[HTML][HTML] CRISPR-Cas9 in vivo gene editing for transthyretin amyloidosis
…, J Taubel, J Kao, M Fontana, ML Maitland… - … England Journal of …, 2021 - Mass Medical Soc
Background Transthyretin amyloidosis, also called ATTR amyloidosis, is a life-threatening
disease characterized by progressive accumulation of misfolded transthyretin (TTR) protein in …
disease characterized by progressive accumulation of misfolded transthyretin (TTR) protein in …
Inflammation, growth factors, and pulmonary vascular remodeling
…, F Grimminger, PL Jones, ML Maitland… - Journal of the american …, 2009 - jacc.org
Inflammatory processes are prominent in various types of human and experimental pulmonary
hypertension (PH) and are increasingly recognized as major pathogenic components of …
hypertension (PH) and are increasingly recognized as major pathogenic components of …
Mitochondrial metabolism, redox signaling, and fusion: a mitochondria-ROS-HIF-1α-Kv1.5 O2-sensing pathway at the intersection of pulmonary hypertension and …
…, M Gomberg-Maitland, ML Maitland… - American Journal …, 2008 - journals.physiology.org
Pulmonary arterial hypertension (PAH) is a lethal syndrome characterized by vascular
obstruction and right ventricular failure. Although the fundamental cause remains elusive, many …
obstruction and right ventricular failure. Although the fundamental cause remains elusive, many …
Initial assessment, surveillance, and management of blood pressure in patients receiving vascular endothelial growth factor signaling pathway inhibitors
ML Maitland, GL Bakris, HR Black… - Journal of the …, 2010 - academic.oup.com
Hypertension is a mechanism-based toxic effect of drugs that inhibit the vascular endothelial
growth factor signaling pathway (VSP). Substantial evidence exists for managing …
growth factor signaling pathway (VSP). Substantial evidence exists for managing …
[HTML][HTML] Carboplatin and paclitaxel in combination with either vorinostat or placebo for first-line therapy of advanced non–small-cell lung cancer
SS Ramalingam, ML Maitland, P Frankel… - Journal of Clinical …, 2010 - ncbi.nlm.nih.gov
Purpose Vorinostat, a histone deacetylase inhibitor, exerts anticancer effects by both histone
and nonhistone–mediated mechanisms. It also enhances the anticancer effects of platinum …
and nonhistone–mediated mechanisms. It also enhances the anticancer effects of platinum …
Cancer pharmacogenomics: strategies and challenges
Genetic variation influences the response of an individual to drug treatments. Understanding
this variation has the potential to make therapy safer and more effective by determining …
this variation has the potential to make therapy safer and more effective by determining …
Ambulatory monitoring detects sorafenib-induced blood pressure elevations on the first day of treatment
ML Maitland, KE Kasza, T Karrison, K Moshier… - Clinical Cancer …, 2009 - AACR
Purpose: Hypertension is a mechanism-based toxicity of sorafenib and other cancer
therapeutics that inhibit the vascular endothelial growth factor (VEGF) signaling pathway. This …
therapeutics that inhibit the vascular endothelial growth factor (VEGF) signaling pathway. This …
A proposed EGFR inhibitor dermatologic adverse event-specific grading scale from the MASCC skin toxicity study group
ME Lacouture, ML Maitland, S Segaert, A Setser… - Supportive Care in …, 2010 - Springer
Background Accurate grading of dermatologic adverse events (AE) due to epidermal growth
factor receptor (EGFR) inhibitors (EGFRIs) is necessary for drug toxicity determinations, …
factor receptor (EGFR) inhibitors (EGFRIs) is necessary for drug toxicity determinations, …
[HTML][HTML] Dose-finding and pharmacokinetic study to optimize the dosing of irinotecan according to the UGT1A1 genotype of patients with cancer
…, R Marsh, T Karrison, ML Maitland… - Journal of clinical …, 2014 - ncbi.nlm.nih.gov
Purpose The risk of severe neutropenia from treatment with irinotecan is related in part to
UGT1A1* 28, a variant that reduces the elimination of SN-38, the active metabolite of irinotecan…
UGT1A1* 28, a variant that reduces the elimination of SN-38, the active metabolite of irinotecan…
Design of phase II cancer trials using a continuous endpoint of change in tumor size: application to a study of sorafenib and erlotinib in non–small-cell lung cancer
TG Karrison, ML Maitland, WM Stadler… - Journal of the National …, 2007 - academic.oup.com
Background The primary objective of phase II cancer clinical trials is to determine whether a
new regimen has sufficient activity to warrant further study, with activity generally defined as …
new regimen has sufficient activity to warrant further study, with activity generally defined as …