Search Results - "Feng, Dairong"

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  1. 1

    Whole‐exome sequencing identified a novel pathogenic mutation of the CYP4F22 gene in a Chinese patient with autosomal recessive congenital ichthyosis and in vitro study of the mutant CYP4F22 protein by Zhao, Lina, Wang, Caixia, Zhang, Yaning, Li, Jinyun, Liu, Huize, Feng, Dairong

    Published in Journal of dermatology (01-05-2022)
    “…Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of rare cornification disorders. Of the 14 genes already known to cause ARCI, CYP4F22…”
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    Journal Article
  2. 2

    Control of alternative splicing by forskolin through hnRNP K during neuronal differentiation by Cao, Wenguang, Razanau, Aleh, Feng, Dairong, Lobo, Vincent G, Xie, Jiuyong

    Published in Nucleic acids research (01-09-2012)
    “…The molecular basis of cell signal-regulated alternative splicing at the 3' splice site remains largely unknown. We isolated a protein kinase A-responsive…”
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    Journal Article
  3. 3

    Increase of a group of PTC+ transcripts by curcumin through inhibition of the NMD pathway by Feng, Dairong, Su, Ruey-Chyi, Zou, Liping, Triggs-Raine, Barbara, Huang, Shangzhi, Xie, Jiuyong

    Published in Biochimica et biophysica acta (01-08-2015)
    “…Nonsense-mediated mRNA decay (NMD), an mRNA surveillance mechanism, eliminates premature termination codon-containing (PTC+) transcripts. For instance, it…”
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    Journal Article
  4. 4

    Aberrant splicing in neurological diseases by Feng, Dairong, Xie, Jiuyong

    Published in Wiley interdisciplinary reviews. RNA (01-11-2013)
    “…Splicing of precursor messenger RNA (pre‐mRNA) removes the intervening sequences (introns) and joins the expressed regions (exons) in the nucleus, before an…”
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    Journal Article
  5. 5

    Multiple effects of curcumin on promoting expression of the exon 7-containing SMN2 transcript by Feng, Dairong, Cheng, Yi, Meng, Yan, Zou, Liping, Huang, Shangzhi, Xie, Jiuyong

    Published in Genes & nutrition (01-11-2015)
    “…Survival of motor neuron 2 (SMN2) is a modifier gene for spinal muscular atrophy (SMA), a neurodegenerative disease caused by insufficient SMN protein mostly…”
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    Journal Article
  6. 6

    Analysis of COL1A1 and COL1A2 gene variants in two fetuses with osteogenesis imperfecta by Zhang, Yaning, Wu, Xinyue, Liu, Qiaoyun, Yan, Xiaona, Liu, Huize, Feng, Dairong

    Published in Zhonghua yi xue yi chuan xue za zhi (10-07-2023)
    “…To explore the genetic basis of two fetuses with an osteogenesis imperfecta (OI) phenotype. Two fetuses diagnosed at the Affiliated Hospital of Weifang Medical…”
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    Journal Article