4.6 Article

Miro1 deficiency in amyotrophic lateral sclerosis

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。
Article Biochemistry & Molecular Biology

MFN2 Couples Glutamate Excitotoxicity and Mitochondrial Dysfunction in Motor Neurons

Wenzhang Wang et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2015)

Article Biochemistry & Molecular Biology

Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models

Jordi Magrane et al.

HUMAN MOLECULAR GENETICS (2014)

Article Multidisciplinary Sciences

Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron disease

Tammy T. Nguyen et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)

Article Biochemistry & Molecular Biology

The ALS disease-associated mutant TDP-43 impairs mitochondrial dynamics and function in motor neurons

Wenzhang Wang et al.

HUMAN MOLECULAR GENETICS (2013)

Review Medicine, General & Internal

Mitochondrial Dynamics - Mitochondrial Fission and Fusion in Human Diseases

Stephen L. Archer

NEW ENGLAND JOURNAL OF MEDICINE (2013)

Editorial Material Neurosciences

Calcium, mitochondria, and the pathogenesis of ALS: the good, the bad, and the ugly

Manoj Kumar Jaiswal

FRONTIERS IN CELLULAR NEUROSCIENCE (2013)

Article Cell Biology

Mitochondrial Trafficking in Neurons

Thomas L. Schwarz

COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2013)

Review Clinical Neurology

The genetics and neuropathology of amyotrophic lateral sclerosis

Ammar Al-Chalabi et al.

ACTA NEUROPATHOLOGICA (2012)

Review Neurosciences

Mitochondrial transport in neurons: impact on synaptic homeostasis and neurodegeneration

Zu-Hang Sheng et al.

NATURE REVIEWS NEUROSCIENCE (2012)

Review Biochemistry & Molecular Biology

Import, Maturation, and Function of SOD1 and Its Copper Chaperone CCS in the Mitochondrial Intermembrane Space

Hibiki Kawamata et al.

ANTIOXIDANTS & REDOX SIGNALING (2010)

Review Biochemistry & Molecular Biology

Mitochondrial dysfunction in amyotrophic lateral sclerosis

Ping Shi et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2010)

Review Biochemistry & Molecular Biology

Abnormal mitochondrial dynamics and neurodegenerative diseases

Bo Su et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2010)

Article Multidisciplinary Sciences

Deficits in axonal transport precede ALS symptoms in vivo

Lynsey G. Bilsland et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Genetics & Heredity

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

Edor Kabashi et al.

NATURE GENETICS (2008)

Article Multidisciplinary Sciences

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

Jemeen Sreedharan et al.

SCIENCE (2008)

Review Cell Biology

Mitochondria and neuronal activity

Oliver Kann et al.

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2007)

Review Biochemistry & Molecular Biology

Mitochondrial morphology and distribution in mammalian cells

Ann E. Frazier et al.

BIOLOGICAL CHEMISTRY (2006)

Article Biochemistry & Molecular Biology

Caspase-3 cleaves and inactivates the glutamate transporter EAAT2

William Boston-Howes et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2006)

Review Neurosciences

Unraveling the mechanisms involved in motor neuron degeneration in ALS

LI Bruijn et al.

ANNUAL REVIEW OF NEUROSCIENCE (2004)

Review Medicine, General & Internal

Medical progress: Amyotrophic lateral sclerosis.

LP Rowland et al.

NEW ENGLAND JOURNAL OF MEDICINE (2001)

Article Clinical Neurology

Activation of p38 kinase links tau phosphorylation, oxidative stress, and cell cycle-related events in Alzheimer disease

XW Zhu et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2000)

Article Cell Biology

Glutamate slows axonal transport of neurofilaments in transfected neurons

S Ackerley et al.

JOURNAL OF CELL BIOLOGY (2000)