相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。The methyltransferase METTL9 mediates pervasive 1-methylhistidine modification in mammalian proteomes
Erna Davydova et al.
NATURE COMMUNICATIONS (2021)
Further delineation of METTL23-associated intellectual disability
Mohammed Almannai et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2020)
Life, death, and autophagy in cancer: NF-κB turns up everywhere
Daniela Verzella et al.
CELL DEATH & DISEASE (2020)
Exome sequencing revealed a novel homozygous METTL23 gene mutation leading to familial mild intellectual disability with dysmorphic features
W. Smaili et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2020)
Dual SMAD inhibition and Wnt inhibition enable efficient and reproducible differentiations of induced pluripotent stem cells into retinal ganglion cells
Venkata R. M. Chavali et al.
SCIENTIFIC REPORTS (2020)
Two Cases of Recessive Intellectual Disability Caused byNDST1andMETTL23Variants
Amjad Khan et al.
GENES (2020)
Roles and regulation of histone methylation in animal development
Ashwini Jambhekar et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2019)
TBK1 at the Crossroads of Inflammation and Energy Homeostasis in Adipose Tissue
Peng Zhao et al.
CELL (2018)
Inhibitors of Protein Methyltransferases and Demethylases
H. Umit Kaniskan et al.
CHEMICAL REVIEWS (2018)
Mechanisms of NF-kappa B p65 and strategies for therapeutic manipulation
Sivagami Giridharan et al.
JOURNAL OF INFLAMMATION RESEARCH (2018)
Genetics of glaucoma
Janey L. Wiggs et al.
HUMAN MOLECULAR GENETICS (2017)
Targeting neuronal gap junctions in mouse retina offers neuroprotection in glaucoma
Abram Akopian et al.
JOURNAL OF CLINICAL INVESTIGATION (2017)
Arginine Methylation: The Coming of Age
Romeo S. Blanc et al.
MOLECULAR CELL (2017)
Histone H3 Methylated at Arginine 17 Is Essential for Reprogramming the Paternal Genome in Zygotes
Yuki Hatanaka et al.
CELL REPORTS (2017)
NF-kappa B signaling in inflammation
Ting Liu et al.
SIGNAL TRANSDUCTION AND TARGETED THERAPY (2017)
Caspases in retinal ganglion cell death and axon regeneration
Chloe N. Thomas et al.
CELL DEATH DISCOVERY (2017)
30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology
Qian Zhang et al.
CELL (2017)
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
Jessica N. Cooke Bailey et al.
NATURE GENETICS (2016)
Significance of optineurin mutations in glaucoma and other diseases
Yuriko Minegishi et al.
PROGRESS IN RETINAL AND EYE RESEARCH (2016)
Linear ubiquitination is involved in the pathogenesis of optineurin-associated amyotrophic lateral sclerosis
Seshiru Nakazawa et al.
NATURE COMMUNICATIONS (2016)
Soluble Tumor Necrosis Factor Alpha Promotes Retinal Ganglion Cell Death in Glaucoma via Calcium-Permeable AMPA Receptor Activation
Jorge L. Cueva Vargas et al.
JOURNAL OF NEUROSCIENCE (2015)
Visual impairment in an optineurin mouse model of primary open-angle glaucoma
Henry C. Tseng et al.
NEUROBIOLOGY OF AGING (2015)
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli et al.
SCIENCE (2015)
METTL23, a transcriptional partner of GABPA, is essential for human cognition
Rachel E. Reiff et al.
HUMAN MOLECULAR GENETICS (2014)
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability
Marie Bernkopf et al.
HUMAN MOLECULAR GENETICS (2014)
Generating genetically modified mice using CRISPR/Cas-mediated genome engineering
Hui Yang et al.
NATURE PROTOCOLS (2014)
Caspase-8 promotes NLRP1/NLRP3 inflammasome activation and IL-1β production in acute glaucoma
Wei Chi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Population-based glaucoma prevalence studies in Asians
Hyun-Kyung Cho et al.
SURVEY OF OPHTHALMOLOGY (2014)
Overexpression of HtrA1 and Exposure to Mainstream Cigarette Smoke Leads to Choroidal Neovascularization and Subretinal Deposits in Aged Mice
Mao Nakayama et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2014)
Enhanced optineurin E50KTBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma
Yuriko Minegishi et al.
HUMAN MOLECULAR GENETICS (2013)
Optineurin suppression causes neuronal cell death via NF-κB pathway
Mayumi Akizuki et al.
JOURNAL OF NEUROCHEMISTRY (2013)
Protein arginine methyltransferases and cancer
Yanzhong Yang et al.
NATURE REVIEWS CANCER (2013)
Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutations
Miranda L. Tradewell et al.
HUMAN MOLECULAR GENETICS (2012)
The kinase TBK1 controls IgA class switching by negatively regulating noncanonical NF-κB signaling
Jin Jin et al.
NATURE IMMUNOLOGY (2012)
Histone H3R17me2a mark recruits human RNA Polymerase-Associated Factor 1 Complex to activate transcription
Jiacai Wu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma
John H. Fingert et al.
HUMAN MOLECULAR GENETICS (2011)
Loss of TFF1 is associated with activation of NF-κB-mediated inflammation and gastric neoplasia in mice and humans
Mohammed Soutto et al.
JOURNAL OF CLINICAL INVESTIGATION (2011)
Retinal ganglion cell death is induced by microglia derived pro-inflammatory cytokines in the hypoxic neonatal retina
Viswanathan Sivakumar et al.
JOURNAL OF PATHOLOGY (2011)
Differences in Rates of Glaucoma among Asian Americans and Other Racial Groups, and among Various Asian Ethnic Groups
Joshua D. Stein et al.
OPHTHALMOLOGY (2011)
Glaucoma: genes, phenotypes, and new directions for therapy
Bao Jian Fan et al.
JOURNAL OF CLINICAL INVESTIGATION (2010)
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
Andrew C. Elden et al.
NATURE (2010)
Mutations of optineurin in amyotrophic lateral sclerosis
Hirofumi Maruyama et al.
NATURE (2010)
Protein structure prediction on the Web: a case study using the Phyre server
Lawrence A. Kelley et al.
NATURE PROTOCOLS (2009)
Brn3a as a Marker of Retinal Ganglion Cells: Qualitative and Quantitative Time Course Studies in Naive and Optic Nerve-Injured Retinas
Francisco M. Nadal-Nicolas et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Enhanced binding of TBK1 by an optineurin mutant that causes a familial form of primary open angle glaucoma
Simon Morton et al.
FEBS LETTERS (2008)
Rapid generation of splicing reporters with pSpliceExpress
Shivendra Kishore et al.
GENE (2008)
Tumor necrosis factor-α mediates oligodendrocyte death and delayed retinal ganglion cell loss in a mouse model of glaucoma
Toru Nakazawa et al.
JOURNAL OF NEUROSCIENCE (2006)
Distribution of Optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United States
Michael A. Hauser et al.
JOURNAL OF GLAUCOMA (2006)
Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene
T Aung et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2005)
Expression of cone-photoreceptor-specific antigens in a cell line derived from retinal tumors in transgenic mice
E Tan et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2004)
NF-κB regulation in the immune system
QT Li et al.
NATURE REVIEWS IMMUNOLOGY (2002)
NF-κB family of transcription factors:: Central regulators of innate and adaptive immune functions
J Caamaño et al.
CLINICAL MICROBIOLOGY REVIEWS (2002)
Adult-onset primary open-angle glaucoma caused by mutations in optineurin
T Rezaie et al.
SCIENCE (2002)
Methylation at arginine 17 of histone H3 is linked to gene activation
UM Bauer et al.
EMBO REPORTS (2002)
分享论文
