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21 Possible Causes for MYOCD, human, protein

Did you mean: MYOCD, human, proteus

  • Idiopathic Pulmonary Fibrosis

    Objective: To determine the effect of recombinant human pentraxin 2 vs placebo on change from baseline to week 28 in mean forced vital capacity (FVC) percentage of predicted[ncbi.nlm.nih.gov] […] 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] […] misfolded proteins when they accumulate.[ncbi.nlm.nih.gov]

  • Alzheimer Disease

    Here we present the first analysis of human neuropathology after immunization with Abeta (AN-1792).[ncbi.nlm.nih.gov] […] 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] 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

    Abstract Mutations in the human gene encoding cadherin23 ( CDH23 ) cause Usher syndrome type 1D ( USH1D ) and nonsyndromic hearing loss.[doi.org] 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] 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]

  • AICA-Ribosiduria

    […] line (HepG2), sarcoma osteogenic cells (Saos-2), human embryonic kidney cells (HEK293), human skin fibroblasts (SF) and primary human keratinocytes (KC) cultured in purine-depleted[ncbi.nlm.nih.gov] 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] AICAR induction of TXNIP depended on MondoA, but was independent of AMPK (AMP-activated protein kinase) activation and calcium.[biochemj.org]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    Human genomes (the complete set of genes or genetic material present in a cell or organism) consist of 3 million DNA base pairs.[dna.universeofatoms.com] 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] […] 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]

  • Nestor-Guillermo Progeria Syndrome

    Less than 1% of human primary somatic cells can usually turn into iPSCs.[aimspress.com] 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] Cell signaling mechanisms often transmit information via posttranslational protein modifications, most importantly reversible protein phosphorylation.[scienceopen.com]

  • Combined Oxidative Phosphorylation Deficiency Type 24

    […] the biology of human nutrition at the molecular, cellular, tissue, and whole-body levels.[books.google.de] 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] View all proteins of this organism that are known to be involved in the pathway polypeptide chain elongation and in Protein biosynthesis .[uniprot.org]

  • Anauxetic Dysplasia

    This information comes from a database called the Human Phenotype Ontology (HPO) .[rarediseases.info.nih.gov] 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] 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]

  • Combined Oxidative Phosphorylation Deficiency Type 3

    Western blot - AIF Human Profiling ELISA Kit (ab126583) Anti-AIF antibody [7F7AB10] ( ab110327 ) at 5 µg/ml Human heart tissue lysate - mitochondrial extract ( ab110337 )[abcam.com] 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] ; decreases the levels of mitochondrial protein synthesis.[uniprot.org]

  • Premature Chromatid Separation Trait

    The sequence of events was haploid groupings of the chromosomes in normal, human metaphase cells, followed by genomic doubling to homozygousdiploidy.[file.scirp.org] 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] Contains 1 protein kinase domain.[abcam.com]