Related references
Note: Only part of the references are listed.Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humans
Nicole J. Van Bergen et al.
HUMAN MOLECULAR GENETICS (2022)
Protein structural and mechanistic basis of progeroid laminopathies
Agathe Marcelot et al.
FEBS JOURNAL (2021)
Dissecting the Structural Dynamics of the Nuclear Pore Complex
Zhanna Hakhverdyan et al.
MOLECULAR CELL (2021)
Epigenetic Small Molecules Rescue Nucleocytoplasmic Transport and DNA Damage Phenotypes in C9ORF72 ALS/FTD
Melina Ramic et al.
BRAIN SCIENCES (2021)
Non-neuronal cells in amyotrophic lateral sclerosis - from pathogenesis to biomarkers
Bjorn F. Vahsen et al.
NATURE REVIEWS NEUROLOGY (2021)
Nuclear lamina invaginations are not a pathological feature of C9orf72 ALS/FTD
Alyssa N. Coyne et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2021)
Interactions between ALS-linked FUS and nucleoporins are associated with defects in the nucleocytoplasmic transport pathway
Yen-Chen Lin et al.
NATURE NEUROSCIENCE (2021)
Nuclear accumulation of CHMP7 initiates nuclear pore complex injury and subsequent TDP-43 dysfunction in sporadic and familial ALS
Alyssa N. Coyne et al.
SCIENCE TRANSLATIONAL MEDICINE (2021)
C9orf72-derived arginine-rich poly-dipeptides impede phase modifiers
Hitoki Nanaura et al.
NATURE COMMUNICATIONS (2021)
Multiple pathways of toxicity induced by c9orf72 dipeptide repeat aggregates and G4C2 RNA in a cellular model
Frederic Frottin et al.
ELIFE (2021)
The ESCRT-III protein VPS4, but not CHMP4B or CHMP2B, is pathologically increased in familial and sporadic ALS neuronal nuclei
Alyssa N. Coyne et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2021)
Measuring and Interpreting Nuclear Transport in Neurodegenerative Disease-The Example of C9orf72 ALS
Marije F. W. Semmelink et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)
Core Components of the Nuclear Pore Bind Distinct States of Chromatin and Contribute to Polycomb Repression
Alejandro Gozalo et al.
MOLECULAR CELL (2020)
C9orf72 arginine-rich dipeptide repeat proteins disrupt karyopherin-mediated nuclear import
Lindsey R. Hayes et al.
ELIFE (2020)
SuperPlots: Communicating reproducibility and variability in cell biology
Samuel J. Lord et al.
JOURNAL OF CELL BIOLOGY (2020)
Nucleoporin 153 links nuclear pore complex to chromatin architecture by mediating CTCF and cohesin binding
Shinichi Kadota et al.
NATURE COMMUNICATIONS (2020)
Spatial control of nucleoporin condensation by fragile X-related proteins
Arantxa Agote-Aran et al.
EMBO JOURNAL (2020)
Amyotrophic lateral sclerosis: a clinical review
P. Masrori et al.
EUROPEAN JOURNAL OF NEUROLOGY (2020)
Correction of amyotrophic lateral sclerosis related phenotypes in induced pluripotent stem cell-derived motor neurons carrying a hexanucleotide expansion mutation in C9orf72 by CRISPR/Cas9 genome editing using homology-directed repair
Nidaa A. Ababneh et al.
HUMAN MOLECULAR GENETICS (2020)
Molecular determinants of large cargo transport into the nucleus
Giulia Paci et al.
ELIFE (2020)
Structural and Mechanical Aberrations of the Nuclear Lamina in Disease
Merel Stiekema et al.
CELLS (2020)
G4C2 Repeat RNA Initiates a POM121-Mediated Reduction in Specific Nucleoporins in C9orf72 ALS/FTD
Alyssa N. Coyne et al.
NEURON (2020)
TPR is required for the efficient nuclear export of mRNAs and lncRNAs from short and intron-poor genes
Eliza S. Lee et al.
NUCLEIC ACIDS RESEARCH (2020)
C9orf72 poly(GR) aggregation induces TDP-43 proteinopathy
Casey N. Cook et al.
SCIENCE TRANSLATIONAL MEDICINE (2020)
Nucleoporin TPR is an integral component of the TREX-2 mRNA export pathway
Vasilisa Aksenova et al.
NATURE COMMUNICATIONS (2020)
The Structure of the Nuclear Pore Complex (An Update)
Daniel H. Lin et al.
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 88 (2019)
NUP214 deficiency causes severe encephalopathy and microcephaly in humans
Hanan E. Shamseldin et al.
HUMAN GENETICS (2019)
Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy
Jeannie Chew et al.
MOLECULAR NEURODEGENERATION (2019)
Cytoplasmic TDP-43 De-mixing Independent of Stress Granules Drives Inhibition of Nuclear Import, Loss of Nuclear TDP-43, and Cell Death
Fatima Gasset-Rosa et al.
NEURON (2019)
Heterochromatin anomalies and double-stranded RNA accumulation underlie C9orf72 poly(PR) toxicity
Yong-Jie Zhang et al.
SCIENCE (2019)
Structure and Assembly of the Nuclear Pore Complex
Bernhard Hampoelz et al.
Annual Review of Biophysics (2019)
An ESCRT-LEM protein surveillance system is poised to directly monitor the nuclear envelope and nuclear transport system
David J. Thaller et al.
ELIFE (2019)
Pathogenic Variants in NUP214 Cause Plugged'' Nuclear Pore Channels and Acute Febrile Encephalopathy
Boris Fichtman et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2019)
Nuclear pores in genome architecture and enhancer function
Pau Pascual-Garcia et al.
CURRENT OPINION IN CELL BIOLOGY (2019)
The neuropathological diagnosis of Alzheimer's disease
Michael A. DeTure et al.
MOLECULAR NEURODEGENERATION (2019)
Modulation of actin polymerization affects nucleocytoplasmic transport in multiple forms of amyotrophic lateral sclerosis
Anthony Giampetruzzi et al.
NATURE COMMUNICATIONS (2019)
Tau-induced nuclear envelope invagination causes a toxic accumulation of mRNA in Drosophila
Garrett L. Cornelison et al.
AGING CELL (2019)
C9orf72-generated poly-GR and poly-PR do not directly interfere with nucleocytoplasmic transport
Joni Vanneste et al.
SCIENTIFIC REPORTS (2019)
Visualization of long-lived proteins reveals age mosaicism within nuclei of postmitotic cells
Brandon H. Toyama et al.
JOURNAL OF CELL BIOLOGY (2019)
CRISPR-Cas9 in genome editing: Its function and medical applications
Saedeh Khadempar et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2019)
Microtubules Deform the Nuclear Membrane and Disrupt Nucleocytoplasmic Transport in Tau-Mediated Frontotemporal Dementia
Francesco Paonessa et al.
CELL REPORTS (2019)
Huntington's disease: a clinical review
P. McColgan et al.
EUROPEAN JOURNAL OF NEUROLOGY (2018)
Nuclear Import Receptor Inhibits Phase Separation of FUS through Binding to Multiple Sites
Takuya Yoshizawa et al.
CELL (2018)
Phase Separation of FUS Is Suppressed by Its Nuclear Import Receptor and Arginine Methylation
Mario Hofweber et al.
CELL (2018)
Stress Granule Assembly Disrupts Nucleocytoplasmic Transport
Ke Zhang et al.
CELL (2018)
Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains
Lin Guo et al.
CELL (2018)
TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD
Ching-Chieh Chou et al.
NATURE NEUROSCIENCE (2018)
Stoichiometry and compositional plasticity of the yeast nuclear pore complex revealed by quantitative fluorescence microscopy
Sasikumar Rajoo et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
The CRISPR tool kit for genome editing and beyond
Mazhar Adli
NATURE COMMUNICATIONS (2018)
Nuclear pore complexes as hubs for gene regulation
Maximiliano A. D'Angelo
NUCLEUS (2018)
Nuclear pore complexes as hubs for gene regulation
Maximiliano A. D'Angelo
NUCLEUS (2018)
Tau Protein Disrupts Nucleocytoplasmic Transport in Alzheimer's Disease
Bahareh Eftekharzadeh et al.
NEURON (2018)
Moonlighting nuclear pore proteins: tissue-specific nucleoporin function in health and disease
Ramona Juhlen et al.
HISTOCHEMISTRY AND CELL BIOLOGY (2018)
Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence
Edith Bonnin et al.
PLOS GENETICS (2018)
Laminopathies; Mutations on single gene and various human genetic diseases
So-mi Kang et al.
BMB REPORTS (2018)
Sense-encoded poly-GR dipeptide repeat proteins correlate to neurodegeneration and uniquely co-localize with TDP-43 in dendrites of repeat-expanded C9orf72 amyotrophic lateral sclerosis
Shahram Saberi et al.
ACTA NEUROPATHOLOGICA (2018)
Cytoplasmic poly-GA aggregates impair nuclear import of TDP-43 in C9orf72 ALS/FTLD
Bahram Khosravi et al.
HUMAN MOLECULAR GENETICS (2017)
The nuclear pore complex: understanding its function through structural insight
Martin Beck et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2017)
Homozygous mutation in NUP107 leads to microcephaly with steroid-resistant nephrotic condition similar to Galloway-Mowat syndrome
Rasim Ozgur Rosti et al.
JOURNAL OF MEDICAL GENETICS (2017)
Antisense Oligonucleotides: Translation from Mouse Models to Human Neurodegenerative Diseases
Kathleen M. Schoch et al.
NEURON (2017)
Polyglutamine-Expanded Huntingtin Exacerbates Age-Related Disruption of Nuclear Integrity and Nucleocytoplasmic Transport
Fatima Gasset-Rosa et al.
NEURON (2017)
Mutant Huntingtin Disrupts the Nuclear Pore Complex
Jonathan C. Grima et al.
NEURON (2017)
Toxic PRn poly-dipeptides encoded by the C9orf72 repeat expansion block nuclear import and export
Kevin Y. Shi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
The function of the inner nuclear envelope protein SUN1 in mRNA export is regulated by phosphorylation
Ping Li et al.
SCIENTIFIC REPORTS (2017)
Nuclear pore complexes and regulation of gene expression
Marcela Raices et al.
CURRENT OPINION IN CELL BIOLOGY (2017)
The nucleus: keeping it together by keeping it apart
C. Patrick Lusk et al.
CURRENT OPINION IN CELL BIOLOGY (2017)
Cytoplasmic protein aggregates interfere with nucleocytoplasmic transport of protein and RNA
Andreas C. Woerner et al.
SCIENCE (2016)
The Nuclear Pore Complex as a Flexible and DynamicGate
Kevin E. Knockenhauer et al.
CELL (2016)
Lamin Dysfunction Mediates Neurodegeneration in Tauopathies
Bess Frost et al.
CURRENT BIOLOGY (2016)
Genetics of Frontotemporal Dementia
Diana A. Olszewska et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2016)
Chm7 and Heh1 collaborate to link nuclear pore complex quality control with nuclear envelope sealing
Brant M. Webster et al.
EMBO JOURNAL (2016)
Nucleoporin genes in human diseases
Valeria Nofrini et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2016)
Evolution of a transcriptional regulator from a transmembrane nucleoporin
Tobias M. Franks et al.
GENES & DEVELOPMENT (2016)
Nuclear envelope rupture is induced by actin-based nucleus confinement
Emily M. Hatch et al.
JOURNAL OF CELL BIOLOGY (2016)
C9ORF72 poly(GA) aggregates sequester and impair HR23 and nucleocytoplasmic transport proteins
Yong-Jie Zhang et al.
NATURE NEUROSCIENCE (2016)
The selective permeability barrier in the nuclear pore complex
Christina Li et al.
NUCLEUS (2016)
The selective permeability barrier in the nuclear pore complex
Christina Li et al.
NUCLEUS (2016)
Energetics of Transport through the Nuclear Pore Complex
Ali Ghavami et al.
PLOS ONE (2016)
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD
Steven Boeynaems et al.
SCIENTIFIC REPORTS (2016)
Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome
Noriko Miyake et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects
Jerome Mertens et al.
CELL STEM CELL (2015)
Nuclear pore proteins and the control of genome functions
Arkaitz Ibarra et al.
GENES & DEVELOPMENT (2015)
The C9orf72 repeat expansion disrupts nucleocytoplasmic transport
Ke Zhang et al.
NATURE (2015)
GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport
Brian D. Freibaum et al.
NATURE (2015)
Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS
Ana Jovicic et al.
NATURE NEUROSCIENCE (2015)
RAN Translation in Huntington Disease
Monica Banez-Coronel et al.
NEURON (2015)
Quantitative Interaction Proteomics of Neurodegenerative Disease Proteins
Fabian Hosp et al.
CELL REPORTS (2015)
Alzheimer's disease
Colin L. Masters et al.
NATURE REVIEWS DISEASE PRIMERS (2015)
Surveillance of Nuclear Pore Complex Assembly by ESCRT-III/Vps4
Brant M. Webster et al.
CELL (2014)
Nup50 is required for cell differentiation and exhibits transcription-dependent dynamics
Abigail L. Buchwalter et al.
MOLECULAR BIOLOGY OF THE CELL (2014)
Tau promotes neurodegeneration through global chromatin relaxation
Bess Frost et al.
NATURE NEUROSCIENCE (2014)
Alzheimer's Disease Genetics: From the Bench to the Clinic
Celeste M. Karch et al.
NEURON (2014)
C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins
Sarah Mizielinska et al.
SCIENCE (2014)
Nucleoporin Nup98 Associates with Trx/MLL and NSL Histone-Modifying Complexes and Regulates Hox Gene Expression
Pau Pascual-Garcia et al.
CELL REPORTS (2014)
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
Maria J. Melia et al.
BRAIN (2013)
Identification of Long-Lived Proteins Reveals Exceptional Stability of Essential Cellular Structures
Brandon H. Toyama et al.
CELL (2013)
Gle1 Functions during mRNA Export in an Oligomeric Complex that Is Altered in Human Disease
Andrew W. Folkmann et al.
CELL (2013)
Cell type-specific nuclear pores: a case in point for context-dependent stoichiometry of molecular machines
Alessandro Ori et al.
MOLECULAR SYSTEMS BIOLOGY (2013)
RNA Toxicity from the ALS/FTD C9ORF72 Expansion Is Mitigated by Antisense Intervention
Christopher J. Donnelly et al.
NEURON (2013)
Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis
Shuo-Chien Ling et al.
NEURON (2013)
Antisense Oligonucleotides: Treating Neurodegeneration at the Level of RNA
Sarah L. DeVos et al.
NEUROTHERAPEUTICS (2013)
Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration
Clotilde Lagier-Tourenne et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
The Nup153-Nup50 Protein Interface and Its Role in Nuclear Import
Masaki Makise et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Neurological features in adult Triple-A (Allgrove) syndrome
Anne-Evelyne Vallet et al.
JOURNAL OF NEUROLOGY (2012)
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
Chi-Hong Wu et al.
NATURE (2012)
Nuclear pore complex composition: a new regulator of tissue-specific and developmental functions
Marcela Raices et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2012)
Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration
Edward B. Lee et al.
NATURE REVIEWS NEUROSCIENCE (2012)
Nuclear Distributions of NUP62 and NUP214 Suggest Architectural Diversity and Spatial Patterning among Nuclear Pore Complexes
Yayoi Kinoshita et al.
PLOS ONE (2012)
Extremely Long-Lived Nuclear Pore Proteins in the Rat Brain
Jeffrey N. Savas et al.
SCIENCE (2012)
Dynamics and diverse functions of nuclear pore complex proteins
Guillaume Chatel et al.
NUCLEUS (2012)
FTD and ALS: A Tale of Two Diseases
R. Ferrari et al.
CURRENT ALZHEIMER RESEARCH (2011)
Gle1 Is a Multifunctional DEAD-box Protein Regulator That Modulates Ded1 in Translation Initiation
Timothy A. Bolger et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Huntington's disease: from molecular pathogenesis to clinical treatment
Christopher A. Ross et al.
LANCET NEUROLOGY (2011)
Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
Peter M. Andersen et al.
NATURE REVIEWS NEUROLOGY (2011)
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
Mariely DeJesus-Hernandez et al.
NEURON (2011)
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Alan E. Renton et al.
NEURON (2011)
Nuclear import impairment causes cytoplasmic trans-activation response DNA-binding protein accumulation and is associated with frontotemporal lobar degeneration
Agnes L. Nishimura et al.
BRAIN (2010)
Chromatin-Bound Nuclear Pore Components Regulate Gene Expression in Higher Eukaryotes
Maya Capelson et al.
CELL (2010)
Triple A syndrome: 32 years experience of a single centre (1977-2008)
Tatjana Milenkovic et al.
EUROPEAN JOURNAL OF PEDIATRICS (2010)
Two Patients with an Identical Novel Mutation in the AAAS Gene and Similar Phenotype of Triple A (Allgrove) Syndrome
I. Krull et al.
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES (2010)
The nuclear pore complex: bridging nuclear transport and gene regulation
Caterina Strambio-De-Castillia et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2010)
Nuclear Pore Proteins Nup153 and Megator Define Transcriptionally Active Regions in the Drosophila Genome
Juan M. Vaquerizas et al.
PLOS GENETICS (2010)
Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2
Derek E. Neilson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Age-Dependent Deterioration of Nuclear Pore Complexes Causes a Loss of Nuclear Integrity in Postmitotic Cells
Maximiliano A. D'Angelo et al.
CELL (2009)
The role of nuclear pores in gene regulation, development and disease
Maya Capelson et al.
EMBO REPORTS (2009)
Evidence for a Shared Nuclear Pore Complex Architecture That Is Conserved from the Last Common Eukaryotic Ancestor
Jeffrey A. DeGrasse et al.
MOLECULAR & CELLULAR PROTEOMICS (2009)
Oxidative Stress Inhibits Nuclear Protein Export by Multiple Mechanisms That Target FG Nucleoporins and Crm1
Noah Crampton et al.
MOLECULAR BIOLOGY OF THE CELL (2009)
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
T. J. Kwiatkowski et al.
SCIENCE (2009)
Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death
Xianqin Zhang et al.
CELL (2008)
Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease
Heidi O. Nousiainen et al.
NATURE GENETICS (2008)
Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype
K. A. Josephs et al.
NEUROLOGY (2008)
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
Jemeen Sreedharan et al.
SCIENCE (2008)
Subdiffraction multicolor imaging of the nuclear periphery with 3D structured illumination microscopy
Lothar Schermelleh et al.
SCIENCE (2008)
Cognitive impairment in familial ALS
M. W. Wheaton et al.
NEUROLOGY (2007)
TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease
Catalina Amador-Ortiz et al.
ANNALS OF NEUROLOGY (2007)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Lamin B1 duplications cause autosomal dominant leukodystrophy
Quasar S. Padiath et al.
NATURE GENETICS (2006)
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Matt Baker et al.
NATURE (2006)
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
Marc Cruts et al.
NATURE (2006)
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis
Lina Basel-Vanagaite et al.
ANNALS OF NEUROLOGY (2006)
Activation of the DExD/H-box protein Dbp5 by the nuclear-pore protein Gle1 and its coactivator InsP6 is required for mRNA export
Christine S. Weirich et al.
NATURE CELL BIOLOGY (2006)
Nuclear pore complex assembly and maintenance in POM121-and gp210-deficient cells
Fabrizia Stavru et al.
JOURNAL OF CELL BIOLOGY (2006)
The relationship between amyotrophic lateral sclerosis and frontotemporal dementia
George M. Ringbolz et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2006)
Nup153 affects entry of messenger and ribosomal ribonucleoproteins into the nuclear basket during export
T Soop et al.
MOLECULAR BIOLOGY OF THE CELL (2005)
Nup50/Npap60 function in nuclear protein import complex disassembly and importin recycling
Y Matsuura et al.
EMBO JOURNAL (2005)
Nup358/RanBP2 attaches to the nuclear pore complex via association with Nup88 and Nup214/CAN and plays a supporting role in CRM1-mediated nuclear protein export
R Bernad et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Mapping the dynamic organization of the nuclear pore complex inside single living cells
G Rabut et al.
NATURE CELL BIOLOGY (2004)
Lamin A truncation in Hutchinson-Gilford progeria
A De Sandre-Giovannoli et al.
SCIENCE (2003)
The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome
JM Cronshaw et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Proteomic analysis of the mammalian nuclear pore complex
JA Cronshaw et al.
JOURNAL OF CELL BIOLOGY (2002)
Npap60/Nup50 is a tri-stable switch that stimulates importin-α:β-mediated nuclear protein import
ME Lindsay et al.
CELL (2002)
Age-associated reduction of nuclear protein import in human fibroblasts
G Pujol et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2002)
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse
A De Sandre-Giovannoli et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Gradient of increasing affinity of importin β for nucleoporins along the pathway of nuclear import
I Ben-Efraim et al.
JOURNAL OF CELL BIOLOGY (2001)
Nup50, a nucleoplasmically oriented nucleoporin with a role in nuclear protein export
TL Guan et al.
MOLECULAR AND CELLULAR BIOLOGY (2000)
The yeast nuclear pore complex: Composition, architecture, and transport mechanism
MP Rout et al.
JOURNAL OF CELL BIOLOGY (2000)
Share Paper
