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1 to 25 of 25  Show
  1. 1
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Gerhard D.S., Wagner L., Feingold E.A., Shenmen C.M., Grouse L.H., Schuler G., Klein S.L., Old S., Rasooly R., Good P., Guyer M., Peck A.M., Derge J.G., Lipman D., Collins F.S., Jang W., Sherry S., Feolo M.
    Malek J.
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
    Category: Sequences.
    Strain: FVB/N.
    Tissue: Mammary tumor. C3.
    Source: UniProtKB/TrEMBL (unreviewed).

    This publication is cited by 50448 other entries.

  2. 2
    Category: Sequences.
    Source: MGI:1922022.

    This publication is cited by 16981 and mapped to 30126 other entries.

  3. 3
    Category: Pathology & Biotech.
    Source: MGI:1922022.

    This publication is mapped to 39464 other entries.

  4. 4
    Category: Sequences.
    Source: MGI:1922022.

    This publication is cited by 2 and mapped to 17 other entries.

  5. 5
    "The transcriptional landscape of the mammalian genome."
    Carninci P., Kasukawa T., Katayama S., Gough J., Frith M.C., Maeda N., Oyama R., Ravasi T., Lenhard B., Wells C., Kodzius R., Shimokawa K., Bajic V.B., Brenner S.E., Batalov S., Forrest A.R., Zavolan M., Davis M.J.
    Hayashizaki Y.
    Science 309:1559-1563(2005) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Source: MGI:1922022.

    This publication is cited by 10625 and mapped to 43846 other entries.

  6. 6
    "Novel genes differentially expressed in cortical regions during late neurogenesis."
    Muhlfriedel S., Kirsch F., Gruss P., Chowdhury K., Stoykova A.
    Eur. J. Neurosci. 26:33-50(2007) [PubMed] [Europe PMC] [Abstract]
    Category: Expression, Sequences.
    Source: MGI:1922022.

    This publication is mapped to 87 other entries.

  7. 7
    Category: Expression.
    Source: MGI:1922022.

    This publication is mapped to 50335 other entries.

  8. 8
    "DLK1 is a novel regulator of bone mass that mediates estrogen deficiency-induced bone loss in mice."
    Abdallah B.M., Ditzel N., Mahmood A., Isa A., Traustadottir G.A., Schilling A.F., Ruiz-Hidalgo M.J., Laborda J., Amling M., Kassem M.
    J. Bone Miner. Res. 26:1457-1471(2011) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Source: MGI:1922022.

    This publication is mapped to 634 other entries.

  9. 9
    Category: Function, Pathology & Biotech.
    Source: MGI:1922022.

    This publication is mapped to 34882 other entries.

  10. 10
    "Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."
    Gaudet P., Livstone M.S., Lewis S.E., Thomas P.D.
    Brief. Bioinformatics 12:449-462(2011) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:1922022.

    This publication is mapped to 57460 other entries.

  11. 11
    "PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity."
    Ramonet D., Podhajska A., Stafa K., Sonnay S., Trancikova A., Tsika E., Pletnikova O., Troncoso J.C., Glauser L., Moore D.J.
    Hum. Mol. Genet. 21:1725-1743(2012) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Annotation: study reveals a number of intriguing neuronal phenotypes due to the loss- or gain-of-function of ATP13A2 that support a role for this protein in regulating intracellular cation homeostasis and neuronal integrity. [GeneRIF:74772].
    Source: GeneRIF:74772, MGI:1922022.

    This publication is mapped to 9 other entries.

  12. 12
    "ATP13A2 regulates mitochondrial bioenergetics through macroautophagy."
    Gusdon A.M., Zhu J., Van Houten B., Chu C.T.
    Neurobiol. Dis. 45:962-972(2012) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: This study showed that ATP13A2 regulates mitochondrial bioenergetics through macroautophagy. [GeneRIF:74772].
    Source: GeneRIF:74772, MGI:1922022.

    This publication is mapped to 3 other entries.

  13. 13
    "Deficiency of ATP13A2 leads to lysosomal dysfunction, alpha-synuclein accumulation, and neurotoxicity."
    Usenovic M., Tresse E., Mazzulli J.R., Taylor J.P., Krainc D.
    J. Neurosci. 32:4240-4246(2012) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Source: MGI:1922022.

    This publication is mapped to 7 other entries.

  14. 14
    Category: Function.
    Annotation: the loss of Atp13a2 causes sensorimotor impairments alpha-synuclein accumulation as occurs in PD and related synucleinopathies and accumulation of lipofuscin deposits characteristic of NCL. [GeneRIF:74772].
    Source: GeneRIF:74772, MGI:1922022.

    This publication is mapped to 4 other entries.

  15. 15
    Category: Function, Pathology & Biotech.
    Source: MGI:1922022.

    This publication is mapped to 4327 other entries.

  16. 16
    "Zn^2⁺ dyshomeostasis caused by loss of ATP13A2/PARK9 leads to lysosomal dysfunction and alpha-synuclein accumulation."
    Tsunemi T., Krainc D.
    Hum. Mol. Genet. 23:2791-2801(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Source: MGI:1922022.

    This publication is mapped to 15 other entries.

  17. 17
    "ATP13A2/PARK9 regulates secretion of exosomes and alpha-synuclein."
    Tsunemi T., Hamada K., Krainc D.
    J. Neurosci. 34:15281-15287(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Source: MGI:1922022.

    This publication is mapped to 16 other entries.

  18. 18
    "alpha-Synuclein-independent histopathological and motor deficits in mice lacking the endolysosomal Parkinsonism protein Atp13a2."
    Kett L.R., Stiller B., Bernath M.M., Tasset I., Blesa J., Jackson-Lewis V., Chan R.B., Zhou B., Di Paolo G., Przedborski S., Cuervo A.M., Dauer W.T.
    J. Neurosci. 35:5724-5742(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Source: MGI:1922022.

    This publication is mapped to 8 other entries.

  19. 19
    "The Parkinson's disease-associated genes ATP13A2 and SYT11 regulate autophagy via a common pathway."
    Bento C.F., Ashkenazi A., Jimenez-Sanchez M., Rubinsztein D.C.
    Nat. Commun. 7:11803-11803(2016) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:1922022.

    This publication is cited by 7 and mapped to 26 other entries.

  20. 20
    "Endolysosomal dysfunction in Parkinson's disease: Recent developments and future challenges."
    Kett L.R., Dauer W.T.
    Mov. Disord. 31:1433-1443(2016) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Source: MGI:1922022.

    This publication is mapped to 3 other entries.

  21. 21
    "Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient Mice."
    Sato S., Koike M., Funayama M., Ezaki J., Fukuda T., Ueno T., Uchiyama Y., Hattori N.
    Am. J. Pathol. 186:3074-3082(2016) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Source: MGI:1922022.

    This publication is mapped to 3 other entries.

  22. 22
    Category: Function, Pathology & Biotech, Expression.
    Annotation: Study shows for the first time in vivo that loss of function of ATP13A2 causes an increased sensitivity to manganese.
    Source: GeneRIF:74772.

    This publication is mapped to 2 other entries.

  23. 23
    "Exacerbation of sensorimotor dysfunction in mice deficient in Atp13a2 and overexpressing human wildtype alpha-synuclein."
    Dirr E.R., Ekhator O.R., Blackwood R., Holden J.G., Masliah E., Schultheis P.J., Fleming S.M.
    Behav. Brain Res. 343:41-49(2018) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Source: MGI:1922022.

    This publication is mapped to 14 other entries.

  24. 24
    "Partial loss of ATP13A2 causes selective gliosis independent of robust lipofuscinosis."
    Rayaprolu S., Seven Y.B., Howard J., Duffy C., Altshuler M., Moloney C., Giasson B.I., Lewis J.
    Mol. Cell. Neurosci. 92:17-26(2018) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: Loss of one functional Atp13a2 allele leads to selective gliosis independent of robust lipofuscinosis. [GeneRIF:74772].
    Source: GeneRIF:74772, MGI:1922022.

    This publication is mapped to 3 other entries.

  25. 25
    "ATP13A2 facilitates HDAC6 recruitment to lysosome to promote autophagosome-lysosome fusion."
    Wang R., Tan J., Chen T., Han H., Tian R., Tan Y., Wu Y., Cui J., Chen F., Li J., Lv L., Guan X., Shang S., Lu J., Zhang Z.
    J. Cell Biol. 218:267-284(2019) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Source: MGI:1922022.

    This publication is mapped to 23 other entries.

1 to 25 of 25  Show
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