Showing results (1-10 of 138) with videos related to
Sort By:
Pageof 14
Genesis (New York, N.Y. : 2000)|August 29, 2012
Strain-specific hyperkyphosis and megaesophagus in Add1 null miceRaymond F Robledo, Kevin L Seburn, Anthony Nicholson, et al.Nature Reviews. Genetics|December 19, 2006
The mouse as a model for human biology: a resource guide for complex trait analysisLuanne L Peters, Raymond F Robledo, Carol J Bult, et al.Blood|August 30, 2008
Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in miceRaymond F Robledo, Steven L Ciciotte, Babette Gwynn, et al.Blood Cells, Molecules & Diseases|December 19, 2020
Rasa3 regulates stage-specific cell cycle progression in murine erythropoiesisElena C Brindley, Julien Papoin, Lauren Kennedy, et al.British Journal of Haematology|June 22, 2011
Comparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in β-adducin null red cellsJason M Wooden, Greg L Finney, Eric Rynes, et al.Blood Cells, Molecules & Diseases|May 20, 2011
Comparative proteomics reveals deficiency of NHE-1 (Slc9a1) in RBCs from the beta-adducin knockout mouse model of hemolytic anemiaDiana M Gilligan, Greg L Finney, Eric Rynes, et al.Proceedings of the National Academy of Sciences of the United States of America|March 17, 2010
Targeted deletion of betaIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypesMichael C Stankewich, Babette Gwynn, Thomas Ardito, et al.Blood|January 9, 2010
Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cellsRaymond F Robledo, Amy J Lambert, Connie S Birkenmeier, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 12, 2006
Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunitMaria Traka, Kevin L Seburn, Brian PopkoScientific Reports|August 26, 2018
Mutant KLF1 in Adult Anemic Nan Mice Leads to Profound Transcriptome Changes and Disordered ErythropoiesisDanitza Nébor, Joel H Graber, Steven L Ciciotte, et al.Pageof 14