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Karl B. Shpargel, Ph.D. - Publications

Affiliations: 
Genetics Case Western Reserve University, Cleveland Heights, OH, United States 
Area:
RNA processing; nuclear cell biology
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23 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Musa RE, Lester KL, Quickstad GA, Vardabasso S, Shumate TV, Salcido RT, Ge K, Shpargel KB. BRD4 binds to active cranial neural crest enhancers to regulate RUNX2 activity during osteoblast differentiation. Development (Cambridge, England). PMID 38063851 DOI: 10.1242/dev.202110  0.345
2021 Mitchell JE, Lund MM, Starmer J, Ge K, Magnuson T, Shpargel KB, Whitmire JK. UTX promotes CD8 T cell-mediated antiviral defenses but reduces T cell durability. Cell Reports. 35: 108966. PMID 33852868 DOI: 10.1016/j.celrep.2021.108966  0.501
2020 Shpargel KB, Mangini CL, Xie G, Ge K, Magnuson T. The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology. Development (Cambridge, England). PMID 32541010 DOI: 10.1242/Dev.187997  0.628
2020 Kalisz M, Bernardo E, Beucher A, Maestro MA, Del Pozo N, Millán I, Haeberle L, Schlensog M, Safi SA, Knoefel WT, Grau V, de Vas M, Shpargel KB, Vaquero E, Magnuson T, et al. HNF1A recruits KDM6A to activate differentiated acinar cell programs that suppress pancreatic cancer. The Embo Journal. e102808. PMID 32154941 DOI: 10.15252/Embj.2019102808  0.606
2017 Wijayatunge R, Liu F, Shpargel KB, Wayne NJ, Chan U, Boua JV, Magnuson T, West AE. The histone demethylase Kdm6b regulates a mature gene expression program in differentiating cerebellar granule neurons. Molecular and Cellular Neurosciences. PMID 29254825 DOI: 10.1016/J.Mcn.2017.11.005  0.594
2017 Shpargel KB, Starmer J, Wang C, Ge K, Magnuson T. UTX-guided neural crest function underlies craniofacial features of Kabuki syndrome. Proceedings of the National Academy of Sciences of the United States of America. 114: E9046-E9055. PMID 29073101 DOI: 10.1073/Pnas.1705011114  0.636
2015 Cook KD, Shpargel KB, Starmer J, Whitfield-Larry F, Conley B, Allard DE, Rager JE, Fry RC, Davenport ML, Magnuson T, Whitmire JK, Su MA. T Follicular Helper Cell-Dependent Clearance of a Persistent Virus Infection Requires T Cell Expression of the Histone Demethylase UTX. Immunity. 43: 703-14. PMID 26431949 DOI: 10.1016/J.Immuni.2015.09.002  0.549
2014 Shi X, Zhang Z, Zhan X, Cao M, Satoh T, Akira S, Shpargel K, Magnuson T, Li Q, Wang R, Wang C, Ge K, Wu J. An epigenetic switch induced by Shh signalling regulates gene activation during development and medulloblastoma growth. Nature Communications. 5: 5425. PMID 25370275 DOI: 10.1038/Ncomms6425  0.6
2014 Shpargel KB, Starmer J, Yee D, Pohlers M, Magnuson T. KDM6 demethylase independent loss of histone H3 lysine 27 trimethylation during early embryonic development. Plos Genetics. 10: e1004507. PMID 25101834 DOI: 10.1371/Journal.Pgen.1004507  0.608
2012 Shpargel KB, Sengoku T, Yokoyama S, Magnuson T. UTX and UTY demonstrate histone demethylase-independent function in mouse embryonic development. Plos Genetics. 8: e1002964. PMID 23028370 DOI: 10.1371/Journal.Pgen.1002964  0.575
2011 Kurima K, Hertzano R, Gavrilova O, Monahan K, Shpargel KB, Nadaraja G, Kawashima Y, Lee KY, Ito T, Higashi Y, Eisenman DJ, Strome SE, Griffith AJ. A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice. Plos Genetics. 7: e1002307. PMID 21980308 DOI: 10.1371/Journal.Pgen.1002307  0.415
2009 Shpargel KB, Praveen K, Rajendra TK, Matera AG. Gemin3 is an essential gene required for larval motor function and pupation in Drosophila. Molecular Biology of the Cell. 20: 90-101. PMID 18923150 DOI: 10.1091/Mbc.E08-01-0024  0.766
2007 Rajendra TK, Gonsalvez GB, Walker MP, Shpargel KB, Salz HK, Matera AG. A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle. The Journal of Cell Biology. 176: 831-41. PMID 17353360 DOI: 10.1083/Jcb.200610053  0.698
2006 Matera AG, Shpargel KB. Pumping RNA: nuclear bodybuilding along the RNP pipeline. Current Opinion in Cell Biology. 18: 317-24. PMID 16632338 DOI: 10.1016/J.Ceb.2006.03.005  0.608
2005 Shpargel KB, Matera AG. Gemin proteins are required for efficient assembly of Sm-class ribonucleoproteins. Proceedings of the National Academy of Sciences of the United States of America. 102: 17372-7. PMID 16301532 DOI: 10.1073/Pnas.0508947102  0.703
2005 Xu H, Pillai RS, Azzouz TN, Shpargel KB, Kambach C, Hebert MD, Schümperli D, Matera AG. The C-terminal domain of coilin interacts with Sm proteins and U snRNPs. Chromosoma. 114: 155-66. PMID 16003501 DOI: 10.1007/S00412-005-0003-Y  0.719
2004 Shpargel KB, Makishima T, Griffith AJ. Col11a1 and Col11a2 mRNA expression in the developing mouse cochlea: implications for the correlation of hearing loss phenotype with mutant type XI collagen genotype. Acta Oto-Laryngologica. 124: 242-8. PMID 15141750 DOI: 10.1080/00016480410016162  0.343
2004 Dundr M, Hebert MD, Karpova TS, Stanek D, Xu H, Shpargel KB, Meier UT, Neugebauer KM, Matera AG, Misteli T. In vivo kinetics of Cajal body components. The Journal of Cell Biology. 164: 831-42. PMID 15024031 DOI: 10.1083/Jcb.200311121  0.715
2003 Shpargel KB, Ospina JK, Tucker KE, Matera AG, Hebert MD. Control of Cajal body number is mediated by the coilin C-terminus. Journal of Cell Science. 116: 303-12. PMID 12482916 DOI: 10.1242/Jcs.00211  0.714
2002 Hebert MD, Shpargel KB, Ospina JK, Tucker KE, Matera AG. Coilin methylation regulates nuclear body formation. Developmental Cell. 3: 329-37. PMID 12361597 DOI: 10.1016/S1534-5807(02)00222-8  0.727
2001 Hebert MD, Szymczyk PW, Shpargel KB, Matera AG. Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein. Genes & Development. 15: 2720-9. PMID 11641277 DOI: 10.1101/Gad.908401  0.757
2001 Tucker KE, Berciano MT, Jacobs EY, LePage DF, Shpargel KB, Rossire JJ, Chan EK, Lafarga M, Conlon RA, Matera AG. Residual Cajal bodies in coilin knockout mice fail to recruit Sm snRNPs and SMN, the spinal muscular atrophy gene product. The Journal of Cell Biology. 154: 293-307. PMID 11470819 DOI: 10.1083/Jcb.200104083  0.673
1999 McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, et al. Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nature Genetics. 23: 413-9. PMID 10581026 DOI: 10.1038/70516  0.332
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