Sara E. Miller

Identification of the orthopoxvirus p4c gene, which encodes a structural protein that directs intracellular mature virus particles into A-type inclusions.

Bioterrorism and electron microscopic differentiation of poxviruses from herpesviruses: dos and don'ts.

Microbial biofilms in the gut: visualization by electron microscopy and by acridine orange staining.

Risk factors for BK polyomavirus nephritis in renal allograft recipients.

Enterotoxigenic Escherichia coli vesicles target toxin delivery into mammalian cells.

Use of sentinel laboratories by clinicians to evaluate potential bioterrorism and emerging infections.

Transgenic mice expressing the myotilin T57I mutation unite the pathology associated with LGMD1A and MFM.

Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice.

Deletion of the protein kinase A/protein kinase G target SMTNL1 promotes an exercise-adapted phenotype in vascular smooth muscle.

Myotilin overexpression enhances myopathology in the LGMD1A mouse model.

Identification of a novel trimeric autotransporter adhesin in the cryptic genospecies of Haemophilus.

Induction of plasma (TRAIL), TNFR-2, Fas ligand, and plasma microparticles after human immunodeficiency virus type 1 (HIV-1) transmission: implications for HIV-1 vaccine design.

Norwalk virus: how infectious is it?

Impaired protein aggregate handling and clearance underlie the pathogenesis of p97/VCP-associated disease.

Kingella kingae expresses type IV pili that mediate adherence to respiratory epithelial and synovial cells.

Quantitation of selective autophagic protein aggregate degradation in vitro and in vivo using luciferase reporters.

Expression of Kingella kingae type IV pili is regulated by sigma54, PilS, and PilR.

The past, present, and future of comprehensive cancer control from the state and tribal perspective.

Modern uses of electron microscopy for detection of viruses.

Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease.

Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1.

Quantitation of selective autophagic protein aggregate degradation in vitro and in vivo using luciferase reporters.

Failure of population recovery in relation to disease in Pacific herring.

Quantitation of "autophagic flux" in mature skeletal muscle.

Public policy action and CCC implementation: benefits and hurdles.

Novel GNE mutations in two phenotypically distinct HIBM2 patients.

Report of a young girl with MYH9 mutation and review of the literature.