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C. Birkenmeier · SciRah

Researcher profile · Semantic Scholar

C. Birkenmeier

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C. Birkenmeier — researcher profile on SciRah

h-index: 14
Works: 24
Citations: 1,149

Most-cited papers

Mutations in a NIMA-related kinase gene, Nek1, cause pleiotropic effects including a progressive polycystic kidney disease in mice.
P. Upadhya, E. Birkenmeier, C. Birkenmeier, J. Barker
2000Proceedings of the National Academy of Sciences of the United States of America188 citations Open access
Semantic Scholar
Human Rhesus-associated glycoprotein mediates facilitated transport of NH(3) into red blood cells.
P. Ripoche, O. Bertrand, P. Gane, C. Birkenmeier +2 more
2004Proceedings of the National Academy of Sciences of the United States of America162 citations Open access
Semantic Scholar
Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes.
D. Bodine, C. Birkenmeier, J. Barker
1984Cell157 citations
Semantic Scholar
Rh-RhAG/Ankyrin-R, a New Interaction Site between the Membrane Bilayer and the Red Cell Skeleton, Is Impaired by Rhnull-associated Mutation*
V. Nicolas, C. Le Van Kim, P. Gane, C. Birkenmeier +3 more
2003Journal of Biological Chemistry120 citations Open access
Semantic Scholar
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice
Luanne L. Peters, C. Birkenmeier, Roderick T. Bronson, Robert A. White +5 more
1991Journal of Cell Biology95 citations Open access
Semantic Scholar
Small, Membrane-bound, Alternatively Spliced Forms of Ankyrin 1 Associated with the Sarcoplasmic Reticulum of Mammalian Skeletal Muscle
Daixing Zhou, C. Birkenmeier, Mcrae W. Williams, J. Sharp +2 more
1997Journal of Cell Biology93 citations Open access
Semantic Scholar
Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin.
R. White, C. Birkenmeier, S. E. Lux, Jane E. Barker
1990Proceedings of the National Academy of Sciences of the United States of America68 citations Open access
Semantic Scholar
Na,K-ATPase in skeletal muscle: two populations of β-spectrin control localization in the sarcolemma but not partitioning between the sarcolemma and the transverse tubules
Mcrae W. Williams, W. G. Resneck, T. Kaysser, J. Ursitti +3 more
2010Journal of Cell Science45 citations Open access
Semantic Scholar
Analysis of the Mobilities of Band 3 Populations Associated with Ankyrin Protein and Junctional Complexes in Intact Murine Erythrocytes*
G. Kodippili, Jeffrey O. Spector, Jacob Hale, Katie M Giger +6 more
2011Journal of Biological Chemistry41 citations Open access
Semantic Scholar
Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibers.
E. Giacomello, Marco Quarta, Cecilia Paolini, R. Squecco +11 more
2015American Journal of Physiology - Cell Physiology36 citations
Semantic Scholar
Changing patterns in cytoskeletal mRNA expression and protein synthesis during murine erythropoiesis in vivo.
Luanne L. Peters, R. White, C. Birkenmeier, M. Bloom +2 more
1992Proceedings of the National Academy of Sciences of the United States of America33 citations Open access
Semantic Scholar
A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis
M. Hughes, Nicole Anderson, S. Maltby, J. Wong +15 more
2010Experimental Hematology30 citations Open access
Semantic Scholar
Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton.
N. Wandersee, C. Birkenmeier, D. Bodine, N. Mohandas +1 more
2003Blood25 citations
Semantic Scholar
Normoblastosis, a murine model for ankyrin-deficient hemolytic anemia, is caused by a hypomorphic mutation in the erythroid ankyrin gene Ank1.
C. Birkenmeier, Elaine J. Gifford, J. Barker
2003The Hematology Journal18 citations
Semantic Scholar
Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells.
R. F. Robledo, A. Lambert, C. Birkenmeier, Marius V Cirlan +4 more
2010Blood14 citations Open access
Semantic Scholar
Urogenital syndrome (us): a developmental mutation on Chromosome 2 of the mouse
P. Lane, C. Birkenmeier
1993Mammalian Genome11 citations
Semantic Scholar
Murine erythrocyte ankyrin cDNA: highly conserved regions of the regulatory domain
Robert A. H. White, C. Birkenmeier, Luanne L. Peters, J. Barker +1 more
2004Mammalian Genome8 citations
Semantic Scholar
Analysis of the mobilities of band 3 populations associated with the ankyrin and junctional complexes in intact murine erythrocytes
G. Kodippili, Jeffrey O. Spector, Jacob Hale, Katie M Giger +7 more
20112 citations
Semantic Scholar
The C-Terminus of Alpha Spectrin Binds Protein 4.2 and Is Necessary for Optimal Spectrin-Actin Binding.
C. Korsgren, C. Birkenmeier, J. Barker, Luanne L. Peters +1 more
20051 citations
Semantic Scholar
Brain β spectrin isoform 235 (Spnb-2) maps to mouse Chromosome 11
M. Bloom, Barbara K. Lee, C. Birkenmeier, Yu-Po Ma +4 more
2004Mammalian Genome1 citations
Semantic Scholar
STUDIES ON mRNA IN RESTING AND GROWING LYMPHOCYTES
S. L. Berger, C. Birkenmeier
19791 citations
Semantic Scholar
the normoblastosis (nb) mutation Fetal compensation of the hemolytic anemia in mice homozygous for
Luanne L. Peters, C. Birkenmeier, J. Barker
20110 citations
Semantic Scholar
skeleton protein levels and spectrin incorporation into the red blood cell membrane-spectrin gene alter spectrin mRNA and α Mutations in the murine erythroid
N. Wandersee, C. Birkenmeier, D. Bodine, M. Narla +1 more
20020 citations
Semantic Scholar
Brain beta spectrin isoform 235 (Spnb-2) maps to mouse chromosome 11.
M. Bloom, B. K. Lee, C. Birkenmeier, Y. Ma +4 more
1992Mammalian Genome0 citations
Semantic Scholar

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