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1 to 25 of 118  Show
  1. 1
    "Isolation of human and murine homologues of the Drosophila minibrain gene: human homologue maps to 21q22.2 in the Down syndrome 'critical region'."
    Song W.J., Sternberg L.R., Kasten-Sportes C., van Keuren M.L., Chung S.H., Slack A.C., Miller D.E., Glover T.W., Chiang P.W., Lou L., Kurnit D.W.
    Genomics 38:331-339(1996) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY.
    Category: Expression, Sequences.
    Strain: Swiss Webster / NIH.
    Tissue: Embryo.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 8 other entries.

  2. 2
    "The murine Dyrk protein maps to chromosome 16, localizes to the nucleus, and can form multimers."
    Song W.J., Chung S.H., Kurnit D.M.
    Biochem. Biophys. Res. Commun. 231:640-644(1997) [PubMed] [Europe PMC] [Abstract]
    Cited for: SUBCELLULAR LOCATION, SUBUNIT.
    Category: Subcellular Location, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 27 other entries.

  3. 3
    "Dyrk1A potentiates steroid hormone-induced transcription via the chromatin remodeling factor Arip4."
    Sitz J.H., Tigges M., Baumgaertel K., Khaspekov L.G., Lutz B.
    Mol. Cell. Biol. 24:5821-5834(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: INTERACTION WITH RAD54L2.
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 and mapped to 26 other entries.

  4. 4
    "Large-scale identification and evolution indexing of tyrosine phosphorylation sites from murine brain."
    Ballif B.A., Carey G.R., Sunyaev S.R., Gygi S.P.
    J. Proteome Res. 7:311-318(2008) [PubMed] [Europe PMC] [Abstract]
    Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT TYR-145, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: PTM / Processing, Sequences.
    Tissue: Brain.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 529 other entries.

  5. 5
    Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-538; SER-748 AND SER-758, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: PTM / Processing, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 25331 other entries.

  6. 6
    "DYRK1A and DYRK3 promote cell survival through phosphorylation and activation of SIRT1."
    Guo X., Williams J.G., Schug T.T., Li X.
    J. Biol. Chem. 285:13223-13232(2010) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, INTERACTION WITH SIRT1, CATALYTIC ACTIVITY.
    Category: Function, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 6 and mapped to 19 other entries.

  7. 7
    "DYRK1A and glycogen synthase kinase 3beta, a dual-kinase mechanism directing proteasomal degradation of CRY2 for circadian timekeeping."
    Kurabayashi N., Hirota T., Sakai M., Sanada K., Fukada Y.
    Mol. Cell. Biol. 30:1757-1768(2010) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, INTERACTION WITH CRY2.
    Category: Function, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 and mapped to 13 other entries.

  8. 8
    "Selectivity, cocrystal structures, and neuroprotective properties of leucettines, a family of protein kinase inhibitors derived from the marine sponge alkaloid leucettamine B."
    Tahtouh T., Elkins J.M., Filippakopoulos P., Soundararajan M., Burgy G., Durieu E., Cochet C., Schmid R.S., Lo D.C., Delhommel F., Oberholzer A.E., Pearl L.H., Carreaux F., Bazureau J.P., Knapp S., Meijer L.
    J. Med. Chem. 55:9312-9330(2012) [PubMed] [Europe PMC] [Abstract]
    Cited for: TISSUE SPECIFICITY.
    Category: Expression.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 4 and mapped to 2 other entries.

  9. 9
    "Behavioral genetics. Fickle mice highlight test problems."
    Enserink M.
    Science 284:1599-1600(1999) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Source: MGI:1330299.

    This publication is mapped to 11 other entries.

  10. 10
    "Large-scale cDNA analysis reveals phased gene expression patterns during preimplantation mouse development."
    Ko M.S.H., Kitchen J.R., Wang X., Threat T.A., Wang X., Hasegawa A., Sun T., Grahovac M.J., Kargul G.J., Lim M.K., Cui Y., Sano Y., Tanaka T.S., Liang Y., Mason S., Paonessa P.D., Sauls A.D., DePalma G.E.
    Doi H.
    Development 127:1737-1749(2000) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Source: MGI:1330299.

    This publication is mapped to 8625 other entries.

  11. 11
    "mDYRK3 kinase is expressed selectively in late erythroid progenitor cells and attenuates colony-forming unit-erythroid development."
    Geiger J.N., Knudsen G.T., Panek L., Pandit A.K., Yoder M.D., Lord K.A., Creasy C.L., Burns B.M., Gaines P., Dillon S.B., Wojchowski D.M.
    Blood 97:901-910(2001) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Source: MGI:1330299.

    This publication is mapped to 15 other entries.

  12. 12
    Category: Sequences.
    Source: MGI:1330299.

    This publication is cited by 16981 and mapped to 30128 other entries.

  13. 13
    "Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21."
    Pletcher M.T., Wiltshire T., Cabin D.E., Villanueva M., Reeves R.H.
    Genomics 74:45-54(2001) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Source: MGI:1330299.

    This publication is mapped to 184 other entries.

  14. 14
    "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., Marti E., Visa J., Guimera J., Oset M., Gonzalez J.R., Florez J., Fillat C., Estivill X.
    Hum. Mol. Genet. 10:1915-1923(2001) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Source: MGI:1330299.

    This publication is mapped to 9 other entries.

  15. 15
    "Mnb/Dyrk1A is transiently expressed and asymmetrically segregated in neural progenitor cells at the transition to neurogenic divisions."
    Hammerle B., Vera-Samper E., Speicher S., Arencibia R., Martinez S., Tejedor F.J.
    Dev. Biol. 246:259-273(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Expression, Sequences.
    Source: MGI:1330299.

    This publication is mapped to 15 other entries.

  16. 16
    "Regulation of Gli1 transcriptional activity in the nucleus by Dyrk1."
    Mao J., Maye P., Kogerman P., Tejedor F.J., Toftgard R., Xie W., Wu G., Wu D.
    J. Biol. Chem. 277:35156-35161(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Subcellular Location.
    Annotation: Gli1 transcriptional activity may be subjected to further regulation in the cell nucleus by a pathway distinct from Shh signaling one mediated by Dyrk1.
    Source: GeneRIF:13548.

    This publication is mapped to 19 other entries.

  17. 17
    "Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice."
    Fotaki V., Dierssen M., Alcantara S., Martinez S., Marti E., Casas C., Visa J., Soriano E., Estivill X., Arbones M.L.
    Mol. Cell. Biol. 22:6636-6647(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Role of Dyrk1A in brain abnormalities and developmental delay. [GeneRIF:13548].
    Source: MGI:1330299, GeneRIF:13548.

    This publication is mapped to 9 other entries.

  18. 18
    "Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs."
    Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R., Suzuki H., Yamanaka I., Kiyosawa H., Yagi K., Tomaru Y., Hasegawa Y., Nogami A., Schonbach C., Gojobori T.
    Hayashizaki Y.
    Nature 420:563-573(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Source: MGI:1330299.

    This publication is cited by 16984 and mapped to 41263 other entries.

  19. 19
    Category: Expression, Sequences.
    Source: MGI:1330299.

    This publication is mapped to 808 other entries.

  20. 20
    Category: Expression.
    Source: MGI:1330299.

    This publication is mapped to 798 other entries.

  21. 21
    Category: Sequences.
    Source: MGI:1330299.

    This publication is mapped to 18613 other entries.

  22. 22
    "Dyrk1A expression pattern supports specific roles of this kinase in the adult central nervous system."
    Marti E., Altafaj X., Dierssen M., de la Luna S., Fotaki V., Alvarez M., Perez-Riba M., Ferrer I., Estivill X.
    Brain Res. 964:250-263(2003) [PubMed] [Europe PMC] [Abstract]
    Category: Subcellular Location.
    Annotation: Dyrk1A is distributed in widespread areas of the adult CNS and in different subcellular compartments. Considering also previous reports demonstrating the involvement of Dyrk1A in developmental events it is suggested that Dyrk1A has several functions. [GeneRIF:13548].
    Source: MGI:1330299, GeneRIF:13548.

    This publication is mapped to 9 other entries.

  23. 23
    "A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome."
    Hansen J., Floss T., Van Sloun P., Fuchtbauer E.M., Vauti F., Arnold H.H., Schnutgen F., Wurst W., von Melchner H., Ruiz P.
    Proc. Natl. Acad. Sci. U.S.A. 100:9918-9922(2003) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Source: MGI:1330299.

    This publication is mapped to 13828 other entries.

  24. 24
    Category: Pathology & Biotech.
    Source: MGI:1330299.

    This publication is mapped to 39458 other entries.

  25. 25
    "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. 15:132-142(2004) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Transgenic mice present DYRK1A overexpression in brain motor areas along with specific motor dysfunction including impairment of motor learning and alteration of the organization of locomotor behavior. [GeneRIF:13548].
    Source: MGI:1330299, GeneRIF:13548.

    This publication is mapped to 9 other entries.

1 to 25 of 118  Show
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