Create issue ticket

6,692 Possible Causes for 4, mouse, neurexin, protein

Show results in: Română

  • Influenza

    Compound 2 shows strong potency versus multiple influenza A strains, including pandemic 2009 H1N1 and avian H5N1 flu strains, and shows an efficacy profile in a mouse influenza[] ., less than 4 days after illness onset).[] Like hemagglutinin and neuraminidase, the M2 protein is an integral membrane protein of the influenza A virus 4 , 5 .[] Fifty per cent mouse infectious dose (MID 50 ) and 50 % mouse lethal dose (MLD 50 ) titres were determined by inoculating groups of eight mice i.n. with serial 10-fold dilutions[]

    Missing: neurexin
  • Rett Syndrome

    Further reading Treating Rett syndrome: from mouse models to human therapies Neeti Vashi & Monica J.[] […] clinical stages, reaching the maximum degree at stage 4, represented by a late motor deterioration.[] Neuroligin 1: a splice site-specific ligand for beta-neurexins. Cell 81(3): 435 -443.[] No information is, to date, available on the inflammatory protein response in CDKL5-RTT. We evaluated, for the first time, the APR protein response in CDKL5-RTT.[]

  • Coxsackie Virus

    We now describe the isolation of cDNAs from human and mouse that encode the human CVB and Ad2 and 5 receptor (HCAR) and the mouse CVB Ad2 and 5 receptor (MCAR).[] Coxsackie virus B 4 should be considered in patients with encephalitis.[] [bsid125147] PodNet: protein-protein interactions in the podocyte PodNet: protein-protein interactions in the podocyte PodNet is a manually curated network of protein-protein[] CAMs such as the cadherins, ephrins, neurexins, and NCAM (a member of the Ig superfamily) play critical roles in general brain homeostasis ( Togashi et al., 2009 ).[]

  • Nephronophthisis 4

    ENCODE transcriptome data Description: RNA profiling data sets generated by the Mouse ENCODE project.[] Mutations in this gene are associated with nephronophthisis type 4, a renal disease, and with Senior-Loken syndrome type 4, a combination of nephronophthisis and retinitis[] 21555462 NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway Habbig, S , Bartram, MP , Müller, RU , Schwarz, R , Andriopoulos, N , Chen, S , Sägmüller[] […] juvenile) homolog (human) (Nphp4) 4930564O18Rik protein nmf192 protein NPHP4 protein POC10 protein SLSN4 protein Protein level used designations for Nephronophthisis 4 Proteins[]

    Missing: neurexin
  • Limb-Girdle Muscular Dystrophy

    LGMD1D mutations in DNAJB6a or DNAJB6b did not alter this localization in mouse muscle.[] Epub 2011 May 4. Author information 1 Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH 43205, USA.[] KEYWORDS: LGMD2A; calpain-3; calpainopathy; genetic diagnosis; immunoblot analysis; limb girdle muscular dystrophy; mutation detection; protein testing[] Neuroligins and neurexins link synaptic function to cognitive disease. Nature. 2008; 455 :903–11. [ PMC free article ] [ PubMed ] [ Google Scholar ] 25.[]

  • LIG4 Syndrome

    […] send to {{ username }} {{geneWatchAttr}} Analyze Gene Strain QTL List Functional Annotation unavailable Annotation Distribution unavailable Genomic Variants unavailble for Mouse[] Abstract DNA ligase 4 deficiency (LIG4-SCID) causes lymphopenia (T-B-NK ) and a radiosensitive SCID (RS-SCID) phenotype.[] Tandem BRCT domains of LigIV mediate a unique mode of protein-protein interaction.[] Term Browser Genes (2) Models (2) Disease References using Mouse Models (2)[]

    Missing: neurexin
  • Oculocutaneous Albinism Type 4

    Conservation of human and mouse MATP proteins. Two-way clustal alignment of human and mouse MATP amino acid sequences is shown.[] No patient had grade 4 foveal hypoplasia.[] Abstract Oculocutaneous albinism type 4 (OCA4) is an autosomal recessive hypopigmentary disorder caused by mutations in the Membrane-Associated Transporter Protein gene (SLC45A2[] Nystagmus is not always present at birth and can develop at 3 to 4 months of age.[]

    Missing: neurexin
  • Osteoporosis

    Black bear parathyroid hormone has been previously reported to enhance bone mass in the dystrophin-deficient mouse.[] Figures and Tables - Analysis 4.2 Comparison 4 Musculoskeletal pain, Outcome 2 Lower limb pain 4 years.[] A similar increase in risk was observed for animal protein, but no association was found for consumption of vegetable protein.[] […] interaction partner [ 87 ] Chinese with low BMD SOD 2 upregulated Located in circulating monocytes (potential osteoclast precursors) [ 89 ] Osteoblast differentiation in mouse[]

    Missing: neurexin
  • Fragile X Syndrome

    Though the genetic cause of FXS is known to be due to the silencing of FMR1 , and the Fmr1 null mouse model representing this lesion has been extensively studied, the contributions[] Gigonzac MA 1, 2, 3, 4 , Teodoro LS 4 , Minasi LB 4 , Vieira TC 1, 3, 4 , da Cruz AD 1, 2, 4 .[] TDP-43 and the Fragile X Syndrome protein FMRP.[] Etherton MR, Blaiss CA, Powell CM, Sudhof TC (2009) Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive[]

  • Upper Respiratory Infection

    […] for respiratory tract infections -- such as coughs, colds, sore throats and ear infections -- is not linked to an increase in the most ... read more Researchers Develop Mouse[] METHODS: This is a case control study of children, age 4-6 years and grouped as: URI, (n   74), URI and wheezing, (URI-wheezing, n   52), and healthy controls (n   51).[] */genetics Receptors, G-Protein-Coupled*/immunology Receptors, G-Protein-Coupled*/metabolism Rhinitis*/genetics Rhinitis*/immunology Rhinitis*/metabolism Rhinitis*/microbiology[] Sixteen percent of family physicians recommended cold remedies for infants 0 to 6 months of age compared to 4% of the pediatricians (P 0.01).[]

    Missing: neurexin