Citations for
1CEP97, DYRK1A, PLK1
CEP97 phosphorylation by Dyrk1a is critical for centriole separation during multiciliogenesis.
Lee M, Nagashima K, Yoon J, Sun J, Wang Z, Carpenter C, Lee HK, Hwang YS, Westlake CJ, Daar IO.
J Cell Biol. Jan 3;221(1):e202102110. doi: 10.1083/jcb.202102110. Epub 2021 Nov 17. 2022
2DYRK1A
DYRK1A: a down syndrome-related dual protein kinase with a versatile role in tumorigenesis
Laham AJ, Saber-Ayad M, El-Awady R.
Cell Mol Life Sci. Jan;78(2):603-619. doi: 10.1007/s00018-020-03626-4. Epub 2020 Sep 1. 2021
3DYRK1A, NFATC1
DYRK1A activates NFATC1 to increase glioblastoma migration
Liu H, Sun Q, Chen S, Chen L, Jia W, Zhao J, Sun X.
Cancer Med. Sep;10(18):6416-6427. doi: 10.1002/cam4.4159. Epub 2021 Jul 26. 2021
4DYRK1A
Dyrk1a from Gene Function in Development and Physiology to Dosage Correction across Life Span in Down Syndrome
Atas-Ozcan H, Brault V, Duchon A, Herault Y.
Genes (Basel). Nov 20;12(11):1833. doi: 10.3390/genes12111833. 2021
5DYRK1A, MEF2D
DYRK1A phosphorylates MEF2D and decreases its transcriptional activity
Wang P, Zhao J, Sun X.
J Cell Mol Med. Jun 9;25(13):6082–93. doi: 10.1111/jcmm.16505. Epub ahead of print. 2021
6DYRK1A, MRD7
Dyrk1a Mutations Cause Undergrowth of Cortical Pyramidal Neurons via Dysregulated Growth Factor Signaling.
Levy JA, LaFlamme CW, Tsaprailis G, Crynen G, Page DT.
Biol Psychiatry. Sep 1;90(5):295-306. doi: 10.1016/j.biopsych.2021.01.012. Epub 2021 Apr 8. 2021
7DYRK1A
The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos
Willsey HR, Xu Y, Everitt A, Dea J, Exner CRT, Willsey AJ, State MW, Harland RM.
Development. Jun 22;147(21):dev189290. doi: 10.1242/dev.189290. Erratum in: Development. 2020 Dec 7;147(23): 2020
8DYRK1A, MET
DYRK1A modulates c-MET in pancreatic ductal adenocarcinoma to drive tumour growth
Luna J, Boni J, Cuatrecasas M, Bofill-De Ros X, Núñez-Manchón E, Gironella M, Vaquero EC, Arbones ML, de la Luna S, Fillat C.
Gut Aug;68(8):1465-1476. doi: 10.1136/gutjnl-2018-316128. Epub 2018 Oct 20. 2019
9DYRK1A, MRD7
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract
Blackburn ATM, Bekheirnia N, Uma VC, Corkins ME, Xu Y, Rosenfeld JA, Bainbridge MN, Yang Y, Liu P, Madan-Khetarpal S, Delgado MR, Hudgins L, Krantz I, Rodriguez-Buritica D, Wheeler PG, Al-Gazali L, Mohamed Saeed Mohamed Al Shamsi A, Gomez-Ospina N, Chao HT, Mirzaa GM, Scheuerle AE, Kukolich MK, Scaglia F, Eng C, Willsey HR, Braun MC, Lamb DJ, Miller RK, Bekheirnia MR.
Genet Med. Dec;21(12):2755-2764. doi: 10.1038/s41436-019-0576-0. Epub 2019 Jul 2. Erratum in: Genet Med. 2020 Apr;22(4):821. 2019
10DYRK1A
The nuclear interactome of DYRK1A reveals a functional role in DNA damage repair.
Guard SE, Poss ZC, Ebmeier CC, Pagratis M, Simpson H, Taatjes DJ, Old WM.
Sci Rep. Apr 25;9(1):6539. doi: 10.1038/s41598-019-42990-5. 2019
11DYRK1A, TRI21
Triple play of DYRK1A kinase in cortical progenitor cells of Trisomy 21
Kurabayashi N, Nguyen MD, Sanada K.
Neurosci Res. Jan;138:19-25. doi: 10.1016/j.neures.2018.09.007. Epub 2018 Sep 15. 2018
12CREBBP, DYRK1A, EP300
DYRK1A interacts with histone acetyl transferase p300 and CBP and localizes to enhancers
Li S, Xu C, Fu Y, Lei PJ, Yao Y, Yang W, Zhang Y, Washburn MP, Florens L, Jaiswal M, Wu M, Mohan M.
Nucleic Acids Res. Nov 30;46(21):11202-11213. doi: 10.1093/nar/gky754. 2018
13DYRK1A
Targeting trisomic treatments: optimizing Dyrk1a inhibition to improve Down syndrome deficits
Stringer M, Goodlett CR, Roper RJ.
Mol Genet Genomic Med. Sep 20;5(5):451-465. doi: 10.1002/mgg3.334. 2017
14CIC, DYRK1A
Minibrain and Wings apart control organ growth and tissue patterning through down-regulation of Capicua.
Yang L, Paul S, Trieu KG, Dent LG, Froldi F, Forés M, Webster K, Siegfried KR, Kondo S, Harvey K, Cheng L, Jiménez G, Shvartsman SY, Veraksa A.
Proc Natl Acad Sci U S A 113(38):10583-8. doi: 10.1073/pnas.1609417113. Epub 2016 Sep 6. 2016
15DYRK1A
DYRK1A inhibition as potential treatment for Alzheimer's disease. 2016 PMID:
Stotani S, Giordanetto F, Medda F.
Future Med Chem. Apr;8(6):681-96. doi: 10.4155/fmc-2016-0013. Epub 2016 Apr 13. 2016
16DYRK1A, MAPT, SNCA
Understanding the Multifaceted Role of Human Down Syndrome Kinase DYRK1A.
Kay LJ, Smulders-Srinivasan TK, Soundararajan M.
Adv Protein Chem Struct Biol. 105:127-71. doi: 10.1016/bs.apcsb.2016.07.001. Epub 2016 Aug 9 2016
17DYRK1A
Dyrk1a regulates the cardiomyocyte cell cycle via D-cyclin-dependent Rb/E2f-signalling
Hille S, Dierck F, Kühl C, Sosna J, Adam-Klages S, Adam D, Lüllmann-Rauch R, Frey N, Kuhn C.
Cardiovasc Res. Jun 1;110(3):381-94. doi: 10.1093/cvr/cvw074. Epub 2016 Apr 7 2016
18CCND3, DYRK1A
DYRK1A controls the transition from proliferation to quiescence during lymphoid development by destabilizing Cyclin D3.
Thompson BJ, Bhansali R, Diebold L, Cook DE, Stolzenburg L, Casagrande AS, Besson T, Leblond B, Désiré L, Malinge S, Crispino JD.
J Exp Med 212(6):953-70. doi: 10.1084/jem.20150002. Epub 2015 May 25. 2015
19DYRK1A
Triplication of DYRK1A causes retinal structural and functional alterations in Down syndrome
Laguna A, Barallobre MJ, Marchena MÁ, Mateus C, Ramírez E, Martínez-Cue C, Delabar JM, Castelo-Branco M, de la Villa P, Arbonés ML.
Hum Mol Genet. Jul 15;22(14):2775-84. doi: 10.1093/hmg/ddt125. Epub 2013 Mar 19. 2013
20DYRK1A, MAPT, SRSF6
Dual-specificity tyrosine phosphorylation-regulated kinase 1A (Dyrk1A) modulates serine/arginine-rich protein 55 (SRp55)-promoted Tau exon 10 inclusion.
Yin X, Jin N, Gu J, Shi J, Zhou J, Gong CX, Iqbal K, Grundke-Iqbal I, Liu F.
J Biol Chem 287(36):30497-506. doi: 10.1074/jbc.M112.355412. Epub 2012 Jul 5. 2012
21DCX, DYRK1A, DYRK3, DYRK4
Dyrk kinases regulate phosphorylation of doublecortin, cytoskeletal organization, and neuronal morphology.
Slepak TI, Salay LD, Lemmon VP, Bixby JL.
Cytoskeleton (Hoboken) 69(7):514-27. doi: 10.1002/cm.21021. Epub 2012 Mar 7. 2012
22APBA1, DYRK1A, STX1A, STXBP1
Phosphorylation of Munc18-1 by Dyrk1A regulates its interaction with Syntaxin 1 and X11α.
Park JH, Jung MS, Kim YS, Song WJ, Chung SH.
J Neurochem 122(5):1081-91. doi: 10.1111/j.1471-4159.2012.07861.x. 2012
23DYRK1A, MRD7
The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy.
Courcet JB, Faivre L, Malzac P, Masurel-Paulet A, Lopez E, Callier P, Lambert L, Lemesle M, Thevenon J, Gigot N, Duplomb L, Ragon C, Marle N, Mosca-Boidron AL, Huet F, Philippe C, Moncla A, Thauvin-Robinet C.
J Med Genet 49(12):731-6. doi: 10.1136/jmedgenet-2012-101251. Epub 2012 Oct 25. 2012
24DYRK1A, REST
REST regulates DYRK1A transcription in a negative feedback loop.
Lu M, Zheng L, Han B, Wang L, Wang P, Liu H, Sun X.
J Biol Chem 286(12):10755-63. Epub 2011 Jan 20. 2011
25DYRK1A, DYRK2, DYRK3, DYRK4
Splice variants of the dual specificity tyrosine phosphorylation-regulated kinase 4 (DYRK4) differ in their subcellular localization and catalytic activity.
Papadopoulos C, Arato K, Lilienthal E, Zerweck J, Schutkowski M, Chatain N, Müller-Newen G, Becker W, de la Luna S.
J Biol Chem 286(7):5494-505. Epub 2010 Dec 2. 2011
26DYRK1A, RCAN1
Regulation of RCAN1 protein activity by Dyrk1A protein-mediated phosphorylation.
Jung MS, Park JH, Ryu YS, Choi SH, Yoon SH, Kwen MY, Oh JY, Song WJ, Chung SH.
J Biol Chem. 286(46):40401-12. 2011
27DYRK1A
DYRK1A binds to an evolutionarily conserved WD40-repeat protein WDR68 and induces its nuclear translocation.
Miyata Y, Nishida E.
Biochim Biophys Acta. 1813(10):1728-39. 2011
28DCAF7, DYRK1A
DYRK1A binds to an evolutionarily conserved WD40-repeat protein WDR68 and induces its nuclear translocation.
Miyata Y, Nishida E.
Biochim Biophys Acta 1813(10):1728-39. doi: 10.1016/j.bbamcr.2011.06.023. Epub 2011 Jul 13. 2011
29DYRK1A, MRD7
Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly.
van Bon BW, Hoischen A, Hehir-Kwa J, de Brouwer AP, Ruivenkamp C, Gijsbers AC, Marcelis CL, de Leeuw N, Veltman JA, Brunner HG, de Vries BB.
Clin Genet 79(3):296-9. doi: 10.1111/j.1399-0004.2010.01544.x. No abstract available. 2011
30DYRK1A, DYRK3, SIRT1
DYRK1A and DYRK3 promote cell survival through phosphorylation and activation of SIRT1.
Guo X, Williams JG, Schug TT, Li X.
J Biol Chem 285(17):13223-32. Epub 2010 Feb 18. 2010
31DEL21QD, DEL21QT, DYRK1A
Microdeletion of the Down syndrome critical region at 21q22.
Fujita H, Torii C, Kosaki R, Yamaguchi S, Kudoh J, Hayashi K, Takahashi T, Kosaki K.
Am J Med Genet A 152A(4):950-3.PMID: 20358607 2010
32DEL21QD, DYRK1A, KCNJ6
Clinical manifestations of the deletion of Down syndrome critical region including DYRK1A and KCNJ6.
Yamamoto T, Shimojima K, Nishizawa T, Matsuo M, Ito M, Imai K.
Am J Med Genet A m J Med Genet A. 2010 Dec 10. [Epub ahead of print]PMID: 21154855 2010
33DYRK1A, SPRED1, SPRED2
Direct association of Sprouty-related protein with an EVH1 domain (SPRED) 1 or SPRED2 with DYRK1A modifies substrate/kinase interactions.
Li D, Jackson RA, Yusoff P, Guy GR.
J Biol Chem 285(46):35374-85. Epub 2010 Aug 24. 2010
34DCAF7, DYRK1A, DYRK1B, HIPK2, MAP3K1
The WD40-repeat protein Han11 functions as a scaffold protein to control HIPK2 and MEKK1 kinase functions.
Ritterhoff S, Farah CM, Grabitzki J, Lochnit G, Skurat AV, Schmitz ML.
EMBO J 29(22):3750-61. Epub 2010 Oct 12. 2010
35DYRK1A, REST, TRI21
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome.
Lepagnol-Bestel AM, Zvara A, Maussion G, Quignon F, Ngimbous B, Ramoz N, Imbeaud S, Loe-Mie Y, Benihoud K, Agier N, Salin PA, Cardona A, Khung-Savatovsky S, Kallunki P, Delabar JM, Puskas LG, Delacroix H, Aggerbeck L, Delezoide AL, Delattre O, Gorwood P, Moalic JM, Simonneau M.
Hum Mol Genet 18(8):1405-1414. 2009
36DYRK1A
Attenuation of Notch signalling by the Down-syndrome-associated kinase DYRK1A.
Fernandez-Martinez J, Vela EM, Tora-Ponsioen M, Ocaña OH, Nieto MA, Galceran J.
J Cell Sci 122(Pt 10):1574-83. Epub 2009 Apr 21. 2009
37DYRK1A
DYRK1A is a novel negative regulator of cardiomyocyte hypertrophy.
Kuhn C, Frank D, Will R, Jaschinski C, Frauen R, Katus HA, Frey N.
J Biol Chem 284(25):17320-7. Epub 2009 Apr 16. 2009
38DYRK1A
Harmine specifically inhibits protein kinase DYRK1A and interferes with neurite formation.
Göckler N, Jofre G, Papadopoulos C, Soppa U, Tejedor FJ, Becker W.
FEBS J 276(21):6324-37. Epub 2009 Oct 1.PMID: 19796173 2009
39DYRK1A
Dyrk1A binds to multiple endocytic proteins required for formation of clathrin-coated vesicles.
Murakami N, Bolton D, Hwang YW.
Biochemistry. 48(39):9297-305 2009
40DYRK1A, RCAN1, TRI21
Mental retardation and associated neurological dysfunctions in Down syndrome: a consequence of dysregulation in critical chromosome 21 genes and associated molecular pathways.
Rachidi M, Lopes C.
Eur J Paediatr Neurol 12(3):168-82. Epub 2007 Oct 22. Review. 2008
41DYRK1A, REST, TRI21
DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome.
Canzonetta C, Mulligan C, Deutsch S, Ruf S, O'Doherty A, Lyle R, Borel C, Lin-Marq N, Delom F, Groet J, Schnappauf F, De Vita S, Averill S, Priestley JV, Martin JE, Shipley J, Denyer G, Epstein CJ, Fillat C, Estivill X, Tybulewicz VL, Fisher EM, Antonarakis SE, Nizetic D.
Am J Hum Genet 83(3):388-400. Epub 2008 Sep 4. 2008
42DYRK1A
Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.
Moller RS, Kubart S, Hoeltzenbein M, Heye B, Vogel I, Hansen CP, Menzel C, Ullmann R, Tommerup N, Ropers HH, TŸmer Z, Kalscheuer VM.
Am J Hum Genet 82(5):1165-70. Epub 2008 Apr 10. 2008
43DYRK1A, TRI21
Targeting Dyrk1A with AAVshRNA attenuates motor alterations in TgDyrk1A, a mouse model of Down syndrome.
Ortiz-Abalia J, Sahún I, Altafaj X, Andreu N, Estivill X, Dierssen M, Fillat C.
Am J Hum Genet 83(4):479-88. 2008
44CASP9, DYRK1A
The protein kinase DYRK1A regulates caspase-9-mediated apoptosis during retina development.
Laguna A, Aranda S, Barallobre MJ, Barhoum R, Fernández E, Fotaki V, Delabar JM, de la Luna S, de la Villa P, Arbonés ML.
Dev Cell 15(6):841-53. 2008
45DYRK1A
The role of overexpressed DYRK1A protein in the early onset of neurofibrillary degeneration in Down syndrome.
Wegiel J, Dowjat K, Kaczmarski W, Kuchna I, Nowicki K, Frackowiak J, Mazur Kolecka B, Wegiel J, Silverman WP, Reisberg B, Deleon M, Wisniewski T, Gong CX, Liu F, Adayev T, Chen-Hwang MC, Hwang YW.
Acta Neuropathol 116(4):391-407. Epub 2008 Aug 12. 2008
46DYRK1A, SPRY2
Sprouty2-mediated inhibition of fibroblast growth factor signaling is modulated by the protein kinase DYRK1A.
Aranda S, Alvarez M, Turró S, Laguna A, de la Luna S.
Mol Cell Biol 28(19):5899-911. Epub 2008 Aug 4. 2008
47DYRK1A, MRD7
Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.
Møller RS, Kübart S, Hoeltzenbein M, Heye B, Vogel I, Hansen CP, Menzel C, Ullmann R, Tommerup N, Ropers HH, Tümer Z, Kalscheuer VM.
Am J Hum Genet 82(5):1165-70. doi: 10.1016/j.ajhg.2008.03.001. Epub 2008 Apr 10. 2008
48DYRK1A, TRI21
Trisomy-driven overexpression of DYRK1A kinase in the brain of subjects with Down syndrome.
Dowjat WK, Adayev T, Kuchna I, Nowicki K, Palminiello S, Hwang YW, Wegiel J.
Neurosci Lett 413(1):77-81. Epub 2006 Dec 4. 2007
49DYRK1A
The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between beta-amyloid production and tau phosphorylation in Alzheimer disease.
Kimura R, Kamino K, Yamamoto M, Nuripa A, Kida T, Kazui H, Hashimoto R, Tanaka T, Kudo T, Yamagata H, Tabara Y, Miki T, Akatsu H, Kosaka K, Funakoshi E, Nishitomi K, Sakaguchi G, Kato A, Hattori H, Uema T, Takeda M.
Hum Mol Genet 16(1):15-23. Epub 2006 Nov 29. 2007
50DYRK1A, TRI21
Familial 4.3 Mb duplication of 21q22 sheds new light on the Down syndrome critical region.
Ronan A, Fagan K, Christie L, Conroy J, Nowak NJ, Turner G.
J Med Genet 44(7):448-51. Epub 2007 Jan 19. 2007
51DYRK1A, TRI21
DYRK1A-mediated hyperphosphorylation of Tau. A functional link between Down syndrome and Alzheimer disease.
Ryoo SR, Jeong HK, Radnaabazar C, Yoo JJ, Cho HJ, Lee HW, Kim IS, Cheon YH, Ahn YS, Chung SH, Song WJ.
J Biol Chem 282(48):34850-7. Epub 2007 Sep 28. 2007
52RCAN1, DYRK1A, NFATC1, NFATC2, NFATC3, NFATC4, TRI21
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21.
Arron JR, Winslow MM, Polleri A, Chang CP, Wu H, Gao X, Neilson JR, Chen L, Heit JJ, Kim SK, Yamasaki N, Miyakawa T, Francke U, Graef IA, Crabtree GR.
Nature 441(7093):595-600. Epub 2006 Mar 22. 2006
53DYRK1A, GMNN, TFAP4, STMN2, REST
A repressor complex, AP4 transcription factor and geminin, negatively regulates expression of target genes in nonneuronal cells.
Kim MY, Jeong BC, Lee JH, Kee HJ, Kook H, Kim NS, Kim YH, Kim JK, Ahn KY, Kim KK.
Proc Natl Acad Sci U S A 103(35):13074-9. Epub 2006 Aug 21. 2006
54DYRK1A,NFATC1,NFATC2,NFATC3,NFATC4
A genome-wide Drosophila RNAi screen identifies DYRK-family kinases as regulators of NFAT.
Gwack Y, Sharma S, Nardone J, Tanasa B, Iuga A, Srikanth S, Okamura H, Bolton D, Feske S, Hogan PG, Rao A.
Nature 441(7093):646-50. Epub 2006 Mar 1. 2006
55RCAN1, DYRK1A, NFAT, TRI21
Down's syndrome: critical genes in a critical region.
Epstein CJ.
Nature 441(7093):582-3. No abstract available. 2006
56DYRK1A, SYNJ1
MNB/DYRK1A phosphorylation regulates the interactions of synaptojanin 1 with endocytic accessory proteins.
Adayev T, Chen-Hwang MC, Murakami N, Wang R, Hwang YW.
Biochem Biophys Res Commun 351(4):1060-5. Epub 2006 Nov 7. 2006
57DYRK1A, SF3B1
The protein kinase DYRK1A phosphorylates the splicing factor SF3b1/SAP155 at Thr434, a novel in vivo phosphorylation site.
de Graaf K, Czajkowska H, Rottmann S, Packman LC, Lilischkis R, Lüscher B, Becker W.
BMC Biochem 7:7. 2006
58DYRK1A, DYRK1B, DYRK2, DYRK3, DYRK4
DYRK gene structure and erythroid-restricted features of DYRK3 gene expression.
Zhang D, Li K, Erickson-Miller CL, Weiss M, Wojchowski DM.
Genomics 85(1):117-30. 2005
59DYRK1A
Dual-specificity tyrosine-phosphorylated and regulated kinase 1A (DYRK1A) interacts with the phytanoyl-CoA alpha-hydroxylase associated protein 1 (PAHX-AP1), a brain specific protein.
Bescond M, Rahmani Z.
Int J Biochem Cell Biol. 37(4):775-83. 2005
60DYRK1A
Raf-1 is a binding partner of DSCR1.
Cho YJ, Abe M, Kim SY, Sato Y.
Arch Biochem Biophys. 439(1):121-8. 2005
61DYRK1A
Motor phenotypic alterations in TgDyrk1a transgenic mice implicate DYRK1A in Down syndrome motor dysfunction.
Martinez de Lagran M, Altafaj X, Gallego X, Marti E, Estivill X, Sahun I, Fillat C, Dierssen M.
Neurobiol Dis 15(1):132-42. 2004
62DYRK1A
Characterization of cyclin L2, a novel cyclin with an arginine/serine-rich domain: phosphorylation by DYRK1A and colocalization with splicing factors.
de Graaf K, Hekerman P, Spelten O, Herrmann A, Packman LC, Büssow K, Müller-Newen G, Becker W.
J Biol Chem. 279(6):4612-24. 2004
63DYRK1A
Regulation of Dyrk1A kinase activity by 14-3-3.
Kim D, Won J, Shin DW, Kang J, Kim YJ, Choi SY, Hwang MK, Jeong BW, Kim GS, Joe CO, Chung SH, Song WJ.
Biochem Biophys Res Commun. 323(2):499-504. 2004
64DYRK1A
Expression patterns and subcellular localization of the Down syndrome candidate protein MNB/DYRK1A suggest a role in late neuronal differentiation.
Hammerle B, Carnicero A, Elizalde C, Ceron J, Martinez S, Tejedor FJ.
Eur J Neurosci 17(11):2277-86. 2003
65DYRK1A
Dual roles of modulatory calcineurin-interacting protein 1 in cardiac hypertrophy.
Vega RB, Rothermel BA, Weinheimer CJ, Kovacs A, Naseem RH, Bassel-Duby R, Williams RS, Olson EN.
Proc Natl Acad Sci U S A. 100(2):669-74. 2003
66DYRK1A
Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice.
Fotaki V, Dierssen M, Alcántara S, Martínez S, Martí E, Casas C, Visa J, Soriano E, Estivill X, Arbonés ML.
Mol Cell Biol. 22(18):6636-47. 2002
67DYRK1A
The kinase DYRK phosphorylates protein-synthesis initiation factor eIF2Bepsilon at Ser539 and the microtubule-associated protein tau at Thr212: potential role for DYRK as a glycogen synthase kinase 3-priming kinase.
Woods YL, Cohen P, Becker W, Jakes R, Goedert M, Wang X, Proud CG.
Biochem J 355(Pt 3):609-15. 2001
68DYRK1A
The kinase DYRK1A phosphorylates the transcription factor FKHR at Ser329 in vitro, a novel in vivo phosphorylation site.
Woods YL, Rena G, Morrice N, Barthel A, Becker W, Guo S, Unterman TG, Cohen P.
Biochem J 355(Pt 3):597-607. 2001
69DYRK1A
Neurodevelopmental delay, motor abnormalities and cognitive deficits in transgenic mice overexpressing Dyrk1A (minibrain), a murine model of Down's syndrome.
Altafaj X, Dierssen M, Baamonde C, Martí E, Visa J, Guimerà J, Oset M, González JR, Flórez J, Fillat C, Estivill X.
Hum Mol Genet. 10(18):1915-23. 2001
70DYRK1A, TRI21
Human minibrain homologue (MNBH/DYRK1): characterization, alternative splicing, differential tissue expression, and overexpression in down syndrome.
Guimera J, et al.
Genomics 57(3):407-18. 1999
71DYRK1A
High level expression of the MNB/DYRK gene in brain and heart during rat early development
Ito F, Okui M, Funakoshi E, Morita K, Ogita K, Yoneda T, Ide T, Kudoh J, Shimizu N.
Cytogenet Cell Genet 86:17 1999
72DYRK1A, EHD1, EMX1, EYA3, JAG2, UBE3A, USP9Y
The embryonic expression pattern of 40 murine cDNAs homologous to Drosophila mutant genes (Dres) : a comparative and topographic approach to predict gene function.
Bulfone A, et al.
Hum Mol Genet 7 : 1997-2006. 1998
73DYRK1A, DYRK2, DYRK3, DYRK4
Sequence characteristics, subcellular localization, and substrate specificity of DYRK-related kinases, a novel family of dual specificity protein kinases.
Becker W, et al.
J Biol Chem 273 : 25893-25902. 1998
74DYRK1A
Identification of two novel 5' noncoding exons in human MNB/DYRK gene and alternatively spliced transcripts.
Wang J, et al.
Biochem Biophys Res Commun 250 : 704-710. 1998
75DYRK1A
Localisation of a human homologue of the Drosophila mnb and rat Dyrk genes to chromosome 21q22.2.
Chen H, et al.
Hum Genet 99 : 262-265. 1997
76DYRK1A, HLCS, KCNJ6, TTC1
Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21.
Ohira M, et al.
Genome Res 7 : 47-58. 1997
77DYRK1A, TRI21
Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome.
Smith DJ, et al.
Nat Genet 16 : 28-36. 1997
78DYRK1A
Minibrain (MNBH) is a single copy gene mapping to human chromosome 21q22.2.
Guimera J, Pritchard M, Nadal M, Estivill X.
Cytogenet Cell Genet 77(3-4):182-4. 1997
79DYRK1A, RCAN1
Genomic organization, alternative splicing, and expression patterns of the DSCR1 (Down syndrome candidate region 1) gene.
Fuentes JJ, Pritchard MA, Estivill X.
Genomics 44(3):358-61. 1997
80TTC3, RCAN1, DYRK1A, KCNJ6
Cosmid contig and transcriptional map of three regions of human chromosome 21q22: identification of 37 novel transcripts by direct selection.
Guimera J, Pucharcos C, Domenech A, Casas C, Solans A, Gallardo T, Ashley J, Lovett M, Estivill X, Pritchard M.
Genomics 45(1):59-67. 1997
81DYRK1A, TRI21
A human homologue of Drosophila minibrain (MNB) is expressed in the neuronal regions affected in Down syndrome and maps to the critical region.
Guimera J, et al.
Hum Mol Genet 5 : 1305-1310. 1996
82DYRK1A
Isolation of human and murine homologues of the Drosophila minibrain gene : human homologue maps to 21q22.2 in the Down syndrome critical region.
Song WJ, et al.
Genomics 38 : 331-339. 1996
83DYRK1A
Cloning of a human homolog of the Drosophila minibrain/rat dyrk gene from the Down syndrome critical region of chromosome 21.
Shindoh N, et al.
Biochem Biophys Res Commun 225 : 92-99. 1996