What is he best known for?
The fields of study he is best known for:
Jim J.-C. Lin mainly investigates Molecular biology, Tropomyosin, Gene isoform, Actin and Microfilament.
Jim J.-C. Lin integrates Molecular biology with Intercalated disc in his study.
Cell biology and Myosin are inextricably linked to his Tropomyosin research.
His research in Gene isoform intersects with topics in 3T3 cells, Actin cytoskeleton and Antigen.
His Actin study integrates concerns from other disciplines, such as Cancer cell, Cell cycle, Caldesmon and Polyclonal antibodies.
In his work, Tropomyosin 3 is strongly intertwined with Rous sarcoma virus, which is a subfield of Microfilament.
His most cited work include:
- Biochemical characterization of the mammalian stress proteins and identification of two stress proteins as glucose- and Ca2+-ionophore-regulated proteins. (376 citations)
- A Defect in the Kv Channel-Interacting Protein 2 (KChIP2) Gene Leads to a Complete Loss of Ito and Confers Susceptibility to Ventricular Tachycardia (368 citations)
- Specification of Actin Filament Function and Molecular Composition by Tropomyosin Isoforms (207 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Cell biology, Tropomyosin, Molecular biology, Actin and Gene isoform.
His work on Myosin as part of general Cell biology research is frequently linked to Intercalated disc, thereby connecting diverse disciplines of science.
Jim J.-C. Lin has researched Tropomyosin in several fields, including Myocyte, Caldesmon, Monoclonal antibody and Microfilament.
His study in Molecular biology is interdisciplinary in nature, drawing from both Cytoplasm, Complementary DNA, Gene expression, Northern blot and Antibody.
His Actin research is multidisciplinary, relying on both Biophysics, Sarcomere, Chinese hamster ovary cell and Cytoskeleton.
Jim J.-C. Lin combines subjects such as Troponin complex, Epithelium, Immunoperoxidase and Exon with his study of Gene isoform.
He most often published in these fields:
- Cell biology (43.20%)
- Tropomyosin (37.60%)
- Molecular biology (37.60%)
What were the highlights of his more recent work (between 2010-2020)?
- Cell biology (43.20%)
- Internal medicine (13.60%)
- Intercalated disc (12.80%)
In recent papers he was focusing on the following fields of study:
His main research concerns Cell biology, Internal medicine, Intercalated disc, Endocrinology and Cardiac muscle.
His biological study spans a wide range of topics, including Mutant and Skeletal muscle.
The study incorporates disciplines such as Null mice and Cardiology in addition to Internal medicine.
His Actin research integrates issues from Cytoplasm, Actin cytoskeleton, Cytoskeleton and Cellular differentiation.
His Western blot research incorporates themes from Tropomyosin and Gene isoform.
His Molecular biology study frequently links to other fields, such as Monoclonal antibody.
Between 2010 and 2020, his most popular works were:
- Quantitative phosphoproteomic study of pressure-overloaded mouse heart reveals dynamin-related protein 1 as a modulator of cardiac hypertrophy (35 citations)
- The Xin repeat-containing protein, mXinβ, initiates the maturation of the intercalated discs during postnatal heart development (31 citations)
- Tropomyosin variants describe distinct functional subcellular domains in differentiated vascular smooth muscle cells. (27 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Internal medicine, Actin, Myocyte, Molecular biology and Western blot.
Within one scientific family, Jim J.-C. Lin focuses on topics pertaining to Endocrinology under Internal medicine, and may sometimes address concerns connected to Phosphorylation.
Actin is a subfield of Cell biology that he explores.
His studies in Cell biology integrate themes in fields like Actin-binding protein, Actin cytoskeleton and Kinocilium, Hair cell, Inner ear.
His Myocyte study combines topics in areas such as Cadherin and Cell junction.
His Molecular biology research incorporates elements of Cellular differentiation, Tropomyosin and Alternative splicing, Gene isoform.
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