C. Birkenmeier

发表

Rh-RhAG/Ankyrin-R, a New Interaction Site between the Membrane Bilayer and the Red Cell Skeleton, Is Impaired by Rhnull-associated Mutation*

P. Gane, J. Cartron, Y. Colin, 2003, Journal of Biological Chemistry.

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

P. Low, K. Ritchie, M. Hughes, 2011, The Journal of Biological Chemistry.

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

P. Gane, J. Cartron, O. Bertrand, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins

C. Birkenmeier, J. Barker, 2004, The Journal of pathology.

The murine mutation jaundiced is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of beta-spectrin.

C. Birkenmeier, J. Barker, M. L. Bloom, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Fetal compensation of the hemolytic anemia in mice homozygous for the normoblastosis (nb) mutation.

L. Peters, C. Birkenmeier, J. Barker, 1992, Blood.

Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.

C. Birkenmeier, J. Barker, E. McFarland-Starr, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Murine erythrocyte ankyrin cDNA: highly conserved regions of the regulatory domain

Robert A. H. White, L. Peters, S. Lux, 2004, Mammalian Genome.

Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene.

N. Mohandas, N. Wandersee, C. Birkenmeier, 2000, The hematology journal : the official journal of the European Haematology Association.

Brain β spectrin isoform 235 (Spnb-2) maps to mouse Chromosome 11

Yupo Ma, W. Zimmer, S. Goodman, 2004, Mammalian Genome.

Changing patterns in cytoskeletal mRNA expression and protein synthesis during murine erythropoiesis in vivo.

R. White, L. Peters, S. Lux, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Remarkable homology among the internal repeats of erythroid and nonerythroid spectrin.

D. Helfman, S. Hughes, D. Bodine, 1985, Proceedings of the National Academy of Sciences of the United States of America.

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

R. Bloch, J. Ursitti, C. Birkenmeier, 2010, Journal of Cell Science.

Characterization of interferon messenger RNA synthesis in Namalva cells.

R. Friedman, K. Zoon, E. Chang, 1980, The Journal of biological chemistry.

Inhibition of intractable nucleases with ribonucleoside--vanadyl complexes: isolation of messenger ribonucleic acid from resting lymphocytes.

S. L. Berger, C. Birkenmeier, 1979, Biochemistry.

Metabolism of polyadenylated mRNA in growing human lymphocytes.

S. L. Berger, C. Birkenmeier, 1979, Biochimica et biophysica acta.

Distinct fetal Ank-1 and Ank-2 related proteins and mRNAs in normal and nb/nb mice

L. Peters, C. Birkenmeier, J. Barker, 1993 .

Distinct fetal Ank-1 and Ank-2 related proteins and mRNAs in normal and nb/nb mice.

L. Peters, C. Birkenmeier, J. Barker, 1993, Blood.

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

A. Lambert, R. Robledo, L. Peters, 2010, Blood.

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

E. Birkenmeier, C. Birkenmeier, J. Barker, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Zinc finger protein gene complexes on mouse chromosomes 8 and 11.

J. Nadeau, K. Chowdhury, C. Birkenmeier, 1990, Genomics.

Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice

R. Bronson, E. Otto, R. White, 1991, The Journal of cell biology.

Normoblastosis, a murine model for ankyrin-deficient hemolytic anemia, is caused by a hypomorphic mutation in the erythroid ankyrin gene Ank1.

C. Birkenmeier, J. Barker, E. Gifford, 2003, The hematology journal : the official journal of the European Haematology Association.

Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton.

D. Bodine, N. Mohandas, N. Wandersee, 2003, Blood.

skeleton protein levels and spectrin incorporation into the red blood cell membrane-spectrin gene alter spectrin mRNA and α Mutations in the murine erythroid

D. Bodine, N. Wandersee, C. Birkenmeier, 2002 .

Spectrin deficient inherited hemolytic anemias in the mouse: Characterization by spectrin synthesis and mRNA activity in reticulocytes

D. Bodine, C. Birkenmeier, J. Barker, 1984, Cell.

Complete nucleotide sequence of the murine erythroid beta-spectrin cDNA and tissue-specific expression in normal and jaundiced mice.

C. Birkenmeier, J. Barker, M. L. Bloom, 1993, Blood.

An alternative first exon in the distal end of the erythroid ankyrin gene leads to production of a small isoform containing an NH2-terminal membrane anchor.

J. J. Sharp, C. Birkenmeier, J. Barker, 1998, Genomics.

the normoblastosis (nb) mutation Fetal compensation of the hemolytic anemia in mice homozygous for

L. Peters, C. Birkenmeier, J. Barker, 2011 .

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

J. J. Sharp, Daixing Zhou, R. Bloch, 1997, Journal of Cell Biology.

Complex patterns of sequence variation and multiple 5' and 3' ends are found among transcripts of the erythroid ankyrin gene.

E. Hall, R. White, L. Peters, 1993, The Journal of biological chemistry.

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, S. Lux, C. Birkenmeier, 1990, Proceedings of the National Academy of Sciences of the United States of America.

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

A. Flenniken, J. Rossant, M. Minden, 2011, Experimental hematology.

Urogenital syndrome (us): a developmental mutation on Chromosome 2 of the mouse

P. Lane, C. Birkenmeier, 1993, Mammalian Genome.

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

J. J. Sharp, Daixing Zhou, R. Bloch, 1997, The Journal of cell biology.

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

E. Birkenmeier, C. Birkenmeier, J. Barker, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Preparation of interferon messenger RNAs with the use of ribonucleoside--vanadyl complexes.

S. L. Berger, G. Siegal, C. Birkenmeier, 1981, Methods in enzymology.