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 82 Citations 33,486 235 World Ranking 2277 National Ranking 1243

Overview

What is he best known for?

The fields of study he is best known for:

  • Enzyme
  • Gene
  • Amino acid

His main research concerns Biochemistry, Presenilin, Amyloid precursor protein secretase, Cell biology and Notch signaling pathway. In his study, Active site and Amyloid beta is strongly linked to Biophysics, which falls under the umbrella field of Biochemistry. His Presenilin research incorporates elements of Membrane protein and Amyloid precursor protein.

His research in Amyloid precursor protein secretase intersects with topics in P3 peptide, Vesicle, Sphingolipid, Protease and Gamma secretase. His Cell biology research is multidisciplinary, incorporating perspectives in Druggability, Proteolytic enzymes and Biotinylation. Michael S. Wolfe has researched Notch signaling pathway in several fields, including Proteolysis, Endoplasmic reticulum and Transmembrane domain.

His most cited work include:

  • Naturally secreted oligomers of amyloid beta protein potently inhibit hippocampal long-term potentiation in vivo. (3673 citations)
  • A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain. (1850 citations)
  • Two transmembrane aspartates in presenilin-1 required for presenilin endoproteolysis and gamma-secretase activity. (1679 citations)

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

His primary scientific interests are in Biochemistry, Presenilin, Amyloid precursor protein secretase, Cell biology and Amyloid precursor protein. His study in Presenilin is interdisciplinary in nature, drawing from both Protease, Membrane protein and Transmembrane protein. His Amyloid precursor protein secretase research integrates issues from Biophysics, P3 peptide and Alpha secretase.

His study focuses on the intersection of Cell biology and fields such as γ secretase with connections in the field of Amyloid β. His Amyloid precursor protein research is multidisciplinary, relying on both Cleavage, Stereochemistry, Aspartate protease, Peptidomimetic and Amyloid. His research in APH-1 tackles topics such as PEN-2 which are related to areas like Gamma-secretase complex.

He most often published in these fields:

  • Biochemistry (48.83%)
  • Presenilin (42.97%)
  • Amyloid precursor protein secretase (32.42%)

What were the highlights of his more recent work (between 2012-2021)?

  • Biochemistry (48.83%)
  • Presenilin (42.97%)
  • Amyloid precursor protein secretase (32.42%)

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

His scientific interests lie mostly in Biochemistry, Presenilin, Amyloid precursor protein secretase, Amyloid precursor protein and Cell biology. His Biochemistry course of study focuses on Amyloid and Neuroscience, Gamma secretase and Apolipoprotein E. His study of Nicastrin is a part of Presenilin.

His Amyloid precursor protein secretase study combines topics from a wide range of disciplines, such as P3 peptide, Proteases, APH-1, Endogeny and Structure–activity relationship. Michael S. Wolfe has included themes like Amyloid beta and Membrane protein in his Amyloid precursor protein study. His Cell biology research focuses on subjects like γ secretase, which are linked to Receptor, Intramembrane protease, Transcription and Pharmacology.

Between 2012 and 2021, his most popular works were:

  • Nicastrin functions to sterically hinder γ-secretase–substrate interactions driven by substrate transmembrane domain (86 citations)
  • Alternative polyadenylation and miR-34 family members regulate tau expression. (84 citations)
  • Alzheimer presenilin-1 mutations dramatically reduce trimming of long amyloid β-peptides (Aβ) by γ-secretase to increase 42-to-40-residue Aβ. (82 citations)

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

  • Enzyme
  • Gene
  • Amino acid

Michael S. Wolfe mainly investigates Transmembrane domain, Amyloid precursor protein secretase, Presenilin, Biochemistry and Cell biology. His Transmembrane domain study incorporates themes from Nicastrin and Transmembrane protein. In Amyloid precursor protein secretase, Michael S. Wolfe works on issues like P3 peptide, which are connected to Biochemistry of Alzheimer's disease.

The Presenilin study combines topics in areas such as Proteases and Amyloid precursor protein. His study in Biochemistry focuses on Proteolysis and Carboxypeptidase. His Cell biology research is multidisciplinary, incorporating elements of Genetics, Polyadenylation, Three prime untranslated region, Regulation of gene expression and Gene isoform.

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

Naturally secreted oligomers of amyloid beta protein potently inhibit hippocampal long-term potentiation in vivo.

Dominic M. Walsh;Igor Klyubin;Julia V. Fadeeva;William K. Cullen.
Nature (2002)

5164 Citations

A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain.

Bart De Strooper;Wim Annaert;Philippe Cupers;Paul Saftig.
Nature (1999)

2618 Citations

Two transmembrane aspartates in presenilin-1 required for presenilin endoproteolysis and gamma-secretase activity.

Michael S. Wolfe;Michael S. Wolfe;Weiming Xia;Beth L. Ostaszewski;Thekla S. Diehl.
Nature (1999)

2342 Citations

c-Myc is an important direct target of Notch1 in T-cell acute lymphoblastic leukemia/lymphoma

Andrew P. Weng;John M. Millholland;Yumi Yashiro-Ohtani;Marie Laure Arcangeli.
Genes & Development (2006)

991 Citations

γ-Secretase is a membrane protein complex comprised of presenilin, nicastrin, aph-1, and pen-2

W. Taylor Kimberly;Matthew J. LaVoie;Beth L. Ostaszewski;Wenjuan Ye.
Proceedings of the National Academy of Sciences of the United States of America (2003)

970 Citations

The surface of articular cartilage contains a progenitor cell population.

Gary P. Dowthwaite;Joanna C. Bishop;Samantha N. Redman;Ilyas M. Khan.
Journal of Cell Science (2004)

859 Citations

Notch mediates TGFα-induced changes in epithelial differentiation during pancreatic tumorigenesis

Yoshiharu Miyamoto;Anirban Maitra;Bidyut Ghosh;Ulrich Zechner.
Cancer Cell (2003)

812 Citations

Transition-state analogue inhibitors of γ-secretase bind directly to presenilin-1

William P. Esler;W. Taylor Kimberly;Beth L. Ostaszewski;Thekla S. Diehl.
Nature Cell Biology (2000)

695 Citations

A Portrait of Alzheimer Secretases--New Features and Familiar Faces

William P. Esler;Michael S. Wolfe.
Science (2001)

682 Citations

Growth suppression of pre-T acute lymphoblastic leukemia cells by inhibition of notch signaling.

Andrew P. Weng;Yunsun Nam;Michael S. Wolfe;Warren S. Pear.
Molecular and Cellular Biology (2003)

512 Citations

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