Showing results (101-110 of 262) with videos related to
Sort By:
Pageof 27
Diabetes/Metabolism Research and Reviews|March 23, 2005
Gly482Ser polymorphism of the peroxisome proliferator-activated receptor-gamma coactivator-1 gene might be a risk factor for diabetic retinopathy in Slovene population (Caucasians) with type 2 diabetes and the Pro12Ala polymorphism of the PPARgamma gene is notMojca Globocnik Petrovic, Tanja Kunej, Borut Peterlin, et al.European Journal of Human Genetics : EJHG|December 19, 2023
Perception of genomic newborn screening among peripartum mothersBernarda Prosenc, Mojca Cizek Sajko, Gorazd Kavsek, et al.Journal of Human Genetics|December 6, 2006
Patients with primary cataract as a genetic pool of DMPK protomutationIgor Medica, Natasa Teran, Marija Volk, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 22, 2009
Gene expression changes in blood as a putative biomarker for Huntington's diseaseLuca Lovrecic, Andrej Kastrin, Jan Kobal, et al.Journal of Assisted Reproduction and Genetics|December 18, 2016
Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortionAnita Barišić, Nina Pereza, Alenka Hodžić, et al.Pflugers Archiv : European Journal of Physiology|February 9, 2017
Angiotensin-converting enzyme gene polymorphism as a cardiovascular risk factor in childrenNataša Marčun Varda, Borut Peterlin, Stanislava Umek Bradač, et al.Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|December 1, 2007
Association of angiotensin-converting enzyme/DD genotype with sarcoidosis susceptibility in Slovenian patientsBarbara Salobir, Igor Medica, Marjeta Tercelj, et al.Andrology|February 26, 2022
Syndromic male subfertility: A network view of genome-phenome associationsŠpela Mikec, Živa Kolenc, Borut Peterlin, et al.Gene|March 26, 2019
Circadian clock genes and myocardial infarction in patients with type 2 diabetes mellitusIvana Škrlec, Jakov Milić, Ines Cilenšek, et al.Journal of Cardiovascular Translational Research|August 19, 2024
Clinical Outcome of Hypertrophic Cardiomyopathy in Probands with the Founder Variant c.913_914del in MYBPC3: A Slovenian Cohort StudyNina Vodnjov, Aleš Maver, Nataša Teran, et al.Pageof 27