Triadopathies: An Emerging Class of Skeletal Muscle Diseases

Por Dowling, James J., Lawlor, Michael W., Dirksen, Robert T.
Publicado no Neurotherapeutics (2014)

USE OF NEUTRON ACTIVATION ANALYSIS FOR STUDYING STABLE IODIDE UPTAKE BY THE THYROID

Por Wagner, Henry N., Nelp, Wil B., Dowling, James H.
Publicado em 1961

Membrane Traffic and Muscle: Lessons from Human Disease

Por Dowling, James J., Gibbs, Elizabeth M., Feldman, Eva L.
Publicado em 2008

Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies

Por Gibbs, Elizabeth M., Horstick, Eric J., Dowling, James J
Publicado em 2013

Phosphoinositide Regulation of Integrin Trafficking Required for Muscle Attachment and Maintenance

Por Ribeiro, Inês, Yuan, Lin, Tanentzapf, Guy, Dowling, James J., Kiger, Amy
Publicado em 2011

Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye

Por Smith, Sarah J., Horstick, Eric J., Davidson, Ann E., Dowling, James
Publicado no J Vis Exp (2015)

Force Measurement During Contraction to Assess Muscle Function in Zebrafish Larvae

Por Sloboda, Darcée D., Claflin, Dennis R., Dowling, James J., Brooks, Susan V.
Publicado em 2013

Congenital Myopathies: An Update

Por Nance, Jessica R., Dowling, James J., Gibbs, Elizabeth M., Bönnemann, Carsten G.
Publicado no Curr Neurol Neurosci Rep (2012)

A novel early onset phenotype in a zebrafish model of merosin deficient congenital muscular dystrophy

Por Smith, Sarah J., Wang, Jeffrey C., Gupta, Vandana A., Dowling, James J.
Publicado no PLoS One (2017)

Kindlin-2 is required for myocyte elongation and is essential for myogenesis

Por Golden Jeffrey, Kim Susie, Vreede Andrew P, Dowling James J, Feldman Eva L
Publicado em 2008-07-01

Kindlin-2 is required for myocyte elongation and is essential for myogenesis

Por Dowling, James J, Vreede, Andrew P, Kim, Susie, Golden, Jeffrey, Feldman, Eva L
Publicado em 2008

A novel intronic mutation in MTM1 detected by RNA analysis in a case of X-linked myotubular myopathy

Por Al-Hashim, Aqeela, Gonorazky, Hernan D., Amburgey, Kimberly, Das, Soma, Dowling, James J.
Publicado no Neurol Genet (2017)

CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1

Por Ward, Amanda J., Rimer, Mendell, Killian, James M., Dowling, James J., Cooper, Thomas A.
Publicado em 2010

neb: a zebrafish model of nemaline myopathy due to nebulin mutation

Por Telfer, William R., Nelson, Darcee D., Waugh, Trent, Brooks, Susan V., Dowling, James J.
Publicado em 2012

Analysis of Embryonic and Larval Zebrafish Skeletal Myofibers from Dissociated Preparations

Por Horstick, Eric J., Gibbs, Elizabeth M., Li, Xingli, Davidson, Ann E., Dowling, James J.
Publicado em 2013

The myopathy-causing mutation DNM2-S619L leads to defective tubulation in vitro and in developing zebrafish

Por Gibbs, Elizabeth M., Davidson, Ann E., Telfer, William R., Feldman, Eva L., Dowling, James J.
Publicado em 2014

Membrane-myofibril cross-talk in myofibrillogenesis and in muscular dystrophy pathogenesis: lessons from the zebrafish

Por Raeker, Maide Ö., Shavit, Jordan A., Dowling, James J., Michele, Daniel E., Russell, Mark W.
Publicado em 2014

A novel approach to study motor neurons from zebrafish embryos and larvae in culture

Por Sakowski, Stacey A., Lunn, J. Simon, Busta, Angela S., Palmer, Madeline, Dowling, James J., Feldman, Eva L.
Publicado em 2012

Transcriptional changes and developmental abnormalities in a zebrafish model of myotonic dystrophy type 1

Por Todd, Peter K., Ackall, Feras Y., Hur, Junguk, Sharma, Kush, Paulson, Henry L., Dowling, James J.
Publicado em 2014

Fluoxetine prevents dystrophic changes in a zebrafish model of Duchenne muscular dystrophy

Por Waugh, Trent A., Horstick, Eric, Hur, Junguk, Jackson, Samuel W., Davidson, Ann E., Li, Xingli, Dowling, James J.
Publicado em 2014