J. Chasis

发表

Erythrocyte membrane deformability and stability: two distinct membrane properties that are independently regulated by skeletal protein associations

N. Mohandas, J. Chasis, N Mohandas, 1986, The Journal of cell biology.

The influence of membrane skeleton on red cell deformability, membrane material properties, and shape.

S B Shohet, N. Mohandas, S. Shohet, 1983, Seminars in hematology.

Cooperative action between band 3 and glycophorin A in human erythrocytes: immobilization of band 3 induced by antibodies to glycophorin A.

D. W. Knowles, D. Knowles, E. Evans, 1994, Biophysical journal.

Identification of a functional role for human erythrocyte sialoglycoproteins beta and gamma.

N. Mohandas, M. Reid, J. Chasis, 1987, Blood.

Molecular and Functional Characterization of Protein 4.1B, a Novel Member of the Protein 4.1 Family with High Level, Focal Expression in Brain*

J. A. Gimm, S. Snyder, J. Conboy, 2000, The Journal of Biological Chemistry.

Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities.

J. Conboy, V. Afzal, B. Coller, 1999, The Journal of clinical investigation.

Deciphering the nuclear import pathway for the cytoskeletal red cell protein 4.1R.

J. Conboy, P. Gascard, L. Walensky, 1999, Molecular biology of the cell.

Differential use of protein 4.1 translation initiation sites during erythropoiesis: implications for a mutation-induced stage-specific deficiency of protein 4.1 during erythroid development.

J. Conboy, N. Mohandas, L. Coulombel, 1996, Blood.

Tissue- and development-specific alternative RNA splicing regulates expression of multiple isoforms of erythroid membrane protein 4.1.

J. Conboy, Y. Kan, N. Mohandas, 1991, The Journal of biological chemistry.

Structural protein 4.1 is located in mammalian centrosomes.

N. Mohandas, G. Krockmalnic, S. Penman, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Glycophorin A dimerization and band 3 interaction during erythroid membrane biogenesis: in vivo studies in human glycophorin A transgenic mice.

C. Huang, N. Mohandas, J. Chasis, 2001, Blood.

Relationship of the human erythrocyte Wrb antigen to an interaction between glycophorin A and band 3.

M. Telen, J. Chasis, M. Telen, 1990, Blood.

Immunofluorescent identification of human megakaryocyte colonies using an antiplatelet glycoprotein antiserum.

R. Hoffman, S. Marchesi, J. Chasis, 1981, Blood.

An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.

J. Conboy, Y. Kan, N. Mohandas, 1993, The Journal of clinical investigation.

Red blood cell deformability, membrane material properties and shape: regulation by transmembrane, skeletal and cytosolic proteins and lipids.

N. Mohandas, J. Chasis, J. Chasis, 1993, Seminars in hematology.

Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3.

D. W. Knowles, J. Conboy, D. Knowles, 1992, The Journal of clinical investigation.

Differentiation-associated switches in protein 4.1 expression. Synthesis of multiple structural isoforms during normal human erythropoiesis.

J. Conboy, Y. Kan, N. Mohandas, 1993, The Journal of clinical investigation.

Red blood cell glycophorins.

N. Mohandas, J. Chasis, J. Chasis, 1992, Blood.

Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.

P. Agre, N. Mohandas, J. Chasis, 1988, The Journal of clinical investigation.

Characterization of multiple isoforms of protein 4.1R expressed during erythroid terminal differentiation.

J. Conboy, P. Gascard, N. Mohandas, 1998, Blood.

between glycophorin A and band 3 Relationship of the human erythrocyte Wrb antigen to an interaction

J. Chasis, M. Telen, 2011 .

Isolation of human platelet glycoproteins.

J. Chasis, S. Marchesi, J. Chasis, 1979, Biochimica et biophysica acta.

Erythrocyte membrane vesiculation: model for the molecular mechanism of protein sorting.

D. W. Knowles, D. Knowles, L. Tilley, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Common structural polymorphisms in human erythrocyte spectrin.

V. Marchesi, S. Marchesi, J. Chasis, 1984, The Journal of clinical investigation.

Identification of a functional role for human erythrocyte sialoglycoproteins beta and gamma.

N. Mohandas, M. Reid, J. Chasis, 1987, Blood.

Erythrocyte membrane rigidity induced by glycophorin A-ligand interaction. Evidence for a ligand-induced association between glycophorin A and skeletal proteins.

N. Mohandas, S. Shohet, J. Chasis, 1985, The Journal of clinical investigation.

Inhibition of malarial parasite invasion by monoclonal antibodies against glycophorin A correlates with reduction in red cell membrane deformability.

M. Tanner, N. Mohandas, D. Anstee, 1989, Blood.

Signal transduction by glycophorin A: role of extracellular and cytoplasmic domains in a modulatable process

N. Mohandas, M. Reid, R. Jensen, 1988, The Journal of cell biology.

The FERM domain: A unique module involved in the linkage of cytoplasmic proteins to the membrane

S. C. Liu, P. Bryant, P. Low, 1998 .

Membrane assembly and remodeling during reticulocyte maturation.

N. Mohandas, J. Chasis, J. Chasis, 1989, Blood.