Showing 1,941 - 1,960 results of 5,147 for search '"codon"', query time: 0.09s Refine Results
  1. 1941

    Complete Genomic Sequence of Bacteriophage Felix O1 by Andrew M. Kropinski, Yi-Min She, Erika J. Lingohr, Vivek Kapur, F. William Pierson, Qing Zhang, Ling Ling Li, Lee A. Weigt, Douglas J. Borris, Jean M. Whichard, Nammalwar Sriranganathan

    Published 2010-03-01
    “…Proteomic analysis indentified structural proteins: Gp23, Gp36 (major tail protein), Gp49, Gp53, Gp54, Gp55, Gp57, Gp58 (major capsid protein), Gp59, Gp63, Gp64, Gp67, Gp68, Gp69, Gp73, Gp74 and Gp77 (tail fiber). Based on phage-host codon differences, 7 tRNAs could affect translation rate during infection. …”
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    Article
  2. 1942

    Clinical case of primary immunodeficiency: X-linked agammaglobulinemia by E. V. Kuvschinova, L. M. Kurtasova, A. G. Borisov, A. R. Schmidt, T. A. Gerasimova

    Published 2020-04-01
    “…The results of molecular genetic studies: gene btk (ex 1-19) genome version GRCh38.p5, transcript version ENST00000308731 single nucleotide substitution identified с.1027С > Т in homozygous state leading to premature stop codon p.Gln343Ter (p.Q343*). The presented clinical case reflects the low alertness of pediatricians for PIDS. …”
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    Article
  3. 1943

    Characterization of the complete mitochondrial genome of Wuhaniligobius polylepis (Gobiiformes: Gobiidae) and phylogenetic studies of Gobiiformes by Li Gong, Bingjian Liu, Zhen-Ming Lü, Li-Qin Liu

    Published 2018-07-01
    “…The 13 PCGs encode 3,802 amino acids in total, twelve of which use the initiation codon ATG except COI, which uses GTG. In order to explore the systematic status of W. polylepis and further phylogenetic study of Gobiiformes, a maximum-likelihood tree was constructed based on the concatenated sequences of 12 PCGs. …”
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    Article
  4. 1944

    Characterization of the complete mitochondrial genome of the false trevally, Lactarius lactarius (Perciformes: Lactariidae) by Nazia Tabassum, Ji-Hyun Lee, Soo Rin Lee, Jeong-Hoon Kim, Hyun-Woo Kim

    Published 2020-04-01
    “…Besides COX1 gene (GTG), all the other protein-coding genes showed typical (ATG) start codon. Incomplete stop condons (TA-/T–) were identified in COX2, COX3, ND2, ND3, ND4 and Cyt B. …”
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    Article
  5. 1945

    The complete mitochondrial genome of Reticulitermes periflaviceps (Isoptera: Rhinotermitidae) by Xin Ye, Yin Hu, Haihong Chen, Yiyuan Liao, Tong Chen, Dayu Zhang

    Published 2019-07-01
    “…The overall A + T among the genome sequence is 65.64%. The start codons of all protein-coding genes are ATN and the stop codon is TAA except TAG for Nad1 and incomplete T for COII and Nad5. …”
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    Article
  6. 1946

    Sickle cell disease complications by Ersi Voskaridou

    Published 2014-12-01
    “…The sickle mutation consists a single nucleotide change (GAT->GTT) in the sixth codon of exon 1 of the β-globin gene coding for the β-globin polypeptide of hemoglobin (Hb) (a2β2). …”
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  7. 1947

    Organization of the mitochondrial genome of Ramulus irregulatiter dentatus (Phasmatidae: Phasmatidae) by Congfen Zhang, Xiaoqiang Guo

    Published 2022-08-01
    “…The base composition and codon usage were typical of Phasmatodea species. …”
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    Article
  8. 1948

    The complete chloroplast genome of Saussurella borneensis (Orthoptera: Tetrigoidea) from China and its phylogenetic analysis by Wei-An Deng, Rong-Jiao Zhang, Xiao-Dong Li, Lei Xin

    Published 2021-09-01
    “…Ten PCGs initiated with a typical ATN codon (one with ATC, two with ATA, two with ATT, and five with ATG) and 13 terminated with complete stop codons. …”
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    Article
  9. 1949

    Nonsense-Mediated mRNA Decay Factor Functions in Human Health and Disease by Lingling Sun, Justine Mailliot, Christiane Schaffitzel

    Published 2023-02-01
    “…Nonsense-mediated mRNA decay (NMD) is a cellular surveillance mechanism that degrades mRNAs with a premature stop codon, avoiding the synthesis of C-terminally truncated proteins. …”
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    Article
  10. 1950

    The complete chloroplast genome sequence of Melampyrum koreanum (Orobanchaceae), an endemic and hemi-parasitic herb in Korea by Dong-Pil Jin, Jin-Seok Kim, Yeon-Bong Ku, Chae Eun Lim

    Published 2021-11-01
    “…Among the identified genes, rpoA and several ndh genes were determined to be pseudogenized due to the stop codon in the middle of the gene. The phylogenetic tree of the family was reconstructed based on 20 protein-coding genes, conserved across studied taxa. …”
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    Article
  11. 1951

    The complete mitochondrial genome of spearnose grenadier, Coelorinchus multispinulosus, Katayama, 1942 (Gadiformes: Macrouridae) by Sapto Andriyono, Ah-Ran Kim, Md. Jobaidul Alam, Hyun Park, Hyun-Woo Kim

    Published 2019-01-01
    “…Incomplete stop codons (TA–/T–) were shown in six genes including COX1, COX2, COX3, ND3, ND4, and ATP6. …”
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    Article
  12. 1952

    New insertions-induced Hb H disease by Marzieh Alipour, Sara Afzali, Khalil Khashei Varnamkhasti

    Published 2021-06-01
    “…One of the insertions, 108/109, is a new findings and another one, codon 44, is the mutation which has been followed for the first time. …”
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    Article
  13. 1953

    The mitochondrial genome of the toothed top shell snail Monodonta labio (Gastropoda: Trochidae): the first complete sequence in the subfamily monodontinae by Haiyan Cong, Yixuan Lei, Lingming Kong

    Published 2020-01-01
    “…All of the protein-coding genes use the standard initiation codon ATN and are terminated by the termination codons TAA and TAG. …”
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    Article
  14. 1954

    Decimative Multiplication of Entropy Arrays, with Application to Influenza by Joel K. Weltman, William A. Thompson, Andy Martwick

    Published 2009-07-01
    “…Because of its dependence upon the periodicity of the codon, the decimative procedure should be generalizable to any biological system.…”
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  15. 1955

    Gene prediction using the Self-Organizing Map: automatic generation of multiple gene models by Smith Terry J, McInerney James O, Mahony Shaun, Golden Aaron

    Published 2004-03-01
    “…The current implementation, named RescueNet, uses relative synonymous codon usage as the indicator of protein-coding potential.…”
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    Article
  16. 1956

    Neuroendocrine effects of the duper mutation in Syrian hamsters: a role for Cryptochrome 1 by Emily N. C. Manoogian, Michael Seifu Bahiru, Emily Jue Wang, Mary Holder, Eric L. Bittman

    Published 2024-02-01
    “…In light of the finding that the duper allele is a stop codon in Cryptochrome 1, our results suggest important neuroendocrine functions of this core circadian clock gene.…”
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    Article
  17. 1957

    Complete mitochondrial genome of the water flea Daphnia magna (Cladocera, Daphniidae) by Chang-Bum Jeong, Bum-Soon Choi, Dae-Sik Hwang, Jinhee Choi, Jae-Seong Lee

    Published 2019-01-01
    “…Of 13 PGCs, five genes (ND2, CO1, CO2, ND4, and ND5) had incomplete stop codons. Furthermore, the stop codons of the remaining eight PGCs were TAG and TAA, while the start codon of CO1 gene was CTA. …”
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    Article
  18. 1958

    The complete mitochondrial genome of Amphinemura bulla Shimizu, 1997 (Plecoptera: Nemouridae) from Japan by Ying Wang, Jinjun Cao, Dávid Murányi, Xiling Chen, Fenming Yan

    Published 2021-03-01
    “…All protein-coding genes (PCGs) use normal initiation codons, except ND1 and ND5 which begin with TTG and GTG. …”
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  19. 1959

    The complete mitochondrial genome of Chlorogomphus shanicus Wilson, 2002 (Anisoptera: Chlorogomphidae), an endemic species in South China by Haojie Wang, Lu Wang, Jian Liao, Bo-Ping Han

    Published 2023-11-01
    “…Twelve PCGs started with ATN codons, except cox1 began with TTG codon. Most transfer RNA genes (tRNAs) were predicted to fold in a typical cloverleaf structure, except the trnS1 (gct), which lacked a dihydrouridine arm that had been simplified to a loop. …”
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    Article
  20. 1960

    A rare homozygous missense mutation of COL7A1 in a Vietnamese family by Nguyen Thuy Duong, Luong Thi Lan Anh, Nguyen Huu Sau, Nguyen Bao Anh, Miyake Noriko, Nong Van Hai, Matsumoto Naomichi

    Published 2022-05-01
    “…Although a heterozygous form of this mutation in combination with a premature termination codon allele has been shown to cause RDEB-I, this is the first report of homozygosity of this mutation as the etiology. …”
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