NGF, nerve growth factor, 4803

N. diseases: 616; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 Biomarker disease BEFREE No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V. 12210794 2002
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 Biomarker disease BEFREE These results provide a basis for elucidating the mechanisms underlying the clinical manifestations of HSAN V patients, and provide a basis for the development of "painless" hNGF molecules with therapeutic potential. 19945432 2010
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE Recently a homozygous missense mutation (R100W) in the NGF gene has been identified in HSAN V patients. 24494679 2014
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE A point mutation (R100W) in the NGFB gene was found in patients with Hereditary Sensory and Autonomic Neuropathy type V (HSAN V), which leads to pain insensitivity. 30612733 2019
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 Biomarker disease BEFREE To prevent the NGF pain-inducing collateral effects, thus avoiding the necessity for local brain injection, we developed painless NGF (hNGFp), based on the human genetic disease Hereditary Sensory and Autonomic Neuropathy type V (HSAN V). hNGFp has similar neurotrophic activity as wild type human NGF, but its pain sensitizing activity is tenfold lower. 30391352 2019
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 Biomarker disease BEFREE We will review neuropathies and clinical presentations that result from the disruption of NGF signalling in HSAN type IV and HSAN type V and review current advances in developing anti-NGF therapy for the clinical management of pain. 23157347 2013
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE A missense mutation (R100W) in the beta-NGF gene was found in hereditary sensory autonomic neuropathy V (HSAN V) patients with severe loss of pain perception but without overt cognitive impairment. 30524266 2018
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE Generation of the human induced pluripotent stem cell line UKWNLi002-A from dermal fibroblasts of a woman with a heterozygous c.608 C>T (p.Thr203Met) mutation in exon 3 of the nerve growth factor gene potentially associated with hereditary sensory and autonomic neuropathy type 5. 30384131 2018
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE The physiological function of NGF as a pain mediator is altered in patients with Hereditary Sensory and Autonomic Neuropathy type V (HSAN V), caused by the 661C>T transition in the <i>Ngf</i> gene, resulting in the R100W missense mutation in mature NGF. 31685654 2019
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE We describe a novel NGF mutation in an individual with typical HSAN5 findings. 30296891 2019
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 Biomarker disease BEFREE It is concluded that the HSAN4 and HSAN5 phenotypes are parts of a phenotypic spectrum caused by changes in the NGF/TRKA signalling pathway. 20978020 2011
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE A family with neurological findings similar to hereditary sensory and autonomic neuropathy type V having a point mutation in the nerve growth factor beta (NGFB) gene was recently described. 18420729 2009
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE We have studied a large Swedish family with a mutation in the nerve growth factor beta (NGFB) gene causing insensitivity to deep pain without anhidrosis (hereditary sensory and autonomic neuropathy, type V; HSAN V). 15468048 2004
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 Biomarker disease BEFREE The integration of both TrkA and p75<sup>NTR</sup> signaling thus appears to regulate neuroplastic effects of NGF in peripheral nociception.<b>SIGNIFICANCE STATEMENT</b> In the present study, we characterized the naturally occurring nerve growth factor NGF<sup>R100W</sup> mutant that is associated with hereditary sensory and autonomic neuropathy type V. We have demonstrated for the first time that NGF<sup>R100W</sup> retains trophic support capability through TrkA, but fails to engage p75<sup>NTR</sup> signaling pathways. 29483280 2018
Hereditary Sensory Autonomic Neuropathy, Type 5
0.800 GeneticVariation disease BEFREE Although those HSAN V patients associated with the NGF<sup>R100W</sup> mutation suffer from severe loss of deep pain, bone fractures and joint destruction, interestingly patients with the NGF<sup>R100W</sup> mutation do not show apparent cognitive deficits, suggesting important trophic support function is preserved. 30632491 2019
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 Biomarker phenotype BEFREE Here we performed long-term evaluation of allodynia and hyperalgesia in a CCI model, and evaluated the effects of NGF and SP on the peripheral and central nervous systems. 28685530 2017
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 AlteredExpression phenotype BEFREE Pressure stimulation, contact heat stimulation, hyperalgesia (pinprick stimulation) and allodynia (brush stimulation) to mechanical stimulation were performed in the area where capsaicin and NGF were injected. 29498480 2018
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 GeneticVariation phenotype BEFREE Intramuscular injection of nerve growth factor (NGF) causes muscle hyperalgesia without immediate pain. 30513347 2019
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 Biomarker phenotype BEFREE Nerve growth factor is an inflammatory mediator that induces long-lasting hyperalgesia, which can partially be attributed to nerve growth factor-induced sensitization of primary afferent nociceptors. 30387376 2019
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 Biomarker phenotype BEFREE This means that NGF-induced hyperalgesia can occur in the absence of the p75 receptor and suggests that the trkA receptor is sufficient to mediate the acute noxious action of NGF. 9835221 1998
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 AlteredExpression phenotype BEFREE Therefore, this study investigated the effect of NGF on ASIC3 expression in the TNC and the role of NGF signaling in chemical dural stimulation-induced hyperalgesia. 30553789 2019
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 GeneticVariation phenotype BEFREE Local injection of nerve growth factor (3 µg/50 µl) or the TRPV1 agonist capsaicin (1 μg/50 μl), but not neurotrophin-3 injection (1 µg/50 µl), resulted in long-lasting facial heat hyperalgesia, which was both significantly reduced by previous neurotrophin-3 local treatment. 31577558 2020
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 Biomarker phenotype BEFREE Hyperalgesia developed after NGF injection in the infrapatellar fat pad, but it was not facilitated by acid provocation. 27634419 2017
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 Biomarker phenotype BEFREE Local pre-treatment with anti-NGF or K252a was effective to prevent ET-1 induced heat hyperalgesia. 28865353 2017
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.600 Biomarker phenotype BEFREE Intraplantar injection of NGF<sup>R100W</sup> into adult rats induced neither TrkA-mediated thermal nor mechanical acute hyperalgesia, but retained the ability to induce chronic hyperalgesia based on agonism for TrkA signaling. 29483280 2018