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Abbreviation : TrJ
Long Form : Trembler-J
No. Year Title Co-occurring Abbreviation
2022 Colocalization Analysis of Peripheral Myelin Protein-22 and Lamin-B1 in the Schwann Cell Nuclei of Wt and TrJ Mice. CMT, EC, HC, PMP22, SC
2022 Cytokines secreted by mesenchymal stem cells reduce demyelination in an animal model of Charcot-Marie-Tooth disease. AREG, CMT, GDF15, MSCs, SCs, WJ-MSCs
2021 Gait parameters as tools for analyzing phenotypic alterations of a mouse model of Charcot-Marie-Tooth disease. CMT, CMT1
2020 Subcellular diversion of cholesterol by gain- and loss-of-function mutations in PMP22. CMT, PMP22, WT
2019 A neutral lipid-enriched diet improves myelination and alleviates peripheral nerve pathology in neuropathic mice. CMT, HFD, PMP22, WT
2019 HSP90 Inhibitor, NVP-AUY922, Improves Myelination in Vitro and Supports the Maintenance of Myelinated Axons in Neuropathic Mice. i.p, PMP22
2018 Differentiation of Human Tonsil-Derived Mesenchymal Stem Cells into Schwann-Like Cells Improves Neuromuscular Function in a Mouse Model of Charcot-Marie-Tooth Disease Type 1A. BDNF, CMT1A, GDNF, GFAP, NGFR, S100B, SC, T-MSC-SCs, T-MSCs
2018 Efficacy of exogenous pyruvate in TremblerJ mouse model of Charcot-Marie-Tooth neuropathy. CMT, MF
2017 Application of differentiated human tonsil-derived stem cells to trembler-J mice. CMT1A, MSCs, T-MSC myocytes, T-MSCs
10  2017 Locomotor and skeletal muscle abnormalities in trembler J neuropathic mice. TA
11  2017 Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo. CMT, siRNA
12  2017 Poly(ADP-ribosylation) is present in murine sciatic nerve fibers and is altered in a Charcot-Marie-Tooth-1E neurodegenerative model. AJ, PAR, PARG, PARPs, SC, WT
13  2014 Rapamycin improves peripheral nerve myelination while it fails to benefit neuromuscular performance in neuropathic mice. CMT1A, PMP22, WT
14  2013 Curcumin facilitates a transitory cellular stress response in Trembler-J mice. ER, UPRs
15  2011 Structural basis for the Trembler-J phenotype of Charcot-Marie-Tooth disease. CMTD, PMP22, TM1, TM2-4
16  2010 Rapamycin activates autophagy and improves myelination in explant cultures from neuropathic mice. Atg12, DRG, PMP22, RM, SCs
17  2009 Intermittent fasting alleviates the neuropathic phenotype in a mouse model of Charcot-Marie-Tooth disease. AL, CMT1A, IF, PMP22
18  2004 Enhancement of Schwann cell myelin formation by K252a in the Trembler-J mouse dorsal root ganglion explant culture. DRG
19  2003 Emerging role for autophagy in the removal of aggresomes in Schwann cells. PMP22, SC
20  2002 Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases. CNX, ER, PMP22
21  2002 Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A. PMP22
22  2002 Matrix metalloproteinase mediated degradation of basement membrane proteins in Trembler J neuropathy nerves. CMT1A, MMPs, PMP22
23  2001 Differential aggregation of the Trembler and Trembler J mutants of peripheral myelin protein 22. PMP22, Tr
24  2000 PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cells. PMP22, Tr
25  1999 Development of early postnatal peripheral nerve abnormalities in Trembler-J and PMP22 transgenic mice. PMP22
26  1999 Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction. PMP22
27  1998 Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22. PMP22, Tr
28  1997 Abnormal Schwann cell/axon interactions in the Trembler-J mouse. PMP22, Tr
29  1997 Upregulation of the endosomal-lysosomal pathway in the trembler-J neuropathy. PMP22
30  1996 A distinct pattern of trophic factor expression in myelin-deficient nerves of Trembler mice: implications for trophic support by Schwann cells. BDNF, CNTF, CST, SC
31  1992 A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse. Tr
32  1992 Molecular genetics and neuropathology of Charcot-Marie-Tooth disease type 1A. CMT, CMT1A, NCV, Tr
33  1983 Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination. Tr