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SIRT1 Gene SNP rs932658 Is Associated With MedicationāRelated Osteonecrosis of the Jaw
Journal of bone and mineral research, ISSN 0884-0431, 02/2021, Volume 36, Issue 2, pp. 347 - 356
OSTEONECROSIS OF THE JAW | BONE MODELING AND REMODELING | ANTIRESORPTIVES | OSTEOBLASTS | PHARMACOGENOMICS | Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Jaw | Reporter gene | Intravenous administration | Linkage disequilibrium | Alleles | Osteonecrosis | Single-nucleotide polymorphism | SIRT1 protein | Bisphosphonates | Index Medicus
Journal Article
Genetics in medicine, ISSN 1098-3600, 06/2018, Volume 20, Issue 6, pp. 655 - 663
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Delivery of Health Care - methods | Precision Medicine - standards | Genomics | Humans | Female | Male | Surveys and Questionnaires | Precision Medicine - methods | Medicine | Working groups | Index Medicus | genomic medicine | consolidated framework | common measures | IGNITE | implementation
Journal Article
Kidney international, ISSN 0085-2538, 03/2011, Volume 79, Issue 5, pp. 563 - 572
human genetics | end-stage renal disease | ethnic minority | polymorphisms | diabetic nephropathy | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Diabetes. Impaired glucose tolerance | Kidneys | Urinary system involvement in other diseases. Miscellaneous | Nephrology. Urinary tract diseases | Biological and medical sciences | Endocrinopathies | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Associated diseases and complications | Genetic Predisposition to Disease | Genome-Wide Association Study | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | African Americans - genetics | Diabetic Nephropathies - genetics | Male | Kidney Failure, Chronic - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Diabetes Mellitus, Type 2 - complications | Index Medicus
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Pharmacoepidemiology and drug safety, ISSN 1053-8569, 11/2020, Volume 29, Issue 11, pp. 1393 - 1401
computable phenotypes | electronic health records | hypertension | resistant hypertension | pharmacoepidemiology | Pharmacology & Pharmacy | Public, Environmental & Occupational Health | Life Sciences & Biomedicine | Science & Technology | Hypertension | Medical research | Algorithms | Electronic records | Medicine, Experimental | Medical records | Genetic aspects | Research institutes | Epidemiology | Genotype & phenotype | Phenotypes | Patients | Electronic medical records | Index Medicus
Journal Article
Scientific reports, ISSN 2045-2322, 11/2019, Volume 9, Issue 1, pp. 17323 - 9
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Hypertension | Metoprolol | Calcineurin | Coronary artery | Calcineurin inhibitors | Association analysis | Genomes | Single-nucleotide polymorphism | Inositol phosphate | Hydrochlorothiazide | Atenolol | NF-AT protein | Chromosome 2 | Proteins | Diuretics | Blood pressure | Ventricle | Protein interaction | Hypertrophy | Pharmacogenomics | Index Medicus
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Genetics in medicine, ISSN 1098-3600, 10/2020, Volume 22, Issue 10, pp. 1729 - 1729
Journal Article
Human genetics, ISSN 0340-6717, 2009, Volume 126, Issue 2, pp. 265 - 275
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Human | Diabetes. Impaired glucose tolerance | Kidneys | Biological and medical sciences | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Urinary system involvement in other diseases. Miscellaneous | Nephrology. Urinary tract diseases | Endocrinopathies | Genetics of eukaryotes. Biological and molecular evolution | Associated diseases and complications | Haplotypes | Genetic Predisposition to Disease | Dipeptidases - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | African Americans | Diabetic Nephropathies - genetics | Male | Diabetic Nephropathies - ethnology | Polymorphism, Genetic | Kidney Failure, Chronic - genetics | Adult | Female | Aged | Genome | Index Medicus | End Stage Renal Disease | nephropathy | DNA polymorphisms | type 2 diabetes | carnosinase
Journal Article
BMC medical genomics, ISSN 1755-8794, 06/2018, Volume 11, Issue 1, pp. 55 - 55
Hypertension | eQTL | Personalized medicine | RNA-Seq | Thiazide diuretics | Pharmacogenomics | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Pharmacogenetics | Genetic research | Genetic aspects | Dosage and administration | Blood pressure | Research | Drug therapy | Thiazides | Pharmacokinetics | Health aspects | Heart failure | Urine | Genomics | Clinical trials | Cardiovascular disease | Genomes | Uric acid | Hydrochlorothiazide | Gene expression | Phosphatase | Metabolism | Kinases | Ribonucleic acid--RNA | Proteins | Diuretics | Chromosome 12 | Potassium | Deoxyribonucleic acid--DNA
Journal Article
The pharmacogenomics journal, ISSN 1470-269X, 2018, Volume 19, Issue 3, pp. 295 - 304
Pharmacology & Pharmacy | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | European Continental Ancestry Group - genetics | Hispanic Americans - genetics | Blood Pressure - genetics | Humans | Middle Aged | Risk Factors | Hypertension - drug therapy | Male | Antihypertensive Agents - therapeutic use | Verapamil - therapeutic use | Polymorphism, Single Nucleotide - genetics | Female | Aged | Blood Pressure - drug effects | Hypertension - genetics | Genome-Wide Association Study - methods | Odds Ratio | Hypertension | Drugs | Stroke | Genes | Coronary artery | Association analysis | Cardiovascular disease | Risk | Genomes | Coronary artery disease | Genetic variance | Msx2 protein | Genetic analysis | Alleles | Verapamil | Blood pressure | Heart diseases | Index Medicus
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Scientific reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 16068 - 8
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