Resources

Last Thursday of the month

5:30 – 6:30 pm
Biology Department conference room, Olsen Hall


2018

Gage Lab – April 26th, 5:30 to 6:30 pm

Myopathies encompass a wide variety of acquired and hereditary disorders.

Presented by Chris Tsiros

The pathomechanisms include structural and functional changes affecting, e.g., myofiber metabolism and contractile properties. In this study, we observed increased passive tension (PT) of skinned myofibers from patients with myofibrillar myopathy (MFM) caused by FLNC mutations (MFM-filaminopathy) and limb-girdle muscular dystrophy type-2A due to CAPN3 mutations (LGMD2A), compared to healthy control myofibers.

      1. Article (PDF)

Moore LabJanuary 30, 2018

Thick Filament in vitro motility

      1. Article (PDF)

2016

Rishel Vohnoutka

Serine 493: The modulation site of Neurofilament Heavy Chain conformation and function within the neuron?

      1. Articles

 

Nugent Lab

Heparan sulfate and heparin interactions with proteins by Divya Tsiros

      1. Articles

Giles Lab

Terahertz Imaging by Dr. Giles and Dr. Joseph

    1. Articles

Moore Lab

Optical Trapping and Myosin Mechanochemistry

      1. Article
      2. Supplement

2015

Gage Lab

Exploring the Role of the Intrinscially Disordered Region of Soluble Guanylyl Cyclase

      1. Articles
      2. PowerPoint Slides

Nugent Lab

Modification of fibronectin structure to regulate function

      1. Article
      2. Background

Gage Lab

Models for Titin’s Role in Active Muscle

      1. Articles

Moore Lab

Expansion Microscopy