Search Results - "Hubbart CS"

BIOCHEMICAL CHARACTERISATION OF FAMILIAL HYPERCHOLESTEROLEMIA: ASSOCIATIONS BETWEEN GENETIC AND LIPID PROFILES.

Alternate Title: BIOHEMIJSKA KARAKTERIZACIJA FAMILIJARNE HIPERHOLESTEROLEMIJE: POVEZANOST GENETIČKIH I LIPIDNIH PARAMETARA.

Authors: Lukač, Sandra Singh Gašić, Vladimir Komazec, Jovana et al.

Source: Journal of Medical Biochemistry. Dec2025, Vol. 44 Issue 9, p2026-2034. 9p.

Familial Hypercholesterolemia: Prevalence and Discrepancy between Genotype and Phenotype: Findings of the Population-based Hamburg City Health Study.

Authors: Riccio, C. Arnold, N. Koliopanos, G. et al.

Source: Deutsches Ärzteblatt International. 9/19/2025, Vol. 122 Issue 19, p511-516. 6p.

PCSK9 and its relationship with HMGB1, TLR4, and TNFα in non-statin and statin-treated coronary artery disease patients.

Authors: Desouky DA Nosair NA Salama MK et al.

Source: Molecular and cellular biochemistry [Mol Cell Biochem] 2025 May; Vol. 480 (5), pp. 2935-2949. Date of Electronic Publication: 2024 Nov 14.

Publication Type: Journal Article

Journal Info: Publisher: Springer Country of Publication: Netherlands NLM ID: 0364456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-4919 (Electronic) Linking ISSN: 03008177 NLM ISO Abbreviation: Mol Cell Biochem Subsets: MEDLINE

Novel start codon variant in the 5'UTR of LDLR associated with familial hypercholesterolaemia.

Authors: Bird M Tung CJ Pittman AM et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2026 Apr; Vol. 34 (4), pp. 522-527. Date of Electronic Publication: 2025 Jul 24.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Assessing accuracy of genotype imputation in the Afrikaner and Brahman cattle breeds of South Africa.

Authors: Mdyogolo, S. MacNeil, M. D. Neser, F. W. C. et al.

Source: Tropical Animal Health & Production. Apr2022, Vol. 54 Issue 2, p1-12. 12p.

Familial Hypercholesterolemia Screening, Diagnosis, Treatment, and Prevention - Current Knowledge and Novel Possibilities in the Region.

Authors: Csép, Katalin Demeter, Orsolya

Source: Bulletin of Medical Sciences. Jul2023, Vol. 96 Issue 1, p13-25. 13p.

Association of glutathione S-transferase M1 and T1 gene polymorphism with oxidative stress in diabetic and nondiabetic chronic kidney disease.

Authors: Datta, Sudip K. Kumar, Vivek Pathak, Rahul et al.

Source: Renal Failure. 2010, Vol. 32 Issue 10, p1189-1195. 7p. 1 Black and White Photograph, 6 Charts, 2 Graphs.

Glutathione S-Transferase Null and Cholesteryl Ester Transfer Protein TaqI B Polymorphisms and Lipid Response to Atorvastatin in Greek Dyslipidaemic Patients.

Authors: Goulas, Antonis Kosmidou, Maria Hatzitolios, Apostolos I. et al.

Source: Basic & Clinical Pharmacology & Toxicology. Jun2008, Vol. 102 Issue 6, p559-562. 4p. 1 Diagram, 2 Charts.

Prevalence of cardiovascular events in genetically confirmed versus unconfirmed familial hypercholesterolaemia.

Authors: Khan, Tina Z. Breen, Jane Neves, Emma et al.

Source: Global Cardiology Science & Practice. 2020, Vol. 2020 Issue 2, p1-12. 12p.

Multimodal lipid-lowering treatment in pediatric patients with homozygous familial hypercholesterolemia—target attainment requires further increase of intensity.

Authors: Klaus, Günter Taylan, Christina Büscher, Rainer et al.

Source: Pediatric Nephrology. Jul2018, Vol. 33 Issue 7, p1199-1208. 10p. 2 Charts, 2 Graphs.

Case-control study on PCSK9 R496W (rs374603772) and D374Y (rs137852912) mutations in Turkish patients with primary dyslipidemia.

Authors: Eroğlu, Zuhal Vardarlı, Aslı Tetik Düzgün, Zekeriya et al.

Source: Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi. May2018, Vol. 19 Issue 5, p334-340. 7p.

PCSK9 inhibitors - from discovery of a single mutation to a groundbreaking therapy of lipid disorders in one decade.

Authors: Jaworski, Krzysztof Jankowski, Piotr Kosior, Dariusz A.

Source: Archives of Medical Science. 2017, Vol. 13 Issue 4, p914-929. 16p. 1 Diagram, 3 Charts.

Evaluation of glutathione S-transferase polymorphism in Iranian patients with type 2 diabetic microangiopathy.

Authors: Hashemi-Soteh, Mohammad Bagher Ahmadzadeh Amiri, Amir Sheikh Rezaee, Majid Reza et al.

Source: Egyptian Journal of Medical Human Genetics. 9/1/2020, Vol. 21 Issue 1, pN.PAG-N.PAG. 1p.

Next-generation-sequencing-based identification of familial hypercholesterolemia-related mutations in subjects with increased LDL–C levels in a latvian population.

Authors: Radovica-Spalvina, Ilze Latkovskis, Gustavs Silamikelis, Ivars et al.

Source: BMC Medical Genetics. 9/29/2015, Vol. 16 Issue 1, p1-9. 9p.

Functional analysis of four LDLR 5′UTR and promoter variants in patients with familial hypercholesterolaemia.

Authors: Khamis, Amna Palmen, Jutta Lench, Nick et al.

Source: European Journal of Human Genetics. Jun2015, Vol. 23 Issue 6, p790-795. 6p.

Functional Characterization of Two Low-Density Lipoprotein Receptor Gene Mutations in Two Chinese Patients with Familial Hypercholesterolemia.

Authors: Wang, Haihong Xu, Shengyuan Sun, Liyuan et al.

Source: PLoS ONE. Mar2014, Vol. 9 Issue 3, p1-10. 10p.

Genetic Polymorphisms in LDLR, APOB, PCSK9 and Other Lipid Related Genes Associated with Familial Hypercholesterolemia in Malaysia.

Authors: Lye, Say-Hean Chahil, Jagdish Kaur Bagali, Pramod et al.

Source: PLoS ONE. Apr2013, Vol. 8 Issue 4, p1-8. 8p.

Evidence for Using Alpha-Lipoic Acid in Reducing Lipoprotein and Inflammatory Related Atherosclerotic Risk.

Authors: Harding, Scott V. Rideout, Todd C. Jones, Peter J. H.

Source: Journal of Dietary Supplements. Jun2012, Vol. 9 Issue 2, p116-127. 12p.

Molecular pathology of familial hypercholesterolemia, related dyslipidemias and therapies beyond the statins.

Authors: Faiz, Fathimath Hooper, Amanda J. van Bockxmeer, Frank M.

Source: Critical Reviews in Clinical Laboratory Sciences. Feb2012, Vol. 49 Issue 1, p1-17. 17p. 6 Diagrams.

Familial hypercholesterolemia: the lipids or the genes.

Authors: Fahed, Akl C Nemer, Georges M

Source: Nutrition & Metabolism. 2011, Vol. 8 Issue 1, p1-12. 12p.