{ "bcoid": "GLY_000256", "title": "Human RefSeq Citations", "description": "The Human RefSeq Citations datasets conatains human [taxid:9606] UniProtKB accessions mapped to publication ...", "filename": "human_protein_citations_refseq.csv", "filetype": "csv", "categories": { "species": "Homo Sapiens", "molecule": "Protein", "tags": "Protein Citations", "file_type": "csv", "status": "Reviewed", "scope": "internal" }, "minitable": { "content": [ [ "Q9Y5H2-1...", "20388442..." ], [ "Q9Y5H2-1...", "15799819..." ] ], "headers": [ "uniprotkb_ca...", "pmid..." ], "colwidth": [ "40%", "20%" ] }, "sampledata": { "type": "table", "data": [ [ { "type": "string", "label": "uniprotkb_canonical_ac" }, { "type": "string", "label": "pmid" }, { "type": "string", "label": "title" }, { "type": "string", "label": "journal_name" }, { "type": "string", "label": "publication_date" }, { "type": "string", "label": "authors" } ], [ "Q9Y5H2-1", "20388442", "[The methylation analysis of EMP3 and PCDH-gamma-A11 gene in human glioma].", "Zhonghua wai ke za zhi [Chinese journal of surgery]", "2010 Feb 15", "Jiang Z, Zhou W, Li XG, Jiang YQ, Wang L, Wang DH, Wang XY, Li XE" ], [ "Q9Y5H2-1", "15799819", "Epigenetic silencing of the protocadherin family member PCDH-gamma-A11 in astrocytomas.", "Neoplasia (New York, N.Y.)", "2005 Mar", "Waha A, Guntner S, Huang TH, Yan PS, Arslan B, Pietsch T, Wiestler OD, Waha A" ], [ "Q9BSR8-1", "27999994", "Functional characterisation of the YIPF protein family in mammalian cells.", "Histochemistry and cell biology", "2017 Apr", "Kranjc T, Dempsey E, Cagney G, Nakamura N, Shields DC, Simpson JC" ], [ "Q96LR9-1", "20628086", "Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.", "Diabetes care", "2010 Oct", "Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S" ], [ "Q96LR9-1", "19913121", "Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.", "American journal of human genetics", "2009 Nov", "Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD" ], [ "Q9UPM8-1", "26542808", "Bivalent Motif-Ear Interactions Mediate the Association of the Accessory Protein Tepsin with the AP-4 Adaptor Complex.", "The Journal of biological chemistry", "2015 Dec 25", "Mattera R, Guardia CM, Sidhu SS, Bonifacino JS" ], [ "Q9UPM8-1", "26544806", "Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering.", "American journal of human genetics", "2015 Nov 5", "Raza MH, Mattera R, Morell R, Sainz E, Rahn R, Gutierrez J, Paris E, Root J, Solomon B, Brewer C, Basra MA, Khan S, Riazuddin S, Braun A, Bonifacino JS, Drayna D" ], [ "Q9UPM8-1", "20972249", "Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability.", "Journal of medical genetics", "2011 Feb", "Moreno-De-Luca A, Helmers SL, Mao H, Burns TG, Melton AM, Schmidt KR, Fernhoff PM, Ledbetter DH, Martin CL" ], [ "Q8NBS9-1", "29749460", "Role of TXNDC5 in tumorigenesis of colorectal cancer cells: In vivo and in vitro evidence.", "International journal of molecular medicine", "2018 Aug", "Tan F, Zhu H, He X, Yu N, Zhang X, Xu H, Pei H" ], [ "Q8NBS9-1", "29784879", "ER-resident protein 46 (ERp46) triggers the mannose-trimming activity of ER degradation-enhancing alpha-mannosidase-like protein 3 (EDEM3).", "The Journal of biological chemistry", "2018 Jul 6", "Yu S, Ito S, Wada I, Hosokawa N" ], [ "Q8NBS9-1", "29131315", "TXNDC5 contributes to rheumatoid arthritis by down-regulating IGFBP1 expression.", "Clinical and experimental immunology", "2018 Apr", "Li J, Xu B, Wu C, Yan X, Zhang L, Chang X" ], [ "Q8NBS9-1", "28604976", "[Progress of research on TXNDC5].", "Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics", "2017 Jun 10", "Li J, Chang X" ], [ "Q8NBS9-1", "26810069", "High TXNDC5 expression predicts poor prognosis in renal cell carcinoma.", "Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine", "2016 Jul", "Mo R, Peng J, Xiao J, Ma J, Li W, Wang J, Ruan Y, Ma S, Hong Y, Wang C, Gao K, Fan J" ], [ "Q8NBS9-1", "17895523", "Differential expression of mimecan and thioredoxin domain-containing protein 5 in colorectal adenoma and cancer: a proteomic study.", "Experimental biology and medicine (Maywood, N.J.)", "2007 Oct", "Wang Y, Ma Y, Lu B, Xu E, Huang Q, Lai M" ], [ "Q8NBS9-1", "12963716", "EndoPDI, a novel protein-disulfide isomerase-like protein that is preferentially expressed in endothelial cells acts as a stress survival factor.", "The Journal of biological chemistry", "2003 Nov 21", "Sullivan DC, Huminiecki L, Moore JW, Boyle JJ, Poulsom R, Creamer D, Barker J, Bicknell R" ], [ "Q9C0K0-1", "29503088", "BCL11B Drives Human Mammary Stem Cell Self-Renewal In Vitro by Inhibiting Basal Differentiation.", "Stem cell reports", "2018 Mar 13", "Miller DH, Jin DX, Sokol ES, Cabrera JR, Superville DA, Gorelov RA, Kuperwasser C, Gupta PB" ], [ "Q9C0K0-1", "29203643", "The N-Terminal CCHC Zinc Finger Motif Mediates Homodimerization of Transcription Factor BCL11B.", "Molecular and cellular biology", "2018 Mar 1", "Grabarczyk P, Winkler P, Delin M, Sappa PK, Bekeschus S, Hildebrandt P, Przybylski GK, Volker U, Hammer E, Schmidt CA" ], [ "Q9C0K0-1", "29039465", "Essential role of microRNA-650 in the regulation of B-cell CLL/lymphoma 11B gene expression following transplantation: A novel mechanism behind the acute rejection of renal allografts.", "International journal of molecular medicine", "2017 Dec", "Jin P, Chen H, Xie J, Zhou C, Zhu X" ], [ "Q9C0K0-1", "28794504", "Promoter hypermethylation of BCL11B gene correlates with downregulation of gene transcription in ankylosing spondylitis patients.", "Genes and immunity", "2017 Sep", "Karami J, Mahmoudi M, Amirzargar A, Gharshasbi M, Jamshidi A, Aslani S, Nicknam MH" ], [ "Q9C0K0-1", "28669733", "BCL11B is frequently downregulated in HTLV-1-infected T-cells through Tax-mediated proteasomal degradation.", "Biochemical and biophysical research communications", "2017 Aug 26", "Permatasari HK, Nakahata S, Ichikawa T, Morishita K" ], [ "Q8N475-1", "26045876", "Down-regulated FSTL5 promotes cell proliferation and survival by affecting Wnt/beta-catenin signaling in hepatocellular carcinoma.", "International journal of clinical and experimental pathology", "2015", "Zhang D, Ma X, Sun W, Cui P, Lu Z" ], [ "Q8N475-1", "21911727", "FSTL5 is a marker of poor prognosis in non-WNT/non-SHH medulloblastoma.", "Journal of clinical oncology : official journal of the American Society of Clinical Oncology", "2011 Oct 10", "Remke M, Hielscher T, Korshunov A, Northcott PA, Bender S, Kool M, Westermann F, Benner A, Cin H, Ryzhova M, Sturm D, Witt H, Haag D, Toedt G, Wittmann A, Schottler A, von Bueren AO, von Deimling A, Rutkowski S, Scheurlen W, Kulozik AE, Taylor MD, Lichter P, Pfister SM" ], [ "O96024-1", "19851445", "High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.", "PLoS genetics", "2009 Oct", "Barcellos LF, May SL, Ramsay PP, Quach HL, Lane JA, Nititham J, Noble JA, Taylor KE, Quach DL, Chung SA, Kelly JA, Moser KL, Behrens TW, Seldin MF, Thomson G, Harley JB, Gaffney PM, Criswell LA" ], [ "P46821-1", "29432744", "A microtubule-associated protein MAP1B binds to and regulates localization of a calcium-binding protein ALG-2.", "Biochemical and biophysical research communications", "2018 Mar 4", "Takahara T, Arai Y, Kono Y, Shibata H, Maki M" ], [ "Q8N1L9-1", "28739720", "Inhibition of Bevacizumab-induced Epithelial-Mesenchymal Transition by BATF2 Overexpression Involves the Suppression of Wnt/beta-Catenin Signaling in Glioblastoma Cells.", "Anticancer research", "2017 Aug", "Huang W, Zhang C, Cui M, Niu J, Ding W" ], [ "Q8N1L9-1", "27785591", "The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveals BATF2 as a poor prognostic marker for childhood medulloblastoma.", "Investigational new drugs", "2017 Feb", "Andrade AF, Borges KS, Suazo VK, Geron L, Correa CA, Castro-Gamero AM, de Vasconcelos EJ, de Oliveira RS, Neder L, Yunes JA, Dos Santos Aguiar S, Scrideli CA, Tone LG" ], [ "Q8N1L9-1", "27926863", "Chronic Infection Depletes Hematopoietic Stem Cells through Stress-Induced Terminal Differentiation.", "Cell reports", "2016 Dec 6", "Matatall KA, Jeong M, Chen S, Sun D, Chen F, Mo Q, Kimmel M, King KY" ], [ "Q8N1L9-1", "26808579", "SARI, a novel target gene of glucocorticoid receptor, plays an important role in dexamethasone-mediated killing of B lymphoma cells.", "Cancer letters", "2016 Apr 1", "Huang Y, Zhou J, Huang Y, He J, Wang Y, Yang C, Liu D, Zhang L, He F" ], [ "Q8N1L9-1", "26977016", "Discovery of a Regulatory Motif for Human Satellite DNA Transcription in Response to BATF2 Overexpression.", "Anticancer research", "2016 Mar", "Bai X, Huang W, Zhang C, Niu J, Ding W" ], [ "Q8N1L9-1", "20473897", "Decreased expression of BATF2 is associated with a poor prognosis in hepatocellular carcinoma.", "International journal of cancer", "2011 Feb 15", "Ma H, Liang X, Chen Y, Pan K, Sun J, Wang H, Wang Q, Li Y, Zhao J, Li J, Chen M, Xia J" ], [ "Q15758-1", "30635397", "Ablation of the ASCT2 (SLC1A5) gene encoding a neutral amino acid transporter reveals transporter plasticity and redundancy in cancer cells.", "The Journal of biological chemistry", "2019 Mar 15", "Broer A, Gauthier-Coles G, Rahimi F, van Geldermalsen M, Dorsch D, Wegener A, Holst J, Broer S" ], [ "Q15758-1", "30272366", "Clinical associations between ASCT2 and pmTOR in the pathogenesis and prognosis of epithelial ovarian cancer.", "Oncology reports", "2018 Dec", "Guo H, Xu Y, Wang F, Shen Z, Tuo X, Qian H, Wang H, Wang K" ], [ "Q15758-1", "30029480", "Targeted Suppression and Knockout of ASCT2 or LAT1 in Epithelial and Mesenchymal Human Liver Cancer Cells Fail to Inhibit Growth.", "International journal of molecular sciences", "2018 Jul 19", "Bothwell PJ, Kron CD, Wittke EF, Czerniak BN, Bode BP" ], [ "Q15758-1", "30071532", "SLC1A5 Silencing Inhibits Esophageal Cancer Growth via Cell Cycle Arrest and Apoptosis.", "Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology", "2018", "Lin J, Yang T, Peng Z, Xiao H, Jiang N, Zhang L, Ca D, Wu P, Pan Q" ], [ "Q9NYL2-1", "30535460", "Long noncoding RNA MLK7AS1 promotes proliferation in human colorectal cancer via downregulation of p21 expression.", "Molecular medicine reports", "2019 Feb", "Zhang R, Li J, Yan X, Jin K, Li W, Liu X, Zhao J, Shang W, Zhao X" ], [ "Q9NYL2-1", "29654619", "Overexpression of ZAKbeta in human osteosarcoma cells enhances ZAKalpha expression, resulting in a synergistic apoptotic effect.", "Cell biochemistry and function", "2018 Jun", "Fu CY, Tseng YS, Chen MC, Hsu HH, Yang JJ, Tu CC, Lin YM, Viswanadha VP, Ding K, Kuo WW, Huang CY" ], [ "Q9NYL2-1", "29071797", "Novel genetic variants in the P38MAPK pathway gene ZAK and susceptibility to lung cancer.", "Molecular carcinogenesis", "2018 Feb", "Feng Y, Wang Y, Liu H, Liu Z, Mills C, Owzar K, Xie J, Han Y, Qian DC, Hung Rj RJ, Brhane Y, McLaughlin J, Brennan P, Bickeboller H, Rosenberger A, Houlston RS, Caporaso N, Landi MT, Bruske I, Risch A, Ye Y, Wu X, Christiani DC, Amos CI, Wei Q" ], [ "Q9NYL2-1", "27816943", "Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion.", "Brain : a journal of neurology", "2017 Jan", "Vasli N, Harris E, Karamchandani J, Bareke E, Majewski J, Romero NB, Stojkovic T, Barresi R, Tasfaout H, Charlton R, Malfatti E, Bohm J, Marini-Bettolo C, Choquet K, Dicaire MJ, Shao YH, Topf A, O'Ferrall E, Eymard B, Straub V, Blanco G, Lochmuller H, Brais B, Laporte J, Tetreault M" ], [ "Q9NYL2-1", "26755636", "Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice.", "Genome research", "2016 Feb", "Spielmann M, Kakar N, Tayebi N, Leettola C, Nurnberg G, Sowada N, Lupianez DG, Harabula I, Flottmann R, Horn D, Chan WL, Wittler L, Yilmaz R, Altmuller J, Thiele H, van Bokhoven H, Schwartz CE, Nurnberg P, Bowie JU, Ahmad J, Kubisch C, Mundlos S, Borck G" ], [ "Q9P0P0-1", "26711259", "Negative Regulation of CARD11 Signaling and Lymphoma Cell Survival by the E3 Ubiquitin Ligase RNF181.", "Molecular and cellular biology", "2015 Dec 28", "Pedersen SM, Chan W, Jattani RP, Mackie dS, Pomerantz JL" ], [ "Q63HQ0-1", "21525240", "Role of AP1 and Gadkin in the traffic of secretory endo-lysosomes.", "Molecular biology of the cell", "2011 Jun 15", "Laulagnier K, Schieber NL, Maritzen T, Haucke V, Parton RG, Gruenberg J" ], [ "Q63HQ0-1", "20332099", "A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts.", "Human molecular genetics", "2010 Jun 15", "Kalsi G, Kuo PH, Aliev F, Alexander J, McMichael O, Patterson DG, Walsh D, Zhao Z, Schuckit M, Nurnberger J Jr, Edenberg H, Kramer J, Hesselbrock V, Tischfield JA, Vladimirov V, Prescott CA, Dick DM, Kendler KS, Riley BP" ], [ "Q63HQ0-1", "19965873", "A novel subtype of AP-1-binding motif within the palmitoylated trans-Golgi network/endosomal accessory protein Gadkin/gamma-BAR.", "The Journal of biological chemistry", "2010 Feb 5", "Maritzen T, Schmidt MR, Kukhtina V, Higman VA, Strauss H, Volkmer R, Oschkinat H, Dotti CG, Haucke V" ], [ "Q63HQ0-1", "19706427", "Regulation of endosomal membrane traffic by a Gadkin/AP-1/kinesin KIF5 complex.", "Proceedings of the National Academy of Sciences of the United States of America", "2009 Sep 8", "Schmidt MR, Maritzen T, Kukhtina V, Higman VA, Doglio L, Barak NN, Strauss H, Oschkinat H, Dotti CG, Haucke V" ], [ "Q9H0N0-1", "28255813", "Gene promoter-associated CpG island hypermethylation in squamous cell carcinoma of the tongue.", "Virchows Archiv : an international journal of pathology", "2017 Apr", "Bhat S, Kabekkodu SP, Jayaprakash C, Radhakrishnan R, Ray S, Satyamoorthy K" ], [ "Q9H0N0-1", "20198315", "Association of genetic variants with hemorrhagic stroke in Japanese individuals.", "International journal of molecular medicine", "2010 Apr", "Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y" ], [ "Q8TE73-1", "28939216", "A targeted next-generation sequencing panel reveals novel mutations in Japanese patients with primary ciliary dyskinesia.", "Auris, nasus, larynx", "2018 Jun", "Takeuchi K, Kitano M, Kiyotoshi H, Ikegami K, Ogawa S, Ikejiri M, Nagao M, Fujisawa T, Nakatani K" ], [ "Q6P4Q7-1", "29421602", "Report of two unrelated families with Jalili syndrome and a novel nonsense heterozygous mutation in CNNM4 gene.", "European journal of medical genetics", "2018 Jul", "Maia CMF, Machado RA, Gil-da-Silva-Lopes VL, Lustosa-Mendes E, Rim PHH, Dias VO, Martelli DRB, Nasser LS, Coletta RD, Martelli-Junior H" ], [ "Q6P4Q7-1", "29322253", "Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1.", "Molecular genetics and genomics : MGG", "2018 Jun", "Li S, Xi Q, Zhang X, Yu D, Li L, Jiang Z, Chen Q, Wang QK, Traboulsi EI" ], [ "Q6P4Q7-1", "29421294", "Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta.", "American journal of ophthalmology", "2018 Apr", "Hirji N, Bradley PD, Li S, Vincent A, Pennesi ME, Thomas AS, Heon E, Bhan A, Mahroo OA, Robson A, Inglehearn CF, Moore AT, Michaelides M" ], [ "Q6P4Q7-1", "28586144", "Co-occurrence of Jalili syndrome and muscular overgrowth.", "American journal of medical genetics. Part A", "2017 Aug", "Wawrocka A, Walczak-Sztulpa J, Badura-Stronka M, Owecki M, Kopczynski P, Mrukwa-Kominek E, Skorczyk-Werner A, Gasperowicz P, Ploski R, Krawczynski MR" ], [ "Q6P4Q7-1", "28246031", "Novel splice site mutation in CNNM4 gene in a family with Jalili syndrome.", "European journal of medical genetics", "2017 May", "Cherkaoui Jaouad I, Lyahyai J, Guaoua S, El Alloussi M, Zrhidri A, Doubaj Y, Boulanouar A, Sefiani A" ], [ "Q9NVM4-1", "28874563", "Epigenetic control via allosteric regulation of mammalian protein arginine methyltransferases.", "Proceedings of the National Academy of Sciences of the United States of America", "2017 Sep 19", "Jain K, Jin CY, Clarke SG" ], [ "Q9NVM4-1", "28587924", "PRMT7 Interacts with ASS1 and Citrullinemia Mutations Disrupt the Interaction.", "Journal of molecular biology", "2017 Jul 21", "Verma M, Charles RCM, Chakrapani B, Coumar MS, Govindaraju G, Rajavelu A, Chavali S, Dhayalan A" ], [ "Q9NVM4-1", "27718516", "Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly.", "Clinical genetics", "2017 May", "Kernohan KD, McBride A, Xi Y, Martin N, Schwartzentruber J, Dyment DA, Majewski J, Blaser S, Boycott KM, Chitayat D" ], [ "Q9NVM4-1", "17709427", "Two distinct arginine methyltransferases are required for biogenesis of Sm-class ribonucleoproteins.", "The Journal of cell biology", "2007 Aug 27", "Gonsalvez GB, Tian L, Ospina JK, Boisvert FM, Lamond AI, Matera AG" ], [ "Q9NVM4-1", "15494416", "PRMT7, a new protein arginine methyltransferase that synthesizes symmetric dimethylarginine.", "The Journal of biological chemistry", "2005 Feb 4", "Lee JH, Cook JR, Yang ZH, Mirochnitchenko O, Gunderson SI, Felix AM, Herth N, Hoffmann R, Pestka S" ], [ "Q9NVM4-1", "15044439", "PRMT7 is a member of the protein arginine methyltransferase family with a distinct substrate specificity.", "The Journal of biological chemistry", "2004 May 28", "Miranda TB, Miranda M, Frankel A, Clarke S" ], [ "P49238-1", "30776726", "Cytokines use different intracellular mechanisms to upregulate the membrane expression of CX3CR1 in human monocytes.", "Molecular immunology", "2019 Apr", "Panek CA, Bruballa AC, Pineda GE, De Brasi C, Fernandez-Brando RJ, Mejias MP, Ramos MV, Palermo MS" ], [ "P49238-1", "30066854", "CX3CL1/fractalkine enhances prostate cancer spinal metastasis by activating the Src/FAK pathway.", "International journal of oncology", "2018 Oct", "Liu P, Liang Y, Jiang L, Wang H, Wang S, Dong J" ], [ "P49238-1", "29485193", "Polymorphisms in the microglial marker molecule CX3CR1 affect the blood volume of the human brain.", "Psychiatry and clinical neurosciences", "2018 Jun", "Sakai M, Takeuchi H, Yu Z, Kikuchi Y, Ono C, Takahashi Y, Ito F, Matsuoka H, Tanabe O, Yasuda J, Taki Y, Kawashima R, Tomita H" ], [ "P49238-1", "29565837", "Polymorphisms in Selected Genes and Their Association with Age-Related Macular Degeneration in a Chinese Population.", "Medical science monitor : international medical journal of experimental and clinical research", "2018 Mar 22", "Huang Q, Xiang Y" ], [ "P49238-1", "30381070", "The Association of Fractalkine Receptor (T280M) Polymorphism in the Pathogenesis of Acute Coronary Syndrome in the Egyptian Population.", "Current pharmaceutical biotechnology", "2018", "Hassan DS, Hashad IM, Abdel Rahman MF, Abdel-Maksoud SM" ], [ "Q9BT67-1", "29333944", "MiR-155 Promotes Uveal Melanoma Cell Proliferation and Invasion by Regulating NDFIP1 Expression.", "Technology in cancer research & treatment", "2017 Dec", "Peng J, Liu H, Liu C" ], [ "Q9BT67-1", "27173227", "Protective effects and mechanisms of Ndfipl on SH-SY5Y cell apoptosis in an in vitro Parkinson's disease model.", "Genetics and molecular research : GMR", "2016 Apr 25", "Xing LF, Guo HP, Wang DT, Sun LH, Pan SY" ], [ "Q9BT67-1", "26363003", "Regulation of the human ether-a-go-go-related gene (hERG) potassium channel by Nedd4 family interacting proteins (Ndfips).", "The Biochemical journal", "2015 Nov 15", "Kang Y, Guo J, Yang T, Li W, Zhang S" ], [ "Q9BT67-1", "26319551", "Nedd4 family interacting protein 1 (Ndfip1) promotes death of pancreatic beta cells.", "Biochemical and biophysical research communications", "2015 Oct 2", "Beck A, Shatz-Azoulay H, Vinik Y, Isaac R, Boura-Halfon S, Zick Y" ], [ "Q9BT67-1", "25631046", "Nedd4 family interacting protein 1 (Ndfip1) is required for ubiquitination and nuclear trafficking of BRCA1-associated ATM activator 1 (BRAT1) during the DNA damage response.", "The Journal of biological chemistry", "2015 Mar 13", "Low LH, Chow YL, Li Y, Goh CP, Putz U, Silke J, Ouchi T, Howitt J, Tan SS" ], [ "Q9BT67-1", "18819914", "Nedd4 family-interacting protein 1 (Ndfip1) is required for the exosomal secretion of Nedd4 family proteins.", "The Journal of biological chemistry", "2008 Nov 21", "Putz U, Howitt J, Lackovic J, Foot N, Kumar S, Silke J, Tan SS" ], [ "Q9HD47-1", "24438356", "The perfect storm? Histiocytoid cardiomyopathy and compound CACNA2D1 and RANGRF mutation in a baby.", "Cardiology in the young", "2015 Jan", "Cataldo S, Annoni GA, Marziliano N" ], [ "Q9HD47-1", "24142675", "Brugada syndrome and p.E61X_RANGRF.", "Cardiology journal", "2014", "Campuzano O, Berne P, Selga E, Allegue C, Iglesias A, Brugada J, Brugada R" ], [ "Q9HD47-1", "21447824", "MOG1: a new susceptibility gene for Brugada syndrome.", "Circulation. 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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_9606.gpff\n URI: https://data.glygen.org/ln2data/releases/data/v-1.4.5/source/refseq_protein_all_9606.gpff\n Name: human_protein_xref_refseq.csv\n URI: https://data.glygen.org/ln2data/releases/data/v-1.4.5/reviewed/human_protein_xref_refseq.csv\n Output Subdomain\n Name: human_protein_citations_refseq.csv\n URI: http://data.glygen.org/ln2data/releases/data/v-1.4.5/reviewed/human_protein_citations_refseq.csv\n Name: human_protein_citations_refseq.stat.csv\n URI: http://data.glygen.org/ln2data/releases/data/v-1.4.5/reviewed/human_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: \"10177\"\n Name: \"title\"\n Description: \"Title of the published article in the journal\"\n Unique Values: \"30961\"\n Name: \"journal_name\"\n Description: \"The name of the journal in which the article is published\"\n Unique Values: \"1903\"\n Name: \"authors\"\n Description: \"\"\n Unique Values: \"30861\"\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: \"4066\"\n Name: \"pmid\"\n Description: \"NCBI PubMed database Identifier\"\n Unique Values: \"30963\"", "downloadurl": "/ln2data/releases/data/v-1.4.5/reviewed/human_protein_citations_refseq.csv" }