2009 - Fellow of the American Association for the Advancement of Science (AAAS)
1991 - Fellow of Alfred P. Sloan Foundation
His primary areas of investigation include Biochemistry, Phospholipase A2, Enzyme, Molecular biology and Stereochemistry. As part of one scientific family, Michael H. Gelb deals mainly with the area of Biochemistry, narrowing it down to issues related to the Cell biology, and often Cell culture. His Phospholipase A2 research incorporates themes from Phospholipase, Inflammation, Arachidonic acid, Eicosanoid and Binding site.
His work deals with themes such as Cloning, Recombinant DNA and Krabbe disease, which intersect with Enzyme. His Molecular biology study combines topics in areas such as Laminopathy, LMNA, Escherichia coli, Receptor and Phosphorylation. His Stereochemistry research also works with subjects such as
Michael H. Gelb spends much of his time researching Biochemistry, Phospholipase A2, Enzyme, Stereochemistry and Newborn screening. His Biochemistry study combines topics from a wide range of disciplines, such as Molecular biology and Cell biology. His Phospholipase A2 study integrates concerns from other disciplines, such as Phospholipid, Phospholipase, Inflammation, Immunology and Arachidonic acid.
His Enzyme study incorporates themes from In vitro and Trypanosoma brucei. His Stereochemistry research is multidisciplinary, incorporating elements of Peptide and Active site. The study incorporates disciplines such as Dried blood, Tandem mass spectrometry, Krabbe disease and Dried blood spot in addition to Newborn screening.
Michael H. Gelb mostly deals with Newborn screening, Tandem mass spectrometry, Dried blood, Biochemistry and Chromatography. His Newborn screening research is multidisciplinary, relying on both Enzyme assay, Multiplex, Krabbe disease and Dried blood spot. His Tandem mass spectrometry study also includes
His Dried blood research incorporates themes from Pathology, Spots, Gastroenterology, Enzyme and Internal medicine. Michael H. Gelb has included themes like Selected reaction monitoring, Cell-Derived Microparticles and Stereochemistry in his Biochemistry study. As a part of the same scientific study, he usually deals with the Phospholipase A2, concentrating on Cell biology and frequently concerns with Calcium and Psoriasis.
Newborn screening, Biochemistry, Phospholipase A2, Dried blood and Tandem mass spectrometry are his primary areas of study. His studies deal with areas such as Dried blood spot, Pseudodeficiency alleles and Leukodystrophy, Krabbe disease as well as Newborn screening. Michael H. Gelb interconnects Cell-Derived Microparticles, Stereochemistry and Molecular biology in the investigation of issues within Biochemistry.
Michael H. Gelb has researched Phospholipase A2 in several fields, including Inflammation, Immunology, Docosahexaenoic acid and Cell biology. The various areas that Michael H. Gelb examines in his Dried blood study include Gastroenterology, Enzyme assay and Multiplex. His Tandem mass spectrometry study combines topics in areas such as Fabry disease, Internal medicine, Mucopolysaccharidosis and Enzyme.
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.
Quantitative analysis of complex protein mixtures using isotope-coded affinity tags
Steven P. Gygi;Beate Rist;Scott A. Gerber;Frantisek Turecek.
Nature Biotechnology (1999)
Computational design of an enzyme catalyst for a stereoselective bimolecular Diels-Alder reaction
Justin B. Siegel;Alexandre Zanghellini;Helena M. Lovick;Gert Kiss.
Interfacial catalysis: the mechanism of phospholipase A2
David L. Scott;Steven P. White;Zbyszek Otwinowski;Wei Yuan.
Biochemistry and physiology of mammalian secreted phospholipases A2.
Gérard Lambeau;Michael H Gelb.
Annual Review of Biochemistry (2008)
Prenyl proteins in eukaryotic cells: a new type of membrane anchor
John A. Glomset;Michael H. Gelb;Christopher C. Farnsworth.
Trends in Biochemical Sciences (1990)
Slow- and tight-binding inhibitors of the 85-kDa human phospholipase A2.
I. P. Street;Hung-Kuei Lin;F. Laliberte;Farideh Ghomashchi.
Platelets release mitochondria serving as substrate for bactericidal group IIA-secreted phospholipase A2 to promote inflammation
Luc H. Boudreau;Anne Claire Duchez;Nathalie Cloutier;Denis Soulet.
Interfacial Enzymology: The Secreted Phospholipase A2-Paradigm
Otto G. Berg;Michael H. Gelb;Ming-Daw Tsai;Mahendra Kumar Jain.
Chemical Reviews (2001)
Fluoro ketone inhibitors of hydrolytic enzymes.
Michael H. Gelb;John P. Svaren;Robert H. Abeles.
Crystal structure of bee-venom phospholipase A2 in a complex with a transition-state analogue.
David L. Scott;Zbyszek Otwinowski;Michael H. Gelb;Paul B. Sigler.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: