Scripps VIVO scripps research logo

  • Index
  • Log in
  • Home
  • People
  • Organizations
  • Research
  • Events
Search form

Academic Article RDF

  • 1
  • 2
  • 3
  • 4
  • 5
  • 6
  • 7
  • 8
  • 9
  • 10
  • 11
  • 12
  • 13
  • 14
  • 15
  • 16
  • 17
  • 18
  • 19
  • 20
  • 21
  • 22
  • 23
  • 24
  • 25
  • 26
  • 27
  • 28
  • 29
  • 30
  • 31
  • 32
  • 33
  • 34
  • 35
  • 36
  • 37
  • 38
  • 39
  • 40
  • more...
  • A general method for site-specific incorporation of unnatural amino acids into proteins
  • A general method to quantify quasi-equivalence in icosahedral viruses
  • A general protocol for addressing speciation of the active catalyst applied to ligand-accelerated enantioselective C(sp(3))-H bond arylation
  • A general purpose RNA-cleaving DNA enzyme
  • A general solid phase method for the preparation of diverse azapeptide probes directed against cysteine proteases
  • A general strategy for construction of both 2,6-cis- and 2,6-trans-disubstituted tetrahydropyrans: Substrate-controlled asymmetric total synthesis of (+)-scanlonenyne
  • A general strategy for the bacterial expression of amyloidogenic peptides using BCL-XL-1/2 fusions
  • A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
  • A general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia-type bromoethers
  • A general strategy for the synthesis of monohydroxyeicosatetraenoic acids - total synthesis of 5(s)-hydroxy-6(e),8,11,14(z)-eicosatetraenoic acid (5-hete) and 12(s)-hydroxy-5,8,14(z),10(e)-eicosatetraenoic acid (12-hete)
  • A general strategy for the total synthesis of the presumed lipoxin structures
  • A general strategy toward s-linked glycopeptides
  • A general system for evaluating the efficiency of chromophore-assisted light inactivation (CALI) of proteins reveals Ru(ii) tris-bipyridyl as an unusually efficient "warhead"
  • A general, polymer-supported acid catalyzed hetero-michael addition
  • A general-approach to enantiomerically pure methylcarbinols - asymmetric-synthesis of antibiotic (-)-a26771b and the wcr sex-pheromone
  • A general-approach to gamma-lactones via osmium-catalyzed asymmetric dihydroxylation - synthesis of (-)-muricatacin and (+)-muricatacin
  • A general-solution to implementing the 4-p participation of 1-aza-1,3-butadienes in Diels-Alder reactions - inverse electron demand Diels-Alder reactions of alpha,beta-unsaturated n-benzenesulfonyl imines
  • A generalized HIV vaccine design strategy for priming of broadly neutralizing antibody responses
  • A genetic analysis of glucocorticoid receptor signaling: Identification and characterization of ligand-effect modulators in Saccharomyces cerevisiae
  • A genetic analysis of lupus
  • A genetic analysis of pax3-fkhr, the oncogene of alveolar rhabdomyosarcoma
  • A genetic approach to the generation of antibodies with enhanced catalytic activities
  • A genetic determinant of the striatal dopamine response to alcohol in men
  • A genetic determinant that specifically regulates the frequency of hematopoietic stem cells
  • A genetic marker in the variable region of light chains of mouse immunoglobulins
  • A genetic model for light-regulated seedling Arabidopsis
  • A genetic network that suppresses genome rearrangements in Saccharomyces cerevisiae and contains defects in cancers
  • A genetic-locus regulates the expression of tissue-specific messenger-rnas from multiple transcription units
  • A genetically amenable platensimycin- and platencin-overproducer as a platform for biosynthetic explorations: a showcase of PtmO4, a long-chain acyl-CoA dehydrogenase
  • A genetically encoded aza-Michael acceptor for covalent cross-linking of protein-receptor complexes
  • 1
  • 2
  • 3
  • 4
  • 5
  • 6
  • 7
  • 8
  • 9
  • 10
  • 11
  • 12
  • 13
  • 14
  • 15
  • 16
  • 17
  • 18
  • 19
  • 20
  • 21
  • 22
  • 23
  • 24
  • 25
  • 26
  • 27
  • 28
  • 29
  • 30
  • 31
  • 32
  • 33
  • 34
  • 35
  • 36
  • 37
  • 38
  • 39
  • 40
  • more...

©2021 The Scripps Research Institute | Terms of Use | Powered by VIVO

  • About
  • Contact Us
  • Support