On the public citation graph
Recent advances in understanding neurotrophin signaling
0 signed · 199 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/neu.10174openalex-snapshot
p75 Neurotrophin receptor mediates neurotrophin activation of NF‐kappa B and induction of iNOS expression in P19 neurons
inferredcites →https://doi.org/10.1007/978-3-642-45106-5_2openalex-snapshot
Deciphering Proneurotrophin Actions
inferredcites →https://doi.org/10.1016/j.cell.2011.07.008openalex-snapshot
Recruitment of Actin Modifiers to TrkA Endosomes Governs Retrograde NGF Signaling and Survival
inferredcites →https://doi.org/10.1016/j.celrep.2015.12.028openalex-snapshot
p75 Neurotrophin Receptor Regulates Energy Balance in Obesity
inferredcites →https://doi.org/10.1016/j.mcn.2010.01.007openalex-snapshot
Trk activation in the secretory pathway promotes Golgi fragmentation
inferredcites →https://doi.org/10.1016/j.molcel.2011.08.033openalex-snapshot
Oxygen-Dependent Cleavage of the p75 Neurotrophin Receptor Triggers Stabilization of HIF-1α
inferredcites →https://doi.org/10.1016/j.neuron.2004.12.040openalex-snapshot
A TNF Receptor Family Member, TROY, Is a Coreceptor with Nogo Receptor in Mediating the Inhibitory Activity of Myelin Inhibitors
inferredcites →https://doi.org/10.1016/j.neuron.2006.03.011openalex-snapshot
Ligand-Dependent Cleavage of the P75 Neurotrophin Receptor Is Necessary for NRIF Nuclear Translocation and Apoptosis in Sympathetic Neurons
inferredcites →https://doi.org/10.1016/j.neuron.2007.11.026openalex-snapshot
Zinc-Mediated Transactivation of TrkB Potentiates the Hippocampal Mossy Fiber-CA3 Pyramid Synapse
inferredcites →https://doi.org/10.1016/j.neuron.2008.07.032openalex-snapshot
p75NTR Mediates Ephrin-A Reverse Signaling Required for Axon Repulsion and Mapping
inferredcites →https://doi.org/10.1016/j.neuron.2009.02.020openalex-snapshot
Activation of the p75 Neurotrophin Receptor through Conformational Rearrangement of Disulphide-Linked Receptor Dimers
inferredcites →https://doi.org/10.1016/j.neuron.2014.04.022openalex-snapshot
SorCS2 Regulates Dopaminergic Wiring and Is Processed into an Apoptotic Two-Chain Receptor in Peripheral Glia
inferredcites →https://doi.org/10.1016/s0021-9258(18)62831-5openalex-snapshot
The Gross Conformation of Protein-Sodium Dodecyl Sulfate Complexes
inferredcites →https://doi.org/10.1016/s0083-6729(03)01011-2openalex-snapshot
Nerve Growth Factor-Dependent Regulation of NADE-Induced Apoptosis
inferredcites →https://doi.org/10.1016/s0896-6273(00)00036-2openalex-snapshot
NRAGE, A Novel MAGE Protein, Interacts with the p75 Neurotrophin Receptor and Facilitates Nerve Growth Factor–Dependent Apoptosis
inferredcites →https://doi.org/10.1016/s0896-6273(00)81114-9openalex-snapshot
Neurotrophin Binding to the p75 Receptor Modulates Rho Activity and Axonal Outgrowth
inferredcites →https://doi.org/10.1016/s0896-6273(01)00526-8openalex-snapshot
NGF Signaling from Clathrin-Coated Vesicles
inferredcites →https://doi.org/10.1016/s0925-4773(98)00024-0openalex-snapshot
Proteolytic processing of the Drosophila Spätzle protein by Easter generates a dimeric NGF-like molecule with ventralising activity
inferredcites →https://doi.org/10.1016/s0959-4388(02)00326-4openalex-snapshot
Retrograde neurotrophin signaling: Trk-ing along the axon
inferredcites →https://doi.org/10.1016/s1359-6101(01)00024-7openalex-snapshot
Distinctive features of Trk neurotrophin receptor transactivation by G protein-coupled receptors
inferredcites →https://doi.org/10.1038/350678a0openalex-snapshot
High-affinity NGF binding requires coexpression of the trk proto-oncogene and the low-affinity NGF receptor
inferredcites →https://doi.org/10.1038/383716a0openalex-snapshot
Death of oligodendrocytes mediated by the interaction of nerve growth factor with its receptor p75
inferredcites →https://doi.org/10.1038/nature01176openalex-snapshot
p75 interacts with the Nogo receptor as a co-receptor for Nogo, MAG and OMgp
inferredcites →https://doi.org/10.1038/nature02319openalex-snapshot
Sortilin is essential for proNGF-induced neuronal cell death
inferredcites →https://doi.org/10.1038/nature07089openalex-snapshot
Crystal structure of the neurotrophin-3 and p75NTR symmetrical complex
inferredcites →https://doi.org/10.1038/nature09336openalex-snapshot
Neurotrophin receptors TrkA and TrkC cause neuronal death whereas TrkB does not
inferredcites →https://doi.org/10.1038/nn.2114openalex-snapshot
Developmental axon pruning mediated by BDNF-p75NTR–dependent axon degeneration
inferredcites →https://doi.org/10.1038/nn.3333openalex-snapshot
EGF transactivation of Trk receptors regulates the migration of newborn cortical neurons
inferredcites →https://doi.org/10.1038/nn.4054openalex-snapshot
Nuclear pore complex remodeling by p75NTR cleavage controls TGF-β signaling and astrocyte functions
inferredcites →https://doi.org/10.1038/nn975openalex-snapshot
A p75NTR and Nogo receptor complex mediates repulsive signaling by myelin-associated glycoprotein
inferredcites →https://doi.org/10.1038/nrn1726openalex-snapshot
The yin and yang of neurotrophin action
inferredcites →https://doi.org/10.1038/sj.emboj.7601017openalex-snapshot
Bex1, a novel interactor of the p75 neurotrophin receptor, links neurotrophin signaling to the cell cycle
inferredcites →https://doi.org/10.1042/bst0340607openalex-snapshot
Mechanisms of neurotrophin receptor signalling
inferredcites →https://doi.org/10.1073/pnas.1103638109openalex-snapshot
p75 neurotrophin receptor regulates glucose homeostasis and insulin sensitivity
inferredcites →https://doi.org/10.1074/jbc.274.5.2597openalex-snapshot
Association of the p75 Neurotrophin Receptor with TRAF6
inferredcites →https://doi.org/10.1074/jbc.m107421200openalex-snapshot
Activation of Trk Neurotrophin Receptor Signaling by Pituitary Adenylate Cyclase-activating Polypeptides
inferredcites →https://doi.org/10.1074/jbc.m109.091041openalex-snapshot
Mutual Regulation of Src Family Kinases and the Neurotrophin Receptor TrkB
inferredcites →https://doi.org/10.1074/jbc.m110929200openalex-snapshot
Amyloid β Binds Trimers as Well as Monomers of the 75-kDa Neurotrophin Receptor and Activates Receptor Signaling
inferredcites →https://doi.org/10.1074/jbc.m112.382903openalex-snapshot
The Effects of Transmembrane Sequence and Dimerization on Cleavage of the p75 Neurotrophin Receptor by γ-Secretase
inferredcites →https://doi.org/10.1074/jbc.m115.679076openalex-snapshot
γ-Secretase Activity Is Required for Regulated Intramembrane Proteolysis of Tumor Necrosis Factor (TNF) Receptor 1 and TNF-mediated Pro-apoptotic Signaling
inferredcites →https://doi.org/10.1074/jbc.m116.723585openalex-snapshot
Structural Basis of p75 Transmembrane Domain Dimerization
inferredcites →https://doi.org/10.1074/jbc.m306028200openalex-snapshot
Regulated Intramembrane Proteolysis of the p75 Neurotrophin Receptor Modulates Its Association with the TrkA Receptor
inferredcites →https://doi.org/10.1074/jbc.m410435200openalex-snapshot
Neurotrophin Receptor Interacting Factor (NRIF) Is an Essential Mediator of Apoptotic Signaling by the p75 Neurotrophin Receptor
inferredcites →https://doi.org/10.1074/jbc.m610458200openalex-snapshot
TrkA Receptor Activation by Nerve Growth Factor Induces Shedding of the p75 Neurotrophin Receptor Followed by Endosomal γ-Secretase-mediated Release of the p75 Intracellular Domain
inferredcites →https://doi.org/10.1083/jcb.140.4.911openalex-snapshot
The p75 Neurotrophin Receptor Mediates Neuronal Apoptosis and Is Essential for Naturally Occurring Sympathetic Neuron Death
inferredcites →https://doi.org/10.1083/jcb.200512013openalex-snapshot
A kinase-deficient TrkC receptor isoform activates Arf6–Rac1 signaling through the scaffold protein tamalin
inferredcites →https://doi.org/10.1083/jcb.200701040openalex-snapshot
p75 neurotrophin receptor regulates tissue fibrosis through inhibition of plasminogen activation via a PDE4/cAMP/PKA pathway
inferredcites →https://doi.org/10.1083/jcb.201306136openalex-snapshot
Death of developing neurons: New insights and implications for connectivity
inferredcites →https://doi.org/10.1083/jcb.201308115openalex-snapshot
Retrograde neurotrophin signaling through Tollo regulates synaptic growth in Drosophila
inferredcites →https://doi.org/10.1083/jcb.201502100openalex-snapshot
BDNF modulates heart contraction force and long-term homeostasis through truncated TrkB.T1 receptor activation
inferredcites →https://doi.org/10.1093/emboj/18.21.6050openalex-snapshot
The zinc finger protein NRIF interacts with the neurotrophin receptor p75NTR and participates in programmed cell death
inferredcites →https://doi.org/10.1101/cshperspect.a020669openalex-snapshot
Neuronal Signaling through Endocytosis
inferredcites →https://doi.org/10.1126/science.1065057openalex-snapshot
Regulation of Cell Survival by Secreted Proneurotrophins
inferredcites →https://doi.org/10.1126/scisignal.2000188openalex-snapshot
Ligand Binding to LRP1 Transactivates Trk Receptors by a Src Family Kinase–Dependent Pathway
inferredcites →https://doi.org/10.1146/annurev.biochem.72.121801.161629openalex-snapshot
Trk Receptors: Roles in Neuronal Signal Transduction
inferredcites →https://doi.org/10.1159/000094082openalex-snapshot
Evolution of the Neurotrophin Signaling System in Invertebrates
inferredcites →https://doi.org/10.1186/1471-2148-9-243openalex-snapshot
The genome sequence of the protostome Daphnia pulex encodes respective orthologues of a neurotrophin, a Trk and a p75NTR: Evolution of neurotrophin signaling components and related proteins in the bilateria
inferredcites →https://doi.org/10.1242/jcs.161745openalex-snapshot
Neuron-type-specific signaling by the p75NTR death receptor regulated by differential proteolytic cleavage
inferredcites →https://doi.org/10.1371/journal.pbio.0060284openalex-snapshot
Drosophila Neurotrophins Reveal a Common Mechanism for Nervous System Formation
inferredcites →https://doi.org/10.1523/jneurosci.0350-08.2008openalex-snapshot
β-Amyloid1–42Induces Neuronal Death through the p75 Neurotrophin Receptor
inferredcites →https://doi.org/10.1523/jneurosci.0591-15.2015openalex-snapshot
Detection of p75NTR Trimers: Implications for Receptor Stoichiometry and Activation
inferredcites →https://doi.org/10.1523/jneurosci.16-24-07950.1996openalex-snapshot
Endocytosis of Activated TrkA: Evidence that Nerve Growth Factor Induces Formation of Signaling Endosomes
inferredcites →https://doi.org/10.1523/jneurosci.19-13-05393.1999openalex-snapshot
Functionally Antagonistic Interactions between the TrkA and p75 Neurotrophin Receptors Regulate Sympathetic Neuron Growth and Target Innervation
inferredcites →https://doi.org/10.1523/jneurosci.23-13-05425.2003openalex-snapshot
Proteolytic Processing of the p75 Neurotrophin Receptor and Two Homologs Generates C-Terminal Fragments with Signaling Capability
inferredcites →https://doi.org/10.1523/jneurosci.4536-15.2016openalex-snapshot
Death Domain Signaling by Disulfide-Linked Dimers of the p75 Neurotrophin Receptor Mediates Neuronal Death in the CNS
inferredcites →https://doi.org/10.1523/jneurosci.5123-04.2005openalex-snapshot
ProBDNF Induces Neuronal Apoptosis via Activation of a Receptor Complex of p75NTRand Sortilin
inferredcites →https://doi.org/10.7554/elife.11692openalex-snapshot
Structural basis of death domain signaling in the p75 neurotrophin receptor
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/cbin.11500openalex-snapshot
Potential role of NGF, BDNF, and their receptors in oligodendrocytes differentiation from neural stem cell: An in vitro study
inferred← citeshttps://doi.org/10.1002/onco.13835openalex-snapshot
Mosaicism for Receptor Tyrosine Kinase Activation in a Glioblastoma Involving Both PDGFRA Amplification and NTRK2 Fusion
inferred← citeshttps://doi.org/10.1002/pro.4563openalex-snapshot
Distinct conformational changes occur within the intrinsically unstructured pro‐domain of pro‐Nerve Growth Factor in the presence of ATP and Mg2+
inferred← citeshttps://doi.org/10.1007/978-1-4939-7571-6_1openalex-snapshot
Neurotrophic Factors: An Overview
inferred← citeshttps://doi.org/10.1007/978-3-031-20792-1_1openalex-snapshot
Overview of CNS Organization and Development
inferred← citeshttps://doi.org/10.1007/978-3-319-27318-1_7-1openalex-snapshot
Receptor Tyrosine Kinases and the Insulin Signaling System
inferred← citeshttps://doi.org/10.1007/978-3-319-44675-2_7openalex-snapshot
Receptor Tyrosine Kinases and the Insulin Signaling System
inferred← citeshttps://doi.org/10.1007/s00213-024-06644-3openalex-snapshot
Unraveling psilocybin’s therapeutic potential: behavioral and neuroplasticity insights in Wistar-Kyoto and Wistar male rat models of treatment-resistant depression
inferred← citeshttps://doi.org/10.1007/s00221-026-07327-5openalex-snapshot
Molecular neurobiological insights on integrative role of Trk neurotrophic receptors and their small-molecule agonists in neurodegenerative conditions
inferred← citeshttps://doi.org/10.1007/s10571-023-01438-1openalex-snapshot
Mutation in the TRKB Cholesterol Recognition Site that blocks Antidepressant Binding does not Influence the Basal or BDNF-Stimulated Activation of TRKB
inferred← citeshttps://doi.org/10.1007/s11033-019-05129-3openalex-snapshot
The cellular and molecular basis of major depressive disorder: towards a unified model for understanding clinical depression
inferred← citeshttps://doi.org/10.1007/s11055-025-01779-yopenalex-snapshot
Poststroke Cognitive Impairment in Young Patients
inferred← citeshttps://doi.org/10.1007/s11064-018-2472-4openalex-snapshot
Berberine Ameliorates MCAO Induced Cerebral Ischemia/Reperfusion Injury via Activation of the BDNF–TrkB–PI3K/Akt Signaling Pathway
inferred← citeshttps://doi.org/10.1007/s12031-019-01450-5openalex-snapshot
Parkinson’s Disease–Associated Changes in the Expression of Neurotrophic Factors and their Receptors upon Neuronal Differentiation of Human Induced Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1007/s12035-022-02966-5openalex-snapshot
A Review of Molecular Interplay between Neurotrophins and miRNAs in Neuropsychological Disorders
inferred← citeshttps://doi.org/10.1007/s40259-021-00504-8openalex-snapshot
Nerve Growth Factor (NGF) Inhibitors and Related Agents for Chronic Musculoskeletal Pain: A Comprehensive Review
inferred← citeshttps://doi.org/10.1016/b978-0-12-814037-6.00006-9openalex-snapshot
Neuroprotective effects of lithium in neuropsychiatric disorders
inferred← citeshttps://doi.org/10.1016/b978-0-12-820472-6.00135-3openalex-snapshot
Receptor Tyrosine Kinases
inferred← citeshttps://doi.org/10.1016/b978-0-443-18677-6.00005-1openalex-snapshot
Growth factors and their receptors
inferred← citeshttps://doi.org/10.1016/bs.ant.2025.03.001openalex-snapshot
Role of glial cells in neurotoxicological effects of alcohol
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2019.06.004openalex-snapshot
Novel targets for parkinsonism-depression comorbidity
inferred← citeshttps://doi.org/10.1016/j.bbi.2020.07.036openalex-snapshot
Lactobacillus plantarum PS128 alleviates neurodegenerative progression in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced mouse models of Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.11.2262openalex-snapshot
The Biased Ligands NGF and NT-3 Differentially Stabilize Trk-A Dimers
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.05.067openalex-snapshot
Full Functional Knockout of Placental Growth Factor by Knockin with an Inactive Variant Able to Heterodimerize with VEGF-A
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113705openalex-snapshot
NGFR regulates stromal cell activation in germinal centers
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.01.010openalex-snapshot
Combined kinesin-1 and kinesin-3 activity drives axonal trafficking of TrkB receptors in Rab6 carriers
inferred← citeshttps://doi.org/10.1016/j.eswa.2024.123469openalex-snapshot
Evolving pathway activation from cancer gene expression data using nature-inspired ensemble optimization
inferred← citeshttps://doi.org/10.1016/j.fct.2018.01.051openalex-snapshot
Anticarcinogenic activities of sulforaphane are influenced by Nerve Growth Factor in human melanoma A375 cells
inferred← citeshttps://doi.org/10.1016/j.gene.2019.144277openalex-snapshot
KLF2 protects BV2 microglial cells against oxygen and glucose deprivation injury by modulating BDNF/TrkB pathway
inferred← citeshttps://doi.org/10.1016/j.humpath.2018.12.003openalex-snapshot
The presence of Y674/Y675 phosphorylated NTRK1 via TP53 repression of PTPN6 expression as a potential prognostic marker in neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.joca.2019.05.028openalex-snapshot
Efficacy and safety of intra-articular injection of tropomyosin receptor kinase A inhibitor in painful knee osteoarthritis: a randomized, double-blind and placebo-controlled study
inferred← citeshttps://doi.org/10.1016/j.joca.2024.08.011openalex-snapshot
Two studies of nerve growth factor (NGF) inhibitors implemented a rigorous mitigation plan to exclude osteoarthritis patients with a risk of joint collapse, but it was still not enough!
inferred← citeshttps://doi.org/10.1016/j.jshs.2019.07.012openalex-snapshot
Updated overview on interplay between physical exercise, neurotrophins, and cognitive function in humans
inferred← citeshttps://doi.org/10.1016/j.neuro.2025.103370openalex-snapshot
Proposed key characteristics of neurotoxic chemicals
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2019.04.057openalex-snapshot
γ-Synuclein Induces Human Cortical Astrocyte Proliferation and Subsequent BDNF Expression and Release
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6c00023openalex-snapshot
Mechanisms and Manifestations of Ligand Bias in Signaling: Focus on Receptor Tyrosine Kinases
inferred← citeshttps://doi.org/10.1021/acsami.3c17108openalex-snapshot
Synergistic Effect of Electrical and Biochemical Stimulation on Human iPSC-Derived Neural Differentiation in a Microfluidic Electrode Array Chip
inferred← citeshttps://doi.org/10.1038/s41419-019-1385-8openalex-snapshot
Neurotrophins and their involvement in digestive cancers
inferred← citeshttps://doi.org/10.1038/s41467-024-53710-7openalex-snapshot
Structural basis for the transmembrane signaling and antidepressant-induced activation of the receptor tyrosine kinase TrkB
inferred← citeshttps://doi.org/10.1038/s41582-019-0257-2openalex-snapshot
Axonal transport and neurological disease
inferred← citeshttps://doi.org/10.1038/s41598-017-05584-7openalex-snapshot
NEAP/DUSP26 suppresses receptor tyrosine kinases and regulates neuronal development in zebrafish
inferred← citeshttps://doi.org/10.1042/bcj20180637openalex-snapshot
Dimerization of the Trk receptors in the plasma membrane: effects of their cognate ligands
inferred← citeshttps://doi.org/10.1042/bcj20200671openalex-snapshot
The biophysical basis of receptor tyrosine kinase ligand functional selectivity: Trk-B case study
inferred← citeshttps://doi.org/10.1042/ns20180066openalex-snapshot
Regulation of cholinergic basal forebrain development, connectivity, and function by neurotrophin receptors
inferred← citeshttps://doi.org/10.1074/jbc.ra119.011312openalex-snapshot
Structural basis of the transmembrane domain dimerization and rotation in the activation mechanism of the TRKA receptor by nerve growth factor
inferred← citeshttps://doi.org/10.1080/00914037.2023.2215376openalex-snapshot
Application of stem cells, growth factors, small molecules, and biological macromolecules on nerve regeneration: a review and future direction
inferred← citeshttps://doi.org/10.1080/08977194.2017.1395420openalex-snapshot
Cardiac autonomic denervation and expression of neurotrophins (NGF and BDNF) and their receptors during experimental Chagas disease
inferred← citeshttps://doi.org/10.1080/14728214.2022.2125506openalex-snapshot
Emerging injectable therapies for osteoarthritis
inferred← citeshttps://doi.org/10.1080/14737175.2020.1800454openalex-snapshot
Therapeutic innovation in Parkinson’s disease: a 2020 update on disease-modifying approaches
inferred← citeshttps://doi.org/10.1080/15384101.2019.1637203openalex-snapshot
From psychology to physicality: how nerve growth factor transduces early life stress into gastrointestinal motility disorders later in life
inferred← citeshttps://doi.org/10.1093/bjd/ljag152openalex-snapshot
Nerve growth factor receptor p75NTR interacts with Toll-like receptor 4 and the alarmins high mobility group box 1 and nucleophosmin: a novel inflammatory mechanism in psoriasis
inferred← citeshttps://doi.org/10.1093/stmcls/sxac060openalex-snapshot
Isolation of an “Early” Transit Amplifying Keratinocyte Population in Human Epidermis: A Role for the Low Affinity Neurotrophin Receptor CD271
inferred← citeshttps://doi.org/10.1097/fbp.0000000000000386openalex-snapshot
Painful neurotrophins and their role in visceral pain
inferred← citeshttps://doi.org/10.1097/j.pain.0000000000001625openalex-snapshot
Nerve growth factor antibody for the treatment of osteoarthritis pain and chronic low-back pain: mechanism of action in the context of efficacy and safety
inferred← citeshttps://doi.org/10.1097/wnr.0000000000000810openalex-snapshot
Expression of brain-derived neurotrophic factors, neurotrophin-3, and neurotrophin-4 in the nucleus accumbens during heroin dependency and withdrawal
inferred← citeshttps://doi.org/10.1101/2020.07.24.216374openalex-snapshot
NT3/TrkC pathway modulates the expression of UCP-1 and adipocyte size in human and murine adipose tissue
inferred← citeshttps://doi.org/10.1101/2023.07.14.548960openalex-snapshot
NGFR regulates germinal center B-cell activation and negative selection
inferred← citeshttps://doi.org/10.1101/2024.01.08.574733openalex-snapshot
CD271 restrains the B1b cell antibody response in a T cell dependent manner
inferred← citeshttps://doi.org/10.1101/2025.10.23.684233openalex-snapshot
Delayed growth of SK-ES-1 Ewing sarcoma tumors associated with reduced expression and activity of Trk receptors, PI3K, and IGF1R
inferred← citeshttps://doi.org/10.1111/cns.14552openalex-snapshot
Efficacy of a benzothiazole‐based LRRK2 inhibitor in oligodendrocyte precursor cells and in a murine model of multiple sclerosis
inferred← citeshttps://doi.org/10.1111/imm.12717openalex-snapshot
Nerve growth factor: a neuroimmune crosstalk mediator for all seasons
inferred← citeshttps://doi.org/10.1111/jgh.70173openalex-snapshot
Advances in Gut Microbiome and Metabolomics Research in the Comorbidity of Inflammatory Bowel Disease and Depressive Disorder
inferred← citeshttps://doi.org/10.1111/nmo.14099openalex-snapshot
Evidence for the presence and release of BDNF in the neuronal and non‐neuronal structures of the internal anal sphincter
inferred← citeshttps://doi.org/10.1126/scisignal.aao4006openalex-snapshot
The receptor tyrosine kinase TrkB signals without dimerization at the plasma membrane
inferred← citeshttps://doi.org/10.1134/s1819712420040066openalex-snapshot
Generation and Characteristics of Glial Cells from Induced Human Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1152/ajpgi.00247.2019openalex-snapshot
BDNF augments rat internal anal sphincter smooth muscle tone via RhoA/ROCK signaling and nonadrenergic noncholinergic relaxation via increased NO release
inferred← citeshttps://doi.org/10.1155/2019/2051235openalex-snapshot
NOX2-Dependent Reactive Oxygen Species Regulate Formyl-Peptide Receptor 1-Mediated TrkA Transactivation in SH-SY5Y Cells
inferred← citeshttps://doi.org/10.1158/0008-5472.can-17-2789openalex-snapshot
Proteolytic Release of the p75NTR Intracellular Domain by ADAM10 Promotes Metastasis and Resistance to Anoikis
inferred← citeshttps://doi.org/10.1159/000499384openalex-snapshot
Tropomyosin-Related Kinase Receptor and Neurotrophin Expression in Cutaneous Melanoma Is Associated with a Poor Prognosis and Decreased Survival
inferred← citeshttps://doi.org/10.1159/000548381openalex-snapshot
Immune Synaptopathy and Sex Differences in Recognition Memory from Neonatal Staphylococcus epidermidis Infection
inferred← citeshttps://doi.org/10.11606/t.22.2022.tde-18082022-102408openalex-snapshot
Estudo de associação entre polimorfismos genéticos e níveis plasmáticos do VEGF, FLT1, KDR e o risco para depressão
inferred← citeshttps://doi.org/10.1177/0300985818781930openalex-snapshot
p75 Neurotrophin Receptor: A Double-Edged Sword in Pathology and Regeneration of the Central Nervous System
inferred← citeshttps://doi.org/10.1177/1759720x231171768openalex-snapshot
Role of imaging for eligibility and safety of a-NGF clinical trials
inferred← citeshttps://doi.org/10.1186/s12974-020-01960-9openalex-snapshot
The effect of insomnia on development of Alzheimer’s disease
inferred← citeshttps://doi.org/10.12688/f1000research.19174.1openalex-snapshot
Recent advances in understanding context-dependent mechanisms controlling neurotrophin signaling and function
inferred← citeshttps://doi.org/10.12731/2658-6649-2023-15-4-370-394openalex-snapshot
FEATURES OF METABOLISM AND THE POTENTIAL ROLE OF NEUROTROPHIC FACTORS OF THE BRAIN IN THE REHABILITATION PROCESS
inferred← citeshttps://doi.org/10.1371/journal.pbio.3000657openalex-snapshot
The receptor tyrosine kinase Ror is required for dendrite regeneration in Drosophila neurons
inferred← citeshttps://doi.org/10.1515/hsz-2017-0163openalex-snapshot
Cystine knot growth factors and their functionally versatile proregions
inferred← citeshttps://doi.org/10.15406/mojgg.2017.01.00031openalex-snapshot
BDNF Integrity in Ageing and Stress
inferred← citeshttps://doi.org/10.17116/jnevro202412408192openalex-snapshot
Post-stroke cognitive impairment in young patients
inferred← citeshttps://doi.org/10.2119/molmed.2016.00229openalex-snapshot
The Transcription Factor XBP1 in Memory and Cognition: implications in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.2174/1570159x18666201116143422openalex-snapshot
Interplay of BDNF and GDNF in the Mature Spinal Somatosensory System and Its Potential Therapeutic Relevance
inferred← citeshttps://doi.org/10.2174/9789815080384123010008openalex-snapshot
Growth Factors and Cancer
inferred← citeshttps://doi.org/10.3103/s009639251604009xopenalex-snapshot
Brain neurotrophic supply in ontogenesis and during development of neurodegenerative diseases
inferred← citeshttps://doi.org/10.3233/jad-190756openalex-snapshot
Differential Effects of Physical Exercise, Cognitive Training, and Mindfulness Practice on Serum BDNF Levels in Healthy Older Adults: A Randomized Controlled Intervention Study
inferred← citeshttps://doi.org/10.32635/2176-9745.rbc.2023v69n4.4262openalex-snapshot
Trk Inhibition Reduces Tumorsphere Formation and Changes Expression of Stemness Markers in SK-ES-1 Ewing Sarcoma Cells
inferred← citeshttps://doi.org/10.3389/fcell.2021.659654openalex-snapshot
Macro, Micro, and Molecular. Changes of the Osteochondral Interface in Osteoarthritis Development
inferred← citeshttps://doi.org/10.3389/fcimb.2019.00154openalex-snapshot
Immunomodulatory Effects of the Neuropeptide Pituitary Adenylate Cyclase-Activating Polypeptide in Acute Toxoplasmosis
inferred← citeshttps://doi.org/10.3389/fendo.2019.00632openalex-snapshot
Toward the Existence of a Sympathetic Neuroplasticity Adaptive Mechanism Influencing the Immune Response. A Hypothetical View—Part I
inferred← citeshttps://doi.org/10.3389/fendo.2021.630097openalex-snapshot
NT3/TrkC Pathway Modulates the Expression of UCP-1 and Adipocyte Size in Human and Rodent Adipose Tissue
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01965openalex-snapshot
Systemic Inflammation and the Increased Risk of Inflamm-Aging and Age-Associated Diseases in People Living With HIV on Long Term Suppressive Antiretroviral Therapy
inferred← citeshttps://doi.org/10.3389/fncel.2019.00231openalex-snapshot
Neuroprotection: Pro-survival and Anti-neurotoxic Mechanisms as Therapeutic Strategies in Neurodegeneration
inferred← citeshttps://doi.org/10.3389/fnins.2019.00446openalex-snapshot
Exploring the Pathogenesis of Alzheimer Disease in Basal Forebrain Cholinergic Neurons: Converging Insights From Alternative Hypotheses
inferred← citeshttps://doi.org/10.3389/fnmol.2018.00325openalex-snapshot
BDNF-Live-Exon-Visualization (BLEV) Allows Differential Detection of BDNF Transcripts in vitro and in vivo
inferred← citeshttps://doi.org/10.3389/fphys.2023.1201328openalex-snapshot
Anti-NGF treatment worsens subchondral bone and cartilage measures while improving symptoms in floor-housed rabbits with osteoarthritis
inferred← citeshttps://doi.org/10.3389/fruro.2022.1037511openalex-snapshot
Effects of pharmacological neurotrophin receptor inhibition on bladder function in female mice with cyclophosphamide-induced cystitis
inferred← citeshttps://doi.org/10.3389/fruro.2022.1089220openalex-snapshot
Changes in nerve growth factor signaling in female mice with cyclophosphamide-induced cystitis
inferred← citeshttps://doi.org/10.3390/biom11060900openalex-snapshot
The Conspicuous Link between Ear, Brain and Heart–Could Neurotrophin-Treatment of Age-Related Hearing Loss Help Prevent Alzheimer’s Disease and Associated Amyloid Cardiomyopathy?
inferred← citeshttps://doi.org/10.3390/biom11111730openalex-snapshot
Do Neurotrophins Connect Neurological Disorders and Heart Diseases?
inferred← citeshttps://doi.org/10.3390/biom12111717openalex-snapshot
Linking Cerebrovascular Dysfunction to Age-Related Hearing Loss and Alzheimer’s Disease—Are Systemic Approaches for Diagnosis and Therapy Required?
inferred← citeshttps://doi.org/10.3390/biomedicines14102249openalex-snapshot
Effects of Acute and Chronic Hyperglycemia on Neurotrophic Factors in the Gut: GDNF and NT3 Expression in Myenteric Ganglia
inferred← citeshttps://doi.org/10.3390/books978-3-03921-314-6openalex-snapshot
Targets, Tracers and Translation – Novel Radiopharmaceuticals Boost Nuclear Medicine
inferred← citeshttps://doi.org/10.3390/cancers11070893openalex-snapshot
Nerves and Pancreatic Cancer: New Insights into A Dangerous Relationship
inferred← citeshttps://doi.org/10.3390/cancers12092542openalex-snapshot
Neurotrophin Signaling in Medulloblastoma
inferred← citeshttps://doi.org/10.3390/cancers16040722openalex-snapshot
A Potential Prognostic Gene Signature Associated with p53-Dependent NTRK1 Activation and Increased Survival of Neuroblastoma Patients
inferred← citeshttps://doi.org/10.3390/cells11111835openalex-snapshot
A Microglial Function for the Nerve Growth Factor: Predictions of the Unpredictable
inferred← citeshttps://doi.org/10.3390/cells15010004openalex-snapshot
Advances in Targeting Growth Factor Signalling in Neuroblastoma and Overcoming Drug Resistance
inferred← citeshttps://doi.org/10.3390/cimb48010003openalex-snapshot
Neurotrophic Control of Puberty: From Molecular Signaling to Disorders of Pubertal Timing
inferred← citeshttps://doi.org/10.3390/ijms18051028openalex-snapshot
NGF and Its Receptors in the Regulation of Inflammatory Response
inferred← citeshttps://doi.org/10.3390/ijms18061143openalex-snapshot
Nerve Growth Factor and Related Substances: A Brief History and an Introduction to the International NGF Meeting Series
inferred← citeshttps://doi.org/10.3390/ijms231911726openalex-snapshot
The Mechanism of Action between Pulsed Radiofrequency and Orthobiologics: Is There a Synergistic Effect?
inferred← citeshttps://doi.org/10.3390/ijms24054871openalex-snapshot
Composite Coatings Based on Recombinant Spidroins and Peptides with Motifs of the Extracellular Matrix Proteins Enhance Neuronal Differentiation of Neural Precursor Cells Derived from Human Induced Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.3390/ph12010007openalex-snapshot
Radioligands for Tropomyosin Receptor Kinase (Trk) Positron Emission Tomography Imaging
inferred← citeshttps://doi.org/10.4103/1673-5374.205084openalex-snapshot
Neurotrophic factors in Alzheimer's and Parkinson's diseases: implications for pathogenesis and therapy
inferred← citeshttps://doi.org/10.4103/1673-5374.306062openalex-snapshot
Topical delivery of nerve growth factor for treatment of ocular and brain disorders
inferred← citeshttps://doi.org/10.47749/t/unicamp.2021.1235306openalex-snapshot
O fator de neurotrófico derivado do cérebro (BDNF) como proteína importante para os efeitos terapêuticos do plasma rico em plaquetas em modelo de osteoartrite experimental
inferred← citeshttps://doi.org/10.47836/mjmhs.20.6.32openalex-snapshot
Evaluation of Serum Brain-derived Neurotrophic Factor (BDNF) in Ambulatory Stroke Survivors With Mild Cognitive Impairment and Normal Cognitive Functions
inferred← citeshttps://doi.org/10.5114/pg.2023.132957openalex-snapshot
Brain-derived neurotrophic factor – a key player in the gastrointestinal system
inferred← citeshttps://doi.org/10.70675/21aba473z09b8z4c23z941fz3b6d04b8b762openalex-snapshot
Implication de la sortiline dans la résistance des cellules cancéreuses au 5-Fluorouracile. Cas du cancer colorectal
inferred← citeshttps://doi.org/10.70675/2f402166z8a8bz4e47z93c4z20ae8f982074openalex-snapshot
Primitive macrophages regulate the development of dorsal root ganglia sensory neurons in mouse embryos
inferred← citeshttps://doi.org/10.70675/38119436z82bez4d08z87f8z67db7c18ad93openalex-snapshot
Expression et rôle du facteur de croissance des nerfs NGF dans l’hypertension pulmonaire
inferred← citeshttps://doi.org/10.70675/47d0433az4375z4bc8za315z0be93e98d476openalex-snapshot
Plasticité des réseaux de récepteurs membranaires dans la signalisation du NGF et de son précurseur dans les cancers du sein
inferred← citeshttps://doi.org/10.7287/peerj.10479v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Expression of the neurotrophic tyrosine kinase receptors, ntrk1 and ntrk2a, precedes expression of other ntrk genes in embryonic zebrafish (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.10479v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Expression of the neurotrophic tyrosine kinase receptors, ntrk1 and ntrk2a, precedes expression of other ntrk genes in embryonic zebrafish (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.10479v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Expression of the neurotrophic tyrosine kinase receptors, ntrk1 and ntrk2a, precedes expression of other ntrk genes in embryonic zebrafish (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.10479v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Expression of the neurotrophic tyrosine kinase receptors, ntrk1 and ntrk2a, precedes expression of other ntrk genes in embryonic zebrafish (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.10479v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Expression of the neurotrophic tyrosine kinase receptors, ntrk1 and ntrk2a, precedes expression of other ntrk genes in embryonic zebrafish (v0.2)"
inferred← citeshttps://doi.org/10.7554/elife.58478openalex-snapshot
circZNF827 nucleates a transcription inhibitory complex to balance neuronal differentiation
inferred← citeshttps://doi.org/10.7717/peerj.10479openalex-snapshot
Expression of the neurotrophic tyrosine kinase receptors, ntrk1 and ntrk2a , precedes expression of other ntrk genes in embryonic zebrafish
inferred← citeshttps://doi.org/10.7759/cureus.35331openalex-snapshot
Mechanisms of Peripheral and Central Sensitization in Osteoarthritis Pain
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.