The Yeast vps Class E Mutants: The Beginning of the Molecular Genetic Analysis of Multivesicular Body Biogenesis

Por Coonrod, Emily M., Stevens, Tom H.
Publicado em 2010

The role of Fis1p–Mdv1p interactions in mitochondrial fission complex assembly

Por Karren, Mary Anne, Coonrod, Emily M., Anderson, Teresa K., Shaw, Janet M.
Publicado em 2005

Clinical analysis of genome next-generation sequencing data using the Omicia platform

Por Coonrod, Emily M, Margraf, Rebecca L, Russell, Archie, Voelkerding, Karl V, Reese, Martin G
Publicado em 2013

VarBin, a novel method for classifying true and false positive variants in NGS data

Por Durtschi, Jacob, Margraf, Rebecca L, Coonrod, Emily M, Mallempati, Kalyan C, Voelkerding, Karl V
Publicado em 2013

Condensation by DNA looping facilitates transfer of large DNA molecules into mammalian cells

Por Montigny, William J., Houchens, Christopher R., Illenye, Sharon, Gilbert, Jonathan, Coonrod, Emily, Chang, Young-Chae, Heintz, Nicholas H.
Publicado em 2001

Homotypic Vacuole Fusion in Yeast Requires Organelle Acidification and not the V-ATPase Membrane Domain

Por Coonrod, Emily M., Graham, Laurie A., Carpp, Lindsay N., Carr, Tom M., Stirrat, Laura, Bowers, Katherine, Bryant, Nia J., Stevens, Tom H.
Publicado em 2013

Arabidopsis Has Two Functional Orthologs of the Yeast V-ATPase Assembly Factor Vma21p

Por Neubert, Christoph, Graham, Laurie A., Black-Maier, Eric W., Coonrod, Emily M., Liu, Tzu-Yin, Stierhof, York-Dieter, Seidel, Thorsten, Stevens, Tom H., Schumacher, Karin
Publicado em 2008

Estimated disease incidence of RAG1/2 mutations: a case report and querying the Exome Aggregation Consortium

Por Kumánovics, Attila, Lee, Yu Nee, Close, Devin W., Coonrod, Emily M., Ujhazi, Boglarka, Chen, Karin, MacArthur, Daniel, Krivan, Gergely, Notarangelo, Luigi D., Walter, Jolan E.
Publicado no J Allergy Clin Immunol (2016)

A Novel Germline PIGA Mutation in Ferro-Cerebro-Cutaneous Syndrome: A Neurodegenerative X-Linked Epileptic Encephalopathy With Systemic Iron-Overload

Por Swoboda, Kathryn J., Margraf, Rebecca L., Carey, John C., Zhou, Holly, Newcomb, Tara M., Coonrod, Emily, Durtschi, Jacob, Mallempati, Kalyan, Kumanovics, Attila, Katz, Ben E., Voelkerding, Karl V., Opitz, John M.
Publicado no Am J Med Genet A (2013)

Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders

Por Buchbinder, David, Baker, Rebecca, Lee, Yu Nee, Ravell, Juan, Zhang, Yu, McElwee, Joshua, Nugent, Diane, Coonrod, Emily M., Durtschi, Jacob D., Augustine, Nancy H., Voelkerding, Karl V., Csomos, Krisztian, Rosen, Lindsey, Browne, Sarah, Walter, Jolan E., Notarangelo, Luigi D., Hill, Harry R., Kumánovics, Attila
Publicado no J Clin Immunol (2014)

Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency

Por Chen, Karin, Coonrod, Emily M., Kumánovics, Attila, Franks, Zechariah F., Durtschi, Jacob D., Margraf, Rebecca L., Wu, Wilfred, Heikal, Nahla M., Augustine, Nancy H., Ridge, Perry G., Hill, Harry R., Jorde, Lynn B., Weyrich, Andrew S., Zimmerman, Guy A., Gundlapalli, Adi V., Bohnsack, John F., Voelkerding, Karl V.
Publicado em 2013