Search Results - "Feng, Dairong"
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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
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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2
Control of alternative splicing by forskolin through hnRNP K during neuronal differentiation
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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3
Increase of a group of PTC+ transcripts by curcumin through inhibition of the NMD pathway
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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Aberrant splicing in neurological diseases
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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Multiple effects of curcumin on promoting expression of the exon 7-containing SMN2 transcript
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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Analysis of COL1A1 and COL1A2 gene variants in two fetuses with osteogenesis imperfecta
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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