PDF) Gene Polymorphisms of the Renin-Angiotensin-Aldosterone System as Risk Factors for the Development of In-Stent Restenosis in Patients with Stable Coronary Artery Disease
The primer set used to amplify KCNJ11, the gene that encodes Kir6.2,... | Download Table
Novel mutations in the CYP11B2 gene causing aldosterone synthase deficiency
Human Peroxisome Assembly Factor-2 (PAF-2): A Gene Responsible for Group C Peroxisome Biogenesis Disorder in Humans
Application of Cas12a and nCas9-activation-induced cytidine deaminase for genome editing and as a non-sexual strategy to generat
Frontiers | Haplotype-specific chromatin looping reveals genetic interactions of regulatory regions modulating gene expression in 8p23.1
Genes | Free Full-Text | Association of Polymorphisms in the Long Non-Coding RNA HOTAIR with Recurrent Pregnancy Loss in a Korean Population | HTML
PDF) Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report
EP0711833A2 - Survival motor neuron (SMN) gene: a gene for spinal muscular atrophy - Google Patents
Genotype–phenotype correlations in recessive titinopathies - ScienceDirect
Genetic Variations and mRNA Expression of Goat DNAH1 and Their Associations with Litter Size
The primer set used to amplify KCNJ11, the gene that encodes Kir6.2,... | Download Table
Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac Death | PLOS ONE
A Novel Missense Mutation in the EDAR Gene and One Missense Mutation in EDA Gene in the Study of HED Patients in Iran
Metabolic and genetic determinants of HDL metabolism and hepatic lipase activity in normolipidemic females - Journal of Lipid Research
Frequencies of the genotypes and alleles of the AGT gene | Download Table
Site-specific gene targeting in mouse embryonic stem cells with intact bacterial artificial chromosomes | Nature Biotechnology
PDF) Cystinosis and two rare mutations in CTNS gene: two case reports
Overexpression of human O6-alkylguanine DNA alkyltransferase (AGT) prevents MNU induced lymphomas in heterozygous p53 deficient mice | Oncogene
The Growth Hormone Receptor Gene is Associated with Mandibular Height in a Chinese Population
PDF) Analysis of reninangiotensin aldosterone system gene polymorphisms in Malaysian essential hypertensive and type 2 diabetic subjects
Predicting chemosensitivity to gemcitabine and cisplatin based on gene polymorphisms and mRNA expression in non-small-cell lung cancer cells | Pharmacogenomics
