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  • A multicenter, randomized, controlled trial comparing Surfaxin (Lucinactant) lavage with standard care for treatment of meconium aspiration syndrome
  • A multicenter, randomized, placebo-controlled trial of a new form of intravenous recombinant tissue-type plasminogen-activator (activase) in acute myocardial-infarction
  • A multidisciplinary intervention to prevent the readmission of elderly patients with congestive-heart-failure
  • A multifunctional bispecific antibody protects against Pseudomonas aeruginosa
  • A multifunctional human monoclonal neutralizing antibody that targets a unique conserved epitope on influenza HA
  • A multifunctional nanocarrier for efficient TRAIL-based gene therapy against hepatocellular carcinoma with desmoplasia in mice
  • A multiplexed single-cell CRISPR screening platform enables systematic dissection of the unfolded protein response
  • A multiscale statistical mechanical framework integrates biophysical and genomic data to assemble cancer networks
  • A multivalent approach towards linked dual-pharmacology prostaglandin F receptor agonist/carbonic anhydrase-II inhibitors for the treatment of glaucoma
  • A multivalent minigene vaccine, containing b-cell, cytotoxic t-lymphocyte, and t-h epitopes from several microbes, induces appropriate responses in vivo and confers protection against more than one pathogen
  • A multivalent probe for AI-2 quorum-sensing receptors
  • A multivalent vaccination strategy for the prevention of old world arenavirus infection in humans
  • A murine lung cancer co-clinical trial identifies genetic modifiers of therapeutic response
  • A murine t-cell receptor gene-complex - isolation, structure and rearrangement
  • A mutagenesis study of a catalytic antibody
  • A mutant mouse with a highly specific contextual fear-conditioning deficit found in an N-ethyl-N-nitrosourea (ENU) mutagenesis screen
  • A mutant of rous sarcoma virus (type o) causing fusiform cell transformation
  • A mutasynthetic library of platensimycin and platencin analogues
  • A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function
  • A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome
  • A mutation in the Arabidopsis DET3 gene uncouples photoregulated leaf development from gene expression and chloroplast biogenesis
  • A mutation in the FHA domain of Coprinus cinereus Nbs1 leads to Spo11-independent meiotic recombination and chromosome segregation
  • A mutation in the human cyclin-dependent kinase interacting protein, ckshs2, interferes with cyclin-dependent kinase binding and biological function, but preserves protein structure and assembly
  • A mutation in the small (alpha) subunit of glycyl-tRNA synthetase affects amino acid activation and subunit association parameters
  • A mutation of Ikbkg causes immune deficiency without impairing degradation of IκBα
  • A mutational study of a Diels-Alderase catalytic antibody
  • A myc-slug (snail2)/twist regulatory circuit directs vascular development
  • A myristoylated pseudosubstrate peptide of PKC-ζ induces degranulation in HMC-1 cells independently of PKC-ζ activity
  • A nanobody:GFP bacterial platform that enables functional enzyme display and easy quantification of display capacity
  • A nanostructure-initiator mass spectrometry-based enzyme activity assay
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