{
    "bcoid": "GLY_000235",
    "title": "Mouse Protein Citations (RefSeq)",
    "description": "The Mouse Protein Citations (RefSeq) datasets contains mouse [taxid:10090] UniProtKB accessions mapped ...",
    "filename": "mouse_protein_citations_refseq.csv",
    "filetype": "csv",
    "categories": {
        "species": "Mus Musculus",
        "molecule": "Protein",
        "tags": "Protein Citations",
        "file_type": "csv",
        "status": "Reviewed",
        "scope": "internal"
    },
    "minitable": {
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                    "label": "title"
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            [
                "Q5F2L2-1",
                "23986452",
                "The Lewis X-related alpha1,3-fucosyltransferase, Fut10, is required for the maintenance of stem cell populations.",
                "The Journal of biological chemistry",
                "2013 Oct 4",
                "Kumar A, Torii T, Ishino Y, Muraoka D, Yoshimura T, Togayachi A, Narimatsu H, Ikenaka K, Hitoshi S"
            ],
            [
                "Q8VBV4-2",
                "29633504",
                "FBXW7 deletion contributes to lung tumor development and confers resistance to gefitinib therapy.",
                "Molecular oncology",
                "2018 Jun",
                "Xiao Y, Yin C, Wang Y, Lv H, Wang W, Huang Y, Perez-Losada J, Snijders AM, Mao JH, Zhang P"
            ],
            [
                "Q8VBV4-2",
                "29475832",
                "Hepatic F-Box Protein FBXW7 Maintains Glucose Homeostasis Through Degradation of Fetuin-A.",
                "Diabetes",
                "2018 May",
                "Zhao J, Xiong X, Li Y, Liu X, Wang T, Zhang H, Jiao Y, Jiang J, Zhang H, Tang Q, Gao X, Li X, Lu Y, Liu B, Hu C, Li X"
            ],
            [
                "Q8VBV4-2",
                "29550488",
                "Genetic Deletion of Fbw7 in the mouse intestinal epithelium aggravated dextran sodium sulfate-induced colitis by modulating the inflammatory response of NF-kappaB pathway.",
                "Biochemical and biophysical research communications",
                "2018 Apr 15",
                "Li H, Liang Y, Lai X, Wang W, Zhang J, Chen S"
            ],
            [
                "Q9JMG3-1",
                "24240191",
                "Different functions of HOPS isoforms in the cell: HOPS shuttling isoform is determined by RIP cleavage system.",
                "Cell cycle (Georgetown, Tex.)",
                "2014",
                "Castelli M, Piobbico D, Bartoli D, Pieroni S, Brunacci C, Bellet MM, Chiacchiaretta M, Della Fazia MA, Servillo G"
            ],
            [
                "Q9JMG3-1",
                "22890319",
                "Hepatocyte odd protein shuttling (HOPS) is a bridging protein in the nucleophosmin-p19 Arf network.",
                "Oncogene",
                "2013 Jul 11",
                "Castelli M, Pieroni S, Brunacci C, Piobbico D, Bartoli D, Bellet MM, Colombo E, Pelicci PG, Della Fazia MA, Servillo G"
            ],
            [
                "Q9JMG3-1",
                "20582322",
                "Transmembrane and ubiquitin-like domain containing 1 (Tmub1) regulates locomotor activity and wakefulness in mice and interacts with CAMLG.",
                "PloS one",
                "2010 Jun 22",
                "Zhang W, Savelieva KV, Suwanichkul A, Small DL, Kirkpatrick LL, Xu N, Lanthorn TH, Ye GL"
            ],
            [
                "Q9JMG3-1",
                "18665261",
                "Transmembrane and ubiquitin-like domain-containing protein 1 (Tmub1/HOPS) facilitates surface expression of GluR2-containing AMPA receptors.",
                "PloS one",
                "2008 Jul 30",
                "Yang H, Takagi H, Konishi Y, Ageta H, Ikegami K, Yao I, Sato S, Hatanaka K, Inokuchi K, Seog DH, Setou M"
            ],
            [
                "Q9JMG3-1",
                "18418082",
                "HOPS is an essential constituent of centrosome assembly.",
                "Cell cycle (Georgetown, Tex.)",
                "2008 May 15",
                "Pieroni S, Della Fazia MA, Castelli M, Piobbico D, Bartoli D, Brunacci C, Bellet MM, Viola-Magni M, Servillo G"
            ],
            [
                "Q9DCN2-1",
                "20927338",
                "Crystal structure of a complex between amino and carboxy terminal fragments of mDia1: insights into autoinhibition of diaphanous-related formins.",
                "PloS one",
                "2010 Sep 30",
                "Nezami A, Poy F, Toms A, Zheng W, Eck MJ"
            ],
            [
                "Q9DCN2-1",
                "20566685",
                "Adenomatous polyposis coli protein nucleates actin assembly and synergizes with the formin mDia1.",
                "The Journal of cell biology",
                "2010 Jun 28",
                "Okada K, Bartolini F, Deaconescu AM, Moseley JB, Dogic Z, Grigorieff N, Gundersen GG, Goode BL"
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            [
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                "30026490",
                "Armadillo repeat containing 12 promotes neuroblastoma progression through interaction with retinoblastoma binding protein 4.",
                "Nature communications",
                "2018 Jul 19",
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            [
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                "PloS one",
                "2018",
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            [
                "O88845-1",
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                "2007 May 15",
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            [
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                "Nature immunology",
                "2013 Sep",
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            ],
            [
                "Q8BHW5-1",
                "17660561",
                "Genomewide discovery and classification of candidate ovarian fertility genes in the mouse.",
                "Genetics",
                "2007 Sep",
                "Gallardo TD, John GB, Shirley L, Contreras CM, Akbay EA, Haynie JM, Ward SE, Shidler MJ, Castrillon DH"
            ],
            [
                "Q3UFT3-1",
                "24003223",
                "A brain-specific Grb2-associated regulator of extracellular signal-regulated kinase (Erk)/mitogen-activated protein kinase (MAPK) (GAREM) subtype, GAREM2, contributes to neurite outgrowth of neuroblastoma cells by regulating Erk signaling.",
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                "2013 Oct 11",
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            [
                "Q5EE38-1",
                "30189268",
                "High-throughput gene expression analysis identifies p53-dependent and -independent pathways contributing to the adrenocortical dysplasia (acd) phenotype.",
                "Gene",
                "2018 Dec 30",
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            [
                "Q5EE38-1",
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                "Cell reports",
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            [
                "Q5EE38-1",
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                "TRF2-tethered TIN2 can mediate telomere protection by TPP1/POT1.",
                "Molecular and cellular biology",
                "2014 Apr",
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                "Hematopoietic stem cells are acutely sensitive to Acd shelterin gene inactivation.",
                "The Journal of clinical investigation",
                "2014 Jan",
                "Jones M, Osawa G, Regal JA, Weinberg DN, Taggart J, Kocak H, Friedman A, Ferguson DO, Keegan CE, Maillard I"
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            [
                "Q5EE38-1",
                "17632522",
                "Telomere protection by mammalian Pot1 requires interaction with Tpp1.",
                "Nature structural &amp; molecular biology",
                "2007 Aug",
                "Hockemeyer D, Palm W, Else T, Daniels JP, Takai KK, Ye JZ, Keegan CE, de Lange T, Hammer GD"
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                "Q5EE38-1",
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                "Urogenital and caudal dysgenesis in adrenocortical dysplasia (acd) mice is caused by a splicing mutation in a novel telomeric regulator.",
                "Human molecular genetics",
                "2005 Jan 1",
                "Keegan CE, Hutz JE, Else T, Adamska M, Shah SP, Kent AE, Howes JM, Beamer WG, Hammer GD"
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                "A SIRT7-dependent acetylation switch of GABPbeta1 controls mitochondrial function.",
                "Cell metabolism",
                "2014 Nov 4",
                "Ryu D, Jo YS, Lo Sasso G, Stein S, Zhang H, Perino A, Lee JU, Zeviani M, Romand R, Hottiger MO, Schoonjans K, Auwerx J"
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                "Q00420-1",
                "22862946",
                "Targeting tetramer-forming GABPbeta isoforms impairs self-renewal of hematopoietic and leukemic stem cells.",
                "Cell stem cell",
                "2012 Aug 3",
                "Yu S, Jing X, Colgan JD, Zhao DM, Xue HH"
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            [
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                "Immunology letters",
                "2011 Dec 30",
                "Hashiguchi M, Hachimura S, Ametani A, Sato T, Kojima H, Kumagai Y, Habu S, Kobata T, Kaminogawa S"
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                "Cancer science",
                "2014 Dec",
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                "Q8CIT9-1",
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                "Developmental dynamics : an official publication of the American Association of Anatomists",
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                "Q8BVZ5-1",
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                "Immunity",
                "2005 Nov",
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                "Mammalian glutaminase Gls2 gene encodes two functional alternative transcripts by a surrogate promoter usage mechanism.",
                "PloS one",
                "2012",
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                "Q571F8-1",
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                "Proceedings of the National Academy of Sciences of the United States of America",
                "2010 Apr 20",
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                "Q9D4J7-1",
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                "PHF6 regulates phenotypic plasticity through chromatin organization within lineage-specific genes.",
                "Genes &amp; development",
                "2017 May 15",
                "Soto-Feliciano YM, Bartlebaugh JME, Liu Y, Sanchez-Rivera FJ, Bhutkar A, Weintraub AS, Buenrostro JD, Cheng CS, Regev A, Jacks TE, Young RA, Hemann MT"
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                "miR-128 regulates neuronal migration, outgrowth and intrinsic excitability via the intellectual disability gene Phf6.",
                "eLife",
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                "Franzoni E, Booker SA, Parthasarathy S, Rehfeld F, Grosser S, Srivatsa S, Fuchs HR, Tarabykin V, Vida I, Wulczyn FG"
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                "Q9D4J7-1",
                "23791194",
                "The X-linked intellectual disability protein PHF6 associates with the PAF1 complex and regulates neuronal migration in the mammalian brain.",
                "Neuron",
                "2013 Jun 19",
                "Zhang C, Mejia LA, Huang J, Valnegri P, Bennett EJ, Anckar J, Jahani-Asl A, Gallardo G, Ikeuchi Y, Yamada T, Rudnicki M, Harper JW, Bonni A"
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            [
                "Q9D4J7-1",
                "17698420",
                "Protein and gene expression analysis of Phf6, the gene mutated in the Borjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity.",
                "Gene expression patterns : GEP",
                "2007 Oct",
                "Voss AK, Gamble R, Collin C, Shoubridge C, Corbett M, Gecz J, Thomas T"
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            [
                "Q149C2-1",
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                "Characterization of mouse IFT complex B.",
                "Cell motility and the cytoskeleton",
                "2009 Aug",
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                "Neuritin Up-regulates Kv4.2 alpha-Subunit of Potassium Channel Expression and Affects Neuronal Excitability by Regulating the Calcium-Calcineurin-NFATc4 Signaling Pathway.",
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                "Molecular and cellular biology",
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    "readme": "Name\n   - Mouse Protein Citations (RefSeq)\n\nVersion\n   - 1.5.12\n\nCreated on\n  - 2019-09-06T14:06:38.962804\n\nModified on\n   - 2019-12-01T15:07:18.213629\n\nCreated by\n   - Jeet Vora [jeetvora@gwu.edu], Rahi Navelkar [rsn13@gwu.edu], Robel Kahsay [rykahsay@gwu.edu], Xavier Holmes [xavierh@email.gwu.edu]\n\nAuthors\n   - \n\nChecksum\n   - \n\nUsability Domain\n   - The Mouse Protein Citations (RefSeq) datasets contains mouse [taxid:10090] UniProtKB accessions mapped to publication information (pmid, title, journal name, publication, date, authors of corresponding RefSeq accessions. The dataset is derived from NCBI RefSeq Release 96, September 9, 2019. If you use this dataset please provide proper attribution to NCBI RefSeq and GlyGen\n\nDescription Domain\n   Keywords\n   - PMID\n   - journal\n   - citations\n   - authors\n   - RefSeq\n   - PubMed\n\n   Pipeline Steps\n   - Step-1: The script parses the NCBI RefSeq gpff files to extract the publication information. The script also maps RefSeq accesion to the UniProtKB Canonical accessions\n\nExecution Domain\n   Scripts   - https://github.com/GW-HIVE/glygen-backend-integration/blob/master/pipeline/integrator/make-protein-dataset.py\n\n\n   Software Prerequisites\n      Name: Python\n      Version: 2.7.5\n      URI: https://www.python.org/download/releases/2.7.5/\n\nI/O Domain\n   Input Subdomain\n      Name: refseq_protein_all_10090.gpff\n      URI: https://data.glygen.org/ln2wwwdata/source/refseq_protein_all_10090.gpff\n      Name: mouse_protein_xref_refseq.csv\n      URI: https://data.glygen.org/ln2wwwdata/reviewed/mouse_protein_xref_refseq.csv\n   Output Subdomain\n      Name: mouse_protein_citations_refseq.csv\n      URI: http://data.glygen.org/ln2wwwdata/reviewed/mouse_protein_citations_refseq.csv\n      Name: mouse_protein_citations_refseq.stat.csv\n      URI: http://data.glygen.org/ln2wwwdata/reviewed/mouse_protein_citations_refseq.stat.csv\n\nFields\n      Name: \"uniprotkb_canonical_ac\"\n     Description: \"Accession assigned to the protein isoform chosen to be the canonical sequence to which all positional annotation refers in UniProtKB database\"\n      Unique Values: \"4595\"\n      Name: \"title\"\n     Description: \"Title of the published article in the journal\"\n      Unique Values: \"7972\"\n      Name: \"journal_name\"\n     Description: \"The name of the journal in which the article is published\"\n      Unique Values: \"740\"\n      Name: \"authors\"\n     Description: \"\"\n      Unique Values: \"7957\"\n      Name: \"publication_date\"\n     Description: \"Contains the full date on which the issue of the journal was published. Sourced from MEDLINE/PubMed data element(fields) description.\"\n      Unique Values: \"2611\"\n      Name: \"pmid\"\n     Description: \"NCBI PubMed database Identifier\"\n      Unique Values: \"7972\"",
    "downloadurl": "/ln2data/releases/data/v-1.5.12/reviewed/mouse_protein_citations_refseq.csv"
}
