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  • Book
    Contents:
    Introduction. Purpose statement
    Patient population
    Settings
    Providers
    Evidence-based guideline development process
    Literature evaluation and scoring
    Significance of late preterm birth. Risk factors
    Neurodevelopmental issues
    Notes
    Evidence-based clinical practice guideline. Gestational age assessment
    Respiratory assessment
    Thermoregulation issues
    Hypoglycemia
    Sepsis
    Jaundice and hyperbilirubinemia
    Feeding challenges
    Parent education and support
    Discharge planning and followup
    Notes
    References
    Appendices. Risk factors for development of severe hyperbilirubinemia in infants of 35 or more weeks of gestation
    Bilirubin nomograms
    Screening and management of postnatal glucose homeostasis in late preterm and term SGA, IDM/LGA infants
    Quick care guide.
    Digital Access R2Library 2017
    Limited to 1 simultaneous user
  • Article
    Hollenberg CP.
    Mol Gen Genet. 1978 Jun 01;162(1):23-34.
    Saccharomyces cerevisiae 2-mum DNA and some of its restriction fragments were integrated in vector pCR1 ,pBR313 or pBR322 and their expression in Escherichia coli P678-54 minicells was analyzed. 2mum DNA inserted at the EcoRI site of pCR1 or pBR313 and at the PstI site of pBR322 promoted the synthesis of polypeptides of 48,000, 37,000, 35,000 and 19,000 daltons. The DNA regions coding for these polypeptides were mapped on the 2-mum DNA molecule by insertion of single EcoRI or HindIII restriction fragments and comparison of the polypeptides produced. For the synthesis of the 37,000 dalton polypeptide, intact sites RIB and H3 were required. The disappearance of the 37,000 dalton polypeptide on interruption of one of these sites by insertion of the vector, was correlated with the appearance of a polypeptide of 22,000 or 23,500 daltons respectively. The DNA sequence coding for the 37,000 daltons polypeptide, therefore, has to be located in the S-loop region close to or overlapping with the site RIB and H3. Assuming that the 22,000 and the 23,500 dalton polypeptides are truncated forms of the 37,000 dalton polypeptide, the last polypeptide can be exactly mapped. The polypeptide of 48,000 daltons was mapped to that half of the L-loop segment containing the sites H1 and H2. If, however, HindIII fragment H1-H2 was expressed, the 48,000 dalton polypeptide was lost and concomitantly a 43,000 dalton polypeptide appeared. We assume that this polypeptide results from early termination of the polypeptide of 48,000 daltons. The 35,000 and 9,000 dalton polypeptides were mapped to the S-loop region. The integrated inverted repeat sequence of yeast 2-mum Dna did not induce any detectable insert-specific polypeptide synthesis.
    Digital Access Access Options
  • Journal
    Print 1962-1974.