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60 Possible Causes for EFG1, human, protein

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  • Candida Albicans

    , Page 1 of 1 Previous page Next page /docserver/preview/fulltext/micro/163/8/1145_micro000499-1.gif Candida albicans is normally a harmless commensal of human beings, but[doi.org] […] interacting proteins ( Kerppola 2009 ).[doi.org] EFG1 was essential for the transcription of both hyphae-specific genes such as HWP1 and HWP2 as well as the yeast form-specific gene YWP1.[ncbi.nlm.nih.gov]

  • Hereditary Myopathy with Lactic Acidosis due to ISCU Deficiency

    Product name Recombinant Human ISCU protein Protein length Full length protein Nature Recombinant Source Escherichia coli Amino Acid Sequence Accession Species Human Sequence[abcam.com] […] of the 70-kD protein suggest a more generalized abnormality of the synthesis, import, processing, or assembly of a group of proteins containing iron-sulfur clusters.[jci.org] […] activity in muscle 57 Molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1[docplayer.net]

  • Alexander Disease

    […] few dogs, a rare condition that in humans has been shown to be caused by dominant mutations in the GFAP gene.[ncbi.nlm.nih.gov] The topological analysis of human protein interaction network strategy to identify highly interconnected sub-network modules from which six proteins are found i.e.[ncbi.nlm.nih.gov] EIF2B4, EIF2B5, ENTPD1, EOGT, ERCC2, ERCC6, ERCC8, FA2H, FAM126A, FBXL4, FGD4, FGFRL1, FIG4, FKRP, FOXC1, FOXG1, FOXRED1, GAA, GALC, GAN, GBE1, GCDH, GDAP1, GFAP, GFM1 (EFG1[genedx.com]

  • X-Linked Sideroblastic Anemia and Ataxia

    Iron Physiology and Pathophysiology in Humans is an excellent new text as well as the most authoritative resource in the field.[books.google.com] In contrast, the expression of mutated ABC7 (E433K) or Atm1p (D398K) proteins in Deltaatm1 cells led to a low efficiency of cytosolic Fe/S protein maturation.[ncbi.nlm.nih.gov] Infantile encephalopathy and defective mitochondrial DNA translation in patients with mutations of mitochondrial elongation factors EFG1 and EFTu.[mitomap.org]

  • Streptococcus Mutans

    Candida albicans is a commensal fungal species commonly colonizing human mucosal surfaces [20] .[doi.org] Recently, bacterial DNA encoding 120-kDa cell surface collagen-binding proteins (CBPs) has frequently been detected from S. mutans -positive IE patients.[ncbi.nlm.nih.gov] This phenotype was independent of hyphae or established fungal-biofilm regulators (EFG1, BCR1).[ncbi.nlm.nih.gov]

  • Lactobacillus

    Abstract Oxidative stress cause serious damages in human organism resulting in multiple diseases.[ncbi.nlm.nih.gov] We previously identified micro integral membrane protein (MIMP) as the smallest domain of surface layer protein from Lactobacillus Plantarum.[ncbi.nlm.nih.gov] The hindrance of biofilm development was characterized by the downregulated expression of C. albicans biofilm-specific genes (ALS3, HWP1, EFG1 and CPH1).[ncbi.nlm.nih.gov]

  • CARASIL

    A human tissue array (AA4 Normal organs; Superbiochips, Korea), containing 59 normal human adult tissues, was also used.[doi.org] The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...[ncbi.nlm.nih.gov] EIF2B4, EIF2B5, ENTPD1, EOGT, ERCC2, ERCC6, ERCC8, FA2H, FAM126A, FBXL4, FGD4, FGFRL1, FIG4, FKRP, FOXC1, FOXG1, FOXRED1, GAA, GALC, GAN, GBE1, GCDH, GDAP1, GFAP, GFM1 (EFG1[genedx.com]

  • TMEM70-Related Mitochondrial Encephalo-Cardio-Myopathy

    Mitochondrial DNA mutations in human disease. Nat Rev Genet. 2005 May;6(5):389-402. PMID: 15861210 Jacobs HT. Disorders of mitochondrial protein synthesis .[humpath.com] […] tagged forms of TMEM70 protein to trypsinfollowed by electrophoretic or microscopic analysis demonstrated theorientation of C- and N- protein termini into mitochondrial matrix[docslide.com.br] Signes A, Ding S, Fearnley IM, Taylor RW, Tiranti V, Arnold S, Fernandez-Vizarra E & Zeviani M (2017) MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human[mrc-mbu.cam.ac.uk]

  • Isolated Complex I Deficiency

    Candidate genes can then be identified and tested for complementation on the basis of information from human and model organism genome projects.[humpath.com] (PMID: 15489334) Gerhard DS … MGC Project Team (Genome research 2004) 3 4 60 Mitochondrial Protein Synthesis Adapts to Influx of Nuclear-Encoded Protein.[genecards.org] Translation factors Mitochondrial ribosomal (mitoribosome) proteins: All encoded by nuclear genes Mammalian initiation factors: IF2 & IF3 Elongation factors: EFTu, EFTs, EFG1[neuromuscular.wustl.edu]

  • Staphylococcus Aureus

    The Human Microbiota and Human Chronic Disease: Dysbioses as a Cause of Human Pathology discusses the role of the microbiota in maintaining human health.[books.google.ro] By a combination of molecular biology and mass spectrometry techniques, the structure of the cell wall anchor of surface proteins in S. aureus was revealed.[doi.org] Ramage G, VandeWalle K, López-Ribot JL, Wickes BL (2002) The filamentation pathway controlled by the Efg1 regulator protein is required for normal biofilm formation and development[doi.org]