BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 37293116)

  • 1. Mouse models of
    Araki Y; Gerber EE; Rajkovich KE; Hong I; Johnson RC; Lee HK; Kirkwood A; Huganir RL
    bioRxiv; 2023 May; ():. PubMed ID: 37293116
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mouse models of
    Araki Y; Gerber EE; Rajkovich KE; Hong I; Johnson RC; Lee HK; Kirkwood A; Huganir RL
    Proc Natl Acad Sci U S A; 2023 Sep; 120(37):e2308891120. PubMed ID: 37669379
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hyperexcitability and translational phenotypes in a preclinical mouse model of
    Fenton TA; Haouchine OY; Hallam EL; Smith EM; Jackson KC; Rahbarian D; Canales C; Adhikari A; Nord AS; Ben-Shalom R; Silverman JL
    Res Sq; 2024 Mar; ():. PubMed ID: 38562838
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Llamosas N; Arora V; Vij R; Kilinc M; Bijoch L; Rojas C; Reich A; Sridharan B; Willems E; Piper DR; Scampavia L; Spicer TP; Miller CA; Holder JL; Rumbaugh G
    J Neurosci; 2020 Oct; 40(41):7980-7994. PubMed ID: 32887745
    [No Abstract]   [Full Text] [Related]  

  • 5. Hyperexcitability and translational phenotypes in a preclinical model of
    Silverman JL; Fenton T; Haouchine O; Hallam E; Smith E; Jackson K; Rahbarian D; Canales C; Adhikari A; Nord A; Ben-Shalom R
    Res Sq; 2023 Sep; ():. PubMed ID: 37790402
    [No Abstract]   [Full Text] [Related]  

  • 6. Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report.
    Prchalova D; Havlovicova M; Sterbova K; Stranecky V; Hancarova M; Sedlacek Z
    BMC Med Genet; 2017 Jun; 18(1):62. PubMed ID: 28576131
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Transcriptome Sequencing Confirms Activation of a Cryptic Splice Site in Suspected
    Brimble E; Lee-Messer C; Nagy PL; Propst J; Ruzhnikov MRZ
    Mol Syndromol; 2019 Jan; 9(6):295-299. PubMed ID: 30800045
    [No Abstract]   [Full Text] [Related]  

  • 8. Hyperexcitability and translational phenotypes in a preclinical model of
    Fenton TA; Haouchine OY; Hallam EL; Smith EM; Jackson KC; Rahbarian D; Canales C; Adhikari A; Nord AS; Ben-Shalom R; Silverman JL
    bioRxiv; 2023 Jul; ():. PubMed ID: 37546838
    [No Abstract]   [Full Text] [Related]  

  • 9. Comprehensive behavioral analysis of heterozygous Syngap1 knockout mice.
    Nakajima R; Takao K; Hattori S; Shoji H; Komiyama NH; Grant SGN; Miyakawa T
    Neuropsychopharmacol Rep; 2019 Sep; 39(3):223-237. PubMed ID: 31323176
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SYNGAP1 mutations: Clinical, genetic, and pathophysiological features.
    Agarwal M; Johnston MV; Stafstrom CE
    Int J Dev Neurosci; 2019 Nov; 78():65-76. PubMed ID: 31454529
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SynGAP regulates synaptic plasticity and cognition independently of its catalytic activity.
    Araki Y; Rajkovich KE; Gerber EE; Gamache TR; Johnson RC; Tran THN; Liu B; Zhu Q; Hong I; Kirkwood A; Huganir R
    Science; 2024 Mar; 383(6686):eadk1291. PubMed ID: 38422154
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of an individual with a SYGNAP1 pathogenic mutation in India.
    Verma V; Mandora A; Botre A; Clement JP
    Mol Biol Rep; 2020 Nov; 47(11):9225-9234. PubMed ID: 33090308
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SYNGAP1: Mind the Gap.
    Jeyabalan N; Clement JP
    Front Cell Neurosci; 2016; 10():32. PubMed ID: 26912996
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability.
    Parker MJ; Fryer AE; Shears DJ; Lachlan KL; McKee SA; Magee AC; Mohammed S; Vasudevan PC; Park SM; Benoit V; Lederer D; Maystadt I; Study D; FitzPatrick DR
    Am J Med Genet A; 2015 Oct; 167A(10):2231-7. PubMed ID: 26079862
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pharmacological intervention in young adolescents rescues synaptic physiology and behavioural deficits in Syngap1
    Verma V; Kumar MJV; Sharma K; Rajaram S; Muddashetty R; Manjithaya R; Behnisch T; Clement JP
    Exp Brain Res; 2022 Jan; 240(1):289-309. PubMed ID: 34739555
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Upregulation of SYNGAP1 expression in mice and human neurons by redirecting alternative splicing.
    Yang R; Feng X; Arias-Cavieres A; Mitchell RM; Polo A; Hu K; Zhong R; Qi C; Zhang RS; Westneat N; Portillo CA; Nobrega MA; Hansel C; Garcia Iii AJ; Zhang X
    Neuron; 2023 May; 111(10):1637-1650.e5. PubMed ID: 36917980
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interneuron-Targeted Disruption of
    Zhao M; Kwon SE
    J Neurosci; 2023 Aug; 43(35):6212-6226. PubMed ID: 37558489
    [No Abstract]   [Full Text] [Related]  

  • 18. Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.
    Kilinc M; Creson T; Rojas C; Aceti M; Ellegood J; Vaissiere T; Lerch JP; Rumbaugh G
    Mol Cell Neurosci; 2018 Sep; 91():140-150. PubMed ID: 29580901
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rescue of Learning and Memory Deficits in the Human Nonsyndromic Intellectual Disability Cereblon Knock-Out Mouse Model by Targeting the AMP-Activated Protein Kinase-mTORC1 Translational Pathway.
    Bavley CC; Rice RC; Fischer DK; Fakira AK; Byrne M; Kosovsky M; Rizzo BK; Del Prete D; Alaedini A; MorĂ³n JA; Higgins JJ; D'Adamio L; Rajadhyaksha AM
    J Neurosci; 2018 Mar; 38(11):2780-2795. PubMed ID: 29459374
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Syngap1 haploinsufficiency damages a postnatal critical period of pyramidal cell structural maturation linked to cortical circuit assembly.
    Aceti M; Creson TK; Vaissiere T; Rojas C; Huang WC; Wang YX; Petralia RS; Page DT; Miller CA; Rumbaugh G
    Biol Psychiatry; 2015 May; 77(9):805-15. PubMed ID: 25444158
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.