| scholarly article | Q13442814 |
| P2093 | author name string | Y Indo | |
| P2860 | cites work | Progress in genetic studies of pain and analgesia | Q24289028 |
| Structure and organization of the human TRKA gene encoding a high affinity receptor for nerve growth factor | Q24310833 | ||
| Neurotrophin-regulated signalling pathways | Q24678332 | ||
| Emotion circuits in the brain | Q27860733 | ||
| Molecular mechanisms of nociception | Q28216291 | ||
| How do you feel? Interoception: the sense of the physiological condition of the body | Q28216765 | ||
| An SCN9A channelopathy causes congenital inability to experience pain | Q28278844 | ||
| A human oncogene formed by the fusion of truncated tropomyosin and protein tyrosine kinase sequences | Q28282360 | ||
| Mice lacking nerve growth factor display perinatal loss of sensory and sympathetic neurons yet develop basal forebrain cholinergic neurons | Q28584797 | ||
| The trk proto-oncogene encodes a receptor for nerve growth factor | Q28609788 | ||
| The trk Proto-Oncogene Product: a Signal Transducing Receptor for Nerve Growth Factor | Q28609789 | ||
| Taking pain out of NGF: a "painless" NGF mutant, linked to hereditary sensory autonomic neuropathy type V, with full neurotrophic activity | Q28742340 | ||
| Molecular and biochemical characterization of the human trk proto-oncogene | Q28854584 | ||
| Cellular and Molecular Mechanisms of Pain | Q29011961 | ||
| How do you feel--now? The anterior insula and human awareness | Q29547250 | ||
| Frontiers in pruritus research: scratching the brain for more effective itch therapy | Q30477216 | ||
| Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor | Q31837528 | ||
| Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies | Q33906447 | ||
| Sustained signaling by phospholipase C-gamma mediates nerve growth factor-triggered gene expression. | Q33967890 | ||
| Trk receptors use redundant signal transduction pathways involving SHC and PLC-gamma 1 to mediate NGF responses | Q34060592 | ||
| Apoptosis in the nervous system | Q34068965 | ||
| A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy | Q34145937 | ||
| The inflammatory reflex | Q34165907 | ||
| A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception | Q34300023 | ||
| Severe sensory and sympathetic neuropathies in mice carrying a disrupted Trk/NGF receptor gene. | Q34338664 | ||
| ??? | Q28213378 | ||
| Familial insensitivity to pain (HSAN V) and a mutation in the NGFB gene. A neurophysiological and pathological study | Q34356401 | ||
| Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor | Q34389720 | ||
| NGF as a mediator of inflammatory pain. | Q34390489 | ||
| Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor | Q34465802 | ||
| Neural regulation of innate immunity: a coordinated nonspecific host response to pathogens | Q34504753 | ||
| Congenital insensitivity to pain with anhydrosis. A unique syndrome in two male siblings | Q34540401 | ||
| Neuronal control of skin function: the skin as a neuroimmunoendocrine organ. | Q34570825 | ||
| Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis | Q34733805 | ||
| Interactions between the immune and nervous systems in pain | Q34799654 | ||
| The cholinergic innervation of the human cerebral cortex | Q35598381 | ||
| Nerve growth factor enhances the excitability of rat sensory neurons through activation of the atypical protein kinase C isoform, PKMζ. | Q35951416 | ||
| Neuroimmunoendocrine circuitry of the 'brain-skin connection'. | Q36306022 | ||
| Novel class of pain drugs based on antagonism of NGF. | Q36352971 | ||
| Neurotrophins in allergic diseases: from neuronal growth factors to intercellular signaling molecules | Q36415921 | ||
| Neurotrophins: mediators and modulators of pain. | Q36507606 | ||
| Pediatric autonomic disorders | Q36526513 | ||
| The development of allergic inflammation | Q36613696 | ||
| Nerve growth factor in treatment and pathogenesis of Alzheimer's disease. | Q36644201 | ||
| A branched signaling pathway for nerve growth factor is revealed by Src-, Ras-, and Raf-mediated gene inductions | Q36684518 | ||
| Nerve growth factor, interoception, and sympathetic neuron: lesson from congenital insensitivity to pain with anhidrosis | Q37388204 | ||
| Animal models of pain: progress and challenges | Q37405925 | ||
| Nerve growth factor, pain, itch and inflammation: lessons from congenital insensitivity to pain with anhidrosis | Q37803223 | ||
| The nerve growth factor 35 years later | Q39667849 | ||
| ERK1/2 mitogen-activated protein kinase phosphorylates sodium channel Na(v)1.7 and alters its gating properties | Q39744096 | ||
| A stop codon mutation in SCN9A causes lack of pain sensation | Q40114322 | ||
| NGF rapidly increases membrane expression of TRPV1 heat-gated ion channels. | Q40345535 | ||
| Structural and functional properties of the TRK family of neurotrophin receptors | Q40374660 | ||
| Functional Interactions of Neurotrophins and Neurotrophin Receptors | Q40441056 | ||
| The hypothalamic-pituitary-adrenal axis and immune-mediated inflammation | Q40506162 | ||
| Nerve growth factor-tyrosine kinase A pathway is involved in thermoregulation and adaptation to stress: studies on patients with hereditary sensory and autonomic neuropathy type IV. | Q40515443 | ||
| Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency | Q40594499 | ||
| A novel point mutation affecting the tyrosine kinase domain of the TRKA gene in a family with congenital insensitivity to pain with anhidrosis | Q40639143 | ||
| Neurogenic vasodilatation and plasma leakage in the skin | Q41697768 | ||
| Nerve growth factor R221W responsible for insensitivity to pain is defectively processed and accumulates as proNGF. | Q42445633 | ||
| Cholinergic innervation of cortex by the basal forebrain: cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (substantia innominata), and hypothalamus in the rhesus monkey | Q42464648 | ||
| Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations | Q42618792 | ||
| A novel NTRK1 mutation associated with congenital insensitivity to pain with anhidrosis | Q42817930 | ||
| 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. | Q44124974 | ||
| Signalling pathways involved in the sensitisation of mouse nociceptive neurones by nerve growth factor | Q44483450 | ||
| Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families. | Q51974122 | ||
| P433 | issue | 4 | |
| P921 | main subject | physiology | Q521 |
| congenital insensitivity to pain with anhidrosis | Q501694 | ||
| congenital disorder | Q727096 | ||
| P304 | page(s) | 341-350 | |
| P577 | publication date | 2012-08-13 | |
| P1433 | published in | Clinical Genetics | Q5133760 |
| P1476 | title | Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis | |
| P478 | volume | 82 |
| Q38623995 | Beyond osteogenesis imperfecta: Causes of fractures during infancy and childhood |
| Q38699127 | Combining Human and Rodent Genetics to Identify New Analgesics |
| Q33835252 | Congenital deafness is associated with specific somatosensory deficits in adolescents |
| Q41361473 | Congenital insensitivity to pain and anhydrosis due to a rare mutation and that is complicated by inflammatory bowel disease and amyloidosis: a case report. |
| Q42085502 | Congenital insensitivity to pain with anhidrosis in Sudanese children |
| Q53640716 | Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype. |
| Q39046528 | Genetic control of the segregation of pain-related sensory neurons innervating the cutaneous versus deep tissues |
| Q55427889 | Hemodynamic Response to Massive Bleeding in a Patient with Congenital Insensitivity to Pain with Anhidrosis. |
| Q51770772 | Hereditary sensory and autonomic neuropathy types IV and V in Japan. |
| Q61811886 | Heterogeneity of clinical features and mutation analysis of in Han Chinese patients with congenital insensitivity to pain with anhidrosis |
| Q41775115 | Identification of a novel nonsense mutation of the neurotrophic tyrosine kinase receptor type 1 gene in two siblings with congenital insensitivity to pain with anhidrosis |
| Q36729840 | Immunosympathectomy as the first phenotypic knockout with antibodies. |
| Q28589735 | In vivo regulation of NGF-mediated functions by Nedd4-2 ubiquitination of TrkA |
| Q35058471 | Lost but making progress--Where will new analgesic drugs come from? |
| Q38185069 | Neurobiology of pain, interoception and emotional response: lessons from nerve growth factor-dependent neurons |
| Q40590626 | Neurotrophic tyrosine kinase receptor 1 is a direct transcriptional and epigenetic target of IL-13 involved in allergic inflammation. |
| Q51107047 | Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis. |
| Q40069818 | Novel NTRK1 mutations associated with congenital insensitivity to pain with anhidrosis verified by functional studies |
| Q54978896 | Novel NTRK1 mutations in Chinese patients with congenital insensitivity to pain with anhidrosis. |
| Q36151639 | Novel and novel de novo mutations in NTRK1 associated with congenital insensitivity to pain with anhidrosis: a case report |
| Q64916585 | Phenotypic and genotypic features of a pair of Chinese identical twins with congenital insensitivity to pain and anhidrosis: A case report. |
| Q52605544 | Phenotypic heterogeneity of intellectual disability in patients with congenital insensitivity to pain with anhidrosis: A case report and literature review. |
| Q41631541 | Recurrent NTRK1 Gene Fusions Define a Novel Subset of Locally Aggressive Lipofibromatosis-like Neural Tumors |
| Q38981486 | The TPM3-NTRK1 rearrangement is a recurring event in colorectal carcinoma and is associated with tumor sensitivity to TRKA kinase inhibition. |
| Q33360470 | The puzzle of orthostatic tolerance in hereditary sensory and autonomic neuropathy, type IV. |
| Q36249565 | Update Review and Clinical Presentation in Congenital Insensitivity to Pain and Anhidrosis |
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