Neurotrophins and their receptors: A convergence point for many signalling pathways
By M. Chao. Nature Reviews Neuroscience, 2003
2,285 citations recorded by the source corpus.
Subfields: Biomaterials, Cellular and Molecular Neuroscience
View Paper: https://www.semanticscholar.org/paper/584fee531197d7bfb25d7dd944de5d508478619a
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biomaterials
In Cellular and Molecular Neuroscience
- B. Lu
- Undurti N. Das
- Siresha Bathina
- B. Hempstead
- Keri Martinowich
- L. Reichardt
- Guang Yang
- Wen-Biao Gan
Citations in the corpus
- Cellular and Molecular Mechanisms of Pain (2009, neutral): “Among its many cellular targets, NGF acts directly on peptidergic C fiber nociceptors, which express the high-affinity NGF receptor tyrosine kinase, TrkA, as well as the low-affinity neurotrophin receptor, p75 (Chao, 2003; Snider and McMahon, 1998).”
- Brain-derived neurotrophic factor and its clinical implications (2015, background): “The secondary messengers which are activated in the spinal cord by BDNF signaling include the MAP/ERK pathway, proto-oncogene c-fos and nitric oxide (NO)-producing neurons [24–26].”
- Microglia promote learning-dependent synapse formation through BDNF (2013, background): “…pro and mature forms of BDNF bind different receptors on the surface of neurons (p75/sortilin and tropomyosin-related kinase receptor B [TrkB], respectively) to affect different cellular processes (Chao, 2003), we asked whether, and in which form, BDNF might be produced and secreted by microglia.”
- Structural and mechanistic insights into nerve growth factor interactions with the TrkA and p75 receptors. (2007, background): “Nerve Growth Factor is the founding member of the neurotrophins, which are a family of secreted proteins essential for the proper development, patterning, and maintenance of the mammalian nervous system (Bothwell, 1995; Chao, 2003; Cohen, 1959; Dechant and Barde, 2002; Roux and Barker, 2002).”
- Socioeconomic status and the brain: mechanistic insights from human and animal research (2010, background): “Licking and grooming of pups increases NMDA ( N -methyl- D -aspartate) receptor levels in the hippocampus and hippocampal expression of growth factors (brain-derived neurotrophic factor and basic fibroblast growth factor), which promote neuronal activation and synaptogenesis, respectivel”
- Mouse and rat BDNF gene structure and expression revisited (2006, background): “All neurotrophins bind to p75NGFR receptor but selectively interact with their individual high-affinity protein kinase receptors of the trk (tropomyosin-related kinase) family (Kaplan and Miller, 2000; Chao, 2003; Teng and Hempstead, 2004).”
- Variant Brain-Derived Neurotrophic Factor (BDNF) (Met66) Alters the Intracellular Trafficking and Activity-Dependent Secretion of Wild-Type BDNF in Neurosecretory Cells and Cortical Neurons (2004, background): “Brain-derived neurotrophic factor (BDNF) has been established to play critical roles in vertebrate nervous system and cardiovascular development and function (Tessarollo, 1998; Huang and Reichardt, 2001; Chao, 2003).”
- Interaction between BDNF and Serotonin: Role in Mood Disorders (2008, background): “Binding of mature BDNF (mBDNF) to TrkB triggers tyrosine phosphorylation in its cytoplasmic domain, leading to activation of at least three signaling pathways: MEK–MAPK, phosphatidylinositol-3-kinase (PI3-K) and phospholipase C-g (PLC-g) (Kaplan and Miller, 2000; Chao, 2003; Huang and Reichardt, 200”
- Neurotrophin-regulated signalling pathways (2006, background): “Several excellent reviews describe recent progress in understanding the developmental and functional roles of these proteins (Bibel & Barde 2000; Huang & Reichardt 2001; Patapoutian & Reichardt 2001; Sofroniew et al. 2001; Dechant & Barde 2002; Chao 2003; Chao & Lee 2004; Lu et al. 2005).”
- Sortilin is essential for proNGF-induced neuronal cell death (2004, background): “NGF regulates cell survival and cell death via binding to two different receptors, TrkA and p75 NTR (ref”