-Chaitan Khosla Researcher Activity Profile

Research Author Detailed Information 

Chaitan Khosla Publication Rate By Year

Chaitan Khosla has published 3 paper(s) in 2003, 2 paper(s) in 2004, 1 paper(s) in 2005, 1 paper(s) in 2006, 20 paper(s) in 2007, 5 paper(s) in 2008, for a total of 32 research publications in total.

Chaitan C Khosla Author Information

LAST NAME: khosla

FIRST NAME: chaitan

INITIALS: C

AFFILIATION:

Papers

Chaitan Khosla's Publication Record

1. Transglutaminase 2 regulates mallory body inclusion formation and injury-associated liver enlargement. Year Published: 2007
Department of Medicine, Palo Alto VA Medical Center, Palo Alto, California, USA.
2. Structure-activity relationship analysis of the selective inhibition of transglutaminase 2 by dihydroisoxazoles. Year Published: 2006
Department of Chemistry, Stanford University, Stanford, California 94305, USA.
3. Bioassay-guided evolution of glycosylated macrolide antibiotics in Escherichia coli. Year Published: 2007
Department of Chemistry, Stanford University, Stanford, California, United States of America.
4. Synthesis and biological activity of novel pyranopyrones derived from engineered aromatic polyketides. Year Published: 2007
5. Substrate tolerance of module 6 of the epothilone synthetase. Year Published: 2007
Department of Chemistry, Stanford University, Stanford, California 94305, USA.
6. Structure-activity relationships of semisynthetic mumbaistatin analogs. Year Published: 2007
Department of Chemistry, Stanford University, Stanford, CA 94305, USA.
7. Structure and mechanism of the 6-deoxyerythronolide B synthase. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, California 94305, USA. khosla@stanford.edu
8. Enhancement of dietary protein digestion by conjugated bile acids. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, California, USA.
9. Structure-based dissociation of a type I polyketide synthase module. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
10. Structure-based design of alpha-amido aldehyde containing gluten peptide analogues as modulators of HLA-DQ2 and transglutaminase 2. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
11. A scaleable manufacturing process for pro-EP-B2, a cysteine protease from barley indicated for celiac sprue. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, California 94305, USA.
12. Combination enzyme therapy for gastric digestion of dietary gluten in patients with celiac sprue. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, California, USA.
13. Structural and mechanistic analysis of protein interactions in module 3 of the 6-deoxyerythronolide B synthase. Year Published: 2007
Department of Chemistry, Keck Building, Stanford University, Stanford, CA 94305, USA.
14. Cyclic and dimeric gluten peptide analogues inhibiting DQ2-mediated antigen presentation in celiac disease. Year Published: 2007
Department of Chemistry, Stanford University, Stanford, CA 94305-5025, USA.
15. Solution structure and proposed domain domain recognition interface of an acyl carrier protein domain from a modular polyketide synthase. Year Published: 2007
Department of Chemistry, Stanford University, Stanford, California 94305, USA.
16. Stereospecificity of ketoreductase domains of the 6-deoxyerythronolide B synthase. Year Published: 2007
Department of Chemistry, Brown University, Providence, RI 02912-9108, USA.
17. Cyclic and dimeric gluten peptide analogues inhibiting DQ2-mediated antigen presentation in celiac disease. Year Published: 2007
Department of Chemistry, Stanford University, Stanford, CA 94305-5025, USA.
18. Structure-based dissociation of a type I polyketide synthase module. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
19. Transglutaminase 2 undergoes a large conformational change upon activation. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, California, United States of America.
20. Stereospecificity of ketoreductase domains of the 6-deoxyerythronolide B synthase. Year Published: 2007
Department of Chemistry, Brown University, Providence, RI 02912-9108, USA.
21. Epothilone C macrolactonization and hydrolysis are catalyzed by the isolated thioesterase domain of epothilone polyketide synthase. Year Published: 2003
Departments of Chemical Engineering, Stanford University, Stanford, California 94305-5025, USA.
22. Polyketide chain length control by chain length factor. Year Published: 2003
Department of Chemistry, Stanford University, Stanford, California 94305, USA.
23. A Switch for the transfer of substrate between nonribosomal peptide and polyketide modules of the rifamycin synthetase assembly line. Year Published: 2003
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 240 Longwood Avenue, Boston, Massachusetts 02115, USA.
24. Precursor-directed biosynthesis of epothilone in Escherichia coli. Year Published: 2004
Departments of Chemical Engineering, Chemistry, and Biochemistry, Stanford University, Stanford, California 94305-5025, USA.
25. Reconstitution and characterization of a new desosaminyl transferase, EryCIII, from the erythromycin biosynthetic pathway. Year Published: 2004
Department of Chemistry, Stanford University, Stanford, California 94305, USA.
26. Stereochemical assignment of intermediates in the rifamycin biosynthetic pathway by precursor-directed biosynthesis. Year Published: 2005
Department of Chemistry, Stanford University, Stanford, California 94305-5025, USA.
27. Transglutaminase 2 undergoes a large conformational change upon activation. Year Published: 2007
Department of Chemical Engineering, Stanford University, Stanford, California, United States of America.
28. A non-human primate model for gluten sensitivity. Year Published: 2008
Department of Biochemistry, Stanford University, Stanford, California, United States of America.
29. Transepithelial transport and enzymatic detoxification of gluten in gluten-sensitive rhesus macaques. Year Published: 2008
Department of Biochemistry, Stanford University, Stanford, California, United States of America.
30. Extracellular transglutaminase 2 is catalytically inactive, but is transiently activated upon tissue injury. Year Published: 2008
Department of Chemical Engineering, Stanford University, Stanford, California, United States of America.
31. Evolution of polyketide synthases in bacteria. Year Published: 2008
Departments of Chemistry, Chemical Engineering, and Biochemistry, Stanford University, Stanford, CA 94305, USA.
32. Evolution of polyketide synthases in bacteria. Year Published: 2008
Departments of Chemistry, Chemical Engineering, and Biochemistry, Stanford University, Stanford, CA 94305, USA.