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The antibody bound specifically to human thrombin and not to murine or bovine thrombin, although these proteins share 86% identity with the human protein. Interestingly, the epitope turned out to be the more structured of two surface regions in which higher sequence variation between the three species is seen.

The genomic results are integrated with the BIOLOGICAL SEQUENCE DATABASES 1. BIOLOGICAL SEQUENCE DATABASES 1 2. NCBI What is NCBI? National center for biotechnology information Established in 1998 Part of national library of medicine at national institute of health Major aim : public database Development of software tools for sequence analysis and disseminate biomedical information 2 The Sequence Revision History tool allows you to see the various gi numbers, version numbers, and update dates for sequences that appeared in a specific GenBank record.. E.g., search for U46667 in the tool to see the old and current identifiers of the nucleotide sequence in that record.

Pubmed sequence

Nucleic Acids Res. 1988 Oct 25;16(20):9775–9787. [PMC free article] [PubMed] [Google Scholar] av C Freitag · 2015 · Citerat av 23 — The contiguity and phase of sequence information are intrinsic to obtain complete 42(10), e85 (2014).10.1093/nar/gku254 [PMC free article] [PubMed] av S Nemes · 2013 · Citerat av 3 — Hazards Models; RNA / chemistry; RNA, Messenger / metabolism; Reproducibility of Results; Sequence Analysis, DNA; Software; Survival Analysis av W Cotton · 1899 — PubMed · Bookshelf · PubMed Central · BLAST · Nucleotide · Genome · SNP Reference Sequences · Gene Expression Omnibus · Genome Data Viewer av MK Cho · 2006 · Citerat av 48 — Human Thiopurine Methyltransferase Pharmacogenetics: Gene Sequence Polymorphisms. Clinical Pharmacology & Therapeutics. 1997;62:60–73. [PubMed] av HB Urnovitz · 1999 · Citerat av 42 — An analysis of the HIV-1vau strain group O env nucleotide sequence disclosed a high frequency of homology with human chromosome 7q31, a fragile site av U Hallberg · 2010 · Citerat av 29 — Humans; Infant; Male; Parent-Child Relations; Parents / psychology*; Professional-Family Relations; Sequence Deletion / genetics*; Sweden av SG Myers · 2009 · Citerat av 108 — in their hypothesized causal sequence explained incremental variance in two different measures of obsessive-compulsive symptoms, with worry controlled. PubMed · Bookshelf · PubMed Central · BLAST · Nucleotide · Genome · SNP Reference Sequences · Gene Expression Omnibus · Genome Data Viewer av S Küry · 2012 · Citerat av 8 — Another widely used method is the bi-directional gene sequencing of all four [PubMed] [Google Scholar]; Wolf B. The neurology of biotinidase av B Yan · 2020 · Citerat av 4 — A comprehensive search was conducted through the online database, including the Cochrane Library, PubMed, EMBASE, SinoMed, CNKI, and av DR Colquhoun · 2006 · Citerat av 47 — Finally, peptide sequencing by tandem mass spectrometry was evaluated as a tool for improving target identification identified the amino acid sequence as TLPDPIEVPLEDVR from norovirus capsid protein (Fig. [PubMed] [Google Scholar].

Sequencing ribosomal RNA (rRNA) genes is currently the method of choice for phylogenetic reconstruction, nucleic acid based detection and quantification of 1. Plant Cell Physiol.

PubMed · Bookshelf · PubMed Central · BLAST · Nucleotide · Genome · SNP Reference Sequences · Gene Expression Omnibus · Genome Data Viewer

Detected in brain, bone, lung and muscle tissues (PubMed:20139355, Immunogen: Expression system for standard: NSO Immunogen sequence: Q22-I354 https://href.li/?https://www.ncbi.nlm.nih.gov/pubmed/?term=berntsson%2C+ronnie the Relaxase PcfG Through Binding and Bending of the oriT Sequence. PubMed via NLM 20 December 2016. Title: F2 Micrognathias[tiab] OR "Pierre Robin Syndrome"[tiab] OR "Robin Sequence"[tiab] OR. "Pierre Robin's PLoS One, 2019.

Find SARS-CoV-2 related resources at NCBI. Download and submit sequences. Explore literature, identify clinical trials, and compounds used in them.

Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls. PubMed; Scopus (216) Google Scholar). These circuits function at a level between the lifeless chemistry of individual molecules and the vibrant dynamic behavior of the living cell. An intracellular protein is sensed by colocalizing its two nanobodies, each attached to a protease or its cleavage sequence, resulting in the release of the Downstream core promoter elements are an expanding class of regulatory sequences that add considerable diversity to the promoter architecture of RNA polymerase II-transcribed genes.

av S Packham · 2015 · Citerat av 11 — Active Transport, Cell Nucleus; Amino Acid Sequence; Cell Line; Cell Nucleus / metabolism*; ErbB Receptors / chemistry; ErbB Receptors av M Paucar · 2020 — The rapid development of massive parallel DNA sequencing and its increased accessibility have enabled for improved diagnostic resolution of av Y Lin · 2018 · Citerat av 6 — RNA sequencing identified 195 differentially expressed genes between R-WT and R-1353 (adjusted P < 1E-100). Most genes were av Z Hu · 1999 · Citerat av 40 — Three novel MDL cDNAs of high sequence identity (designated MDL2, MDL4, and Comparison of these sequences suggests that black cherry MDL is encoded by [PubMed] [Google Scholar]; Sambrook J, Fritsch EF, Maniatis T. Molecular av DM Özata · 2017 · Citerat av 35 — and normal testes using small RNA sequencing, and identified several deregulated miRNAs in TGCTs, including the miR-506~514 cluster. View and Analyze sequences in NCBI Virus · ICTV homepage Information from sequence entries.
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2019-06-03 · The application of advanced methodologies such as next-generation sequencing (NGS) and mass spectrometry (MS) to the characterization of cell lines and recombinant proteins has enabled the highly sensitive detection of sequence variants (SVs). However, while these approaches can be leveraged to provide deep insight into product micro-heterogeneity caused by SVs, they are not used in a - the full sequence of the insert(s), together with (at least) the base pairs of the host flanking sequences needed to establish an event-specific detection method, - the full sequence of the species-specific target (reference gene) and/ its GenBank accession number if available. Whole-genome sequencing (WGS) can provide excellent resolution in global and local epidemiological investigations of Staphylococcus aureus outbreaks.

You can see 0 articles in Pubmed Central that av ENLAV KLINISKA · 2019 — Metod: Litteratusökning utfördes i databaserna PubMed, Cochrane, Medline och 8a) Method used to generate the random allocation sequence. Nej. Nej. Nej. Björn Olsen's publications in PubMed Jan Sjölin's publications in PubMed Finnish Campylobacter jejuni strains of multilocus sequence type ST-22 complex Nuclear localisation prediction for Eukaryotic protein sequences. PubMed id: 17332022.
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The Nucleotide database is a collection of sequences from several sources, including GenBank, RefSeq, TPA and PDB. Genome, gene and transcript sequence data provide the foundation for biomedical research and discovery.

Results: We analyzed 10 Background: In a previous paper, we introduced MUSCLE, a new program for creating multiple alignments of protein sequences, giving a brief summary of the G-quadruplexes are higher-order DNA and RNA structures formed from G-rich sequences that are built around tetrads of hydrogen-bonded guanine bases. Sequencing ribosomal RNA (rRNA) genes is currently the method of choice for phylogenetic reconstruction, nucleic acid based detection and quantification of 1. Plant Cell Physiol.

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Pseudomonas plecoglossicida is a lethal pathogen of ayu (Plecoglossus altivelis) in Japan and is responsible for substantial economic costs to ayu culture. Previously, we demonstrated the efficacy of phage therapy against P. plecoglossicida infection using two lytic phages (PPpW-3 and PPpW-4) (S. C. Park, I. Shimamura, M. Fukunaga, K. Mori, and T. Nakai, Appl Environ Microbiol 66:1416–1422

Nucleotide sequence of human preproinsulin complementary DNA. Recombinant bacterial plasmids that contain DNA complementary to human preproinsulin messenger RNA have been constructed. One clone contains the entire preproinsulin coding region, as well as the 3' untranslated region of the messenger RNA and eight nucleotides of the 5' untranslated RefSeq release 201 is public. RefSeq release 201 is accessible online, via FTP and through NCBI’s Entrez programming utilities, E-utilities. This full release incorporates genomic, transcript, and protein data available as of July 6, 2020, and contains 246,016,651 records, including 178,304,046 proteins, 32,462,009 RNAs, and sequences from 103,293 associated sequence accession: M11313[accn] gene name (symbol) BRCA1[sym] publication (PubMed ID) 11331580[PMID] Gene Ontology (GO) terms or identifiers "cell adhesion"[GO] 10030[GO] genes with short variants of medical interest "clinvar gene specific"[Filter] chromosome and species: Y[CHR] AND human[ORGN] Enzyme Commission (EC) numbers: 1.9.3.1[EC] Search a BLAST database of Betacoronavirus nucleotide sequences. Run BLAST. Search, retrieve, and analyze sequences and other content in the NCBI Virus SARS-CoV-2 Data Hub. Explore in NCBI Virus.

PubMed · Bookshelf · PubMed Central · BLAST · Nucleotide · Genome · SNP Reference Sequences · Gene Expression Omnibus · Genome Data Viewer

Comments and questions to info@ncbi.nlm.nih.gov av M Annertz · 2017 — including a whole lower body coronal STIR sequence or computed tomography with radiation dose adapted to indication and patient age. av X Li · 2020 · Citerat av 10 — Literature search and eligibility criteria. We searched PubMed, medRxiv and the WHO COVID-19 database on 21 June 2020 with entry date limits av C Hedberg-Oldfors · 2017 · Citerat av 5 — Further analysis of the grandfather revealed equal amounts of DNA with the wild-type sequence and DNA with the c.646_648dupGTT variant in five different av MG Worku · 2020 · Citerat av 3 — PubMed, direct Google, advanced Google Scholar, and Cochrane the prevalence of brown adipose tissue after the sequential omission. Browse BY. Family of Virus · Virus Name · Gene Name · Pubmed Id · VsiRNAid; Total number of Results for EBNA1 are 25. Results from 0 - 25. siRNA sequence av U Kõljalg · 2020 · Citerat av 4 — Databases and open data of the International Nucleotide Sequence Database For the calculations of SHs, two datasets of eukaryote rDNA ITS sequences were [Google Scholar] [CrossRef] [PubMed]; Hawksworth, D.L.; Lücking, R. Fungal (2002) Complete genome sequence of the model actinomycete Streptomyces coelicolor A3 (2). Nature 417(6885): 141-147.

For a nucleotide sequence select nucleotide blast from the Basic BLAST section of the BLAST home page. For a protein sequence, select the protein blast service.