Mutations in a NIMA-related kinase gene, Nek1, cause pleiotropic effects including a progressive polycystic kidney disease in mice

Por Upadhya, Poornima, Birkenmeier, Edward H., Birkenmeier, Connie S., Barker, Jane E.
Publicado em 2000

Human Rhesus-associated glycoprotein mediates facilitated transport of NH(3) into red blood cells

Por Ripoche, Pierre, Bertrand, Olivier, Gane, Pierre, Birkenmeier, Connie, Colin, Yves, Cartron, Jean-Pierre
Publicado em 2004

Small, Membrane-bound, Alternatively Spliced Forms of Ankyrin 1 Associated with the Sarcoplasmic Reticulum of Mammalian Skeletal Muscle

Por Zhou, Daixing, Birkenmeier, Connie S., Williams, McRae W., Sharp, John J., Barker, Jane E., Bloch, Robert J.
Publicado em 1997

Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in α-spectrin–deficient red cells

Por Robledo, Raymond F., Lambert, Amy J., Birkenmeier, Connie S., Cirlan, Marius V., Cirlan, Andreea Flavia M., Campagna, Dean R., Lux, Samuel E., Peters, Luanne L.
Publicado em 2010

Analysis of the Mobilities of Band 3 Populations Associated with Ankyrin Protein and Junctional Complexes in Intact Murine Erythrocytes

Por Kodippili, Gayani C., Spector, Jeff, Hale, Jacob, Giger, Katie, Hughes, Michael R., McNagny, Kelly M., Birkenmeier, Connie, Peters, Luanne, Ritchie, Ken, Low, Philip S.
Publicado em 2012

A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis

Por Hughes, Michael R., Anderson, Nicole, Maltby, Steven, Wong, Justin, Berberovic, Zorana, Birkenmeier, Connie S., Haddon, D. James, Garcha, Kamal, Flenniken, Ann, Osborne, Lucy R., Adamson, S. Lee, Rossant, Janet, Peters, Luanne L., Minden, Mark D., Paulson, Robert F., Wang, Chen, Barber, Dwayne L., McNagny, Kelly M., Stanford, William L.
Publicado em 2010