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1,924 Possible Causes for complex, glycine tRNA, ligase, location

  • LIG4 Syndrome

    Term Name: DNA ligase IV deficiency Search Ontology: Synonyms: LIG4 Syndrome Definition: A combined T cell and B cell immunodeficiency that has material basis in a mutation[] Important User Information: Remote access to EBSCO's databases is permitted to patrons of subscribing institutions accessing from remote locations for personal, non-commercial[] […] size range anticipated for LIG4/XRCC4 complexes (data not shown).[] Gene LIG4 Chromosomal Location 13q22-q34 Allelic Variant 2 601837.0002 ; LIG4 SYNDROME Identified Mutation ARG814TER ; O'Driscoll et al. [Molec.[]

    Missing: glycine tRNA
  • Influenza

    RNA ligation RNA was circularized overnight at 4  C with T4 RNA ligase (Epicentre).[] The incidence of influenza A(H1N1)pdm09 was higher in Ras Tanura city compared to other locations in the Eastern Province.[] Each genomic RNA segment exists in the form of a ribonucleoprotein complex (RNP) in association with nucleoproteins and an RNA-dependent RNA polymerase in virions.[] […] all types of influenza viruses, each vRNA segment binds to an RNA-dependent RNA polymerase and multiple copies of nucleoprotein (NP), forming a rod-like ribonucleoprotein complex[]

    Missing: glycine tRNA
  • Isolated Complex I Deficiency

    Provision of succinyl-CoA by KGDHC is essential for generation of matrix ATP (or GTP) by substrate-level phosphorylation catalyzed by succinyl-CoA ligase.[] , Syndromes , Muscle , NMJ , Nerve , Spinal , Ataxia , Antibody & Biopsy , Patient Info PATHWAYS: MITOCHONDRIAL OXIDATIVE PHOSPHORYLATION Mitochondrial respiratory chain Location[] Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA (glycine) gene.[] Further biochemical analysis of subject fibroblasts revealed a severe complex I deficiency caused by defective assembly.[]

  • Autosomal Recessive Juvenile Parkinson Disease

    Parkin is a ubiquitin ligase that ubiquitinates misfolded proteins targeted for the proteasome-dependent protein degradation pathway.[] SNP-rs9347684, located 3.5 kb upstream region of the PARK2 gene; and SNP-rs10945859, located within the 6.67 kb upstream region of PACRG gene, were cloned in pGL3 promoter[] Part of a SCF-like complex, consisting of PARK2, CUL1 and FBXW7. Part of a complex, including STUB1, HSP70 and GPR37.[] This gene encodes for F-box protein 7, another component of the ubiquitin ligase complex.[]

    Missing: glycine tRNA
  • Lafora Disease

    Here, we demonstrate that malin is a single subunit E3 ubiquitin (Ub) ligase and that its RING domain is necessary and sufficient to mediate ubiquitination.[] Laforin-positive polyglucosan bodies were located in neurofilament-positive neurons but not in GFAP-positive astrocytes.[] These results suggest that the modification introduced by the laforin-malin complex could affect the subcellular distribution of AMPK beta subunits.[] In addition, we found that malin shares significant identity with the E3-ubiquitin ligase TRIM32.[]

    Missing: glycine tRNA
  • Malignant Neoplasm

    After circularization with T4 DNA ligase, plasmids were used to electrotransform Escherichia coli C (Δ LacZ , galE ‐) cells by electroporation.[] RESULTS: In addition to the case we present, 12 case reports were located (n 13). The mean age of patients was 59.6 (SD, 14.98 years) years.[] The complex role of radiation, cytotoxic drugs and genes in the development of a second malignant neoplasm in association with retinoblasma is also discussed.[] Zheng, Zhenping Chen, Liwei Sun, Hailong Wang, Yuanxiang Zhu, Jing Zhang, Shuyan Yang, Yi Lu, Qinmiao Sun, Yi Tao, Feng Liu, Yun Zhao and Dahua Chen , Activation of Smurf E3 Ligase[]

    Missing: glycine tRNA
  • Tuberculosis

    The ubiquitin ligase parkin mediates resistance to intracellular pathogens.[] Intravenous drug users: choose own location versus treatment centre[] Bone and soft tissue samples from 85 ancient Egyptian mummies were analyzed for the presence of ancient Mycobacterium tuberculosis complex DNA (aDNA) and further characterized[] […] sequencing analysis Automated molecular testing Microscopic-observation drug susceptibility (MODS) and thin-layer agar (TLA) assays Additional rapid tests (eg, BACTEC-460, ligase[]

    Missing: glycine tRNA
  • Leber's Hereditary Optic Neuropathy

    […] chemistry Tyrosine-tRNA Ligase/genetics* Tyrosine-tRNA Ligase/metabolism Substances DNA, Mitochondrial Mitochondrial Proteins Cyclooxygenase 2 PTGS2 protein, human Electron[] Find a Doctor Find a doctor by specialty or location. Care Locations Find primary and specialty care near you.[] A nucleotide exchange was detected at position 14568 replacing a glycine by serine in the ND6 gene.[] […] between complex I and its substrate ubiquinone in the heteroplasmic condition (asymptomatic state), and the catalytic function of complex I, as mutated mDNA turns toward the[]

  • Infectious Mononucleosis

    After being purified, gp350 either was aliquoted and then frozen at 70 C until required for ELISA or was biotinylated (gp350-biotin) using biotin ligase (Avidity).[] Lifespan Locations Featured Lifespan Locations Additional Lifespan Locations Centers & Services Lifespan Centers & Services Browse By Popular Category Lifespan Living Featured[] Our physicians provide care for both outpatients and inpatients with complex problems involving a wide variety of infectious diseases.[] Need help finding a location?[]

    Missing: glycine tRNA
  • Sarcosinemia

    Alaninemia Alpha ketoadipic aciduria Aminomethyltransferase deficiency Aromatic amino acid decarboxylase deficiency Beta-hydroxyisobutyryl-CoA deacylase deficiency Biotin- ligase[] […] recessive manner, which means the defective gene responsible for the disorder is located on an autosome (chromosome 9 is an autosome), and two copies of the defective gene[] CHEBI:16015 ChEBI 439161 PubChem-compound C00430 KEGG Compound Glycine--tRNA ligase L-Arginine CHEBI:30314 ChEBI Ammonia 439153 PubChem-compound 57 ChemSpider 50 ChemSpider[] Title Other Names: Sarcosine dehydrogenase complex deficiency; SARD deficiency; Hypersarcosinemia; Sarcosine dehydrogenase complex deficiency; SARD deficiency; Hypersarcosinemia[]