BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 12616675)

  • 21. Filamin a, periventricular nodular heterotopia, and West syndrome.
    Robertson SP
    Epilepsia; 2006 Jun; 47(6):1082; author reply 1082-3. PubMed ID: 16822260
    [No Abstract]   [Full Text] [Related]  

  • 22. Missense mutations resulting in type 1 lissencephaly.
    Reiner O; Coquelle FM
    Cell Mol Life Sci; 2005 Feb; 62(4):425-34. PubMed ID: 15719169
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Autosomal recessive form of periventricular heterotopia.
    Sheen VL; Topçu M; Berkovic S; Yalnizoglu D; Blatt I; Bodell A; Hill RS; Ganesh VS; Cherry TJ; Shugart YY; Walsh CA
    Neurology; 2003 Apr; 60(7):1108-12. PubMed ID: 12682315
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. RELN and VLDLR mutations underlie two distinguishable clinico-radiological phenotypes.
    Valence S; Garel C; Barth M; Toutain A; Paris C; Amsallem D; Barthez MA; Mayer M; Rodriguez D; Burglen L
    Clin Genet; 2016 Dec; 90(6):545-549. PubMed ID: 27000652
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.
    Fox JW; Lamperti ED; Ekşioğlu YZ; Hong SE; Feng Y; Graham DA; Scheffer IE; Dobyns WB; Hirsch BA; Radtke RA; Berkovic SF; Huttenlocher PR; Walsh CA
    Neuron; 1998 Dec; 21(6):1315-25. PubMed ID: 9883725
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Epilepsy and genetic malformations of the cerebral cortex.
    Guerrini R; Carrozzo R
    Am J Med Genet; 2001; 106(2):160-73. PubMed ID: 11579436
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Genetic landmarks through philately - autism spectrum disorders: a genetic update.
    Chudley AE
    Clin Genet; 2004 May; 65(5):352-7. PubMed ID: 15099341
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mechanisms and disturbances of neuronal migration.
    Gressens P
    Pediatr Res; 2000 Dec; 48(6):725-30. PubMed ID: 11102537
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Development. New hints into the biological basis of autism.
    Stokstad E
    Science; 2001 Oct; 294(5540):34-7. PubMed ID: 11588233
    [No Abstract]   [Full Text] [Related]  

  • 32. Life is a journey: a genetic look at neocortical development.
    Gupta A; Tsai LH; Wynshaw-Boris A
    Nat Rev Genet; 2002 May; 3(5):342-55. PubMed ID: 11988760
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Normal and abnormal neuronal migration in the developing cerebral cortex.
    Sun XZ; Takahashi S; Cui C; Zhang R; Sakata-Haga H; Sawada K; Fukui Y
    J Med Invest; 2002 Aug; 49(3-4):97-110. PubMed ID: 12323012
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Developmental neurobiology. A real gene for reeler.
    Goffinet AM
    Nature; 1995 Apr; 374(6524):675-6. PubMed ID: 7715721
    [No Abstract]   [Full Text] [Related]  

  • 35. Reelin, lipoprotein receptors and synaptic plasticity.
    Herz J; Chen Y
    Nat Rev Neurosci; 2006 Nov; 7(11):850-9. PubMed ID: 17053810
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Filamins in cardiovascular development.
    Zhou X; Borén J; Akyürek LM
    Trends Cardiovasc Med; 2007 Oct; 17(7):222-9. PubMed ID: 17936203
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The reeler mouse as a model of brain development.
    Lambert de Rouvroit C; Goffinet AM
    Adv Anat Embryol Cell Biol; 1998; 150():1-106. PubMed ID: 9816727
    [No Abstract]   [Full Text] [Related]  

  • 38. Developmental abnormality contributes to cortex-dependent motor impairments and higher intracortical current requirement in the reeler homozygous mutants.
    Nishibe M; Katsuyama Y; Yamashita T
    Brain Struct Funct; 2018 Jul; 223(6):2575-2587. PubMed ID: 29536172
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Molecular pathways controlling the sequential steps of cortical projection neuron migration.
    Hippenmeyer S
    Adv Exp Med Biol; 2014; 800():1-24. PubMed ID: 24243097
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.