Related references
Note: Only part of the references are listed.The SINEB1 element in the long non-coding RNA Malat1 is necessary for TDP-43 proteostasis
Tuan M. Nguyen et al.
NUCLEIC ACIDS RESEARCH (2020)
FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retention
Jack Humphrey et al.
NUCLEIC ACIDS RESEARCH (2020)
The role of hnRNPs in frontotemporal dementia and amyotrophic lateral sclerosis
Alexander Bampton et al.
ACTA NEUROPATHOLOGICA (2020)
A large-scale binding and functional map of human RNA-binding proteins
Eric L. Van Nostrand et al.
NATURE (2020)
Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia
Mercedes Prudencio et al.
JOURNAL OF CLINICAL INVESTIGATION (2020)
Stress-Specific Spatiotemporal Responses of RNA-Binding Proteins in Human Stem Cell-Derived Motor Neurons
Jasmine Harley et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)
Heterogeneous nuclear ribonucleoproteins R and Q accumulate in pathological inclusions in FTLD-FUS
Lauren M. Gittings et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2019)
Molecular pathology of neurodegenerative diseases: principles and practice
Gabor G. Kovacs
JOURNAL OF CLINICAL PATHOLOGY (2019)
C9-ALS/FTD-linked proline-arginine dipeptide repeat protein associates with paraspeckle components and increases paraspeckle formation
Hiroaki Suzuki et al.
CELL DEATH & DISEASE (2019)
Heavy-tailed prior distributions for sequence count data: removing the noise and preserving large differences
Anqi Zhu et al.
BIOINFORMATICS (2019)
ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair
Joseph R. Klim et al.
NATURE NEUROSCIENCE (2019)
Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration
Ze'ev Melamed et al.
NATURE NEUROSCIENCE (2019)
Review: Clinical, genetic and neuroimaging features of frontotemporal dementia
R. Convery et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2019)
GENCODE reference annotation for the human and mouse genomes
Adam Frankish et al.
NUCLEIC ACIDS RESEARCH (2019)
Annotation-free quantification of RNA splicing using LeafCutter
Yang I. Li et al.
NATURE GENETICS (2018)
Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis
Pietro Fratta et al.
EMBO JOURNAL (2018)
Progress and Challenges in Frontotemporal Dementia Research: A 20-Year Review
John R. Hodges et al.
JOURNAL OF ALZHEIMERS DISEASE (2018)
TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTD
Matthew A. White et al.
NATURE NEUROSCIENCE (2018)
HnRNP L represses cryptic exons
Sean P. McClory et al.
RNA (2018)
Frontotemporal dementia: latest evidence and clinical implications
Juan Joseph Young et al.
THERAPEUTIC ADVANCES IN PSYCHOPHARMACOLOGY (2018)
Heterogeneous nuclear ribonucleoprotein K is associated with poor prognosis and regulates proliferation and apoptosis in bladder cancer
Xu Chen et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2017)
TDP-43 mutations causing amyotrophic lateral sclerosis are associated with altered expression of RNA-binding protein hnRNP K and affect the Nrf2 antioxidant pathway
Diane Moujalled et al.
HUMAN MOLECULAR GENETICS (2017)
Major hnRNP proteins act as general TDP-43 functional modifiers both in Drosophila and human neuronal cells
Chiara Appocher et al.
NUCLEIC ACIDS RESEARCH (2017)
Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene
Yvonne S. Davidson et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2017)
Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar Degeneration
Yvonne S. Davidson et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2017)
Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration
Edward B. Lee et al.
ACTA NEUROPATHOLOGICA (2017)
Quantitative analysis of cryptic splicing associated with TDP-43 depletion
Jack Humphrey et al.
BMC MEDICAL GENOMICS (2017)
The hnRNP family: insights into their role in health and disease
Thomas Geuens et al.
HUMAN GENETICS (2016)
Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models
Qiumin Tan et al.
HUMAN MOLECULAR GENETICS (2016)
PTBP1 and PTBP2 Repress Nonconserved Cryptic Exons
Jonathan P. Ling et al.
CELL REPORTS (2016)
Splicing repression allows the gradual emergence of new Alu-exons in primate evolution
Jan Attig et al.
ELIFE (2016)
hnRNP K Overexpression Drives AML Progression By Altering Pathways Critical for Myeloid Proliferation and Differentiation
Marisa J. Hornbaker et al.
BLOOD (2016)
Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations
T. Lashley et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2015)
TDP-43 repression of nonconserved cryptic exons is compromised in ALS-FTD
Jonathan P. Ling et al.
SCIENCE (2015)
Phosphorylation of hnRNP K by cyclin-dependent kinase 2 controls cytosolic accumulation of TDP-43
Diane Moujalled et al.
HUMAN MOLECULAR GENETICS (2015)
Sequestration of multiple RNA recognition motif-containing proteins by C9orf72 repeat expansions
Johnathan Cooper-Knock et al.
BRAIN (2014)
Emerging roles of heterogeneous nuclear ribonucleoprotein K (hnRNP K) in cancer progression
Paola Barboro et al.
CANCER LETTERS (2014)
Loss of hnRNP K Impairs Synaptic Plasticity in Hippocampal Neurons
Alessandra Folci et al.
JOURNAL OF NEUROSCIENCE (2014)
C9orf72 nucleotide repeat structures initiate molecular cascades of disease
Aaron R. Haeusler et al.
NATURE (2014)
Frontotemporal dementia: diagnosis, deficits and management
Nicholas T. Bott et al.
NEURODEGENERATIVE DISEASE MANAGEMENT (2014)
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Michael I. Love et al.
GENOME BIOLOGY (2014)
STAR: ultrafast universal RNA-seq aligner
Alexander Dobin et al.
BIOINFORMATICS (2013)
Direct Competition between hnRNP C and U2AF65 Protects the Transcriptome from the Exonization of Alu Elements
Kathi Zarnack et al.
CELL (2013)
Frontotemporal dementia
Jason D. Warren et al.
BMJ-BRITISH MEDICAL JOURNAL (2013)
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies
Daniah Trabzuni et al.
HUMAN MOLECULAR GENETICS (2012)
Alteration of POLDIP3 Splicing Associated with Loss of Function of TDP-43 in Tissues Affected with ALS
Atsushi Shiga et al.
PLOS ONE (2012)
Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2011)
RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome
Bo Li et al.
BMC BIOINFORMATICS (2011)
hnRNP K post-transcriptionally co-regulates multiple cytoskeletal genes needed for axonogenesis
Yuanyuan Liu et al.
DEVELOPMENT (2011)
Analysis of alternative splicing associated with aging and neurodegeneration in the human brain
James R. Tollervey et al.
GENOME RESEARCH (2011)
Translation of myelin basic protein mRNA in oligodendrocytes is regulated by integrin activation and hnRNP-K
Lisbeth S. Laursen et al.
JOURNAL OF CELL BIOLOGY (2011)
Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies
Daniah Trabzuni et al.
JOURNAL OF NEUROCHEMISTRY (2011)
BigWig and BigBed: enabling browsing of large distributed datasets
W. J. Kent et al.
BIOINFORMATICS (2010)
Detection of nonneutral substitution rates on mammalian phylogenies
Katherine S. Pollard et al.
GENOME RESEARCH (2010)
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
Manuela Neumann et al.
ACTA NEUROPATHOLOGICA (2009)
hnRNP K interacts with RNA binding motif protein 42 and functions in the maintenance of cellular ATP level during stress conditions
Toshiyuki Fukuda et al.
GENES TO CELLS (2009)
MEME SUITE: tools for motif discovery and searching
Timothy L. Bailey et al.
NUCLEIC ACIDS RESEARCH (2009)
TDP-43 Overexpression Enhances Exon 7 Inclusion during the Survival of Motor Neuron Pre-mRNA Splicing
Jayarama Krishnan Bose et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Heterogeneous nuclear ribonucleoprotein K is over expressed, aberrantly localised and is associated with poor prognosis in colorectal cancer
B. Carpenter et al.
BRITISH JOURNAL OF CANCER (2006)
Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene
PA Mercado et al.
NUCLEIC ACIDS RESEARCH (2005)
Cooperative binding of the hnRNP K three KH domains to mRNA targets
A Paziewska et al.
FEBS LETTERS (2004)
HnRNP K: One protein multiple processes
K Bomsztyk et al.
BIOESSAYS (2004)
The UCSC Table Browser data retrieval tool
D Karolchik et al.
NUCLEIC ACIDS RESEARCH (2004)
A novel set of nuclear localization signals determine distributions of the αCP RNA-binding proteins
AN Chkheidze et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)