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Extending the Faultline Model to Geographically Dispersed Teams: How Colocated Subgroups can Impair Group Functioning
We theorize that in geographically dispersed teams, members' geographic locations are likely to activate “faultlines” (hypothetical dividing lines that split a group into subgroups) that impair teamExpand
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Limbic system fos expression associated with paternal behavior
Axon-sparing lesions of the medial nucleus of the amygdala (MeA) decrease male parental behavior in the highly social prairie vole. To assess further the role of the amygdala in paternal behavior,Expand
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A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V.
Osteogenesis imperfecta (OI) is a heterogenous group of genetic disorders of bone fragility. OI type V is an autosomal-dominant disease characterized by calcification of the forearm interosseousExpand
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Survey of Klebsiella pneumoniae Strains Producing Extended-Spectrum β-Lactamases: Prevalence of SHV-12 and SHV-2a in Korea
ABSTRACT Fifty-three clinical isolates of extended-spectrum β-lactamase (ESBL)-producing Klebsiella pneumoniae collected from three hospitals in Korea were investigated for phenotypical andExpand
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The evaluation of resin infiltration for masking labial enamel white spot lesions.
OBJECTIVE The aim of this study was to clinically assess the effectiveness of masking white spot enamel lesions using a resin infiltration technique that was recently developed to arrest incipientExpand
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Safety and Efficacy of Fast-track Surgery in Laparoscopic Distal Gastrectomy for Gastric Cancer: A Randomized Clinical Trial
BackgroundFast-track surgery has been shown to enhance postoperative recovery in several surgical fields. This study aimed to evaluate the safety and efficacy of fast-track surgery in laparoscopicExpand
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Mutational spectrum of FAM83H: the C‐terminal portion is required for tooth enamel calcification
Dental enamel forms through the concerted activities of specialized extracellular matrix proteins, including amelogenin, enamelin, MMP20, and KLK4. Defects in the genes encoding these proteins causeExpand
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Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II
The current system for the classification of hereditary defects of tooth dentin is based upon clinical and radiographic findings and consists of two types of dentin dysplasia (DD) and three types ofExpand
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Novel FAM20A mutations in hypoplastic amelogenesis imperfecta
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects without any other nonoral symptoms. Recently, a disease‐causing nonsense mutationExpand
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Nonsyndromic multiple mandibular supernumerary premolars.
  • H. Hyun, S. Lee, +4 authors J. Kim
  • Medicine
  • Journal of oral and maxillofacial surgery…
  • 1 July 2008
PURPOSE The purpose of this study was to estimate the frequency of and describe the clinical characteristics and complications of patients with nonsyndromic multiple mandibular supernumeraryExpand
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