Search Results - "Jia, Yichang"
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Dual-gRNA approach with limited off-target effect corrects C9ORF72 repeat expansion in vivo
Published in Scientific reports (05-04-2022)“…C9ORF72 GGGGCC repeat expansion is the most common genetic cause for amyotrophic lateral sclerosis and frontotemporal dementia, which generates abnormal DNA…”
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Three-dimensional surface motion capture of multiple freely moving pigs using MAMMAL
Published in Nature communications (25-11-2023)“…Understandings of the three-dimensional social behaviors of freely moving large-size mammals are valuable for both agriculture and life science, yet…”
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Activity-induced histone modifications govern Neurexin-1 mRNA splicing and memory preservation
Published in Nature neuroscience (01-05-2017)“…Relatively little is known about the mechanisms that preserve memories during long-term storage. The authors found that neural activation during learning…”
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An L1 retrotransposon insertion–induced deafness mouse model for studying the development and function of the cochlear stria vascularis
Published in Proceedings of the National Academy of Sciences - PNAS (05-10-2021)“…Dysregulation of ion and potential homeostasis in the scala media is the most prevalent cause of hearing loss in mammals. However, it is not well understood…”
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Mutation of a U2 snRNA Gene Causes Global Disruption of Alternative Splicing and Neurodegeneration
Published in Cell (20-01-2012)“…Although uridine-rich small nuclear RNAs (U-snRNAs) are essential for pre-mRNA splicing, little is known regarding their function in the regulation of…”
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Critical role of TRPC6 channels in the formation of excitatory synapses
Published in Nature neuroscience (01-07-2008)“…The transient receptor potential canonical (TRPC) channels are Ca2+-permeable, nonselective cation channels with different biological functions, but their…”
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An ENU-induced mutation in Twist1 transactivation domain causes hindlimb polydactyly with complete penetrance and dominant-negatively impairs E2A-dependent transcription
Published in Scientific reports (12-02-2020)“…Twist1 encodes a basic helix-loop-helix transcription factor (TF), which forms homodimer or heterodimer with other TFs, like E2A, to regulate target genes’…”
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Identification of a Novel ENU-Induced Mutation in Mouse Tbx1 Linked to Human DiGeorge Syndrome
Published in Neural plasticity (01-01-2016)“…The patients with DiGeorge syndrome (DGS), caused by deletion containing dozens of genes in chromosome 22, often carry cardiovascular problem and hearing loss…”
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TCF7L2 acts as a molecular switch in midbrain to control mammal vocalization through its DNA binding domain but not transcription activation domain
Published in Molecular psychiatry (01-04-2023)“…Vocalization is an essential medium for social signaling in birds and mammals. Periaqueductal gray (PAG) a conserved midbrain structure is believed to be…”
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Expression of TCF7L2 in midbrain Vglut2-positive neurons
Published in Molecular psychiatry (01-04-2023)Get full text
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TRPC Channels and Neuron Development, Plasticity, and Activities
Published in Advances in experimental medicine and biology (01-01-2017)“…In this chapter, we mainly focus on the functions of TRPC channels in brain development, including neural progenitor proliferation, neurogenesis, neuron…”
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TRPC Channels and Programmed Cell Death
Published in Advances in experimental medicine and biology (01-01-2017)“…Neurotrophins, including nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF), bind to their high-affinity receptors to promote neuronal…”
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Disruption of ER ion homeostasis maintained by an ER anion channel CLCC1 contributes to ALS-like pathologies
Published in Cell research (01-07-2023)“…Although anion channel activities have been demonstrated in sarcoplasmic reticulum/endoplasmic reticulum (SR/ER), their molecular identities and functions…”
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In vivo stress granule misprocessing evidenced in a FUS knock-in ALS mouse model
Published in Brain (London, England : 1878) (01-05-2020)“…Many RNA-binding proteins, including TDP-43, FUS, and TIA1, are stress granule components, dysfunction of which causes amyotrophic lateral sclerosis (ALS)…”
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A molecular brake that modulates spliceosome pausing at detained introns contributes to neurodegeneration
Published in Protein & cell (08-05-2023)“…Emerging evidence suggests that intron-detaining transcripts (IDTs) are a nucleus-detained and polyadenylated mRNA pool for cell to quickly and effectively…”
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Loss of Clcc1 results in ER stress, misfolded protein accumulation, and neurodegeneration
Published in The Journal of neuroscience (18-02-2015)“…Folding of transmembrane and secretory proteins occurs in the lumen of the endoplasmic reticulum (ER) before transportation to the cell surface and is…”
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TRPC channels promote cerebellar granule neuron survival
Published in Nature neuroscience (01-05-2007)“…Channels formed by the transient receptor potential (TRP) family of proteins have a variety of physiological functions. Here we report that two members of the…”
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Global Disruption of Alternative Splicing and Neurodegeneration Is Caused by Mutation of a U2 snRNA Gene
Published in Cell (20-01-2012)“…Although uridine-rich small nuclear RNAs (U-snRNAs) are essential for pre-mRNA splicing, little is known regarding their function in the regulation of…”
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Characterization of ZNF23, a KRAB-containing protein that is downregulated in human cancers and inhibits cell cycle progression
Published in Experimental cell research (15-01-2007)“…The Krupple-associated box-containing zinc-finger proteins (KRAB–ZFPs) make up one of the largest family of transcription factors. Several members of the…”
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