Muscle regulates mTOR dependent axonal local translation in motor neurons via CTRP3 secretion: implications for a neuromuscular disorder, spinal muscular atrophy (Q90728074)

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scientific article published on 15 October 2019

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English	Muscle regulates mTOR dependent axonal local translation in motor neurons via CTRP3 secretion: implications for a neuromuscular disorder, spinal muscular atrophy	scientific article published on 15 October 2019

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15 April 2020

Muscle regulates mTOR dependent axonal local translation in motor neurons via CTRP3 secretion: implications for a neuromuscular disorder, spinal muscular atrophy (English)

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15 April 2020

spinal muscular atrophy

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muscular atrophy

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15 April 2020

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Wiebke A Rehorst

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15 April 2020

Maximilian P Thelen

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15 April 2020

Hendrik Nolte

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15 April 2020

Clara Türk

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Sebahattin Cirak

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15 April 2020

Jonathan M Peterson

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15 April 2020

G William Wong

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15 April 2020

Brunhilde Wirth

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Marcus Krüger

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15 April 2020

Dominic Winter

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15 October 2019

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15 April 2020

Acta Neuropathologica Communications

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15 April 2020

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15 April 2020

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15 April 2020

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15 April 2020

Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Myogenic cell lines derived from transgenic mice carrying a thermolabile T antigen: a model system for the derivation of tissue-specific and mutation-specific cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Correlation between severity and SMN protein level in spinal muscular atrophy

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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A mouse model for spinal muscular atrophy

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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VAP-A binds promiscuously to both v- and tSNAREs

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Sorting of internalized neurotrophins into an endocytic transcytosis pathway via the Golgi system: Ultrastructural analysis in retinal ganglion cells.

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Stable isotope labeling by amino acids in cell culture, SILAC, as a simple and accurate approach to expression proteomics

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Stop and go extraction tips for matrix-assisted laser desorption/ionization, nanoelectrospray, and LC/MS sample pretreatment in proteomics

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Conserved roles for Slit and Robo proteins in midline commissural axon guidance

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Role of myokines in exercise and metabolism

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Defective Ca2+ channel clustering in axon terminals disturbs excitability in motoneurons in spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Molecular, biochemical and functional characterizations of C1q/TNF family members: adipose-tissue-selective expression patterns, regulation by PPAR-gamma agonist, cysteine-mediated oligomerizations, combinatorial associations and metabolic functions

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Endocytosis of adiponectin receptor 1 through a clathrin- and Rab5-dependent pathway.

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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SUnSET, a nonradioactive method to monitor protein synthesis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Vascular perfusion abnormalities in infants with spinal muscular atrophy

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Role of muscle-derived growth factors in bone formation

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Gemin5 delivers snRNA precursors to the SMN complex for snRNP biogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Muscle-derived collagen XIII regulates maturation of the skeletal neuromuscular junction.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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C1q/TNF-related protein-3 (CTRP3), a novel adipokine that regulates hepatic glucose output

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Conserved Genes Act as Modifiers of Invertebrate SMN Loss of Function Defects

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Increased IGF-1 in muscle modulates the phenotype of severe SMA mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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TSC1/TSC2 signaling in the CNS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Activation of mTORC2 by Association with the Ribosome

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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The survival of motor neuron (SMN) protein interacts with the mRNA-binding protein HuD and regulates localization of poly(A) mRNA in primary motor neuron axons.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Interaction of survival of motor neuron (SMN) and HuD proteins with mRNA cpg15 rescues motor neuron axonal deficits.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72,400 specimens

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Reversible molecular pathology of skeletal muscle in spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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IGF-1 delivery to CNS attenuates motor neuron cell death but does not improve motor function in type III SMA mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Glucose metabolism and pancreatic defects in spinal muscular atrophy

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Selective enrichment of newly synthesized proteins for quantitative secretome analysis

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Spinal muscular atrophy: going beyond the motor neuron

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https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Morphological characteristics of motor neurons do not determine their relative susceptibility to degeneration in a mouse model of severe spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction, termed MaxLFQ.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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SMN regulates axonal local translation via miR-183/mTOR pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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The Neuromuscular Junction: Aging at the Crossroad between Nerves and Muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Motor neuron cell bodies are actively positioned by Slit/Robo repulsion and Netrin/DCC attraction

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Molecular and Genetic Analyses of Collagen Type IV Mutant Mouse Models of Spontaneous Intracerebral Hemorrhage Identify Mechanisms for Stroke Prevention

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Moving towards treatments for spinal muscular atrophy: hopes and limits

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Mechanisms Regulating Neuromuscular Junction Development and Function and Causes of Muscle Wasting

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Impaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetases

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Lower Circulating C1q/TNF-Related Protein-3 (CTRP3) Levels Are Associated with Obesity: A Cross-Sectional Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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IGF-1R Reduction Triggers Neuroprotective Signaling Pathways in Spinal Muscular Atrophy Mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Responses to Fasting and Glucose Loading in a Cohort of Well Children with Spinal Muscular Atrophy Type II.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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CTRP3 deficiency reduces liver size and alters IL-6 and TGFβ levels in obese mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extracellular and Luminal pH Regulation by Vacuolar H+-ATPase Isoform Expression and Targeting to the Plasma Membrane and Endosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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The Perseus computational platform for comprehensive analysis of (prote)omics data

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased function of survival motor neuron protein impairs endocytic pathways.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Motor neuron mitochondrial dysfunction in spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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The Power of Human Protective Modifiers: PLS3 and CORO1C Unravel Impaired Endocytosis in Spinal Muscular Atrophy and Rescue SMA Phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of Putative Receptors for the Novel Adipokine CTRP3 Using Ligand-Receptor Capture Technology

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Altered mRNA Splicing in SMN-Depleted Motor Neuron-Like Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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C1q/Tumor Necrosis Factor-Related Protein-3 Attenuates Brain Injury after Intracerebral Hemorrhage via AMPK-Dependent Pathway in Rat

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurocalcin Delta Suppression Protects against Spinal Muscular Atrophy in Humans and across Species by Restoring Impaired Endocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CTRP3 attenuates cardiac dysfunction, inflammation, oxidative stress and cell death in diabetic cardiomyopathy in rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - a literature review.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Molecular control of local translation in axon development and maintenance

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Collagen VI is required for the structural and functional integrity of the neuromuscular junction

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Transgenic overexpression of CTRP3 prevents alcohol-induced hepatic triglyceride accumulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

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Neuronal activity regulates DROSHA via autophagy in spinal muscular atrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Instant Clue: A Software Suite for Interactive Data Visualization and Analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired myogenic development, differentiation and function in hESC-derived SMA myoblasts and myotubes

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further refinement of COL4A1 and COL4A2 related cortical malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ALS/FTD-Linked Mutation in FUS Suppresses Intra-axonal Protein Synthesis and Drives Disease Without Nuclear Loss-of-Function of FUS

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurologic phenotypes associated with / mutations: Expanding the spectrum of disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ALS mutations of FUS suppress protein translation and disrupt the regulation of nonsense-mediated decay

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic reduction of eEF2 kinase alleviates pathophysiology in Alzheimer's disease model mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum levels of CTRP3 in diabetic nephropathy and its relationship with insulin resistance and kidney function

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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COL4A1 Mutations Cause Neuromuscular Disease with Tissue-Specific Mechanistic Heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/31615574

12 December 2020

based on heuristic

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Investigation of Oligodendrocyte Precursor Cell Differentiation by Quantitative Proteomics

1 reference

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12 December 2020

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Identifiers

10.1186/S40478-019-0806-3

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