His primary areas of study are Cell biology, Biochemistry, Membrane-associated guanylate kinase, PDZ domain and Molecular biology. He interconnects Calpain, Membrane protein and Gene isoform in the investigation of issues within Cell biology. Biochemistry is represented through his Glycophorin, Glycophorin C, Peptide sequence, Protein primary structure and Red blood cell research.
Athar H. Chishti has researched Peptide sequence in several fields, including Receptor clustering and Peptide. His Membrane-associated guanylate kinase course of study focuses on Binding site and Fusion protein. His Molecular biology research includes themes of Tyrosine, In vitro, Recombinant DNA, Receptor and Signal transduction.
His main research concerns Cell biology, Molecular biology, Biochemistry, Calpain and Plasmodium falciparum. His Cell biology study combines topics from a wide range of disciplines, such as Cytoskeleton, Spectrin and Membrane protein. His Molecular biology research incorporates elements of Tyrosine, Peptide sequence, Gene, PDZ domain and Glycophorin.
His research investigates the connection between Peptide sequence and topics such as Membrane-associated guanylate kinase that intersect with problems in SH3 domain. His Calpain research is multidisciplinary, relying on both Platelet, Internal medicine, Immunology and Endocrinology. Athar H. Chishti combines subjects such as Receptor, Band 3, Phage display and Virology with his study of Plasmodium falciparum.
Athar H. Chishti mainly focuses on Cell biology, Calpain, Immunology, Plasmodium falciparum and Platelet. His Cell biology research incorporates themes from Cytoskeleton, Spectrin, Band 3 and Biochemistry. His study in Calpain is interdisciplinary in nature, drawing from both Humanized mouse, Molecular biology, Disease and Transgene.
His Immunology study incorporates themes from Endocrinology, Macrophage and Internal medicine. The various areas that he examines in his Plasmodium falciparum study include Heat shock protein, Signal peptide peptidase, Virology, Receptor and Epitope. His research investigates the connection between Platelet and topics such as Whole blood that intersect with issues in Clot retraction.
His primary scientific interests are in Cell biology, Calpain, Disease, Cytoskeleton and Phenotype. His biological study spans a wide range of topics, including Band 3, Membrane protein, Biochemistry and Plasmodium falciparum. His Calpain study integrates concerns from other disciplines, such as Mast cell, Tumor necrosis factor alpha, Cytokine, Calcium flux and MAPK/ERK pathway.
The Disease study combines topics in areas such as Cell, Cleavage, Cysteine protease, Humanized mouse and Gene isoform. His work carried out in the field of Cytoskeleton brings together such families of science as Erythropoiesis, Actin, Protein kinase A and Peripheral membrane protein. His Phenotype research is multidisciplinary, incorporating perspectives in Proteases, Cancer research and Model organism.
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Recognition of unique carboxyl-terminal motifs by distinct PDZ domains
Z. Songyang;A. S. Fanning;C. Fu;J. Xu.
The FERM domain: A unique module involved in the linkage of cytoplasmic proteins to the membrane
Athar H. Chishti;Anthony C. Kim;Shirin M. Marfatia;Mohini Lutchman.
Trends in Biochemical Sciences (1998)
Cloning and characterization of hdlg: the human homologue of the Drosophila discs large tumor suppressor binds to protein 4.1
Robert A. Lue;Shirin M. Marfatia;Daniel Branton;Athar H. Chishti.
Proceedings of the National Academy of Sciences of the United States of America (1994)
Human CASK/LIN-2 Binds Syndecan-2 and Protein 4.1 and Localizes to the Basolateral Membrane of Epithelial Cells
Alexandra R. Cohen;Daniel F. Wood;Shirin M. Marfatia;Zenta Walther.
Journal of Cell Biology (1998)
Crystal structure of a PDZ domain
João H. Morais Cabral;Carlo Petosa;Michael J. Sutcliffe;Sami Raza.
Disruption of the Mouse μ-Calpain Gene Reveals an Essential Role in Platelet Function
Mohammad Azam;Shaida S. Andrabi;Kenneth E. Sahr;Lakshmi Kamath.
Molecular and Cellular Biology (2001)
μ-Calpain is essential for postmortem proteolysis of muscle proteins,
G. H. Geesink;S. Kuchay;A. H. Chishti;M. Koohmaraie.
Journal of Animal Science (2006)
Identification of the Protein 4.1 Binding Interface on Glycophorin C and p55, a Homologue of the Drosophila discs-large Tumor Suppressor Protein
Shirin M. Marfatia;Robert A. Lue;Daniel Branton;Athar H. Chishti.
Journal of Biological Chemistry (1995)
Band 3 is a host receptor binding merozoite surface protein 1 during the Plasmodium falciparum invasion of erythrocytes.
Vikas K. Goel;Xuerong Li;Huiqing Chen;Shih-Chun Liu.
Proceedings of the National Academy of Sciences of the United States of America (2003)
Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton
Christopher D. Southgate;Athar H. Chishti;Betsy Mitchell;Scott J. Yi.
Nature Genetics (1996)
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