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 *

169 related articles for article (PubMed ID: 34597683)

  • 1. Mutation of the murine Prickle1 (R104Q) causes phenotypes analogous to human symptoms of epilepsy and autism.
    Ban Y; Yu T; Wang J; Wang X; Liu C; Baker C; Zou Y
    Exp Neurol; 2022 Jan; 347():113880. PubMed ID: 34597683
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prickle1 is expressed in distinct cell populations of the central nervous system and contributes to neuronal morphogenesis.
    Liu C; Lin C; Whitaker DT; Bakeri H; Bulgakov OV; Liu P; Lei J; Dong L; Li T; Swaroop A
    Hum Mol Genet; 2013 Jun; 22(11):2234-46. PubMed ID: 23420014
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder.
    Todd BP; Bassuk AG
    J Neurogenet; 2018 Dec; 32(4):313-315. PubMed ID: 29790814
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders.
    Paemka L; Mahajan VB; Skeie JM; Sowers LP; Ehaideb SN; Gonzalez-Alegre P; Sasaoka T; Tao H; Miyagi A; Ueno N; Takao K; Miyakawa T; Wu S; Darbro BW; Ferguson PJ; Pieper AA; Britt JK; Wemmie JA; Rudd DS; Wassink T; El-Shanti H; Mefford HC; Carvill GL; Manak JR; Bassuk AG
    PLoS One; 2013; 8(12):e80737. PubMed ID: 24312498
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mechanisms of prickle1a function in zebrafish epilepsy and retinal neurogenesis.
    Mei X; Wu S; Bassuk AG; Slusarski DC
    Dis Model Mech; 2013 May; 6(3):679-88. PubMed ID: 23324328
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chondrocyte Polarity During Endochondral Ossification Requires Protein-Protein Interactions Between Prickle1 and Dishevelled2/3.
    Wan Y; Szabo-Rogers HL
    J Bone Miner Res; 2021 Dec; 36(12):2399-2412. PubMed ID: 34423861
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene.
    Algahtani H; Al-Hakami F; Al-Shehri M; Shirah B; Al-Qahtani MH; Abdulkareem AA; Naseer MI
    Seizure; 2019 Jul; 69():133-139. PubMed ID: 31035234
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyria.
    Bassuk AG; Sherr EH
    J Neurogenet; 2015; 29(4):174-7. PubMed ID: 26727662
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neurobiological Mechanisms of Autism Spectrum Disorder and Epilepsy, Insights from Animal Models.
    Sierra-Arregui T; Llorente J; Giménez Minguez P; Tønnesen J; Peñagarikano O
    Neuroscience; 2020 Oct; 445():69-82. PubMed ID: 32147509
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function.
    Gilbert J; O'Connor M; Templet S; Moghaddam M; Di Via Ioschpe A; Sinclair A; Zhu LQ; Xu W; Man HY
    J Neurosci; 2020 Jan; 40(1):237-254. PubMed ID: 31704787
    [TBL] [Abstract][Full Text] [Related]  

  • 11. PRICKLE1-related early onset epileptic encephalopathy.
    Mastrangelo M; Tolve M; Martinelli M; Di Noia SP; Parrini E; Leuzzi V
    Am J Med Genet A; 2018 Dec; 176(12):2841-2845. PubMed ID: 30345727
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autism spectrum disorder phenotype and intellectual disability in females with epilepsy and PCDH-19 mutations.
    Breuillard D; Leunen D; Chemaly N; Auclair L; Pinard JM; Kaminska A; Desguerre I; Ouss L; Nabbout R
    Epilepsy Behav; 2016 Jul; 60():75-80. PubMed ID: 27179713
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification and characterization of human PRICKLE1 and PRICKLE2 genes as well as mouse Prickle1 and Prickle2 genes homologous to Drosophila tissue polarity gene prickle.
    Katoh M; Katoh M
    Int J Mol Med; 2003 Feb; 11(2):249-56. PubMed ID: 12525887
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prickle1 is required for EMT and migration of zebrafish cranial neural crest.
    Ahsan K; Singh N; Rocha M; Huang C; Prince VE
    Dev Biol; 2019 Apr; 448(1):16-35. PubMed ID: 30721665
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Replicable in vivo physiological and behavioral phenotypes of the
    Dhamne SC; Silverman JL; Super CE; Lammers SHT; Hameed MQ; Modi ME; Copping NA; Pride MC; Smith DG; Rotenberg A; Crawley JN; Sahin M
    Mol Autism; 2017; 8():26. PubMed ID: 28638591
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in prickle orthologs cause seizures in flies, mice, and humans.
    Tao H; Manak JR; Sowers L; Mei X; Kiyonari H; Abe T; Dahdaleh NS; Yang T; Wu S; Chen S; Fox MH; Gurnett C; Montine T; Bird T; Shaffer LG; Rosenfeld JA; McConnell J; Madan-Khetarpal S; Berry-Kravis E; Griesbach H; Saneto RP; Scott MP; Antic D; Reed J; Boland R; Ehaideb SN; El-Shanti H; Mahajan VB; Ferguson PJ; Axelrod JD; Lehesjoki AE; Fritzsch B; Slusarski DC; Wemmie J; Ueno N; Bassuk AG
    Am J Hum Genet; 2011 Feb; 88(2):138-49. PubMed ID: 21276947
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Vangl2 interaction plays a role in the proteasomal degradation of Prickle2.
    Nagaoka T; Furuse M; Ohtsuka T; Tsuchida K; Kishi M
    Sci Rep; 2019 Feb; 9(1):2912. PubMed ID: 30814664
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transcriptomics of Gabra4 knockout mice reveals common NMDAR pathways underlying autism, memory, and epilepsy.
    Fan C; Gao Y; Liang G; Huang L; Wang J; Yang X; Shi Y; Dräger UC; Zhong M; Gao TM; Yang X
    Mol Autism; 2020 Feb; 11(1):13. PubMed ID: 32033586
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comorbid epilepsy in autism spectrum disorder: Implications of postnatal inflammation for brain excitability.
    Lewis ML; Kesler M; Candy SA; Rho JM; Pittman QJ
    Epilepsia; 2018 Jul; 59(7):1316-1326. PubMed ID: 29858515
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.
    Bassuk AG; Wallace RH; Buhr A; Buller AR; Afawi Z; Shimojo M; Miyata S; Chen S; Gonzalez-Alegre P; Griesbach HL; Wu S; Nashelsky M; Vladar EK; Antic D; Ferguson PJ; Cirak S; Voit T; Scott MP; Axelrod JD; Gurnett C; Daoud AS; Kivity S; Neufeld MY; Mazarib A; Straussberg R; Walid S; Korczyn AD; Slusarski DC; Berkovic SF; El-Shanti HI
    Am J Hum Genet; 2008 Nov; 83(5):572-81. PubMed ID: 18976727
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.