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1 to 25 of 28  Show
  1. 1
    "The t(3;5)(q25.1;q34) of myelodysplastic syndrome and acute myeloid leukemia produces a novel fusion gene, NPM-MLF1."
    Yoneda-Kato N., Look A.T., Kirstein M.N., Valentine M.B., Raimondi S.C., Cohen K.J., Carroll A.J., Morris S.W.
    Oncogene 12:265-275(1996) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), CHROMOSOMAL TRANSLOCATION.
    Category: Pathology & Biotech, Sequences.
    Tissue: Skeletal muscle and Testis.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  2. 2
    Feng X., Ling S., Zhang H., Song X., Wang G., Chen K., Zhu C.
    Submitted (DEC-2004) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 2 AND 5).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  3. 3
    "Complete sequencing and characterization of 21,243 full-length human cDNAs."
    Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.
    , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
    Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 3; 4 AND 5).
    Category: Sequences.
    Tissue: Brain and Skeletal muscle.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12924 other entries.

  4. 4
    "The DNA sequence, annotation and analysis of human chromosome 3."
    Muzny D.M., Scherer S.E., Kaul R., Wang J., Yu J., Sudbrak R., Buhay C.J., Chen R., Cree A., Ding Y., Dugan-Rocha S., Gill R., Gunaratne P., Harris R.A., Hawes A.C., Hernandez J., Hodgson A.V., Hume J.
    , Jackson A., Khan Z.M., Kovar-Smith C., Lewis L.R., Lozado R.J., Metzker M.L., Milosavljevic A., Miner G.R., Morgan M.B., Nazareth L.V., Scott G., Sodergren E., Song X.-Z., Steffen D., Wei S., Wheeler D.A., Wright M.W., Worley K.C., Yuan Y., Zhang Z., Adams C.Q., Ansari-Lari M.A., Ayele M., Brown M.J., Chen G., Chen Z., Clendenning J., Clerc-Blankenburg K.P., Chen R., Chen Z., Davis C., Delgado O., Dinh H.H., Dong W., Draper H., Ernst S., Fu G., Gonzalez-Garay M.L., Garcia D.K., Gillett W., Gu J., Hao B., Haugen E., Havlak P., He X., Hennig S., Hu S., Huang W., Jackson L.R., Jacob L.S., Kelly S.H., Kube M., Levy R., Li Z., Liu B., Liu J., Liu W., Lu J., Maheshwari M., Nguyen B.-V., Okwuonu G.O., Palmeiri A., Pasternak S., Perez L.M., Phelps K.A., Plopper F.J., Qiang B., Raymond C., Rodriguez R., Saenphimmachak C., Santibanez J., Shen H., Shen Y., Subramanian S., Tabor P.E., Verduzco D., Waldron L., Wang J., Wang J., Wang Q., Williams G.A., Wong G.K.-S., Yao Z., Zhang J., Zhang X., Zhao G., Zhou J., Zhou Y., Nelson D., Lehrach H., Reinhardt R., Naylor S.L., Yang H., Olson M., Weinstock G., Gibbs R.A.
    Nature 440:1194-1198(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3693 other entries.

  5. 5
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  6. 6
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
    Category: Sequences.
    Tissue: Urinary bladder.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50492 other entries.

  7. 7
    "cDNA cloning and characterization of a novel gene encoding the MLF1-interacting protein MLF1IP."
    Hanissian S.H., Akbar U., Teng B., Janjetovic Z., Hoffmann A., Hitzler J.K., Iscove N., Hamre K., Du X., Tong Y., Mukatira S., Robertson J.H., Morris S.W.
    Oncogene 23:3700-3707(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: INTERACTION WITH CENPU.
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 and mapped to 10 other entries.

  8. 8
    "Myeloid leukemia factor 1 regulates p53 by suppressing COP1 via COP9 signalosome subunit 3."
    Yoneda-Kato N., Tomoda K., Umehara M., Arata Y., Kato J.-Y.
    EMBO J. 24:1739-1749(2005) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, INTERACTION WITH COPS3.
    Category: Function, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).
  9. 9
    "Toward a comprehensive characterization of a human cancer cell phosphoproteome."
    Zhou H., Di Palma S., Preisinger C., Peng M., Polat A.N., Heck A.J., Mohammed S.
    J. Proteome Res. 12:260-271(2013) [PubMed] [Europe PMC] [Abstract]
    Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-8 AND SER-32, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: PTM / Processing, Sequences.
    Tissue: Erythroleukemia.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12975 other entries.

  10. 10
    "Structural insights of the MLF1/14-3-3 interaction."
    Molzan M., Weyand M., Rose R., Ottmann C.
    FEBS J. 279:563-571(2012) [PubMed] [Europe PMC] [Abstract]
    Cited for: X-RAY CRYSTALLOGRAPHY (1.8 ANGSTROMS) OF 29-42 IN COMPLEX WITH YWHAE, PHOSPHORYLATION AT SER-34.
    Category: PTM / Processing, Interaction, Structure.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 12 other entries.

  11. 11
    "MADM, a novel adaptor protein that mediates phosphorylation of the 14-3-3 binding site of myeloid leukemia factor 1."
    Lim R., Winteringham L.N., Williams J.H., McCulloch R.K., Ingley E., Tiao J.Y.-H., Lalonde J.-P., Tsai S., Tilbrook P.A., Sun Y., Wu X., Morris S.W., Klinken S.P.
    J. Biol. Chem. 277:40997-41008(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Annotation: phosphorylation of 14-3-3 binding site by MADMImported.
    Source: GeneRIF:4291, IntAct:P58340.

    This publication is cited by 3 and mapped to 47 other entries.

  12. 12
    "Detection of NPM/MLF1 fusion in t(3;5)-positive acute myeloid leukemia and myelodysplasia."
    Arber D.A., Chang K.L., Lyda M.H., Bedell V., Spielberger R., Slovak M.L.
    Hum. Pathol. 34:809-813(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: These findings suggest that an NPM/MLF1 fusion is the primary molecular abnormality in t(3;5) MDS and AML with multilineage dysplasia and that cases with NPM/MLF1 may be clinically distinct from other MDS-associated diseaseImported.
    Source: GeneRIF:4291.

    This publication is mapped to 15 other entries.

  13. 13
    Category: Interaction.
    Source: IntAct:P58340.

    This publication is mapped to 1658 other entries.

  14. 14
    Category: Interaction.
    Source: IntAct:P58340.

    This publication is mapped to 1506 other entries.

  15. 15
    "Non-pathogenic protein aggregates in skeletal muscle in MLF1 transgenic mice."
    Li Z.F., Wu X., Jiang Y., Liu J., Wu C., Inagaki M., Izawa I., Mizisin A.P., Engvall E., Shelton G.D.
    J. Neurol. Sci. 264:77-86(2008) [PubMed] [Europe PMC] [Abstract]
    Annotation: Over-expression of MLF1 has little impact on skeletal muscle function in mice; progressive formation of protein aggregates in muscle are not necessarily pathogenic; MLF1 and MRJ may function together to ameliorate the toxic effects of mutant proteins.Imported.
    Source: GeneRIF:4291.

    This publication is mapped to 11 other entries.

  16. 16
    "Shuttling imbalance of MLF1 results in p53 instability and increases susceptibility to oncogenic transformation."
    Yoneda-Kato N., Kato J.Y.
    Mol. Cell. Biol. 28:422-434(2008) [PubMed] [Europe PMC] [Abstract]
    Annotation: shuttling of MLF1 is critical for the regulation of cell proliferation and a disturbance in the shuttling balance increases the cell's susceptibility to oncogenic transformationImported.
    Source: GeneRIF:4291.

    This publication is mapped to 31 other entries.

  17. 17
    "Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study."
    Shiffman D., O'Meara E.S., Bare L.A., Rowland C.M., Louie J.Z., Arellano A.R., Lumley T., Rice K., Iakoubova O., Luke M.M., Young B.A., Malloy M.J., Kane J.P., Ellis S.G., Tracy R.P., Devlin J.J., Psaty B.M.
    Arterioscler. Thromb. Vasc. Biol. 28:173-179(2008) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:4291.

    This publication is mapped to 219 other entries.

  18. 18
    "Gene variants associated with ischemic stroke: the cardiovascular health study."
    Luke M.M., O'Meara E.S., Rowland C.M., Shiffman D., Bare L.A., Arellano A.R., Longstreth W.T. Jr., Lumley T., Rice K., Tracy R.P., Devlin J.J., Psaty B.M.
    Stroke 40:363-368(2009) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:4291.

    This publication is mapped to 214 other entries.

  19. 19
    "Detection of t(3;5) and NPM1/MLF1 rearrangement in an elderly patient with acute myeloid leukemia: clinical and laboratory study with review of the literature."
    Lim G., Choi J.R., Kim M.J., Kim S.Y., Lee H.J., Suh J.T., Yoon H.J., Lee J., Lee S., Lee W.I., Park T.S.
    Cancer Genet. Cytogenet. 199:101-109(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: MLF1 gene rearrangement is associated with acute myeloid leukemia.Imported.
    Source: GeneRIF:4291.

    This publication is mapped to 15 other entries.

  20. 20
    "NPM-MLF1 synergizes with Npm haploinsufficiency to enhance myeloid progenitor activity."
    Lee W.H., Salek-Ardakani S., Pandolfi P.P., Brady H.J., de Boer J., Williams O.
    Leukemia 26:1110-1112(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: changes in the subcellular localization of NPM due to alterations in the relative abundance of NPM and NPM-MLF1 proteins may contribute to the enhanced myeloid progenitor activity of Npm +/- cellsImported.
    Source: GeneRIF:4291.

    This publication is mapped to 15 other entries.

  21. 21
    "Subcellular localization of full-length human myeloid leukemia factor 1 (MLF1) is independent of 14-3-3 proteins."
    Molzan M., Ottmann C.
    Cell. Mol. Biol. Lett. 18:137-148(2013) [PubMed] [Europe PMC] [Abstract]
    Annotation: The subcellular localization of full-length human MLF1 is 14-3-3epsilon-independent.Imported.
    Source: GeneRIF:4291.

    This publication is mapped to 7 other entries.

  22. 22
    "Acute myeloid leukemia with translocation t(3;5): new molecular insights."
    Dumezy F., Renneville A., Mayeur-Rousse C., Nibourel O., Labis E., Preudhomme C.
    Haematologica 98:e52-4(2013) [PubMed] [Europe PMC] [Abstract]
    Annotation: Data indicte that acute myeloid leukemia (AML) with NPM1-MLF1 and AML with NPM1 mutations showed similar immunophenotypical and molecular features including gene mutation patterns and gene expression profiling (GEP).Imported.
    Source: GeneRIF:4291.

    This publication is mapped to 15 other entries.

  23. 23
    "A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactome."
    Blandin G., Marchand S., Charton K., Daniele N., Gicquel E., Boucheteil J.B., Bentaib A., Barrault L., Stockholm D., Bartoli M., Richard I.
    Skelet Muscle 3:3-3(2013) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:P58340.

    This publication is mapped to 498 other entries.

  24. 24
    "A quantitative chaperone interaction network reveals the architecture of cellular protein homeostasis pathways."
    Taipale M., Tucker G., Peng J., Krykbaeva I., Lin Z.Y., Larsen B., Choi H., Berger B., Gingras A.C., Lindquist S.
    Cell 158:434-448(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:P58340.

    This publication is mapped to 689 other entries.

  25. 25
    "Modulation of mutant Huntingtin aggregates and toxicity by human myeloid leukemia factors."
    Banerjee M., Datta M., Bhattacharyya N.P.
    Int. J. Biochem. Cell Biol. 82:1-9(2017) [PubMed] [Europe PMC] [Abstract]
    Annotation: Mutation in HTT causes Huntington's disease (HD); aggregates of mutated HTT cause apoptosis in neurons of HD patients. Data suggest that both MLF1 and MLF2 preferentially interact with mutated N-terminal HTT; MLF1/MLF2 reduce number of neurons (Neuro2A cell line) containing mutant HTT aggregates and subsequent apoptosis. (HTT = Huntingtin protein; MLF = myeloid leukemia factor)Imported.
    Source: GeneRIF:4291.

    This publication is mapped to 10 other entries.

1 to 25 of 28  Show