronald C, Graff-Radford Neill R, Bennett David A, Crook Julia E, Younkin Steven G, Estus Stev |
Array-based resequencing for mutations causing familial hypercholesterolemia. Atherosclerosis 2011 Jun 216 (2): 383-9. Chiou Kuan-Rau, Charng Min-Ji, Chang Hua-M |
Ayurgenomics for stratified medicine: TRISUTRA consortium initiative across ethnically and geographically diverse Indian populations. Journal of ethnopharmacology 2016 Jul . Prasher Bhavana, Varma Binuja, Kumar Arvind, Khuntia Bharat Krushna, Pandey Rajesh, Narang Ankita, Tiwari Pradeep, Kutum Rintu, Guin Debleena, Kukreti Ritushree, Dash Debasis, , Mukerji Mita |
Familial hypercholesterolemia: experience from France. Current opinion in lipidology 2018 2 29 (2): 65-71. Rabès Jean-Pierre, Béliard Sophie, Carrié Ala |
Genetic variations in familial hypercholesterolemia and cascade screening in East Asians. Molecular genetics & genomic medicine 2018 12 7 (2): e00520. Chan Melody Lok-Yi, Cheung Ching-Lung, Lee Alan Chun-Hong, Yeung Chun-Yip, Siu Chung-Wah, Leung Jenny Yin-Yan, Pang Ho-Kwong, Tan Kathryn Choon-Be |
The Prevalence and Genetic Spectrum of Familial Hypercholesterolemia in Qatar Based on Whole Genome Sequencing of 14,000 Subjects. Frontiers in genetics 2022 8 13 927504. Diboun Ilhame, Al-Sarraj Yasser, Toor Salman M, Mohammed Shaban, Qureshi Nadeem, Al Hail Moza S H, Jayyousi Amin, Al Suwaidi Jassim, Albagha Omar M |
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- Page last updated:Dec 04, 2023
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