Dr. Michael S Glickman MD
Infectious Disease Specialist | Infectious Disease
1275 York Ave New York NY, 10021About
I am an infectious diseases specialist and a Fellow of the Infectious Diseases Society of America (FIDSA), and am involved in both patient care and laboratory research. I care for patients with a wide ...
Education and Training
Columbia Univ Coll of Physicians And Surgeons, New York Ny 1993
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM- Infectious Disease
Internal MedicineAmerican Board of Internal MedicineABIM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- A novel mycolic acid cyclopropane synthetase is required for cording, persistence, and virulence of Mycobacterium tuberculosis.
- The Mycobacterium tuberculosis cmaA2 gene encodes a mycolic acid trans-cyclopropane synthetase.
- Microbial pathogenesis of Mycobacterium tuberculosis: dawn of a discipline.
- Crystal structures of mycolic acid cyclopropane synthases from Mycobacterium tuberculosis.
- The mmaA2 gene of Mycobacterium tuberculosis encodes the distal cyclopropane synthase of the alpha-mycolic acid.
- Efficient allelic exchange and transposon mutagenesis in Mycobacterium avium by specialized transduction.
- Mycobacterium tuberculosis controls host innate immune activation through cyclopropane modification of a glycolipid effector molecule.
- Mechanism of nonhomologous end-joining in mycobacteria: a low-fidelity repair system driven by Ku, ligase D and ligase C.
- Regulation of Mycobacterium tuberculosis cell envelope composition and virulence by intramembrane proteolysis.
- Atomic structure and nonhomologous end-joining function of the polymerase component of bacterial DNA ligase D.
- Site-2 proteases in prokaryotes: regulated intramembrane proteolysis expands to microbial pathogenesis.
- Trans-cyclopropanation of mycolic acids on trehalose dimycolate suppresses Mycobacterium tuberculosis -induced inflammation and virulence.
- Mycobacterial nonhomologous end joining mediates mutagenic repair of chromosomal double-strand DNA breaks.
- Bacterial DNA repair by non-homologous end joining.
Fellowships
- Albert Einstein College of Medicine/ Montefiore Medical Center
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