4 results match your criteria: "3 Novartis Institutes for BioMedical Research[Affiliation]"
J R Soc Interface
February 2019
2 Mathematical Institute, University of Oxford, Oxford OX2 6GG , UK.
We introduce a tensor-based clustering method to extract sparse, low-dimensional structure from high-dimensional, multi-indexed datasets. This framework is designed to enable detection of clusters of data in the presence of structural requirements which we encode as algebraic constraints in a linear program. Our clustering method is general and can be tailored to a variety of applications in science and industry.
View Article and Find Full Text PDFAm J Respir Crit Care Med
May 2019
6 Department of Respiratory Medicine, Hannover Medical School, Hannover, Germany.
In the CLAIM study, dual bronchodilation with indacaterol/glycopyrronium (IND/GLY) significantly reduced hyperinflation, which translated into improved cardiac function, measured by left ventricular end-diastolic volume and cardiac output. Pulmonary microvascular blood flow (PMBF) is reduced in chronic obstructive pulmonary disease (COPD); however, the effect of reduced lung hyperinflation on PMBF remains unknown. To determine the effect of lung deflation with IND/GLY on PMBF and regional pulmonary ventilation using magnetic resonance imaging (MRI) in hyperinflated patients with COPD.
View Article and Find Full Text PDFAm J Respir Crit Care Med
February 2019
3 Novartis Institutes for BioMedical Research, Cambridge, Massachusetts.
Rationale: Bimagrumab is a fully human monoclonal antibody that blocks the activin type II receptors, preventing the activity of myostatin and other negative skeletal muscle regulators.
Objectives: To assess the effects of bimagrumab on skeletal muscle mass and function in patients with chronic obstructive pulmonary disease (COPD) and reduced skeletal muscle mass.
Methods: Sixty-seven patients with COPD (mean FEV, 1.
Toxicol Pathol
December 2016
1 Novartis Institutes for BioMedical Research, Cambridge, Massachusetts, USA.
Naphthoquine phosphate (NP) was considered as a partner drug with a promising antimalarial drug candidate. Here we report unexpected adverse clinical signs and microscopic findings in a canine pilot toxicology study with NP. Male and female dogs were dosed daily by oral gavage with NP at 2, 10, or 50 mg/kg/day for a maximum of 14 days.
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