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。Improving mitochondria and ER stability helps eliminate upper motor neuron degeneration that occurs due to mSOD1 toxicity and TDP-43 pathology
Baris Genc et al.
CLINICAL AND TRANSLATIONAL MEDICINE (2021)
Neuropathological profile of long-duration amyotrophic lateral sclerosis in military Veterans
Keith R. Spencer et al.
BRAIN PATHOLOGY (2020)
Quantitative patterns of motor cortex proteinopathy across ALS genotypes
Matthew Nolan et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2020)
Morphology and Distribution of TDP-43 Pre-inclusions in Primary Progressive Aphasia
Garam Kim et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2019)
An autopsy case of early-stage amyotrophic lateral sclerosis with TDP-43 immunoreactive neuronal, but not glial, inclusions
Tomoya Kon et al.
NEUROPATHOLOGY (2019)
Mitochondria, ER, and nuclear membrane defects reveal early mechanisms for upper motor neuron vulnerability with respect to TDP-43 pathology
Mukesh Gautam et al.
ACTA NEUROPATHOLOGICA (2019)
Colocalization of Bunina bodies and TDP-43 inclusions in a case of sporadic amyotrophic lateral sclerosis with Lewy body-like hyaline inclusions
Yasuo Miki et al.
NEUROPATHOLOGY (2018)
Pathological TDP-43 changes in Betz cells differ from those in bulbar and spinal α-motoneurons in sporadic amyotrophic lateral sclerosis
Heiko Braak et al.
ACTA NEUROPATHOLOGICA (2017)
Heat Shock-induced Phosphorylation of TAR DNA-binding Protein 43 (TDP-43) by MAPK/ERK Kinase Regulates TDP-43 Function
Wen Li et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2017)
Spinal motor neuron protein supersaturation patterns are associated with inclusion body formation in ALS
Prajwal Ciryam et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Protein quality control at the endoplasmic reticulum
Kathleen McCaffrey et al.
PROTEOSTASIS (2016)
Quantification of the Relative Contributions of Loss-of-function and Gain-of-function Mechanisms in TAR DNA-binding Protein 43 (TDP-43) Proteinopathies
Roberta Cascella et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2016)
TDP-43 skeins show properties of amyloid in a subset of ALS cases
John L. Robinson et al.
ACTA NEUROPATHOLOGICA (2013)
Stages of pTDP-43 Pathology in Amyotrophic Lateral Sclerosis
Johannes Brettschneider et al.
ANNALS OF NEUROLOGY (2013)
National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease: a practical approach
Thomas J. Montine et al.
ACTA NEUROPATHOLOGICA (2012)
Amyotrophic Lateral Sclerosis with Demyelinating Neuropathy
Haruo Nishijima et al.
INTERNAL MEDICINE (2012)
Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration
Edward B. Lee et al.
NATURE REVIEWS NEUROSCIENCE (2012)
Autophagy in Spinal Cord Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis
Shoichi Sasaki
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2011)
Enhancement of native and phosphorylated TDP-43 immunoreactivity by proteinase K treatment following autoclave heating
Fumiaki Mori et al.
NEUROPATHOLOGY (2011)
Hyperphosphorylation as a Defense Mechanism to Reduce TDP-43 Aggregation
Huei-Ying Li et al.
PLOS ONE (2011)
Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form
Aaron Kerman et al.
ACTA NEUROPATHOLOGICA (2010)
Endoplasmic Reticulum Stress in Motor Neurons of the Spinal Cord in Sporadic Amyotrophic Lateral Sclerosis
Shoichi Sasaki
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2010)
Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology
Yasushi Nishihira et al.
ACTA NEUROPATHOLOGICA (2009)
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies
Manuela Neumann et al.
ACTA NEUROPATHOLOGICA (2009)
Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions
Yasushi Nishihira et al.
ACTA NEUROPATHOLOGICA (2008)
Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia
Fumiaki Mori et al.
ACTA NEUROPATHOLOGICA (2008)
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Masato Hasegawa et al.
ANNALS OF NEUROLOGY (2008)
Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis
Felix Geser et al.
ARCHIVES OF NEUROLOGY (2008)
Structural determinants of the cellular localization and shuttling of TDP-43
Youhna M. Ayala et al.
JOURNAL OF CELL SCIENCE (2008)
Anterior horn cells with abnormal TDP-43 immunoreactivities show fragmentation of the Golgi apparatus in ALS
Yukio Fujita et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2008)
Spinal anterior horn cells in sporadic amyotrophic lateral sclerosis show ribosomal detachment from, and cisternal distention of the rough endoplasmic reticulum
K. Oyanagi et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2008)
Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease
Nicholas J. Brandmeir et al.
ACTA NEUROPATHOLOGICA (2008)
Evidence that TDP-43 is not the major ubiquitinated target within the pathological inclusions of amyotrophic lateral sclerosis
Teresa Sanelli et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2007)
Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43
Yvonne Davidson et al.
ACTA NEUROPATHOLOGICA (2007)
分享论文
