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21 Possible Causes for Myocd, mouse, protein

Did you mean: Myocd, morus, proteus

  • Idiopathic Pulmonary Fibrosis

    […] based potential FFLs, an important observation was that two miRNA-FFLs were consisted of miR-210 targeting matrix metalloproteinase gene (MMP16) in combination with TFs MYOCD[nature.com] Penn researchers develop first mouse model of idiopathic pulmonary fibrosis The biggest hurdle to finding effective therapies for idiopathic pulmonary fibrosis (IPF) – a life-threatening[news-medical.net] […] misfolded proteins when they accumulate.[ncbi.nlm.nih.gov]

  • Alzheimer Disease

    […] we have identified two vascularly restricted genes, GAX (growth arrest-specific homeobox), which controls LRP1 expression in brain capillaries and brain angiogenesis, and MYOCD[doi.org] By analyzing every eighth section from 0.8 to 2.8 mm from bregma for each mouse (total of 8 to 10 sections per mouse), we found that the cortical area occupied by plaques[dx.doi.org] Recently, evidence was reported that γ-secretase activating protein (GSAP, 16 kDa), derived from a larger precursor protein (98 kDa), plays a role in Aβ metabolism through[ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1D

    CTNNA3, CTSD, DGKB, DLST, EPHA1, EXOC3L2, FAS, FLG, FPR2, GAB2, GSK3B, GSTO1, HFE, HSD11B1, IDE, IL1A, IL1B, IL8, KIF3A, KLK6, LDLR, LRP1, MEOX2, MPO, MS4A10, MTFR1, MTHFR, MYOCD[e-icm.net] […] inner ear, but not in the mouse retina.[ncbi.nlm.nih.gov] Symbol Name Synonyms Organism USH1G Usher syndrome 1G (autosomal recessive) ANKS4A, FLJ33924, Sans, SANS, Scaffold protein containing ankyrin repeats and SAM domain, Usher[ihop-net.org]

  • Nestor-Guillermo Progeria Syndrome

    Glaucoma, early-onset, digenic (3) MYOCD G:606127 . . MYOD1 G:159970 . . MYOF G:604603 . . MYOG G:159980 . . MYOM1 G:603508 . . MYOM2 G:603509 . .[usegalaxy.org] Phenotype associations for Rpgrip1l Significant Not Significant Not tested All Phenotypes Summary Based on automated MP annotations supported by experiments on knockout mouse[mousephenotype.org] Cell signaling mechanisms often transmit information via posttranslational protein modifications, most importantly reversible protein phosphorylation.[scienceopen.com]

  • AICA-Ribosiduria

    Glaucoma, early-onset, digenic (3) MYOCD G:606127 . . MYOD1 G:159970 . . MYOF G:604603 . . MYOG G:159980 . . MYOM1 G:603508 . . MYOM2 G:603509 . .[usegalaxy.org] […] and mouse monoclonal IgG anti-ATIC (Abcam Antibodies).[academic.oup.com] AICAR induction of TXNIP depended on MondoA, but was independent of AMPK (AMP-activated protein kinase) activation and calcium.[biochemj.org]

  • Spondyloperipheral Dysplasia

    […] and TCF3 might modulate the primary chondrogenesis by associating with the SOX9-related transcriptional complex, and by binding to the conserved E-box on COL2A1 promoter MYOCD[genatlas.medecine.univ-paris5.fr] Phenotype associations for Pth Significant Not Significant Not tested All Phenotypes Summary Based on automated MP annotations supported by experiments on knockout mouse models[mousephenotype.org] Instead of forming collagen molecules, the abnormal protein builds up in cartilage cells (chondrocytes).[en.wikipedia.org]

  • Anauxetic Dysplasia

    MYH15, MYH2, MYH3, MYH6, MYH7, MYH8, MYH9, MYL2, MYL3, MYLIP, MYLK, MYLK2, MYO15A, MYO18B, MYO1A, MYO1C, MYO1E, MYO1F, MYO3A, MYO5A, MYO5B, MYO6, MYO7A, MYO7B, MYO9B, MYOC, MYOCD[inteligene.com.br] 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]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    Glaucoma, early-onset, digenic (3) MYOCD G:606127 . . MYOD1 G:159970 . . MYOF G:604603 . . MYOG G:159980 . . MYOM1 G:603508 . . MYOM2 G:603509 . .[usegalaxy.org] Read More Mixed Neurodevelopmental and Neurodegenerative Pathology in -Null Mouse Model of Christianson Syndrome. eNeuro 2017 Nov-Dec;4(6). Epub 2018 Jan 17.[pubfacts.com] […] in InterPro IPR036236 Znf_C2H2_sf IPR013087 Znf_C2H2_type SMART i View protein in SMART SM00355 ZnF_C2H2, 13 hits SUPFAM i SSF57667 SSF57667, 7 hits PROSITE i View protein[uniprot.org]

  • Combined Oxidative Phosphorylation Deficiency Type 3

    Glaucoma, early-onset, digenic (3) MYOCD G:606127 . . MYOD1 G:159970 . . MYOF G:604603 . . MYOG G:159980 . . MYOM1 G:603508 . . MYOM2 G:603509 . .[usegalaxy.org] Phenotype associations for Zfp13 Significant Not Significant Not tested All Phenotypes Summary Based on automated MP annotations supported by experiments on knockout mouse[mousephenotype.org] ; decreases the levels of mitochondrial protein synthesis.[uniprot.org]

  • Combined Oxidative Phosphorylation Deficiency Type 24

    Glaucoma, early-onset, digenic (3) MYOCD G:606127 . . MYOD1 G:159970 . . MYOF G:604603 . . MYOG G:159980 . . MYOM1 G:603508 . . MYOM2 G:603509 . .[usegalaxy.org] 1 - 7 of 7 Abreviews or Q&A Application Immunohistochemistry (Frozen sections) Sample Mouse Tissue sections (Skeletal muscle) Permeabilization Yes - 0.5% triton X-100 Specification[abcam.com] View all proteins of this organism that are known to be involved in the pathway polypeptide chain elongation and in Protein biosynthesis .[uniprot.org]