BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 15045646)

  • 1. Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patients.
    Couillard-Despres S; Uyanik G; Ploetz S; Karl C; Koch H; Winkler J; Aigner L
    Neurogenetics; 2004 Jun; 5(2):83-93. PubMed ID: 15045646
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.
    Tsai MH; Kuo PW; Myers CT; Li SW; Lin WC; Fu TY; Chang HY; Mefford HC; Chang YC; Tsai JW
    Eur J Paediatr Neurol; 2016 Sep; 20(5):788-94. PubMed ID: 27292316
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Different Doublecortin (DCX) Patient Alleles Show Distinct Phenotypes in Cultured Neurons: EVIDENCE FOR DIVERGENT LOSS-OF-FUNCTION AND "OFF-PATHWAY" CELLULAR MECHANISMS.
    Yap CC; Digilio L; McMahon L; Roszkowska M; Bott CJ; Kruczek K; Winckler B
    J Biol Chem; 2016 Dec; 291(52):26613-26626. PubMed ID: 27799303
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Colocalization of doublecortin with the microtubules: an ex vivo colocalization study of mutant doublecortin.
    Yoshiura K; Noda Y; Kinoshita A; Niikawa N
    J Neurobiol; 2000 May; 43(2):132-9. PubMed ID: 10770842
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structural studies of the doublecortin family of MAPs.
    Fourniol F; Perderiset M; Houdusse A; Moores C
    Methods Cell Biol; 2013; 115():27-48. PubMed ID: 23973064
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pathogenic E2K mutation of doublecortin X (DCX) alters microtubule stabilisation and actin filament association.
    Moslehi M; Ng DCH; Bogoyevitch MA
    Biochem Biophys Res Commun; 2019 Jun; 513(3):540-545. PubMed ID: 30979500
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.
    Bahi-Buisson N; Souville I; Fourniol FJ; Toussaint A; Moores CA; Houdusse A; Lemaitre JY; Poirier K; Khalaf-Nazzal R; Hully M; Leger PL; Elie C; Boddaert N; Beldjord C; Chelly J; Francis F;
    Brain; 2013 Jan; 136(Pt 1):223-44. PubMed ID: 23365099
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.
    D'Agostino MD; Bernasconi A; Das S; Bastos A; Valerio RM; Palmini A; Costa da Costa J; Scheffer IE; Berkovic S; Guerrini R; Dravet C; Ono J; Gigli G; Federico A; Booth F; Bernardi B; Volpi L; Tassinari CA; Guggenheim MA; Ledbetter DH; Gleeson JG; Lopes-Cendes I; Vossler DG; Malaspina E; Franzoni E; Sartori RJ; Mitchell MH; Mercho S; Dubeau F; Andermann F; Dobyns WB; Andermann E
    Brain; 2002 Nov; 125(Pt 11):2507-22. PubMed ID: 12390976
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration.
    Tanaka T; Serneo FF; Higgins C; Gambello MJ; Wynshaw-Boris A; Gleeson JG
    J Cell Biol; 2004 Jun; 165(5):709-21. PubMed ID: 15173193
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Antagonistic effects of doublecortin and MARK2/Par-1 in the developing cerebral cortex.
    Sapir T; Shmueli A; Levy T; Timm T; Elbaum M; Mandelkow EM; Reiner O
    J Neurosci; 2008 Nov; 28(48):13008-13. PubMed ID: 19036994
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Doublecortin recognizes the 13-protofilament microtubule cooperatively and tracks microtubule ends.
    Bechstedt S; Brouhard GJ
    Dev Cell; 2012 Jul; 23(1):181-92. PubMed ID: 22727374
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Doublecortin mutations cluster in evolutionarily conserved functional domains.
    Sapir T; Horesh D; Caspi M; Atlas R; Burgess HA; Wolf SG; Francis F; Chelly J; Elbaum M; Pietrokovski S; Reiner O
    Hum Mol Genet; 2000 Mar; 9(5):703-12. PubMed ID: 10749977
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect.
    Yap CC; Digilio L; Kruczek K; Roszkowska M; Fu XQ; Liu JS; Winckler B
    J Biol Chem; 2018 Dec; 293(49):18890-18902. PubMed ID: 30291144
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DCAMKL1 encodes a protein kinase with homology to doublecortin that regulates microtubule polymerization.
    Lin PT; Gleeson JG; Corbo JC; Flanagan L; Walsh CA
    J Neurosci; 2000 Dec; 20(24):9152-61. PubMed ID: 11124993
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phosphorylation of doublecortin by protein kinase A orchestrates microtubule and actin dynamics to promote neuronal progenitor cell migration.
    Toriyama M; Mizuno N; Fukami T; Iguchi T; Toriyama M; Tago K; Itoh H
    J Biol Chem; 2012 Apr; 287(16):12691-702. PubMed ID: 22367209
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes.
    Friocourt G; Kappeler C; Saillour Y; Fauchereau F; Rodriguez MS; Bahi N; Vinet MC; Chafey P; Poirier K; Taya S; Wood SA; Dargemont C; Francis F; Chelly J
    Mol Cell Neurosci; 2005 Jan; 28(1):153-64. PubMed ID: 15607950
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel DCX mutation-caused lissencephaly in a boy and very mild heterotopia in his mother.
    Takeshita S; Higuchi M; Suyama M; Koide W; Maki K; Ushijima K; Ban K; Saito M; Kato M; Saitoh S
    Pediatr Int; 2015 Apr; 57(2):321-3. PubMed ID: 25868952
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Doublecortin-like kinase is associated with microtubules in neuronal growth cones.
    Burgess HA; Reiner O
    Mol Cell Neurosci; 2000 Nov; 16(5):529-41. PubMed ID: 11083916
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons.
    Gleeson JG; Lin PT; Flanagan LA; Walsh CA
    Neuron; 1999 Jun; 23(2):257-71. PubMed ID: 10399933
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The location of DCX mutations predicts malformation severity in X-linked lissencephaly.
    Leger PL; Souville I; Boddaert N; Elie C; Pinard JM; Plouin P; Moutard ML; des Portes V; Van Esch H; Joriot S; Renard JL; Chelly J; Francis F; Beldjord C; Bahi-Buisson N
    Neurogenetics; 2008 Oct; 9(4):277-85. PubMed ID: 18685874
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.