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21 Possible Causes for Hcrtr2, mouse, protein

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  • Narcolepsy

    It is unclear what causes the orexin neurons to die, but our strategy has been to place the gene for orexin into surrogate neurons in the validated mouse models of narcolepsy[ncbi.nlm.nih.gov] proteins in the central nervous system.[ncbi.nlm.nih.gov] Anti-HCRTR2 autoantibodies were detected using three strategies: (1) Human embryonic kidney (HEK) 293T cells with transient expression of HCRTR2 were stained with human sera[ncbi.nlm.nih.gov]

  • Nortriptyline

    In this study, we used a cell viability assay to demonstrate that NTP is cytotoxic to human TCCSUP and mouse MBT-2 bladder cancer cells in a concentration and time-dependent[ncbi.nlm.nih.gov] proteins, perhaps due to adsorption of proteins on the liposomes.[ncbi.nlm.nih.gov] Hcrtr1 is more selective for hypocretin 1 than for hypocretin 2, while hcrtr2 systej equally selective for both of the hypocretins. That reduces the download time.[harekrishnaforex.com]

  • Sphenopalatine Neuralgia

    Much work has recently been done on the HCRTR2 gene (hypocretin receptor 2) polymorphism [ 39 , 40 ], suggesting a role of this gene in CH susceptibility.[ojrd.biomedcentral.com] […] all possible variations for your translation, Voice Recognition for dictation capabilities and Voice Commands that allow you to call out the tasks you need without using mouse[wordmagicsoft.com] A whole foods diet with adequate protein, carbohydrates, and fats that also includes yeast, liver, wheat germ, and foods that are high in B vitamins may be helpful.[medical-dictionary.thefreedictionary.com]

  • Anauxetic Dysplasia

    Models phenotype-based associations Disease phenotypes are compared with mouse phenotypes, with each mouse model contributing one point to the diagram.[mousephenotype.org] POP1 Human Genome Epidemiology (HuGE) Navigator POP1 Atlas of Genetics and Cytogenetics in Oncology and Haematology: POP1 No data available for Genatlas for POP1 Gene RNA-protein[genecards.org] HAMP, HAND1, HAND2, HARS, HARS2, HAS1, HAVCR1, HAX1, HBA1, HBA2, HBB, HBD, HBE1, HBEGF, HBG1, HBG2, HBM, HBS1L, HBZ, HCCS, HCK, HCLS1, HCN1, HCN2, HCN4, HCP5, HCRT, HCRTR1, HCRTR2[inteligene.com.br]

  • Idiopathic Hypersomnia

    Tanaka S, Honda Y, Inoue Y, Honda M (2006) Detection of autoantibodies against hypocretin, hcrtrl, and hcrtr2 in narcolepsy: anti-Hcrt system antibody in narcolepsy.[journals.plos.org] Abnormally low levels of acylcarnitine have been observed in patients with narcolepsy. [50] These same low levels have been associated with primary hypersomnia in general in mouse[en.wikipedia.org] Analysis of cerebral spinal fluid demonstrates moderate lymphocytosis (30-50 cells/µL with mild to moderate elevation in protein).[emedicine.medscape.com]

  • Focal Nonepidermolytic Palmoplantar Keratoderma

    Yeast artificial chromosomes: an alternative approach to the molecular analysis of mouse developmental mutations . Genet. Res. 56 , 203–208 (1990). 54.[nature.com] The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins.[genecards.org] Neonatal Encephalopathy with Seizures (NEWS) (ATF2) Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) Narcolepsy (HCRTR2[embarkvet.com]

  • Familial Episodic Pain Syndrome 2

    Autonomic Neuropathy Type IIB (HSAN2B) 3 GCH1 GTP cyclohydrolase 1 14 55,308,724: 55,369,542 rate-limiting enzyme for BH4 synthesis acute and chronic pain, experimental pain 13 HCRTR2[painresearchforum.org] This is confirmed by two knock-in mouse models of the disease carrying the human FHM1 R192Q or S218L mutations, which showed a reduced threshold and increased velocity of[jci.org] The properties of the channel formed by the encoded transmembrane protein can be altered by interaction with different beta subunits.[genecards.org]

  • Prekallikrein Deficiency, Congenital, Autosomal Recessive

    […] also be activated by thrombin on the surface of activated platelets, a pathway that is the most likely mechanism of in vivo activation in vivo during hemostasis. [6] In a mouse[emedicine.medscape.com] S , Protein C and Protein Z .[es.w3eacademy.com] Neonatal Encephalopathy with Seizures (NEWS) (ATF2) Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) Narcolepsy (HCRTR2[embarkvet.com]

  • Immunodeficiency with Factor I Anomaly

    A similar phenotype is seen in the Chy mouse, which carries a spontaneous heterozygous point mutation in Vegfr3 and is a model to study the pathophysiology and to perform[jci.org] In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within[genecards.org] Neonatal Encephalopathy with Seizures (NEWS) (ATF2) Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) Narcolepsy (HCRTR2[embarkvet.com]

  • Osteosclerosis-Ichthyosis-Premature Ovarian Failure Syndrome

    Phenotype associations for Babam2 Significant Not Significant Not tested All Phenotypes Summary Based on automated MP annotations supported by experiments on knockout mouse[mousephenotype.org] PRB1 deficiency PRB1 Proline-rich protein PRB3 deficiency PRB3 Proline-rich protein PRB4 deficiency PRB4 Hypotonia-Cystinuria syndrome PREPL Haemophagocytic lymphohistiocytosis[springer.com] Premature ovarian failure is part of the BPES Type I variant of the syndrome but not of the BPES Type II variant. [20] DNA repair deficiency [ edit ] BRCA1 protein plays an[en.wikipedia.org]