D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 98 Citations 36,964 379 World Ranking 1088 National Ranking 666

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Internal medicine

The scientist’s investigation covers issues in Biochemistry, Internal medicine, Endocrinology, Phosphorylation and Protein biosynthesis. Scot R. Kimball works in the field of Internal medicine, namely Skeletal muscle. Scot R. Kimball interconnects Stimulation, Insulin and Protein metabolism in the investigation of issues within Skeletal muscle.

His Phosphorylation research is multidisciplinary, incorporating elements of Leucine and Signal transduction. His Protein biosynthesis research incorporates elements of Amino acid, Phenylalanine, Eukaryotic translation, Messenger RNA and Metabolism. His biological study spans a wide range of topics, including eIF2B, Translational regulation, EIF4EBP1, P70-S6 Kinase 1 and Cell biology.

His most cited work include:

  • AMP-activated protein kinase suppresses protein synthesis in rat skeletal muscle through down-regulated mammalian target of rapamycin (mTOR) signaling. (708 citations)
  • Leucine Stimulates Translation Initiation in Skeletal Muscle of Postabsorptive Rats via a Rapamycin-Sensitive Pathway (652 citations)
  • Diabetic retinopathy: seeing beyond glucose-induced microvascular disease. (547 citations)

What are the main themes of his work throughout his whole career to date?

Internal medicine, Endocrinology, Protein biosynthesis, Skeletal muscle and Biochemistry are his primary areas of study. His Internal medicine research includes themes of Diabetes mellitus, Protein kinase B, PI3K/AKT/mTOR pathway and Ribosomal protein s6. His Endocrinology study incorporates themes from mTORC1, Protein kinase A, Phosphorylation and P70-S6 Kinase 1.

Scot R. Kimball combines subjects such as Signal transduction and Kinase with his study of Phosphorylation. His Protein biosynthesis research integrates issues from Translation, Eukaryotic translation, Messenger RNA and Eukaryotic initiation factor. In Eukaryotic initiation factor, Scot R. Kimball works on issues like eIF2B, which are connected to eIF2.

He most often published in these fields:

  • Internal medicine (49.60%)
  • Endocrinology (49.33%)
  • Protein biosynthesis (37.20%)

What were the highlights of his more recent work (between 2014-2021)?

  • Internal medicine (49.60%)
  • Endocrinology (49.33%)
  • Cell biology (26.68%)

In recent papers he was focusing on the following fields of study:

His scientific interests lie mostly in Internal medicine, Endocrinology, Cell biology, Skeletal muscle and mTORC1. His work deals with themes such as Regulation of gene expression, Alternative splicing and Protein kinase A, which intersect with Internal medicine. His study explores the link between Endocrinology and topics such as Phosphorylation that cross with problems in Ceramide.

Scot R. Kimball focuses mostly in the field of Cell biology, narrowing it down to matters related to Eukaryotic initiation factor and, in some cases, Initiation factor. His study in Skeletal muscle is interdisciplinary in nature, drawing from both TNNT3, Protein biosynthesis, Hindlimb, Anabolism and Muscle hypertrophy. His Protein biosynthesis study combines topics in areas such as Leucine, EIF4E and Sepsis.

Between 2014 and 2021, his most popular works were:

  • A Unique ISR Program Determines Cellular Responses to Chronic Stress (63 citations)
  • Leucine induced dephosphorylation of Sestrin2 promotes mTORC1 activation. (50 citations)
  • ALCAT1 controls mitochondrial etiology of fatty liver diseases, linking defective mitophagy to steatosis. (49 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Enzyme
  • Internal medicine

Scot R. Kimball focuses on Internal medicine, Endocrinology, mTORC1, Skeletal muscle and Phosphorylation. His Internal medicine research is multidisciplinary, relying on both Autophagy, Protein kinase B, Mechanistic target of rapamycin, PI3K/AKT/mTOR pathway and Regulation of gene expression. Scot R. Kimball has included themes like Signal transduction and Kinase in his Endocrinology study.

His studies deal with areas such as Carcinogenesis, Senescence and Protein biosynthesis as well as mTORC1. Protein biosynthesis is a subfield of Biochemistry that Scot R. Kimball studies. His studies in Phosphorylation integrate themes in fields like Translational attenuation, Eukaryotic initiation factor and Initiation factor.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky;Amal Kamal Abdel-Aziz;Sara Abdelfatah;Mahmoud Abdellatif.
Autophagy (2021)

8964 Citations

AMP-activated protein kinase suppresses protein synthesis in rat skeletal muscle through down-regulated mammalian target of rapamycin (mTOR) signaling.

Douglas R. Bolster;Stephen J. Crozier;Scot R. Kimball;Leonard S. Jefferson.
Journal of Biological Chemistry (2002)

1155 Citations

Leucine Stimulates Translation Initiation in Skeletal Muscle of Postabsorptive Rats via a Rapamycin-Sensitive Pathway

Joshua C. Anthony;Fumiaki Yoshizawa;Tracy Gautsch Anthony;Thomas C. Vary.
Journal of Nutrition (2000)

905 Citations

Diabetic retinopathy: seeing beyond glucose-induced microvascular disease.

David A. Antonetti;Alistair J. Barber;Sarah K. Bronson;Willard M. Freeman.
Diabetes (2006)

888 Citations

Signaling Pathways and Molecular Mechanisms through which Branched-Chain Amino Acids Mediate Translational Control of Protein Synthesis

Scot R. Kimball;Leonard S. Jefferson.
Journal of Nutrition (2006)

728 Citations

Phosphorylation of the cap-binding protein eukaryotic translation initiation factor 4E by protein kinase Mnk1 in vivo.

Andrew Jan Waskiewicz;Jeffrey C. Johnson;Bennett Penn;Bennett Penn;Malathy Mahalingam.
Molecular and Cellular Biology (1999)

579 Citations

Orally Administered Leucine Stimulates Protein Synthesis in Skeletal Muscle of Postabsorptive Rats in Association with Increased eIF4F Formation

Joshua C. Anthony;Tracy Gautsch Anthony;Scot R. Kimball;Thomas C. Vary.
Journal of Nutrition (2000)

564 Citations

Signaling Pathways Involved in Translational Control of Protein Synthesis in Skeletal Muscle by Leucine

Joshua C. Anthony;Tracy G. Anthony;Scot R. Kimball;Leonard S. Jefferson.
Journal of Nutrition (2001)

561 Citations

The GCN2 eIF2α Kinase Is Required for Adaptation to Amino Acid Deprivation in Mice

Peichuan Zhang;Peichuan Zhang;Barbara C. McGrath;Jamie Reinert;De Anne S. Olsen.
Molecular and Cellular Biology (2002)

486 Citations

Oral Leucine Administration Stimulates Protein Synthesis in Rat Skeletal Muscle

Stephen J. Crozier;Scot R. Kimball;Sans W. Emmert;Joshua C. Anthony.
Journal of Nutrition (2005)

464 Citations

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