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 53 Citations 13,604 84 World Ranking 11400 National Ranking 823

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Genetics

His primary areas of study are Cell biology, ADAM10, Sheddase, Molecular biology and Disintegrin. Dieter Hartmann has researched Cell biology in several fields, including ADAM17 Protein, Ectodomain and TGF alpha. As part of one scientific family, he deals mainly with the area of ADAM10, narrowing it down to issues related to the ADAM Proteins, and often Chemokine, Transmembrane protein and Cleavage.

His Sheddase course of study focuses on Amphiregulin and Heparin-binding EGF-like growth factor and ADAM9. His studies in Molecular biology integrate themes in fields like Enzyme activator, Ceramide and Protein kinase C, Rottlerin. His Disintegrin research is multidisciplinary, incorporating elements of Cytoplasm and Catenin.

His most cited work include:

  • Distinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligands (800 citations)
  • Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice (713 citations)
  • Mitochondrial Rhomboid PARL Regulates Cytochrome c Release during Apoptosis via OPA1-Dependent Cristae Remodeling (584 citations)

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

Dieter Hartmann focuses on Cell biology, Molecular biology, Biochemistry, ADAM10 and Metachromatic leukodystrophy. Dieter Hartmann combines subjects such as Cell growth, Regulated Intramembrane Proteolysis, Ectodomain, Presenilin and Alpha secretase with his study of Cell biology. As a part of the same scientific study, Dieter Hartmann usually deals with the Molecular biology, concentrating on ADAM17 Protein and frequently concerns with TGF alpha and Signal transduction.

His Biochemistry study combines topics in areas such as P3 peptide and Neurodegeneration. The various areas that Dieter Hartmann examines in his ADAM10 study include Phorbol, ADAM Proteins and Sheddase. His study in Sheddase is interdisciplinary in nature, drawing from both Epidermal growth factor, Epidermal growth factor receptor and Amphiregulin.

He most often published in these fields:

  • Cell biology (51.69%)
  • Molecular biology (20.22%)
  • Biochemistry (17.98%)

What were the highlights of his more recent work (between 2008-2021)?

  • Cell biology (51.69%)
  • Myelin (11.24%)
  • Sphingolipid (11.24%)

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

The scientist’s investigation covers issues in Cell biology, Myelin, Sphingolipid, Biochemistry and Molecular biology. His Cell biology research includes elements of Regulated Intramembrane Proteolysis, Sheddase, APH-1, ADAM10 and Alpha secretase. His biological study deals with issues like Genetics, which deal with fields such as Astrogliosis.

His studies deal with areas such as Endocrinology, Lipid metabolism, Ceramide synthase, Ceramide synthase 2 and Epidermis as well as Sphingolipid. His Biochemistry study combines topics from a wide range of disciplines, such as Cerebellum and Neurodegeneration. His Molecular biology research incorporates elements of Amino acid, Receptor, Peptide sequence, Alzheimer's disease and Amyloid precursor protein secretase.

Between 2008 and 2021, his most popular works were:

  • Critical role of the disintegrin metalloprotease ADAM17 for intestinal inflammation and regeneration in mice (216 citations)
  • Adult ceramide synthase 2 (CerS2) deficient mice exhibit myelin sheath defects, cerebellar degeneration and hepatocarcinomas (193 citations)
  • ADAM10, the Rate-limiting Protease of Regulated Intramembrane Proteolysis of Notch and Other Proteins, Is Processed by ADAMS-9, ADAMS-15, and the γ-Secretase * (141 citations)

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

  • Gene
  • Enzyme
  • Genetics

His main research concerns Cell biology, Biochemistry, Alpha secretase, Presenilin and ADAM10. Dieter Hartmann is studying Endoplasmic reticulum, which is a component of Cell biology. His research in Endoplasmic reticulum tackles topics such as Calpain which are related to areas like Signal transduction.

He has included themes like Regulated Intramembrane Proteolysis, APH-1, Sheddase and Ectodomain in his Alpha secretase study. His work is dedicated to discovering how Cerebellum, Ceramide synthase are connected with Myelin and Cerebellar Degeneration and other disciplines. His research integrates issues of Intestinal mucosa, Inflammation, TGF alpha, Molecular biology and Metalloproteinase in his study of Tumor necrosis factor alpha.

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

Distinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligands

Umut Sahin;Gisela Weskamp;Kristine Kelly;Kristine Kelly;Hong-Ming Zhou.
Journal of Cell Biology (2004)

1074 Citations

Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice

Yoshitaka Tanaka;Yoshitaka Tanaka;Gundula Guhde;Anke Suter;Eeva Liisa Eskelinen;Eeva Liisa Eskelinen;Eeva Liisa Eskelinen.
Nature (2000)

1027 Citations

The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts.

Dieter Hartmann;Bart De Strooper;Lutgarde Serneels;Kathleen Craessaerts.
Human Molecular Genetics (2002)

812 Citations

Mitochondrial Rhomboid PARL Regulates Cytochrome c Release during Apoptosis via OPA1-Dependent Cristae Remodeling

Sara Cipolat;Tomasz Rudka;Dieter Hartmann;Veronica Costa.
Cell (2006)

800 Citations

ADAM10 cleavage of N‐cadherin and regulation of cell–cell adhesion and β‐catenin nuclear signalling

Karina Reiss;Thorsten Maretzky;Andreas Ludwig;Thomas Tousseyn.
The EMBO Journal (2005)

583 Citations

The transmembrane CXC-chemokine ligand 16 is induced by IFN-gamma and TNF-alpha and shed by the activity of the disintegrin-like metalloproteinase ADAM10.

Soeren Abel;Christian Hundhausen;Rolf Mentlein;Alexander Schulte.
Journal of Immunology (2004)

474 Citations

Cellular Cholesterol Depletion Triggers Shedding of the Human Interleukin-6 Receptor by ADAM10 and ADAM17 (TACE)

Vance Matthews;Björn Schuster;Stefan Schütze;Ingo Bussmeyer.
Journal of Biological Chemistry (2003)

442 Citations

Phenotypic and Biochemical Analyses of BACE1- and BACE2-deficient Mice

Diana Dominguez;Jos Tournoy;Dieter Hartmann;Tobias Huth.
Journal of Biological Chemistry (2005)

424 Citations

Lipids revert inert Aβ amyloid fibrils to neurotoxic protofibrils that affect learning in mice

Ivo Cristiano Martins;Inna Kuperstein;Hannah Wilkinson;Elke Maes.
The EMBO Journal (2008)

380 Citations

The disintegrins ADAM10 and TACE contribute to the constitutive and phorbol ester-regulated normal cleavage of the cellular prion protein.

Bruno Vincent;Erwan Paitel;Paul Saftig;Yveline Frobert.
Journal of Biological Chemistry (2001)

348 Citations

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