Publications by authors named "Wen-Lang Lin"

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Capillary basal lamina in human brain and spinal cord has fibrillar collagen type I and type III: Ignorance may not be bliss.
Wen-Lang Lin, Dennis W Dickson

Free Neuropathol· January 2025

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Assessment of Skin Biopsy as a Diagnostic Biomarker in CSF1R-Related Disorder.
Jaroslaw Dulski, Peizhou Jiang, Wen-Lang Lin, Dennis W Dickson, Zbigniew K Wszolek

Neurology· June 2024

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Vascular Collagen Type-IV in Hypertension and Cerebral Small Vessel Disease.
Apoorva A Kumar, Natalie Yeo, Max Whittaker, Priya Attra, Thomas R Barrick, Wen Lang Lin

Stroke· December 2022

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Mitophagy alterations in Alzheimer's disease are associated with granulovacuolar degeneration and early tau pathology.
Xu Hou, Jens O Watzlawik, Casey Cook, Chia-Chen Liu, Silvia S Kang, Wen-Lang Lin

Alzheimers Dement· October 2020

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Neuronal intermediate filament inclusion disease may be incorrectly classified as a subtype of FTLD-FUS.
Kevin F Bieniek, Keith A Josephs, Wen-Lang Lin, Dennis W Dickson

Free Neuropathol· March 2020

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Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease.
Xu Hou, Fabienne C Fiesel, Dominika Truban, Monica Castanedes Casey, Wen-Lang Lin, Linda G Rousseau

Autophagy· October 2019

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Combining P301L and S320F tau variants produces a novel accelerated model of tauopathy.
Emily J Koller, Elsa Gonzalez De La Cruz, Timothy Machula, Kristen R Ibanez, Wen-Lang Lin

Hum Mol Genet· October 2019

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X-Linked Lymphoproliferative Syndrome Presenting as Adult-Onset Multi-Infarct Dementia.
Patrick R Blackburn, Wen-Lang Lin, David A Miller, Oswaldo Lorenzo-Betancor, Emily S Edwards

J Neuropathol Exp Neurol· May 2019

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rAAV-based brain slice culture models of Alzheimer's and Parkinson's disease inclusion pathologies.
Cara L Croft, Pedro E Cruz, Daniel H Ryu, Carolina Ceballos-Diaz, Kevin H Strang, Wen-Lang Lin

J Exp Med· March 2019

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Heterochromatin anomalies and double-stranded RNA accumulation underlie poly(PR) toxicity.
Yong-Jie Zhang, Lin Guo, Patrick K Gonzales, Tania F Gendron, Yanwei Wu, Ruilin Tian, Wen-Lang Lin, Christopher D Link

Science· February 2019

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Tangential Flow Filtration for Highly Efficient Concentration of Extracellular Vesicles from Large Volumes of Fluid.
Sara Busatto, George Vilanilam, Taylor Ticer, Wen-Lang Lin, Dennis W Dickson

Cells· December 2018

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FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G.
Pawel Tacik, Michael A DeTure, Yari Carlomagno, Wen-Lang Lin, Melissa E Murray

Brain Pathol· September 2017

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p62 Pathology Model in the Rat Substantia Nigra with Filamentous Inclusions and Progressive Neurodegeneration.
Kasey L Jackson, Wen-Lang Lin, Sumitra Miriyala, Robert D Dayton, Manikandan Panchatcharam

PLoS One· August 2017

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Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy.
Takayasu Mishima, Shunsuke Koga, Wen-Lang Lin, Koji Kasanuki, Monica Castanedes-Casey

J Neuropathol Exp Neurol· August 2017

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C9ORF72 poly(GA) aggregates sequester and impair HR23 and nucleocytoplasmic transport proteins.
Yong-Jie Zhang, Tania F Gendron, Jonathan C Grima, Hiroki Sasaguri, Karen Jansen-West, Wen-Lang Lin, Christopher D Link

Nat Neurosci· May 2016

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Tau deposition drives neuropathological, inflammatory and behavioral abnormalities independently of neuronal loss in a novel mouse model.
Casey Cook, Silvia S Kang, Yari Carlomagno, Wen-Lang Lin, Mei Yue, Linda Rousseau

Hum Mol Genet· November 2015

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A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease.
Pawel Tacik, Michael DeTure, Kelly M Hinkle, Wen-Lang Lin, Monica Sanchez-Contreras

J Neuropathol Exp Neurol· November 2015

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ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function.
Tetsuro Murakami, Seema Qamar, Julie Qiaojin Lin, Gabriele S Kaminski Schierle, Eric Rees, Wen-Lang Lin

Neuron· November 2015

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A novel tau mutation, p.K317N, causes globular glial tauopathy.
Pawel Tacik, Michael DeTure, Wen-Lang Lin, Monica Sanchez Contreras, Aleksandra Wojtas

Acta Neuropathol· August 2015

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A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration.
Masataka Nakamura, Kevin F Bieniek, Wen-Lang Lin, Neill R Graff-Radford, Melissa E Murray

Acta Neuropathol· July 2015

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Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein.
Naoya Aoki, Philip J Boyer, Cheryl Lund, Wen-Lang Lin, Shunsuke Koga

Acta Neuropathol· July 2015

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Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress.
Yong-Jie Zhang, Karen Jansen-West, Ya-Fei Xu, Tania F Gendron, Kevin F Bieniek, Wen-Lang Lin

Acta Neuropathol· October 2014

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Nutrient deprivation induces α-synuclein aggregation through endoplasmic reticulum stress response and SREBP2 pathway.
Peizhou Jiang, Ming Gan, Wen-Lang Lin, Shu-Hui C Yen

Front Aging Neurosci· October 2014

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Optineurin immunoreactivity in neuronal and glial intranuclear inclusions in adult-onset neuronal intranuclear inclusion disease.
Masataka Nakamura, Melissa E Murray, Wen-Lang Lin, Hirofumi Kusaka, Dennis W Dickson

Am J Neurodegener Dis· September 2014

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Concurrent variably protease-sensitive prionopathy and amyotrophic lateral sclerosis.
Ashley Cannon, Kevin F Bieniek, Wen-Lang Lin, Silvio Notari, Wen-Quan Zou

Acta Neuropathol· August 2014

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