Gap Junctions Couple Astrocytes and Oligodendrocytes

Por Orthmann-Murphy, Jennifer L., Abrams, Charles K., Scherer, Steven S.
Publicado em 2008

Loss-of-function connexin47 mutations cause Pelizaeus-Merzbacher-like disease

Por Orthmann-Murphy, Jennifer L., Enriquez, Alan D., Abrams, Charles K., Scherer, Steven S.
Publicado em 2007

Service to Others in Sobriety (SOS)

Por Pagano, Maria E., Krentzman, Amy R., Onder, Casey C., Baryak, Justina L., Murphy, Jennifer L., Zywiak, William H., Stout, Robert L.
Publicado em 2010

Pain Psychology: A Global Needs Assessment and National Call to Action

Por Darnall, Beth D., Scheman, Judith, Davin, Sara, Burns, John W., Murphy, Jennifer L., Wilson, Anna C., Kerns, Robert D., Mackey, Sean C.
Publicado no Pain Med (2016)

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

Por Orthmann-Murphy, Jennifer L., Salsano, Ettore, Abrams, Charles K., Bizzi, Alberto, Uziel, Graziella, Freidin, Mona M., Lamantea, Eleonora, Zeviani, Massimo, Scherer, Steven S., Pareyson, Davide
Publicado em 2009

A Cluster Randomized Controlled Evaluation of the Health Impact of a Novel Antimicrobial Hand Towel on the Health of Children Under 2 Years Old in Rural Communities in Nyanza Provi...

Por Slayton, Rachel B., Murphy, Jennifer L., Morris, Jamae, Faith, Sitnah Hamidah, Oremo, Jared, Odhiambo, Aloyce, Ayers, Tracy, Feinman, Shawna J., Brown, Allison C., Quick, Robert E.
Publicado no Am J Trop Med Hyg (2016)

Microbes in Pool Filter Backwash as Evidence of the Need for Improved Swimmer Hygiene — Metro-Atlanta, Georgia, 2012

Por Hutcheson,, Christopher, Cira, Ryan, Gaines, Stanley L., Jones, Kevin R., Howard, Walter, Hornsby, David, Redmond, Maurice, Rustin, Chris, Hlavsa, Michele C., Murphy, Jennifer L., Narayanan, Jothikumar, Miller, Candace D., Cantrell, Brittany, Hill, Vincent R., Beach, Michael J.
Publicado no MMWR Morb Mortal Wkly Rep (2013)

Chinese hamster ovary cells can produce galactose-α-1,3-galactose antigens on proteins

Por Bosques, Carlos J, Collins, Brian E, Meador, James W, Sarvaiya, Hetal, Murphy, Jennifer L, DelloRusso, Guy, Bulik, Dorota A, Hsu, I-Hsuan, Washburn, Nathaniel, Sipsey, Sandra F, Myette, James R, Raman, Rahul, Shriver, Zachary, Sasisekharan, Ram, Venkataraman, Ganesh
Publicado em 2010

Loss-of-Function Alanyl-tRNA Synthetase Mutations Cause an Autosomal-Recessive Early-Onset Epileptic Encephalopathy with Persistent Myelination Defect

Por Simons, Cas, Griffin, Laurie B., Helman, Guy, Golas, Gretchen, Pizzino, Amy, Bloom, Miriam, Murphy, Jennifer L.P., Crawford, Joanna, Evans, Sarah H., Topper, Scott, Whitehead, Matthew T., Schreiber, John M., Chapman, Kimberly A., Tifft, Cyndi, Lu, Katrina B., Gamper, Howard, Shigematsu, Megumi, Taft, Ryan J., Antonellis, Anthony, Hou, Ya-Ming, Vanderver, Adeline
Publicado no Am J Hum Genet (2015)