Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Victoria M Pratt

Showing results (21-30 of 89) with videos related to

Pageof 9
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2012
Laboratory testing of CYP2D6 alleles in relation to tamoxifen therapyElaine Lyon, Julie Gastier Foster, Glenn E Palomaki, et al.
The Journal of Molecular Diagnostics : JMD|November 27, 2024
Twenty-Five Years of Germline Genetic Testing and What May Lie AheadVictoria M Pratt, Sara Akhavanfard, Jane Houldsworth, et al.
The Journal of Molecular Diagnostics : JMD|February 23, 2019
Analytical Validation of Variants to Aid in Genotype-Guided Therapy for OncologyMarelize Swart, Wesley M Stansberry, Victoria M Pratt, et al.
The Journal of Molecular Diagnostics : JMD|March 28, 2009
Identification of cystic fibrosis variants by polymerase chain reaction/oligonucleotide ligation assayKaren M Schwartz, Lisa L Pike-Buchanan, Kasinathan Muralidharan, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 1, 2020
Influence of Uridine Diphosphate Glucuronosyltransferase Family 1 Member A1 and Solute Carrier Organic Anion Transporter Family 1 Member B1 Polymorphisms and Efavirenz on Bilirubin Disposition in Healthy VolunteersKimberly S Collins, Ingrid F Metzger, Brandon T Gufford, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotypeJia-Chi Wang, Mary Vaccarello-Cruz, Leslie Ross, et al.
Clinical and Translational Science|July 24, 2020
Tracheal Aspirate as an Alternative Biologic Sample for Pharmacogenomics Testing in Mechanically Ventilated Pediatric PatientsKatherine A Hargreaves, Victoria M Pratt, Elizabeth B Medeiros, et al.
Nature Communications|February 28, 2018
Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genesIbrahim Numanagić, Salem Malikić, Michael Ford, et al.
The Journal of Molecular Diagnostics : JMD|May 11, 2019
Recommendations for Clinical CYP2C9 Genotyping Allele Selection: A Joint Recommendation of the Association for Molecular Pathology and College of American PathologistsVictoria M Pratt, Larisa H Cavallari, Andria L Del Tredici, et al.
JCO Precision Oncology|September 14, 2020
Severe Capecitabine Toxicity Associated With a Rare <i>DPYD</i> Variant Identified Through Whole-Genome SequencingReynold C Ly, Remington E Schmidt, Patrick J Kiel, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2012
Laboratory testing of CYP2D6 alleles in relation to tamoxifen therapyElaine Lyon, Julie Gastier Foster, Glenn E Palomaki, et al.
The Journal of Molecular Diagnostics : JMD|November 27, 2024
Twenty-Five Years of Germline Genetic Testing and What May Lie AheadVictoria M Pratt, Sara Akhavanfard, Jane Houldsworth, et al.
The Journal of Molecular Diagnostics : JMD|February 23, 2019
Analytical Validation of Variants to Aid in Genotype-Guided Therapy for OncologyMarelize Swart, Wesley M Stansberry, Victoria M Pratt, et al.
The Journal of Molecular Diagnostics : JMD|March 28, 2009
Identification of cystic fibrosis variants by polymerase chain reaction/oligonucleotide ligation assayKaren M Schwartz, Lisa L Pike-Buchanan, Kasinathan Muralidharan, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 1, 2020
Influence of Uridine Diphosphate Glucuronosyltransferase Family 1 Member A1 and Solute Carrier Organic Anion Transporter Family 1 Member B1 Polymorphisms and Efavirenz on Bilirubin Disposition in Healthy VolunteersKimberly S Collins, Ingrid F Metzger, Brandon T Gufford, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotypeJia-Chi Wang, Mary Vaccarello-Cruz, Leslie Ross, et al.
Clinical and Translational Science|July 24, 2020
Tracheal Aspirate as an Alternative Biologic Sample for Pharmacogenomics Testing in Mechanically Ventilated Pediatric PatientsKatherine A Hargreaves, Victoria M Pratt, Elizabeth B Medeiros, et al.
Nature Communications|February 28, 2018
Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genesIbrahim Numanagić, Salem Malikić, Michael Ford, et al.
The Journal of Molecular Diagnostics : JMD|May 11, 2019
Recommendations for Clinical CYP2C9 Genotyping Allele Selection: A Joint Recommendation of the Association for Molecular Pathology and College of American PathologistsVictoria M Pratt, Larisa H Cavallari, Andria L Del Tredici, et al.
JCO Precision Oncology|September 14, 2020
Severe Capecitabine Toxicity Associated With a Rare <i>DPYD</i> Variant Identified Through Whole-Genome SequencingReynold C Ly, Remington E Schmidt, Patrick J Kiel, et al.
Pageof 9