K. John

发表

Analysis of the ternary interaction of the red cell membrane skeletal proteins spectrin, actin, and 4.1.

V. Ohanian, W. Gratzer, L. Wolfe, 1984, Biochemistry.

Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins

Samuel E. Lux, Vann Bennett, V. Bennett, 1990, Nature.

A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles.

Yeang H. Ch'ng, P. Devarajan, L. Peters, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1).

H. Lodish, R. Kopito, K. John, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Anion Exchanger 1 (Band 3) Is Required to Prevent Erythrocyte Membrane Surface Loss but Not to Form the Membrane Skeleton

S. Orkin, R. Shivdasani, S. Alper, 1996, Cell.

Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice.

D. Golan, C. Brugnara, N. Mohandas, 1999, The Journal of clinical investigation.

A New Spectrin, βIV, Has a Major Truncated Isoform That Associates with Promyelocytic Leukemia Protein Nuclear Bodies and the Nuclear Matrix*

A. Kung, O. Jin, L. Peters, 2001, The Journal of Biological Chemistry.

Irreversible deformation of the spectrin-actin lattice in irreversibly sickled cells.

M. Karnovsky, K. John, S. Lux, 1976, The Journal of clinical investigation.

Amino acid sequence of human apoLp-Gln-II (apoA-II), an apolipoprotein isolated from the high-density lipoprotein complex.

H. Brewer, K. John, S. Lux, 1972, Proceedings of the National Academy of Sciences of the United States of America.

Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S.

D. Vandorpe, D. E. Bauer, S. Alper, 2011, American journal of physiology. Cell physiology.

Cloning and characterization of band 3 , the human erythrocyte anion-exchange protein ( AE 1 ) ( anion antiporter / DNA cloning / erythrocyte membrane )

K. John, S. Lux, Harvey F. LODISHt, 2022 .

Identification of the lipid-binding cyanogen bromide fragment from the cystine-containing high density apolipoprotein, APOLP-GLN-II.

A. Gotto, S. Fleischer, R. Jackson, 1972, Biochemical and biophysical research communications.

Isolation and characterization of the tryptic and cyanogen bromide peptides of apoLp-Gln-II (apoA-II), plasma high density apolipoprotein.

H. Brewer, K. John, S. Lux, 1972, The Journal of biological chemistry.

THE ROLE OF SPECTRIN AND ACTIN IN IRREVERSIBLY SICKLED CELLS: UNSICKLING OF “IRREVERSIBLY” SICKLED GHOSTS BY CONDITIONS WHICH INTERFERE WITH SPECTRIN-ACTIN POLYMERIZATION

K. John, S. Lux, 1978 .

Isolation and partial characterization of a high molecular weight red cell membrane protein complex normally removed by the spleen.

K. John, S. Lux, 1977, Blood.

A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.

L. Wolfe, K. John, S. Lux, 1982, The New England journal of medicine.

Diminished spectrin extraction from ATP-depleted human erythrocytes. Evidence relating spectrin to changes in erythrocyte shape and deformability.

K. John, S. Lux, T. Ukena, 1978, The Journal of clinical investigation.

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

F. Collins, D. Ward, U. Francke, 1990, Nature.

Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.

K. John, S. Lux, M. Tomaselli, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain

A. Otsuka, L. Peters, S E Lux, 1995, The Journal of cell biology.

Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis.

O. Shalev, K. John, S. Lux, 1993, Blood.

Hemolytic anemias associated with deficient or dysfunctional spectrin.

K. John, S. Lux, M. Tomaselli, 1979, Progress in clinical and biological research.

Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.

P. Agre, F. Costa, P. Watkins, 1990, The New England journal of medicine.

Isolation and characterization of apoLp-Gln-II (apoA-II), a plasma high density apolipoprotein containing two identical polypeptide chains.

H. Brewer, K. John, S. Lux, 1972, The Journal of biological chemistry.

Further characterization of the polymorphic forms of a human high density apolipoprotein, apoLP-Gln-I (apoA-I).

K. John, S. Lux, 1972, Biochimica et biophysica acta.

Diminished Spectrin Extraction from ATP-Depleted

K. John, E. Lux, T. Ukena, 1978 .