2006 - Fellow of Alfred P. Sloan Foundation
His main research concerns Genetics, Fragile X syndrome, Cell biology, Neurogenesis and Molecular biology. In most of his Genetics studies, his work intersects topics such as Neurodegeneration. His studies in Fragile X syndrome integrate themes in fields like Polysome, Messenger RNA, RNA-binding protein and FMR1.
His Messenger RNA research incorporates elements of Synaptic plasticity and microRNA. His biological study deals with issues like Regulation of gene expression, which deal with fields such as Neuropathology. His biological study spans a wide range of topics, including RNA, RNA splicing, Amyloid precursor protein, HEK 293 cells and 5-Hydroxymethylcytosine.
Peng Jin mainly investigates Genetics, Epigenetics, Cell biology, DNA methylation and Fragile X syndrome. His work on Genetics deals in particular with microRNA, Gene, Gene expression, RNA and Trinucleotide repeat expansion. His RNA study typically links adjacent topics like Messenger RNA.
His Epigenetics study combines topics from a wide range of disciplines, such as Enhancer, 5-Hydroxymethylcytosine, Embryonic stem cell and Computational biology. His work deals with themes such as Molecular biology, Cellular differentiation and Induced pluripotent stem cell, which intersect with Cell biology. His Fragile X syndrome study incorporates themes from Drosophila melanogaster, Drosophila Protein, Polysome and FMR1.
Peng Jin focuses on Epigenetics, Computational biology, Gene, Genetics and DNA. His Epigenetics study integrates concerns from other disciplines, such as Methylation, Enhancer, Gene expression, DNA methylation and Cytosine. He has researched Gene in several fields, including Age at menopause and Menopause.
His work on Genetics is being expanded to include thematically relevant topics such as Pathogenesis. His FMR1 research integrates issues from Phenotype, Ovulation and RNA, Untranslated region. His research in Neurodegeneration intersects with topics in Ataxia and Cell biology.
Genetics, Methylation, DNA methylation, Epigenetics and Disease are his primary areas of study. The concepts of his Genetics study are interwoven with issues in Cerebellum, Tau protein and Pathogenesis. His Pathogenesis research includes elements of Fragile X-associated tremor/ataxia syndrome, FMR1, Sphingolipid, Ataxia and Genetic screen.
His Methylation research is multidisciplinary, incorporating perspectives in Translation, Messenger RNA, Untranslated region and Nervous system. His study in DNA methylation is interdisciplinary in nature, drawing from both Cytosine, Frontal lobe, Computational biology and Mutation rate. His Epigenetics research is multidisciplinary, relying on both Marker selection and DNA Hydroxymethylation.
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Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome
Victoria Brown;Victoria Brown;Peng Jin;Peng Jin;Stephanie Ceman;Stephanie Ceman;Jennifer C. Darnell.
Cell (2001)
Zika Virus Infects Human Cortical Neural Progenitors and Attenuates Their Growth
Hengli Tang;Christy Hammack;Sarah C. Ogden;Zhexing Wen.
Cell Stem Cell (2016)
Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure
Xuyu Qian;Ha Nam Nguyen;Mingxi M. Song;Christopher Hadiono.
Cell (2016)
Fragile X Mental Retardation Protein Targets G Quartet mRNAs Important for Neuronal Function
Jennifer C. Darnell;Kirk B. Jensen;Peng Jin;Victoria Brown.
Cell (2001)
Selective chemical labeling reveals the genome-wide distribution of 5-hydroxymethylcytosine
Chun Xiao Song;Keith E. Szulwach;Ye Fu;Qing Dai.
Nature Biotechnology (2011)
Base-Resolution Analysis of 5-Hydroxymethylcytosine in the Mammalian Genome
Miao Yu;Gary C. Hon;Keith E. Szulwach;Chun Xiao Song.
Cell (2012)
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
Peng Jin;Daniela C Zarnescu;Stephanie Ceman;Stephanie Ceman;Mika Nakamoto.
Nature Neuroscience (2004)
5-hmC–mediated epigenetic dynamics during postnatal neurodevelopment and aging
Keith E. Szulwach;Xuekun Li;Yujing Li;Chun Xiao Song.
Nature Neuroscience (2011)
Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA
Ranhui Duan;ChangHui Pak;Peng Jin.
Human Molecular Genetics (2007)
Genome-wide Profiling of 5-Formylcytosine Reveals Its Roles in Epigenetic Priming
Chun-Xiao Song;Keith E. Szulwach;Qing Dai;Ye Fu.
Cell (2013)
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