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British Journal of Clinical Pharmacology
|
March 21, 2017
Pharmacogenomic screening for anthracycline-induced cardiotoxicity in childhood cancer
Folefac Aminkeng, Colin J D Ross, Shahrad R Rassekh, et al.
Molecular Therapy. Nucleic Acids
|
April 20, 2026
sgRNA amount is a limiting factor in adenine base editing using RNA LNPs
Alexandra Birkenshaw, Tyler Thomson, Mai P Truong, et al.
Pharmacogenetics and Genomics
|
October 8, 2015
Genetic diversity of variants involved in drug response and metabolism in Sri Lankan populations: implications for clinical implementation of pharmacogenomics
Sze Ling Chan, Nilakshi Samaranayake, Colin J D Ross, et al.
Journal of Clinical Pharmacology
|
July 25, 2025
Four Pharmacogenomic Variants Strongly Linked to Corticosteroid-Induced Avascular Necrosis in Children with Cancer
Miguel Cordova-Delgado, Erika N Scott, Shahrad R Rassekh, et al.
Stem Cell Research
|
August 2, 2023
Generation of a human induced pluripotent stem cell line from a patient with hypomyelinating leukodystrophy 22 (HLD22)
Oguz K Ozgoren, Glen Lester Sequiera, Costanza Ferrari Bardile, et al.
JACC. Cardiooncology
|
July 3, 2023
<i>RBL2</i> Regulates Cardiac Sensitivity to Anthracycline Chemotherapy
Peng Xia, Jingrui Chen, Yadav Sapkota, et al.
Human Molecular Genetics
|
September 8, 2020
Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington disease
Galen E B Wright, Nicholas S Caron, Bernard Ng, et al.
Pediatrics
|
September 15, 2010
Fatal hydrocodone overdose in a child: pharmacogenetics and drug interactions
Parvaz Madadi, Doris Hildebrandt, Inna Y Gong, et al.
Therapeutic Drug Monitoring
|
March 14, 2023
Role of Cisplatin Dose Intensity and TPMT Variation in the Development of Hearing Loss in Children
Angela Siemens, Beth Brooks, S Rod Rassekh, et al.
Orphanet Journal of Rare Diseases
|
February 12, 2017
Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease
Maja Tarailo-Graovac, Britt I Drögemöller, Wyeth W Wasserman, et al.
Page
of 23
Search research articles
Search
Showing results (161-170 of 225) with videos related to
Sort By:
Page
of 23
British Journal of Clinical Pharmacology
|
March 21, 2017
Pharmacogenomic screening for anthracycline-induced cardiotoxicity in childhood cancer
Folefac Aminkeng, Colin J D Ross, Shahrad R Rassekh, et al.
Molecular Therapy. Nucleic Acids
|
April 20, 2026
sgRNA amount is a limiting factor in adenine base editing using RNA LNPs
Alexandra Birkenshaw, Tyler Thomson, Mai P Truong, et al.
Pharmacogenetics and Genomics
|
October 8, 2015
Genetic diversity of variants involved in drug response and metabolism in Sri Lankan populations: implications for clinical implementation of pharmacogenomics
Sze Ling Chan, Nilakshi Samaranayake, Colin J D Ross, et al.
Journal of Clinical Pharmacology
|
July 25, 2025
Four Pharmacogenomic Variants Strongly Linked to Corticosteroid-Induced Avascular Necrosis in Children with Cancer
Miguel Cordova-Delgado, Erika N Scott, Shahrad R Rassekh, et al.
Stem Cell Research
|
August 2, 2023
Generation of a human induced pluripotent stem cell line from a patient with hypomyelinating leukodystrophy 22 (HLD22)
Oguz K Ozgoren, Glen Lester Sequiera, Costanza Ferrari Bardile, et al.
JACC. Cardiooncology
|
July 3, 2023
<i>RBL2</i> Regulates Cardiac Sensitivity to Anthracycline Chemotherapy
Peng Xia, Jingrui Chen, Yadav Sapkota, et al.
Human Molecular Genetics
|
September 8, 2020
Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington disease
Galen E B Wright, Nicholas S Caron, Bernard Ng, et al.
Pediatrics
|
September 15, 2010
Fatal hydrocodone overdose in a child: pharmacogenetics and drug interactions
Parvaz Madadi, Doris Hildebrandt, Inna Y Gong, et al.
Therapeutic Drug Monitoring
|
March 14, 2023
Role of Cisplatin Dose Intensity and TPMT Variation in the Development of Hearing Loss in Children
Angela Siemens, Beth Brooks, S Rod Rassekh, et al.
Orphanet Journal of Rare Diseases
|
February 12, 2017
Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease
Maja Tarailo-Graovac, Britt I Drögemöller, Wyeth W Wasserman, et al.
Page
of 23