Showing 161 - 180 results of 28,335 for search '(( significant cause case ) OR ( significant ((genes decrease) OR (teer decrease)) ))', query time: 2.77s Refine Results
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    Table_1_Case Report: Exome Sequencing Identified a Novel Compound Heterozygous Variation in PLOD2 Causing Bruck Syndrome Type 2.DOC by Jing Zhang (23775)

    Published 2021
    “…And the result of immunohistochemistry (IHC) indicated that the expression of PLOD2 protein in the proband's osteochondral tissue was significantly decreased. These findings in our study expanded the variation spectrum of PLOD2 gene, provided solid evidence for the family's counseling in regard to future pregnancies, strongly supported the application of WES in prenatal diagnosis, and might give insight into the understanding of PLOD2 function.…”
  14. 174

    Case selection flow chart. by Daniel Koehler (5079566)

    Published 2023
    “…An acquired antibiotic resistance was detected in 36.0% of all significant isolates, occurring especially in CoNS (68.3%) and gram-negative species (24.0%).…”
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