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Severe Vincristine-Induced Neuropathic Pain: A Case Report with Pharmacogenetic Analysis and Literature Review.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 1029, doi. 10.2147/PGPM.S389197
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- Article
Decreased Expression of a Novel lncRNA FAM181A-AS1 is Associated with Poor Prognosis and Immune Infiltration in Lung Adenocarcinoma.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 985, doi. 10.2147/PGPM.S384901
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- Article
Clinical Characteristics and Gene Mutations of Two Families with MODY 3 in Inner Mongolia.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 1019, doi. 10.2147/PGPM.S371141
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- Article
AZGP1 Up-Regulation is a Potential Target for Andrographolide Reversing Radioresistance of Colorectal Cancer.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 999, doi. 10.2147/PGPM.S360147
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- Article
The Role of Single Nucleotide Polymorphisms in Transporter Proteins and the Folate Metabolism Pathway in Delayed Methotrexate Excretion: A Case Report and Literature Review.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 919, doi. 10.2147/PGPM.S376797
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- Article
CES1 and SLC6A2 Genetic Variants As Predictors of Response To Methylphenidate in Autism Spectrum Disorders.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 951, doi. 10.2147/PGPM.S377210
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- Article
Utilizing Pharmacogenomics Results to Determine Opioid Appropriateness and Improve Pain Management in a Patient with Osteoarthritis.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 943, doi. 10.2147/PGPM.S385272
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- Article
Next-Generation Sequencing and Bioinformatics-Based Protocol for the Full-Length CYP2E1 Gene Polymorphism Analysis.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 959, doi. 10.2147/PGPM.S371709
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- Article
Germline PRDM1 Variant rs2185379 in Long-Term Recurrence-Free Survivors of Advanced Ovarian Cancer.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 977, doi. 10.2147/PGPM.S387120
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- Article
Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 913, doi. 10.2147/PGPM.S380908
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- Article
What Personalized Medicine Humans Need and Way to It ——also on the Practical Significance and Scientific Limitations of Precision Medicine.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 927, doi. 10.2147/PGPM.S380767
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- Article
Utilization of Drugs with Pharmacogenetic Dosing Recommendations in Switzerland: A Descriptive Study Using the Helsana Database.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 967, doi. 10.2147/PGPM.S382214
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- Article
Drug–Drug–Gene Interactions in Cardiovascular Medicine.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 879, doi. 10.2147/PGPM.S338601
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- Article
Shwachman Diamond Syndrome with Arrhythmia as the First Manifestation a Case Report and Literature Review.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 867, doi. 10.2147/PGPM.S381695
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- Article
Risk Factors and Predictive Model for Dermatomyositis Associated with Rapidly Progressive Interstitial Lung Disease.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 775, doi. 10.2147/PGPM.S369556
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- Article
Downregulation of Crystallin Lambda 1 is a New Independent Prognostic Marker in Clear Cell Renal Cell Carcinoma.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 857, doi. 10.2147/PGPM.S382564
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- Article
Contribution of ZBTB20 Polymorphisms to Esophageal Cancer Risk Among the Chinese Han Population.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 827, doi. 10.2147/PGPM.S370963
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- Article
PFKP and GPC6 Variants Were Correlated with Alcohol-Induced Femoral Head Necrosis Risk in the Chinese Han Population.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 797, doi. 10.2147/PGPM.S369957
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- Article
The Association Between Genetic Polymorphisms of Transporter Genes and Prognosis of Platinum-Based Chemotherapy in Lung Cancer Patients.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 817, doi. 10.2147/PGPM.S375284
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- Article
Neurofibromatosis Type 1 and Hypospadias in a Male 46, XY with a Mutation in the NF1 Gene and a Mutation in NR5A1.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 873, doi. 10.2147/PGPM.S380796
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- Article
Expression Profile and Bioinformatics Analysis of Circular RNAs in Patients with Vitiligo.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 785, doi. 10.2147/PGPM.S371107
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- Article
Association of CYP7A1 and CYP2E1 Polymorphisms with Type 2 Diabetes in the Chinese Han Populations.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 843, doi. 10.2147/PGPM.S367806
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- Article
A Study on the Molecular Mechanism of High Altitude Heart Disease in Children.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 721, doi. 10.2147/PGPM.S356206
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- Article
Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 743, doi. 10.2147/PGPM.S361809
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- Article
Prescription Advice Based on Data of Drug-Drug-Gene Interaction of Patients with Polypharmacy.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 765, doi. 10.2147/PGPM.S368606
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- Article
Cuproptosis-Related Gene – SLC31A1, FDX1 and ATP7B – Polymorphisms are Associated with Risk of Lung Cancer.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 733, doi. 10.2147/PGPM.S372824
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- Article
IL-10 rs1800896 Polymorphism: A Risk Factor for Adult Acute Lymphoblastic Leukemia.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 809, doi. 10.2147/PGPM.S377356
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- Article
Identification of a Novel OFD1 Variant in a Patient with Primary Ciliary Dyskinesia.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 697, doi. 10.2147/PGPM.S365740
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- Article
Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 705, doi. 10.2147/PGPM.S366826
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- Article
Inducible Nitric Oxide Synthase iNOS-954-G>C and Ex16+14-C>T Gene Polymorphisms and Susceptibility to Vitiligo in the Saudi Population.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 603, doi. 10.2147/PGPM.S344415
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- Article
The Impact of Pharmacogenetics on Pharmacokinetics and Pharmacodynamics in Neonates and Infants: A Systematic Review.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 675, doi. 10.2147/PGPM.S350205
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- Article
Examining an Association of Single Nucleotide Polymorphisms with Hyperuricemia in Chinese Flight Attendants.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 589, doi. 10.2147/PGPM.S364206
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- Article
Pharmacogenetics of Breast Cancer Treatments: A Sub-Saharan Africa Perspective.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 613, doi. 10.2147/PGPM.S308531
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Effective Treatment of Low-Grade Myofibroblastic Sarcoma with Apatinib: A Case Report and Literature Review.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 573, doi. 10.2147/PGPM.S359492
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- Article
Impact of HOXB4 and PRDM16 Gene Expressions on Prognosis and Treatment Response in Acute Myeloid Leukemia Patients.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 663, doi. 10.2147/PGPM.S368640
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- Article
Effect of Genetic Variations in Drug-Metabolizing Enzymes and Drug Transporters on the Pharmacokinetics of Rifamycins: A Systematic Review.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 561, doi. 10.2147/PGPM.S363058
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- Article
Compound Heterozygous Mutations in TGM1 Causing a Severe Form of Lamellar Ichthyosis: A Case Report.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 583, doi. 10.2147/PGPM.S361350
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- Article
Italian Real-Life Experience of Patients with Hereditary Transthyretin Amyloidosis Treated with Patisiran.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 499, doi. 10.2147/PGPM.S359851
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- Article
An Integrative Analysis Identifying RAB40C as an Oncogenic Immune Protein and Prognostic Marker of Lung Squamous Cell Carcinoma.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 525, doi. 10.2147/PGPM.S357166
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- Article
Psoriasis Patients with Specific HLA-Cw Alleles and Lower Plasma IL-17 Level Show Improved Response to Topical Lindioil Treatment.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 515, doi. 10.2147/PGPM.S351452
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- Article
Missense Variant rs28362680 in BTNL2 Reduces Risk of Coronary Heart Disease.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 449, doi. 10.2147/PGPM.S353085
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- Article
Is Pharmacogenetic Panel Testing Applicable to Low-Dose Methotrexate in Rheumatoid Arthritis? – A Case Report.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 465, doi. 10.2147/PGPM.S354011
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- Article
Effect of Apolipoprotein E ϵ4 Allele on the Progression of Carotid Atherosclerosis Through Apolipoprotein Levels.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 653, doi. 10.2147/PGPM.S367471
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- Article
Genetic Variations of CARMN Modulate Glioma Susceptibility and Prognosis in a Chinese Han Population.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 487, doi. 10.2147/PGPM.S345764
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- Article
Identification of NFASC and CHL1 as Two Novel Hub Genes in Endometriosis Using Integrated Bioinformatic Analysis and Experimental Verification.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 377, doi. 10.2147/PGPM.S354957
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- Article
Gene Polymorphisms of m6A Erasers FTO and ALKBH1 Associated with Susceptibility to Gastric Cancer.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 547, doi. 10.2147/PGPM.S360912
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- Article
Correlation Between Angiotensin Receptor Type 1 Polymorphisms and Atherosclerotic Cerebral Infarction Risk.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 477, doi. 10.2147/PGPM.S364648
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- Article
Cancer Metastases from Lung Adenocarcinoma Disappeared After Molecular Targeted Therapy: A Successfully Clinical Treatment Experience.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 539, doi. 10.2147/PGPM.S367978
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- Article
Associations Between Genetic Polymorphisms Within Transporter Genes and Clinical Response to Methotrexate in Chinese Rheumatoid Arthritis Patients: A Pilot Study.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 327, doi. 10.2147/PGPM.S350417
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- Article
Susceptibility of Genetic Variations in Methylation Pathway to Gastric Cancer.
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- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 441, doi. 10.2147/PGPM.S340941
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- Article