J. Justin Hsuan mostly deals with Biochemistry, Molecular biology, Complementary DNA, Proto-oncogene tyrosine-protein kinase Src and Receptor. His work in Peptide sequence, Phosphatidylinositol, Kinase, Receptor tyrosine kinase and Binding protein is related to Biochemistry. His research in Peptide sequence intersects with topics in Deamination and Recombinant DNA.
The concepts of his Molecular biology study are interwoven with issues in RNA, RNA-binding protein, Internal ribosome entry site and Gene product. His Proto-oncogene tyrosine-protein kinase Src research incorporates elements of Tyrosine kinase and NADPH oxidase. His study in Receptor is interdisciplinary in nature, drawing from both Plasma protein binding and Binding site.
The scientist’s investigation covers issues in Biochemistry, Cell biology, Molecular biology, Phosphatidylinositol and Peptide sequence. His Biochemistry study is mostly concerned with Complementary DNA, Phospholipase C, Phosphorylation, Amino acid and Tyrosine kinase. His work in the fields of Cell biology, such as Signal transduction, overlaps with other areas such as Phosphatidylinositol transfer protein.
J. Justin Hsuan usually deals with Molecular biology and limits it to topics linked to Cell culture and Proteome. His research integrates issues of Inositol, Endoplasmic reticulum and Kinase activity in his study of Phosphatidylinositol. His study on Conserved sequence is often connected to Actin-Related Protein 2-3 Complex, Lamellipodium and Actin-Related Protein 3 as part of broader study in Peptide sequence.
J. Justin Hsuan focuses on Phosphatidylinositol, Kinase, Cell biology, Molecular biology and Biochemistry. Many of his studies involve connections with topics such as Caveolae and Phosphatidylinositol. J. Justin Hsuan interconnects splice, Gene, Locus, Exon and Phosphorylation in the investigation of issues within Kinase.
His Molecular biology research is multidisciplinary, incorporating perspectives in Blood proteins, Proteome, Cell culture and Haptoglobin. His research combines Alpha and Biochemistry. His work in the fields of Signal transduction, such as Kinase activity, intersects with other areas such as Neurodegeneration.
His primary areas of investigation include Cell biology, Phosphatidylinositol, Phosphatidylinositol 4-phosphate, Kinase and Signal transduction. His work carried out in the field of Cell biology brings together such families of science as Cell fractionation and Membrane. J. Justin Hsuan has researched Phosphatidylinositol in several fields, including Lipid raft and Hereditary spastic paraplegia.
His research in Phosphatidylinositol 4-phosphate intersects with topics in Transport protein, Fluorescence recovery after photobleaching, Cell membrane, Apical membrane and Membrane glycoproteins. Kinase is the subject of his research, which falls under Biochemistry. His biological study spans a wide range of topics, including Molecular biology, Gene knockdown and Phosphorylation.
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Interleukin-1 activates a novel protein kinase cascade that results in the phosphorylation of hsp27
Norman W. Freshney;Lesley Rawlinson;François Guesdon;Elizabeth Jones.
Eotaxin: a potent eosinophil chemoattractant cytokine detected in a guinea pig model of allergic airways inflammation.
P J Jose;D A Griffiths-Johnson;P D Collins;D T Walsh.
Journal of Experimental Medicine (1994)
Glial growth factors are alternatively spliced erbB2 ligands expressed in the nervous system.
Mark A. Marchionni;Andrew D. J. Goodearl;Maio Su Chen;Olivia Bermingham-McDonogh.
Characterization of two 85 kd proteins that associate with receptor tyrosine kinases, middle-T/pp60c-src complexes, and PI3-kinase.
Masayuki Otsu;Ian Hiles;Ivan Gout;Michael J. Fry.
Phosphatidylinositol 3-kinase : structure and expression of the 110 kd catalytic subunit
Ian D. Hiles;Masayuki Otsu;Stefano Volinia;Michael J. Fry.
Phospholipase D: a downstream effector of ARF in granulocytes
Shamshad Cockcroft;Geraint M. H. Thomas;Amanda Fensome;Blandine Geny.
Human lysozyme gene mutations cause hereditary systemic amyloidosis
M. B. Pepys;P. N. Hawkins;D. R. Booth;D. M. Vigushin.
The GTPase dynamin binds to and is activated by a subset of SH3 domains.
Ivan Gout;Ritu Dhand;Ian D. Hiles;Michael J. Fry.
Bcr encodes a GTPase-activating protein for p21rac.
Dagmar Diekmann;Suzanne Brill;Michelle D. Garrett;Nicholas Totty.
GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells
Fabio Palombo;Paola Gallinari;Ingram Iaccarino;Teresa Lettieri.
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