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4,426 Possible Causes for (S, 4, REX4,, RNA, exonuclease, homolog

Show results in: Română

  • Influenza

    , Ryuto M , Sakaguchi S , Sakayori S , Sasaki Y , Sato S , Sato T , Sato Y , Sato Y , Segawa Y , Shibasaki A , Shimamoto E , Shimomura H , Sugiura T , Suzuki S , Suzuki T[ncbi.nlm.nih.gov] Older: 0/1/2/3 127/66/23/1 134/63/15/1 0.59 4 Younger: 0/1/2/3/4 109/75/29/4/0 108/75/25/4/1 0.87 4 Starting age of nursery school [ n (%)] 0.21 4 6 (35) 61 (29) 3 y 138[ajcn.org] Most RNA viruses that lack a DNA phase replicate in the cytoplasm.[ncbi.nlm.nih.gov] Amplicons were prepared for sequencing by incubating them at 37  C for 60 min with 0.5 U of shrimp alkaline phosphatase (Amersham) and 1 U of exonuclease I (Amersham) to inactivate[dx.doi.org] Heterologous mean HI titers were normalized to mean homologous HI titers (mean heterologous titers/mean homologous titers).[doi.org] Perdigão AC 1, 2, 3 , Ramalho IL 1, 2 , Guedes MI 2 , Braga DN 4, 5 , Cavalcanti LP 4 , Melo ME 1 , Araújo RM 6 , Lima EG 1, 2 , Silva LA 1 , Araújo Lde C 7 , Araújo FM 1,[ncbi.nlm.nih.gov]

    Missing: REX4
  • LIG4 Syndrome

    .}, author {S. C. Unal and Karen Cerosaletti and Duygu Uçkan-Çetinkaya and M.[semanticscholar.org] Abstract DNA ligase 4 deficiency (LIG4-SCID) causes lymphopenia (T-B-NK ) and a radiosensitive SCID (RS-SCID) phenotype.[bloodadvances.org] Structure-guided mutational analysis of T4 RNA ligase 1. RNA 12 , 2126–2134 (2006). 39. Yin, S., Ho, C. K. & Shuman, S. Structure-function analysis of T4 RNA ligase 2.[nature.com] Sarcoma, Avian DNA ligase and exonuclease activities in virions of rous sarcoma virus.[brenda-enzymes.org] LIG4 syndrome is conferred by hypomorphic mutations in DNA ligase IV, an essential component of DNA non-homologous end-joining (NHEJ), and is associated with pancytopaenia[ncbi.nlm.nih.gov] .; Weitzman, S.; Nezarati, M. M. : A patient with mutations in DNA ligase IV: clinical features and overlap with Nijmegen breakage syndrome. Am. J. Med.[humpath.com]

    Missing: REX4
  • Werner Syndrome

    Genet. 62 , 25–30 (1982). 32 Samantray, S. K., Samantray, S., Johnson, S. C. & Bhaktaviziam, A. Aust. N.Z. J. Med. 7 , 309–311 (1977). 33 Sparkes, R. S. et al.[dx.doi.org] Kamiya H 1, 2, 3, 4 , Yamazaki D 1 , Nakamura E 2 , Makino T 2, 4 , Kobayashi M 3 , Matsuoka I 3 , Harashima H 1 .[ncbi.nlm.nih.gov] It has been suggested that, in addition to RNA pol II, RNA pol I activity is affected in WS cells ( 33 ).[doi.org] Both Pol δ and WRN encode 3' 5' DNA exonuclease activities.[ncbi.nlm.nih.gov] Such homology does not necessarily mean that WRN encodes an active helicase.[ncbi.nlm.nih.gov] , 0.1 µg/µl BSA and 4 mM ATP].[doi.org]

    Missing: REX4
  • Hepatitis C Virus

    Kaito, M, Watanabe, S, Tsukiyama-Kohara, K, Yamaguchi, K, Kobayashi, Y, Konishi, M, Yokoi, M, Ishida, S, Suzuki, S, Kohara, M 1994 Hepatitis C virus particle detected by immunoelectron[doi.org] However, hepatitis C virus genotype 4 (HCV GT-4) has rarely been reported in Brazil. HCV GT-4 demonstrates high sustained virological response (SVR).[ncbi.nlm.nih.gov] , Small Interfering/metabolism RNA, Viral/metabolism Virus Replication/genetics Substances MIRN122 microRNA, human MicroRNAs RNA, Small Interfering RNA, Viral Exoribonucleases[ncbi.nlm.nih.gov] Comparative phylogenetic analysis of the canine hepacivirus (CHV) confirmed it to be the most genetically similar animal virus homolog of HCV.[ncbi.nlm.nih.gov] To address this challenge, we searched for homologous viruses in small mammals, including wild rodents.[ncbi.nlm.nih.gov] BACKGROUND: Aspartate transaminase-to-platelet ratio index (APRI) and fibrosis-4 (FIB-4) are well known as representative indirect serum biomarkers related to liver fibrosis[ncbi.nlm.nih.gov]

    Missing: REX4
  • Saccharomyces Cerevisiae

    RESULTS: S. boulardii and S. cerevisiae helped to mediate the effects of stress on the small and large intestine.[ncbi.nlm.nih.gov] Michael CF 1, 2 , Waters CM 3 , LeMessurier KS 1, 2 , Samarasinghe AE 1, 2 , Song CY 4 , Malik KU 4 , Lew DB 1, 2 .[ncbi.nlm.nih.gov] Mutations in three genes (TCOF1, POLR1C and POLR1D) involved in RNA polymerase I (Pol I) transcription account for more than 90% of disease cases.[ncbi.nlm.nih.gov] Only variants directly altering the DNA binding cleft in the exonuclease domain elevated the mutation rate.[ncbi.nlm.nih.gov] Coupled with previous evidence, this suggests that MRX drives expansions of short TNRs through a process distinct from homologous recombination.[ncbi.nlm.nih.gov] To more fully characterize the global response to hypoxia, we exposed yeast to hypoxic conditions, extracted RNA at different times, and performed RNA sequencing (RNA-seq)[ncbi.nlm.nih.gov]

    Missing: REX4
  • Infectious Mononucleosis

    Alfred S.[nytimes.com] Panikkar A 1 , Smith C 2 , Hislop A 3 , Tellam N 4 , Dasari V 4 , Hogquist KA 5 , Wykes M 4 , Moss DJ 4 , Rickinson A 3 , Balfour HH Jr 6 , Khanna R 2 .[ncbi.nlm.nih.gov] In-situ hybridization for EBV-encoded RNA with immunostaining against CD20 was used for evaluation of EBV infection.[ncbi.nlm.nih.gov] The Epstein-Barr virus alkaline exonuclease BGLF5 serves pleiotropic functions in virus replication. J. Virol. 83 : 4952 -4962. Fingeroth, J. D., J. J. Weis, T. F.[dx.doi.org] On in situ hybridization, numerous Epstein-Barr virus (EBV)-encoded small RNA (EBER)-positive cells were demonstrated in the germinal center, as well as in interfollicular[ncbi.nlm.nih.gov] Sutcliffe S 1, 2 , Nevin RL 3 , Pakpahan R 1 , Elliott DJ 4 , Langston ME 5 , De Marzo AM 4, 6, 7 , Gaydos CA 8 , Isaacs WB 6, 7 , Nelson WG 4, 6, 7, 9 , Sokoll LJ 4, 6, 7[ncbi.nlm.nih.gov]

    Missing: REX4
  • Lassa Virus

    RNA copies/ml serum, which corresponds to 4 to 30 S RNA copies/assay.[ncbi.nlm.nih.gov] Safronetz D 1, 2 , Sogoba N 3 , Diawara SI 3 , Bane S 3 , Rosenke K 4 , Maiga O 3 , Boisen M 5 , Garry RF 6 , Branco LM 5 , Lindsay LR 1, 2 , Traoré SF 3 , Feldmann H 1, 4[ncbi.nlm.nih.gov] Here, we present crystal structures of the RNA-binding domain of Lassa virus NP in complex with ssRNA.[ncbi.nlm.nih.gov] Although the fold of the NP enzyme is conserved and the active site completely conserved with other exonucleases in its DEDDh family, NP is atypical among exonucleases in[ncbi.nlm.nih.gov] It was found that while the GPC extravirion domains were readily exchangeable, homologous stable signal peptide (SSP) and G2 transmembrane and cytoplasmic tail domains were[ncbi.nlm.nih.gov] With the Nigeria strain of Lassa virus the levels of homology were 100% for two of these epitopes and 85% for three of them, whereas homology with the respective Mopeia epitopes[ncbi.nlm.nih.gov]

    Missing: REX4
  • Streptococcus Lactis

    Table 1: General features of S. thermophilus CNRZ1066 and LMG18311 genomes Inactive S. thermophilus genes Unexpectedly, 10% of the S. thermophilus genes are not functional[dx.doi.org] […] deliver/fulltext/micro/161/4/701.html?[doi.org] […] the c is -encoded RNAs or antisense RNAs (asRNAs).[doi.org] Read a second time 845 4/15/2010 Asm. Ordered to a third reading 845 4/15/2010 Asm. Rules suspended 845 4/15/2010 Asm.[docs.legis.wisconsin.gov] Google Scholar Moineau S, Fortier J, Ackermann H-W& Pandian S (1992) Characterization of lactococcal bacteriophages from Québec cheese plants. Can. J.[doi.org] […] biology umbel:isLike ; # RNA biology . # RNA biology a schema:Periodical ; schema:issn " 1547-6286 " ; schema:name " RNA biology " ; umbel:isLike ; . # RNA biology a schema[worldcat.org]

    Missing: REX4
  • Acute Gastroenteritis

    Previously reported cases of S. algae have mainly been associated with direct contact with seawater.[ncbi.nlm.nih.gov] Braz J Infect Dis. 2017 Jul - Aug;21(4):472-476. doi: 10.1016/j.bjid.2017.03.012. Epub 2017 May 10.[ncbi.nlm.nih.gov] Extracted viral RNA was separated by polyacrylamide gel electrophoresis (PAGE) and the specific rotavirus VP4 (P-types) and VP7 (G-types) determined.[ncbi.nlm.nih.gov] Sequencing of a portion of the capsid gene and the ORF1/ORF2 overlap was used to assess DNA sequence homology, phylogeny, and recombination using pairwise alignments, MEGA[ncbi.nlm.nih.gov] Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved.[ncbi.nlm.nih.gov] Sequence analysis of the RNA-dependent RNA polymerase (RdRp) and capsid protein of the viral isolates from these outbreaks confirmed that this GII.P16-GII.2 strain was the[ncbi.nlm.nih.gov]

    Missing: REX4 exonuclease
  • Rotavirus

    S. Bresee, M. Greenwald, S. Cullen, H. D. Davies, C. Trevenen, S. R. Zaki, and R. I. Glass. 2003.[ncbi.nlm.nih.gov] […] and Dentistry, Rochester, New York, USA. [email protected] Abstract In 2009, three children were hospitalized in Rochester, NY, with sequence-confirmed G8P[4][ncbi.nlm.nih.gov] Viral proteins involved in RNA replication include the RNA polymerase (VP1), the core scaffold protein (VP2) and the non-structural RNA-binding proteins (NSP2 and NSP5).[ncbi.nlm.nih.gov] Subsequently, the 7-methylguanosine cap was found to protect mRNA from degradation by exonuclease activity [ 40 ].[doi.org] […] responses produced after both natural infection and vaccination, and the fact that animal models do not fully mimic the human immunologic responses, even when inoculated with homologous[doi.org] The genotype composition of GER1H-09 (G8-P[4]-I2-R2-C2-M2-A2-N2-T2-E2-H2) suggests the occurrence of reassortment events between G8 genotypes and human DS-1-like G2P[4] rotaviruses[ncbi.nlm.nih.gov]

    Missing: REX4