{ "bcoid": "GLY_000256", "title": "Human Protein Citations (RefSeq)", "description": "The Human Protein Citations (RefSeq) datasets contains human [taxid:9606] UniProtKB accessions mapped ...", "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": [ [ "Q8WTX9-1...", "23687301..." ], [ "Q8WTX9-1...", "20549515..." ] ], "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" } ], [ "Q8WTX9-1", "23687301", "In silico screening for palmitoyl substrates reveals a role for DHHC1/3/10 (zDHHC1/3/11)-mediated neurochondrin palmitoylation in its targeting to Rab5-positive endosomes.", "The Journal of biological chemistry", "2013 Jul 5", "Oku S, Takahashi N, Fukata Y, Fukata M" ], [ "Q8WTX9-1", "20549515", "Genome-wide searching of rare genetic variants in WTCCC data.", "Human genetics", "2010 Sep", "Feng T, Zhu X" ], [ "Q86YM7-1", "30219717", "Associations of Homer Scaffolding Protein 1 gene and psychological correlates with suicide attempts in Chinese: A pilot study of multifactorial risk model.", "Gene", "2018 Dec 30", "Rao S, Siu CO, Shi M, Zhang J, Lam MHB, Yu M, Wing YK, Waye MMY" ], [ "Q86YM7-1", "29923011", "Homer 1a Induces Calcium Channel Activation, but Does Not Change Their Properties in A431 Cells.", "Bulletin of experimental biology and medicine", "2018 Jun", "Shalygin AV, Ryazantseva MA, Glushankova LN, Gusev KO, Kolesnikov DO, Vigont VA, Skopin AY, Skobeleva KV, Kaznacheeva EV" ], [ "Q86YM7-1", "29079138", "A Homer 1 gene variant influences brain structure and function, lithium effects on white matter, and antidepressant response in bipolar disorder: A multimodal genetic imaging study.", "Progress in neuro-psychopharmacology & biological psychiatry", "2018 Feb 2", "Benedetti F, Poletti S, Locatelli C, Mazza E, Lorenzi C, Vitali A, Riberto M, Brioschi S, Vai B, Bollettini I, Melloni E, Aggio V, Falini A, De Bartolomeis A, Colombo C" ], [ "Q86YM7-1", "28815330", "Homer1a protein expression in schizophrenia, bipolar disorder, and major depression.", "Journal of neural transmission (Vienna, Austria : 1996)", "2017 Oct", "Leber SL, Llenos IC, Miller CL, Dulay JR, Haybaeck J, Weis S" ], [ "Q9BRX8-1", "26438880", "Adipocyte-derived PAMM suppresses macrophage inflammation by inhibiting MAPK signalling.", "The Biochemical journal", "2015 Dec 15", "Guo F, He H, Fu ZC, Huang S, Chen T, Papasian CJ, Morse LR, Xu Y, Battaglino RA, Yang XF, Jiang Z, Xin HB, Fu M" ], [ "Q9BRX8-1", "26402163", "A short report: PAMM, a novel antioxidant protein, induced by oxidative stress.", "Redox biology", "2015 Dec", "Xu Y, Morse LR, da Silva RAB, Wang D, Battaglino RA" ], [ "Q9BRX8-1", "19951071", "PAMM: a redox regulatory protein that modulates osteoclast differentiation.", "Antioxidants & redox signaling", "2010 Jul 1", "Xu Y, Morse LR, da Silva RA, Odgren PR, Sasaki H, Stashenko P, Battaglino RA" ], [ "Q9BQ52-1", "28441660", "The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous ELAC2 Mutation.", "Cardiology", "2017", "Shinwari ZMA, Almesned A, Alakhfash A, Al-Rashdan AM, Faqeih E, Al-Humaidi Z, Alomrani A, Alghamdi M, Colak D, Alwadai A, Rababh M, Al-Fayyadh M, Al-Hassnan ZN" ], [ "Q9BQ52-1", "27769300", "A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement.", "Orphanet journal of rare diseases", "2016 Oct 21", "Akawi NA, Ben-Salem S, Hertecant J, John A, Pramathan T, Kizhakkedath P, Ali BR, Al-Gazali L" ], [ "Q9BQ52-1", "27318894", "Association between RNASEL, MSR1, and ELAC2 single nucleotide polymorphisms and gene expression in prostate cancer risk.", "Urologic oncology", "2016 Oct", "Alvarez-Cubero MJ, Pascual-Geler M, Martinez-Gonzalez LJ, Exposito Ruiz M, Saiz M, Cozar JM, Lorente JA" ], [ "Q9BQ52-1", "16636667", "ELAC2, a putative prostate cancer susceptibility gene product, potentiates TGF-beta/Smad-induced growth arrest of prostate cells.", "Oncogene", "2006 Sep 14", "Noda D, Itoh S, Watanabe Y, Inamitsu M, Dennler S, Itoh F, Koike S, Danielpour D, ten Dijke P, Kato M" ], [ "Q9BQ52-1", "11254449", "HPC2 variants and screen-detected prostate cancer.", "American journal of human genetics", "2001 Apr", "Vesprini D, Nam RK, Trachtenberg J, Jewett MA, Tavtigian SV, Emami M, Ho M, Toi A, Narod SA" ], [ "Q9BQ52-1", "11254448", "Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer.", "American journal of human genetics", "2001 Apr", "Xu J, Zheng SL, Carpten JD, Nupponen NN, Robbins CM, Mestre J, Moses TY, Faith DA, Kelly BD, Isaacs SD, Wiley KE, Ewing CM, Bujnovszky P, Chang B, Bailey-Wilson J, Bleecker ER, Walsh PC, Trent JM, Meyers DA, Isaacs WB" ], [ "Q9BQ52-1", "11175785", "A candidate prostate cancer susceptibility gene at chromosome 17p.", "Nature genetics", "2001 Feb", "Tavtigian SV, Simard J, Teng DH, Abtin V, Baumgard M, Beck A, Camp NJ, Carillo AR, Chen Y, Dayananth P, Desrochers M, Dumont M, Farnham JM, Frank D, Frye C, Ghaffari S, Gupte JS, Hu R, Iliev D, Janecki T, Kort EN, Laity KE, Leavitt A, Leblanc G, McArthur-Morrison J, Pederson A, Penn B, Peterson KT, Reid JE, Richards S, Schroeder M, Smith R, Snyder SC, Swedlund B, Swensen J, Thomas A, Tranchant M, Woodland AM, Labrie F, Skolnick MH, Neuhausen S, Rommens J, Cannon-Albright LA" ], [ "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" ], [ "Q7Z7M0-1", "23063620", "Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.", "American journal of human genetics", "2012 Nov 2", "Twigg SR, Lloyd D, Jenkins D, Elcioglu NE, Cooper CD, Al-Sannaa N, Annagur A, Gillessen-Kaesbach G, Huning I, Knight SJ, Goodship JA, Keavney BD, Beales PL, Gileadi O, McGowan SJ, Wilkie AO" ], [ "Q13049-1", "28465353", "TRIM24 protein promotes and TRIM32 protein inhibits cardiomyocyte hypertrophy via regulation of dysbindin protein levels.", "The Journal of biological chemistry", "2017 Jun 16", "Borlepawar A, Rangrez AY, Bernt A, Christen L, Sossalla S, Frank D, Frey N" ], [ "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", "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" ], [ "Q9NRY2-1", "29150435", "Biochemical characterization of INTS3 and C9ORF80, two subunits of hNABP1/2 heterotrimeric complex in nucleic acid binding.", "The Biochemical journal", "2018 Jan 2", "Vidhyasagar V, He Y, Guo M, Talwar T, Singh RS, Yadav M, Katselis G, Vizeacoumar FJ, Lukong KE, Wu Y" ], [ "Q9NRY2-1", "19786574", "INTS3 controls the hSSB1-mediated DNA damage response.", "The Journal of cell biology", "2009 Oct 5", "Skaar JR, Richard DJ, Saraf A, Toschi A, Bolderson E, Florens L, Washburn MP, Khanna KK, Pagano M" ], [ "Q9NRY2-1", "19605351", "HSSB1 and hSSB2 form similar multiprotein complexes that participate in DNA damage response.", "The Journal of biological chemistry", "2009 Aug 28", "Li Y, Bolderson E, Kumar R, Muniandy PA, Xue Y, Richard DJ, Seidman M, Pandita TK, Khanna KK, Wang W" ], [ "Q9NRY2-1", "19683501", "SOSS complexes participate in the maintenance of genomic stability.", "Molecular cell", "2009 Aug 14", "Huang J, Gong Z, Ghosal G, Chen J" ], [ "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" ], [ "Q71RC2-1", "30520539", "circLARP4 induces cellular senescence through regulating miR-761/RUNX3/p53/p21 signaling in hepatocellular carcinoma.", "Cancer science", "2019 Feb", "Chen Z, Zuo X, Pu L, Zhang Y, Han G, Zhang L, Wu J, Wang X" ], [ "Q71RC2-1", "30686809", "La-Related Protein 4 as a Suppressor for Motility of Ovarian Cancer Cells.", "The Tohoku journal of experimental medicine", "2019 Jan", "Egiz M, Usui T, Ishibashi M, Zhang X, Shigeta S, Toyoshima M, Kitatani K, Yaegashi N" ], [ "Q71RC2-1", "21098120", "La-related protein 4 binds poly(A), interacts with the poly(A)-binding protein MLLE domain via a variant PAM2w motif, and can promote mRNA stability.", "Molecular and cellular biology", "2011 Feb", "Yang R, Gaidamakov SA, Xie J, Lee J, Martino L, Kozlov G, Crawford AK, Russo AN, Conte MR, Gehring K, Maraia RJ" ], [ "Q71RC2-1", "16682284", "Detection of abnormalities of PRV-1, TPO, and c-MPL genes detected by fluorescence in situ hybridization in essential thrombocythemia.", "Cancer genetics and cytogenetics", "2006 May", "Puigdecanet E, Espinet B, Villa O, Florensa L, Besses C, Serrano S, Sole F" ], [ "Q71RC2-1", "15572213", "Molecular pathogenesis of Philadelphia chromosome negative myeloproliferative disorders.", "Blood reviews", "2005 Jan", "Kralovics R, Skoda RC" ], [ "Q12879-1", "30260902", "No association of GRIN2A polymorphisms with the major depressive disorder in the Chinese Han origin.", "Psychiatric genetics", "2018 Dec", "Hu J, Bi Y, Shi L, Xu F, Yuan F, Niu W, Ren D, Guo Z, Yang F, He L, He G" ], [ "Q12879-1", "29958946", "Segregating polymorphism in the NMDA receptor gene GRIN2A, schizotypy, and mental rotation among healthy individuals.", "Neuropsychologia", "2018 Aug", "Jha S, Read S, Hurd P, Crespi B" ], [ "Q12879-1", "29896722", "[Study of GRIN2A mutation in epilepsy-aphasia spectrum disorders].", "Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics", "2018 Jun 10", "Qian P, Yang X, Xu X, Liu X, Zhang Y, Yang Z" ], [ "Q12879-1", "29358611", "Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.", "European journal of human genetics : EJHG", "2018 Feb", "Bobbili DR, Lal D, May P, Reinthaler EM, Jabbari K, Thiele H, Nothnagel M, Jurkowski W, Feucht M, Nurnberg P, Lerche H, Zimprich F, Krause R, Neubauer BA, Reinthaler EM, Zimprich F, Feucht M, Steinbock H, Neophytou B, Geldner J, Gruber-Sedlmayr U, Haberlandt E, Ronen GM, Altmuller J, Lal D, Nurnberg P, Sander T, Thiele H, Krause R, May P, Balling R, Lerche H, Neubauer BA" ], [ "P17858-1", "30409970", "TAp73-induced phosphofructokinase-1 transcription promotes the Warburg effect and enhances cell proliferation.", "Nature communications", "2018 Nov 8", "Li L, Li L, Li W, Chen T, Bin Zou, Zhao L, Wang H, Wang X, Xu L, Liu X, Wang D, Li B, Mak TW, Du W, Yang X, Jiang P" ], [ "P17858-1", "28646105", "The glycolytic enzyme phosphofructokinase-1 assembles into filaments.", "The Journal of cell biology", "2017 Aug 7", "Webb BA, Dosey AM, Wittmann T, Kollman JM, Barber DL" ], [ "P17858-1", "22923583", "Phosphofructokinase 1 glycosylation regulates cell growth and metabolism.", "Science (New York, N.Y.)", "2012 Aug 24", "Yi W, Clark PM, Mason DE, Keenan MC, Hill C, Goddard WA 3rd, Peters EC, Driggers EM, Hsieh-Wilson LC" ], [ "Q9Y294-1", "29478807", "The Histone Chaperones ASF1 and CAF-1 Promote MMS22L-TONSL-Mediated Rad51 Loading onto ssDNA during Homologous Recombination in Human Cells.", "Molecular cell", "2018 Mar 1", "Huang TH, Fowler F, Chen CC, Shen ZJ, Sleckman B, Tyler JK" ], [ "Q9Y294-1", "28943310", "ASF1a Promotes Non-homologous End Joining Repair by Facilitating Phosphorylation of MDC1 by ATM at Double-Strand Breaks.", "Molecular cell", "2017 Oct 5", "Lee KY, Im JS, Shibata E, Dutta A" ], [ "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", "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" ], [ "Q9UM22-1", "27805251", "In silico RNA-seq and experimental analyses reveal the differential expression and splicing of EPDR1 and ZNF518B genes in relation to KRAS mutations in colorectal cancer cells.", "Oncology reports", "2016 Dec", "Riffo-Campos AL, Castillo J, Vallet-Sanchez A, Ayala G, Cervantes A, Lopez-Rodas G, Franco L" ], [ "Q9UM22-1", "27245865", "Dupuytren's disease susceptibility gene, EPDR1, is involved in myofibroblast contractility.", "Journal of dermatological science", "2016 Aug", "Staats KA, Wu T, Gan BS, O'Gorman DB, Ophoff RA" ], [ "Q9UM22-1", "24089297", "Common variants of the EPDR1 gene and the risk of Dupuytren's disease.", "Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V...", "2013 Oct", "Debniak T, Zyluk A, Puchalski P, Serrano-Fernandez P" ], [ "Q9UM22-1", "16954209", "Demonstration of lysosomal localization for the mammalian ependymin-related protein using classical approaches combined with a novel density shift method.", "The Journal of biological chemistry", "2006 Nov 17", "Della Valle MC, Sleat DE, Sohar I, Wen T, Pintar JE, Jadot M, Lobel P" ], [ "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" ], [ "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" ], [ "Q8IYT3-1", "26928228", "Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.", "Nature genetics", "2016 Apr", "Dunning AM, Michailidou K, Kuchenbaecker KB, Thompson D, French JD, Beesley J, Healey CS, Kar S, Pooley KA, Lopez-Knowles E, Dicks E, Barrowdale D, Sinnott-Armstrong NA, Sallari RC, Hillman KM, Kaufmann S, Sivakumaran H, Moradi Marjaneh M, Lee JS, Hills M, Jarosz M, Drury S, Canisius S, Bolla MK, Dennis J, Wang Q, Hopper JL, Southey MC, Broeks A, Schmidt MK, Lophatananon A, Muir K, Beckmann MW, Fasching PA, Dos-Santos-Silva I, Peto J, Sawyer EJ, Tomlinson I, Burwinkel B, Marme F, Guenel P, Truong T, Bojesen SE, Flyger H, Gonzalez-Neira A, Perez JI, Anton-Culver H, Eunjung L, Arndt V, Brenner H, Meindl A, Schmutzler RK, Brauch H, Hamann U, Aittomaki K, Blomqvist C, Ito H, Matsuo K, Bogdanova N, Dork T, Lindblom A, Margolin S, Kosma VM, Mannermaa A, Tseng CC, Wu AH, Lambrechts D, Wildiers H, Chang-Claude J, Rudolph A, Peterlongo P, Radice P, Olson JE, Giles GG, Milne RL, Haiman CA, Henderson BE, Goldberg MS, Teo SH, Yip CH, Nord S, Borresen-Dale AL, Kristensen V, Long J, Zheng W, Pylkas K, Winqvist R, Andrulis IL, Knight JA, Devilee P, Seynaeve C, Figueroa J, Sherman ME, Czene K, Darabi H, Hollestelle A, van den Ouweland AM, Humphreys K, Gao YT, Shu XO, Cox A, Cross SS, Blot W, Cai Q, Ghoussaini M, Perkins BJ, Shah M, Choi JY, Kang D, Lee SC, Hartman M, Kabisch M, Torres D, Jakubowska A, Lubinski J, Brennan P, Sangrajrang S, Ambrosone CB, Toland AE, Shen CY, Wu PE, Orr N, Swerdlow A, McGuffog L, Healey S, Lee A, Kapuscinski M, John EM, Terry MB, Daly MB, Goldgar DE, Buys SS, Janavicius R, Tihomirova L, Tung N, Dorfling CM, van Rensburg EJ, Neuhausen SL, Ejlertsen B, Hansen TV, Osorio A, Benitez J, Rando R, Weitzel JN, Bonanni B, Peissel B, Manoukian S, Papi L, Ottini L, Konstantopoulou I, Apostolou P, Garber J, Rashid MU, Frost D, Izatt L, Ellis S, Godwin AK, Arnold N, Niederacher D, Rhiem K, Bogdanova-Markov N, Sagne C, Stoppa-Lyonnet D, Damiola F, Sinilnikova OM, Mazoyer S, Isaacs C, Claes KB, De Leeneer K, de la Hoya M, Caldes T, Nevanlinna H, Khan S, Mensenkamp AR, Hooning MJ, Rookus MA, Kwong A, Olah E, Diez O, Brunet J, Pujana MA, Gronwald J, Huzarski T, Barkardottir RB, Laframboise R, Soucy P, Montagna M, Agata S, Teixeira MR, Park SK, Lindor N, Couch FJ, Tischkowitz M, Foretova L, Vijai J, Offit K, Singer CF, Rappaport C, Phelan CM, Greene MH, Mai PL, Rennert G, Imyanitov EN, Hulick PJ, Phillips KA, Piedmonte M, Mulligan AM, Glendon G, Bojesen A, Thomassen M, Caligo MA, Yoon SY, Friedman E, Laitman Y, Borg A, von Wachenfeldt A, Ehrencrona H, Rantala J, Olopade OI, Ganz PA, Nussbaum RL, Gayther SA, Nathanson KL, Domchek SM, Arun BK, Mitchell G, Karlan BY, Lester J, Maskarinec G, Woolcott C, Scott C, Stone J, Apicella C, Tamimi R, Luben R, Khaw KT, Helland A, Haakensen V, Dowsett M, Pharoah PD, Simard J, Hall P, Garcia-Closas M, Vachon C, Chenevix-Trench G, Antoniou AC, Easton DF, Edwards SL" ], [ "Q8IYT3-1", "20200978", "Replication of previous genome-wide association studies of bone mineral density in premenopausal American women.", "Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research", "2010 Aug", "Ichikawa S, Koller DL, Padgett LR, Lai D, Hui SL, Peacock M, Foroud T, Econs MJ" ], [ "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" ], [ "Q02548-1", "30643249", "PAX5-driven subtypes of B-progenitor acute lymphoblastic leukemia.", "Nature genetics", "2019 Feb", "Gu Z, Churchman ML, Roberts KG, Moore I, Zhou X, Nakitandwe J, Hagiwara K, Pelletier S, Gingras S, Berns H, Payne-Turner D, Hill A, Iacobucci I, Shi L, Pounds S, Cheng C, Pei D, Qu C, Newman S, Devidas M, Dai Y, Reshmi SC, Gastier-Foster J, Raetz EA, Borowitz MJ, Wood BL, Carroll WL, Zweidler-McKay PA, Rabin KR, Mattano LA, Maloney KW, Rambaldi A, Spinelli O, Radich JP, Minden MD, Rowe JM, Luger S, Litzow MR, Tallman MS, Racevskis J, Zhang Y, Bhatia R, Kohlschmidt J, Mrozek K, Bloomfield CD, Stock W, Kornblau S, Kantarjian HM, Konopleva M, Evans WE, Jeha S, Pui CH, Yang J, Paietta E, Downing JR, Relling MV, Zhang J, Loh ML, Hunger SP, Mullighan CG" ], [ "Q02548-1", "30583670", "Expression of PAX-5 in B Cell Hodgkin and Non Hodgkin Lymphoma", "Asian Pacific journal of cancer prevention : APJCP", "2018 Dec 25", "Khan MR, Ahmad A, Kayani N, Minhas K" ], [ "Q02548-1", "30257940", "PAX5-ELN oncoprotein promotes multistep B-cell acute lymphoblastic leukemia in mice.", "Proceedings of the National Academy of Sciences of the United States of America", "2018 Oct 9", "Jamrog L, Chemin G, Fregona V, Coster L, Pasquet M, Oudinet C, Rouquie N, Prade N, Lagarde S, Cresson C, Hebrard S, Nguyen Huu NS, Bousquet M, Quelen C, Brousset P, Mancini SJC, Delabesse E, Khamlichi AA, Gerby B, Broccardo C" ], [ "Q02548-1", "30194145", "Pax-5 Inhibits Breast Cancer Proliferation Through MiR-215 Up-regulation.", "Anticancer research", "2018 Sep", "Leblanc N, Harquail J, Crapoulet N, Ouellette RJ, Robichaud GA" ], [ "Q6UXS9-1", "28380444", "Caspase 12 degrades IkappaBalpha protein and enhances MMP-9 expression in human nasopharyngeal carcinoma cell invasion.", "Oncotarget", "2017 May 16", "Chu WK, Hsu CC, Huang SF, Hsu CC, Chow SE" ] ] }, "readme": "Name\n - Human Protein Citations (RefSeq)\n\nVersion\n - 1.5.12\n\nCreated on\n - 2019-09-06T14:06:38.983152\n\nModified on\n - 2019-12-01T15:08:14.010693\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 Human Protein Citations (RefSeq) datasets contains human [taxid:9606] 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_9606.gpff\n URI: https://data.glygen.org/ln2data/releases/data/v-1.5.12/source/refseq_protein_all_9606.gpff\n Name: human_protein_xref_refseq.csv\n URI: https://data.glygen.org/ln2data/releases/data/v-1.5.12/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-1.5.12/reviewed/human_protein_citations_refseq.csv\n Name: human_protein_citations_refseq.stat.csv\n URI: http://data.glygen.org/ln2data/releases/data/v-1.5.12/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: \"11167\"\n Name: \"title\"\n Description: \"Title of the published article in the journal\"\n Unique Values: \"27461\"\n Name: \"journal_name\"\n Description: \"The name of the journal in which the article is published\"\n Unique Values: \"1801\"\n Name: \"authors\"\n Description: \"\"\n Unique Values: \"27370\"\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: \"3992\"\n Name: \"pmid\"\n Description: \"NCBI PubMed database Identifier\"\n Unique Values: \"27463\"", "downloadurl": "/ln2data/releases/data/v-1.5.12/reviewed/human_protein_citations_refseq.csv" }