Here, we report the sequencing of cDNA clones spanning 9,992 nucleotides encoding the murine HD homologue (hd), which exhibits 90% peptide sequence identity, including conservation of the CAG and adjacent CCG repeats. In addition, we show that the CCG is polymorphic in the mouse.
2018-6-7
av D Goldman · 1987 · Citerat av 83 — The derived phylogenetic tree indicated a branching sequence, from oldest to most recent, of cercopithecoids (Macaca fascicularis), gibbon-siamang, orangutan, av KD Lardizabal · 2001 · Citerat av 405 — Using coding sequences from acyl CoA:cholesterol acyltransferase (ACAT), expressed sequence tag data bases were searched and a gene identified that or protein name, organism, unique identifier (e.g., accession number, sequence ID, PubMed ID), and other terms, depending on the database being searched. However, standards for how sequence databases are organized and presented are currently insufficient. Here, we propose five strategies to address fundamental issues in the annotation of sequence databases: (i) to PubMed. 27528420 15 dec. 2015 — Recent massive next-generation sequencing (NGS)-based consortium efforts such as the 1000 Genomes Project (1000G) and the Exome shown are described using the NM_139276.2 transcript reference sequence. variant could not be associated with disease phenotype, PubMed: Vogelaar av JK Yuvaraj · 2021 · Citerat av 7 — The tree is based on a MAFFT alignment of amino acid sequences, The sources of sequence data and explanation of receptor suffixes are Title, Sequence analysis of HIV-1 isolates from Guinea-Bissau: selection of vaccine epitopes relevant in URL, http://www.ncbi.nlm.nih.gov/pubmed/?term=.
The DMSO reductase structural operon was shown to consist of three open reading frames, namely dmsABC, encoding polypeptides with predicted molecular weights of 87,350, 23,070, and 30,789 Daltons, respectively. 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. Here, we report the sequencing of cDNA clones spanning 9,992 nucleotides encoding the murine HD homologue (hd), which exhibits 90% peptide sequence identity, including conservation of the CAG and adjacent CCG repeats. In addition, we show that the CCG is polymorphic in the mouse. Show these sequence matches individually on genome browser (activates track "Individual matches for article") Position: chr14:95,562,199-95,582,045 Genomic Size: 19,847 The National Library of Medicine (NLM), on the NIH campus in Bethesda, Maryland, is the world's largest biomedical library and the developer of electronic information services that delivers data to millions of scientists, health professionals and members of the public around the globe, every day. The National Center for Biotechnology Information (NCBI) provides a large suite of online resources for biological information and data, including the GenBank ® nucleic acid sequence database and the PubMed database of citations and abstracts published in life science journals.
Björn Olsen's publications in PubMed Jan Sjölin's publications in PubMed Finnish Campylobacter jejuni strains of multilocus sequence type ST-22 complex
Subject sequence(s) to be used for a BLAST search should be pasted in the text area. It automatically determines the format or the input.
av W Cotton · 1899 — PubMed · Bookshelf · PubMed Central · BLAST · Nucleotide · Genome · SNP Reference Sequences · Gene Expression Omnibus · Genome Data Viewer
The National Center for Biotechnology Information (NCBI) provides a large suite of online resources for biological information and data, including the GenBank® nucleic acid sequence database and the PubMed database of citations and abstracts published in life science journals. The Entrez system provides search and retrieval operations for most of these data from 38 distinct databases. Subject sequence(s) to be used for a BLAST search should be pasted in the text area. It automatically determines the format or the input. To allow this feature there are certain conventions required with regard to the input of identifiers. The Basic Local Alignment Search Tool (BLAST) finds regions of local similarity between sequences.
However, whole-genome short read sequencing does not yield haplotype information spanning whole chromosomes directly. Computational assembly of shorter haplotype fragments is …
Krishna et al. dissect the immune microenvironment and TCR clonotype dynamics in multiregional clear cell renal cell carcinoma (ccRCC) samples at single-cell resolution. They show that CD8+ tissue-resident T cells and distinct tumor-associated macrophage (TAM) populations are associated with response and resistance to immune checkpoint blockade (ICB) in ccRCC.
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BLAST provides sequence similarity searches of GenBank and other sequence databases. There is a paucity of complete genome sequence information for human respiratory syncytial virus (HRSV). To this end, we sequenced the complete genome sequences of HRSV genotype A (HRSV-A/IC688/12) and genotype B (HRSV-B/GW0047/14 and HRSV-B/IC0027/14). This information will increase the understanding of HRSV genetic diversity, evolution, pathogenicity, antigenicity, and transmissibility.
However, standards for how sequence databases are organized and presented are currently insufficient.
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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.
Here, we report the sequencing of cDNA clones spanning 9,992 nucleotides encoding the murine HD homologue (hd), which exhibits 90% peptide sequence identity, including conservation of the CAG and adjacent CCG repeats. In addition, we show that the CCG is polymorphic in the mouse. Show these sequence matches individually on genome browser (activates track "Individual matches for article") Position: chr14:95,562,199-95,582,045 Genomic Size: 19,847 The National Library of Medicine (NLM), on the NIH campus in Bethesda, Maryland, is the world's largest biomedical library and the developer of electronic information services that delivers data to millions of scientists, health professionals and members of the public around the globe, every day. The National Center for Biotechnology Information (NCBI) provides a large suite of online resources for biological information and data, including the GenBank ® nucleic acid sequence database and the PubMed database of citations and abstracts published in life science journals. Valid sequencing data were aligned to the human reference genome sequence from the National Center for Biotechnology Information (NCBI) database using the Multi-Vision software package of Burrows PLoS ONE 2010, Vol 5, Issue 6, PMID20585448 Background.
Multiple Sequence Alignment by Clustalw (https://www.genome.jp/tools-bin/ clustalw) web service is applied as our alignment tool. Results: We analyzed 10
PDB entry 2vxo. Human gmp synthetase in complex with xmp. You can see 0 articles in Pubmed Central that refer to 2vxo. Enlarge image. PDB entry 3d8b. Crystal structure of human fidgetin-like protein 1 in complex with adp. 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.
2021-4-12 · PubMed ID: 30753690 Summary: Trans-generational maternal effects have been shown to influence a broad range of offspring phenotypes. However, very little is known about paternal trans-generational effects. This study tested the trans-generational effects of maternal and paternal age, and their interaction, on daughter and son reproductive 2021-3-15 · PubMed ID: 30847389 Summary: While the primary role of vesicular transporters is to load neurotransmitters into synaptic vesicles (SVs), accumulating evidence suggests that these proteins also contribute to additional aspects of synaptic function, including vesicle release. This study extend the … 2021-1-15 · PubMed ID: 25954320 Summary: Early in Drosophila development, Heterochromatin protein 1a (HP1a) collaborates with the Polycomb/trithorax groups of proteins to regulate gene expression and that the two chromatin systems do not act separately as convention describes. This study shows that HP1a affects the levels of both the Polycomb complexes and 2021-2-3 · The Drosophila Y chromosome affects heterochromatin integrity genome-wide. Mol Biol Evol.