Involvement of neuronal and muscular Trk-fused gene (TFG) defects in the development of neurodegenerative diseases

Proteogenomics analysis unveils a TFG-RET gene fusion and druggable targets in papillary thyroid carcinomas

(2020) Aswini Krishnan et al.   Nature Communications

Multiple MuSK signaling pathways and the aging neuromuscular junction

(2020) Lauren A. Fish et al.   NEUROSCIENCE LETTERS

Tropomyosin-receptor kinase fused gene (TFG) regulates lipid production in human sebocytes

(2019) So-Ra Choi et al.   Scientific Reports

Novel TFG ‐ RET Fusion in Spindle Cell Tumour with S100 and CD 34 Co‐Expresssion

(2019) Shihleone Loong et al.   HISTOPATHOLOGY

Neuromuscular Junction Formation, Aging, and Disorders

(2018) Lei Li et al.   Annual Review of Physiology

TFG-RARA: A Novel Fusion Gene in Acute Promyelocytic Leukemia that is Responsive to All-Trans Retinoic Acid

(2018) Mei-Ling Chong et al.   LEUKEMIA RESEARCH

Pathogenic TFG Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking and Axon Fasciculation

(2018) Erin L. Slosarek et al.   Cell Reports

TFG facilitates outer coat disassembly on COPII transport carriers to promote tethering and fusion with ER–Golgi intermediate compartments

(2017) Michael G. Hanna et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Proteasome impairment in neural cells derived from HMSN-P patient iPSCs

(2017) Nagahisa Murakami et al.   Molecular Brain

Trk-fused gene (TFG) regulates pancreatic β cell mass and insulin secretory activity

(2017) Takeshi Yamamotoya et al.   Scientific Reports

Reappraisal of VAChT-Cre: Preference in slow motor neurons innervating type I or IIa muscle fibers

(2016) Hidemi Misawa et al.   GENESIS

Novel Genetic, Clinical, and Pathomechanistic Insights into TFG-Associated Hereditary Spastic Paraplegia

(2016) Gaurav V. Harlalka et al.   HUMAN MUTATION

Selective Expression of Osteopontin in ALS-resistant Motor Neurons is a Critical Determinant of Late Phase Neurodegeneration Mediated by Matrix Metalloproteinase-9

(2016) Yuta Morisaki et al.   Scientific Reports

TFG clusters COPII-coated transport carriers and promotes early secretory pathway organization

(2015) A. Johnson et al.   EMBO JOURNAL

Innervation and neuromuscular control in ageing skeletal muscle

(2015) Russell T. Hepple et al.   JOURNAL OF PHYSIOLOGY-LONDON

Evidence of TRK-Fused Gene (TFG1) function in the ubiquitin–proteasome system

(2014) Takuya Yagi et al.   NEUROBIOLOGY OF DISEASE

A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function

(2014) P.-C. Tsai et al.   NEUROLOGY

Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure

(2013) C. Beetz et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement

(2012) Hiroyuki Ishiura et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Investigation of the freely available easy-to-use software ‘EZR’ for medical statistics

(2012) Y Kanda   BONE MARROW TRANSPLANTATION

Myocardial deletion of Smad4 using a novel α skeletal muscle actin Cre recombinase transgenic mouse causes misalignment of the cardiac outflow tract

(2012) Mohamad Azhar et al.   International Journal of Biological Sciences

Agrin and Synaptic Laminin Are Required to Maintain Adult Neuromuscular Junctions

(2012) Melanie A. Samuel et al.   PLoS One

TFG-1 function in protein secretion and oncogenesis

(2011) Kristen Witte et al.   NATURE CELL BIOLOGY

Motor Neuron Diversity in Development and Disease

(2010) Kevin C. Kanning et al.   Annual Review of Neuroscience

Increased superoxide in vivo accelerates age-associated muscle atrophy through mitochondrial dysfunction and neuromuscular junction degeneration

(2009) Youngmok C. Jang et al.   FASEB JOURNAL

Role of IGF-I in skeletal muscle mass maintenance

(2009) David R. Clemmons   TRENDS IN ENDOCRINOLOGY AND METABOLISM

Nerve-dependent changes in skeletal muscle myosin heavy chain after experimental denervation and cross-reinnervation and in a demyelinating mouse model of Charcot-Marie-Tooth disease type 1A

(2008) Alison M. Maggs et al.   MUSCLE & NERVE