These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 19023603)

  • 1. An interrupted beta-propeller and protein disorder: structural bioinformatics insights into the N-terminus of alsin.
    Soares DC; Barlow PN; Porteous DJ; Devon RS
    J Mol Model; 2009 Feb; 15(2):113-22. PubMed ID: 19023603
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function.
    Panzeri C; De Palma C; Martinuzzi A; Daga A; De Polo G; Bresolin N; Miller CC; Tudor EL; Clementi E; Bassi MT
    Brain; 2006 Jul; 129(Pt 7):1710-9. PubMed ID: 16670179
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular and cellular function of ALS2/alsin: implication of membrane dynamics in neuronal development and degeneration.
    Hadano S; Kunita R; Otomo A; Suzuki-Utsunomiya K; Ikeda JE
    Neurochem Int; 2007; 51(2-4):74-84. PubMed ID: 17566607
    [TBL] [Abstract][Full Text] [Related]  

  • 4. RCC1-like repeat proteins: a pangenomic, structurally diverse new superfamily of beta-propeller domains.
    Stevens TJ; Paoli M
    Proteins; 2008 Feb; 70(2):378-87. PubMed ID: 17680689
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The 1.7 A crystal structure of the regulator of chromosome condensation (RCC1) reveals a seven-bladed propeller.
    Renault L; Nassar N; Vetter I; Becker J; Klebe C; Roth M; Wittinghofer A
    Nature; 1998 Mar; 392(6671):97-101. PubMed ID: 9510255
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Model of the ran-RCC1 interaction using biochemical and docking experiments.
    Azuma Y; Renault L; García-Ranea JA; Valencia A; Nishimoto T; Wittinghofer A
    J Mol Biol; 1999 Jun; 289(4):1119-30. PubMed ID: 10369786
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The RCC1 superfamily: from genes, to function, to disease.
    Hadjebi O; Casas-Terradellas E; Garcia-Gonzalo FR; Rosa JL
    Biochim Biophys Acta; 2008 Aug; 1783(8):1467-79. PubMed ID: 18442486
    [TBL] [Abstract][Full Text] [Related]  

  • 8. C-terminal domain of gyrase A is predicted to have a beta-propeller structure.
    Qi Y; Pei J; Grishin NV
    Proteins; 2002 May; 47(3):258-64. PubMed ID: 11948780
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Structural basis for guanine nucleotide exchange on Ran by the regulator of chromosome condensation (RCC1).
    Renault L; Kuhlmann J; Henkel A; Wittinghofer A
    Cell; 2001 Apr; 105(2):245-55. PubMed ID: 11336674
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alsin and the molecular pathways of amyotrophic lateral sclerosis.
    Chandran J; Ding J; Cai H
    Mol Neurobiol; 2007 Dec; 36(3):224-31. PubMed ID: 17955197
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Three-dimensional context rather than NLS amino acid sequence determines importin α subtype specificity for RCC1.
    Sankhala RS; Lokareddy RK; Begum S; Pumroy RA; Gillilan RE; Cingolani G
    Nat Commun; 2017 Oct; 8(1):979. PubMed ID: 29042532
    [TBL] [Abstract][Full Text] [Related]  

  • 12. p619, a giant protein related to the chromosome condensation regulator RCC1, stimulates guanine nucleotide exchange on ARF1 and Rab proteins.
    Rosa JL; Casaroli-Marano RP; Buckler AJ; Vilaró S; Barbacid M
    EMBO J; 1996 Aug; 15(16):4262-73. PubMed ID: 8861955
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel missense mutation in ALS2 gene results in infantile ascending hereditary spastic paralysis.
    Eymard-Pierre E; Yamanaka K; Haeussler M; Kress W; Gauthier-Barichard F; Combes P; Cleveland DW; Boespflug-Tanguy O
    Ann Neurol; 2006 Jun; 59(6):976-80. PubMed ID: 16718699
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Crystal structure of human WBSCR16, an RCC1-like protein in mitochondria.
    Koyama M; Sasaki T; Sasaki N; Matsuura Y
    Protein Sci; 2017 Sep; 26(9):1870-1877. PubMed ID: 28608466
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Altered oligomeric states in pathogenic ALS2 variants associated with juvenile motor neuron diseases cause loss of ALS2-mediated endosomal function.
    Sato K; Otomo A; Ueda MT; Hiratsuka Y; Suzuki-Utsunomiya K; Sugiyama J; Murakoshi S; Mitsui S; Ono S; Nakagawa S; Shang HF; Hadano S
    J Biol Chem; 2018 Nov; 293(44):17135-17153. PubMed ID: 30224357
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The N-terminal intrinsically disordered region mediates intracellular localization and self-oligomerization of ALS2.
    Shimakura K; Sato K; Mitsui S; Ono S; Otomo A; Hadano S
    Biochem Biophys Res Commun; 2021 Sep; 569():106-111. PubMed ID: 34243065
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alsin is a Rab5 and Rac1 guanine nucleotide exchange factor.
    Topp JD; Gray NW; Gerard RD; Horazdovsky BF
    J Biol Chem; 2004 Jun; 279(23):24612-23. PubMed ID: 15033976
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alsin, the product of ALS2 gene, suppresses SOD1 mutant neurotoxicity through RhoGEF domain by interacting with SOD1 mutants.
    Kanekura K; Hashimoto Y; Niikura T; Aiso S; Matsuoka M; Nishimoto I
    J Biol Chem; 2004 Apr; 279(18):19247-56. PubMed ID: 14970233
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ALS2/alsin knockout mice and motor neuron diseases.
    Cai H; Shim H; Lai C; Xie C; Lin X; Yang WJ; Chandran J
    Neurodegener Dis; 2008; 5(6):359-66. PubMed ID: 18714162
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T.
    Wakil SM; Ramzan K; Abuthuraya R; Hagos S; Al-Dossari H; Al-Omar R; Murad H; Chedrawi A; Al-Hassnan ZN; Finsterer J; Bohlega S
    Gene; 2014 Feb; 536(1):217-20. PubMed ID: 24315819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.