BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 18514414)

  • 1. Pafah1b2 mutations suppress the development of hydrocephalus in compound Pafah1b1; Reln and Pafah1b1; Dab1 mutant mice.
    Assadi AH; Zhang G; McNeil R; Clark GD; D'Arcangelo G
    Neurosci Lett; 2008 Jul; 439(1):100-5. PubMed ID: 18514414
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Differential interaction of the Pafah1b alpha subunits with the Reelin transducer Dab1.
    Zhang G; Assadi AH; Roceri M; Clark GD; D'Arcangelo G
    Brain Res; 2009 Apr; 1267():1-8. PubMed ID: 19272360
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interaction of reelin signaling and Lis1 in brain development.
    Assadi AH; Zhang G; Beffert U; McNeil RS; Renfro AL; Niu S; Quattrocchi CC; Antalffy BA; Sheldon M; Armstrong DD; Wynshaw-Boris A; Herz J; D'Arcangelo G; Clark GD
    Nat Genet; 2003 Nov; 35(3):270-6. PubMed ID: 14578885
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Pafah1b complex interacts with the reelin receptor VLDLR.
    Zhang G; Assadi AH; McNeil RS; Beffert U; Wynshaw-Boris A; Herz J; Clark GD; D'Arcangelo G
    PLoS One; 2007 Feb; 2(2):e252. PubMed ID: 17330141
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development.
    Sweeney KJ; Clark GD; Prokscha A; Dobyns WB; Eichele G
    Mech Dev; 2000 Apr; 92(2):263-71. PubMed ID: 10727864
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aberrant dentate gyrus cytoarchitecture and fiber lamination in Lis1 mutant mice.
    Wang Y; Baraban SC
    Hippocampus; 2008; 18(8):758-65. PubMed ID: 18446829
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Histological study in the brain of the reelin/Dab1-compound mutant mouse.
    Yamamoto T; Setsu T; Okuyama-Yamamoto A; Terashima T
    Anat Sci Int; 2009 Sep; 84(3):200-9. PubMed ID: 19221860
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Developmental dynamics of PAFAH1B subunits during mouse brain development.
    Escamez T; Bahamonde O; Tabares-Seisdedos R; Vieta E; Martinez S; Echevarria D
    J Comp Neurol; 2012 Dec; 520(17):3877-94. PubMed ID: 22522921
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Migration of sympathetic preganglionic neurons in the spinal cord is regulated by Reelin-dependent Dab1 tyrosine phosphorylation and CrkL.
    Yip YP; Kronstadt-O'Brien P; Capriotti C; Cooper JA; Yip JW
    J Comp Neurol; 2007 Jun; 502(4):635-43. PubMed ID: 17394141
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dab1 (Disable homolog-1) reelin adaptor protein is overexpressed in the olfactory bulb at early postnatal stages.
    Martín-López E; Blanchart A; De Carlos JA; López-Mascaraque L
    PLoS One; 2011; 6(10):e26673. PubMed ID: 22046330
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intersectin 1 is a component of the Reelin pathway to regulate neuronal migration and synaptic plasticity in the hippocampus.
    Jakob B; Kochlamazashvili G; Jäpel M; Gauhar A; Bock HH; Maritzen T; Haucke V
    Proc Natl Acad Sci U S A; 2017 May; 114(21):5533-5538. PubMed ID: 28484035
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reelin promotes hippocampal dendrite development through the VLDLR/ApoER2-Dab1 pathway.
    Niu S; Renfro A; Quattrocchi CC; Sheldon M; D'Arcangelo G
    Neuron; 2004 Jan; 41(1):71-84. PubMed ID: 14715136
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reelin-induced tyrosine [corrected] phosphorylation of disabled 1 during neuronal positioning.
    Howell BW; Herrick TM; Cooper JA
    Genes Dev; 1999 Mar; 13(6):643-8. PubMed ID: 10090720
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare RELN variants affect Reelin-DAB1 signal transduction in autism spectrum disorder.
    Sánchez-Sánchez SM; Magdalon J; Griesi-Oliveira K; Yamamoto GL; Santacruz-Perez C; Fogo M; Passos-Bueno MR; Sertié AL
    Hum Mutat; 2018 Oct; 39(10):1372-1383. PubMed ID: 29969175
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic enhancement of the Lis1+/- phenotype by a heterozygous mutation in the adenomatous polyposis coli gene.
    Hebbar S; Guillotte AM; Mesngon MT; Zhou Q; Wynshaw-Boris A; Smith DS
    Dev Neurosci; 2008; 30(1-3):157-70. PubMed ID: 18075263
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression of DISC1 binding partners is reduced in schizophrenia and associated with DISC1 SNPs.
    Lipska BK; Peters T; Hyde TM; Halim N; Horowitz C; Mitkus S; Weickert CS; Matsumoto M; Sawa A; Straub RE; Vakkalanka R; Herman MM; Weinberger DR; Kleinman JE
    Hum Mol Genet; 2006 Apr; 15(8):1245-58. PubMed ID: 16510495
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reelin mouse mutants as models of cortical development disorders.
    D'Arcangelo G
    Epilepsy Behav; 2006 Feb; 8(1):81-90. PubMed ID: 16266828
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Importance of Reelin C-terminal region in the development and maintenance of the postnatal cerebral cortex and its regulation by specific proteolysis.
    Kohno T; Honda T; Kubo K; Nakano Y; Tsuchiya A; Murakami T; Banno H; Nakajima K; Hattori M
    J Neurosci; 2015 Mar; 35(11):4776-87. PubMed ID: 25788693
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dorsal Forebrain-Specific Deficiency of Reelin-Dab1 Signal Causes Behavioral Abnormalities Related to Psychiatric Disorders.
    Imai H; Shoji H; Ogata M; Kagawa Y; Owada Y; Miyakawa T; Sakimura K; Terashima T; Katsuyama Y
    Cereb Cortex; 2017 Jul; 27(7):3485-3501. PubMed ID: 26762856
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ndel1 and Reelin Maintain Postnatal CA1 Hippocampus Integrity.
    Jiang Y; Gavrilovici C; Chansard M; Liu RH; Kiroski I; Parsons K; Park SK; Teskey GC; Rho JM; Nguyen MD
    J Neurosci; 2016 Jun; 36(24):6538-52. PubMed ID: 27307241
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.