1,467 results on '"Patrinos, George P."'
Search Results
252. Development of Rapid Pharmacogenomic Testing Assay in a Mobile Molecular Biology Laboratory (2MoBiL)
253. High frequency of concomitant nm23-H1 and E-cadherin transcriptional inactivation in primary non-inheriting colorectal carcinomas
254. Understanding Tandem Base Substitutions
255. Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy
256. A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and β-thalassemia compound heterozygotes
257. Human variome project country nodes: Documenting genetic information within a country
258. Microattribution and nanopublication as means to incentivize the placement of human genome variation data into the public domain
259. Molecular Diagnostics
260. Preface – Second Edition
261. Contributors
262. Mutation Detection by Single Strand Conformation Polymorphism and Heteroduplex Analysis
263. Preface – First Edition
264. Allele-Specific Mutation Detection
265. Locus-Specific and National/Ethnic Mutation Databases
266. Horizon Scanning: Teaching Genomics and Personalized Medicine in the Digital Age.
267. A novel variant in DYNC1H1 could contribute to human amyotrophic lateral sclerosis-frontotemporal dementia spectrum.
268. KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients
269. Genetics, genomics and society: the responsibilities of scientists for science communication and education
270. Pharmacogenomics and public health: implementing ‘populationalized’ medicine
271. Conference Scene: Golden Helix Pharmacogenomics Days: educational activities on pharmacogenomics and personalized medicine
272. Institutional Profile: Golden Helix Institute of Biomedical Research: interdisciplinary research and educational activities in pharmacogenomics and personalized medicine
273. Ascertainment and critical assessment of the views of the general public and healthcare professionals on nutrigenomics in Greece
274. 6-mercaptopurine influences TPMT gene transcription in a TPMT gene promoter variable number of tandem repeats-dependent manner
275. A novel 23-bp deletion in exon 5 of the p53 tumor suppressor gene
276. Evidence for association of an ACCN1 gene variant with response to lithium treatment in Sardinian patients with bipolar disorder
277. A critical view of the general public’s awareness and physicians’ opinion of the trends and potential pitfalls of genetic testing in Greece
278. Critical appraisal of the private genetic and pharmacogenomic testing environment in Greece
279. Genetic Analysis in Translational Medicine: The 2010 GOLDEN HELIX Symposium
280. Transcriptional regulation and pharmacogenomics
281. Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion
282. Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase
283. FINDbase: a worldwide database for genetic variation allele frequencies updated
284. Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection
285. Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations
286. Knowledge and Attitudes of Medical and Health Science Students in the United Arab Emirates toward Genomic Medicine and Pharmacogenomics: A Cross-Sectional Study
287. Roadmap for Establishing Large-Scale Genomic Medicine Initiatives in Low- and Middle-Income Countries
288. Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology
289. Genomics and Pharmacogenomics Knowledge, Attitude and Practice of Pharmacists Working in United Arab Emirates: Findings from Focus Group Discussions—A Qualitative Study
290. Costing Methods as a Means to Measure the Costs of Pharmacogenomics Testing
291. Editorial: Pharmacogenetics Research and Clinical Applications: An International Landscape of the Accomplishments, Challenges, and Opportunities
292. CYP3A5 Gene-Guided Tacrolimus Treatment of Living-Donor Egyptian Kidney Transplanted Patients
293. Toward High-Throughput Fungal Electroculturomics and New Omics Methodologies in 21st-Century Microbiology and Ecology
294. Towards harmonizing guidance for genome-informed drug treatment interventions: The show must go on
295. Screening for the C9ORF72 Expansion in Greek Huntington Disease Phenocopies and Controls and Meta-analysis of Current Data
296. Exome-Wide Analysis of the DiscovEHR Cohort Reveals Novel Candidate Pharmacogenomic Variants for Clinical Pharmacogenomics
297. Nutrigenetics and nutrigenomics: ready for clinical use or still a way to go?
298. Toxicity and Pharmacogenomic Biomarkers in Breast Cancer Chemotherapy
299. Documentation of clinically relevant genomic biomarker allele frequencies in the next‐generation FINDbase worldwide database
300. Multiomics Analysis Coupled with Text Mining Identify Novel Biomarker Candidates for Recurrent Cardiovascular Events
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