BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 29423132)

  • 1. Significant transcriptional changes in 15q duplication but not Angelman syndrome deletion stem cell-derived neurons.
    Urraca N; Hope K; Victor AK; Belgard TG; Memon R; Goorha S; Valdez C; Tran QT; Sanchez S; Ramirez J; Donaldson M; Bridges D; Reiter LT
    Mol Autism; 2018; 9():6. PubMed ID: 29423132
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.
    LaSalle JM; Reiter LT; Chamberlain SJ
    Epigenomics; 2015 Oct; 7(7):1213-28. PubMed ID: 26585570
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1.
    Germain ND; Chen PF; Plocik AM; Glatt-Deeley H; Brown J; Fink JJ; Bolduc KA; Robinson TM; Levine ES; Reiter LT; Graveley BR; Lalande M; Chamberlain SJ
    Mol Autism; 2014; 5():44. PubMed ID: 25694803
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome.
    Meguro-Horike M; Yasui DH; Powell W; Schroeder DI; Oshimura M; Lasalle JM; Horike S
    Hum Mol Genet; 2011 Oct; 20(19):3798-810. PubMed ID: 21725066
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders.
    Baker EK; Butler MG; Hartin SN; Ling L; Bui M; Francis D; Rogers C; Field MJ; Slee J; Gamage D; Amor DJ; Godler DE
    Transl Psychiatry; 2020 Oct; 10(1):362. PubMed ID: 33116122
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndrome.
    Copping NA; Christian SGB; Ritter DJ; Islam MS; Buscher N; Zolkowska D; Pride MC; Berg EL; LaSalle JM; Ellegood J; Lerch JP; Reiter LT; Silverman JL; Dindot SV
    Hum Mol Genet; 2017 Oct; 26(20):3995-4010. PubMed ID: 29016856
    [TBL] [Abstract][Full Text] [Related]  

  • 7. IPSC Models of Chromosome 15Q Imprinting Disorders: From Disease Modeling to Therapeutic Strategies.
    Germain ND; Levine ES; Chamberlain SJ
    Adv Neurobiol; 2020; 25():55-77. PubMed ID: 32578144
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples.
    Scoles HA; Urraca N; Chadwick SW; Reiter LT; Lasalle JM
    Mol Autism; 2011 Dec; 2(1):19. PubMed ID: 22152151
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transcriptomic and proteomic profiling of glial versus neuronal Dube3a overexpression reveals common molecular changes in gliopathic epilepsies.
    Hope KA; Johnson D; Miller PW; Lopez-Ferrer D; Kakhniashvili D; Reiter LT
    Neurobiol Dis; 2020 Jul; 141():104879. PubMed ID: 32344153
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletion.
    Neubert G; von Au K; Drossel K; Tzschach A; Horn D; Nickel R; Kaindl AM
    Gene; 2013 Jan; 512(2):453-5. PubMed ID: 23124039
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The role of UBE3A in the autism and epilepsy-related Dup15q syndrome using patient-derived, CRISPR-corrected neurons.
    Elamin M; Dumarchey A; Stoddard C; Robinson TM; Cowie C; Gorka D; Chamberlain SJ; Levine ES
    Stem Cell Reports; 2023 Apr; 18(4):884-898. PubMed ID: 36898382
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.
    Bittel DC; Kibiryeva N; Talebizadeh Z; Driscoll DJ; Butler MG
    Genomics; 2005 Jan; 85(1):85-91. PubMed ID: 15607424
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic dissection identifies Necdin as a driver gene in a mouse model of paternal 15q duplications.
    Tamada K; Fukumoto K; Toya T; Nakai N; Awasthi JR; Tanaka S; Okabe S; Spitz F; Saitow F; Suzuki H; Takumi T
    Nat Commun; 2021 Jul; 12(1):4056. PubMed ID: 34210967
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gastrointestinal problems in 15q duplication syndrome.
    Shaaya EA; Pollack SF; Boronat S; Davis-Cooper S; Zella GC; Thibert RL
    Eur J Med Genet; 2015 Mar; 58(3):191-3. PubMed ID: 25573720
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
    Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.
    Kuroda Y; Ohashi I; Saito T; Nagai J; Ida K; Naruto T; Wada T; Kurosawa K
    Am J Med Genet A; 2014 Nov; 164A(11):2873-8. PubMed ID: 25099823
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hyperexcitable Phenotypes in Induced Pluripotent Stem Cell-Derived Neurons From Patients With 15q11-q13 Duplication Syndrome, a Genetic Form of Autism.
    Fink JJ; Schreiner JD; Bloom JE; James J; Baker DS; Robinson TM; Lieberman R; Loew LM; Chamberlain SJ; Levine ES
    Biol Psychiatry; 2021 Dec; 90(11):756-765. PubMed ID: 34538422
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bioinformatics Analyses of the Transcriptome Reveal Ube3a-Dependent Effects on Mitochondrial-Related Pathways.
    Panov J; Simchi L; Feuermann Y; Kaphzan H
    Int J Mol Sci; 2020 Jun; 21(11):. PubMed ID: 32532103
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A genome-wide enhancer/suppressor screen for Dube3a interacting genes in Drosophila melanogaster.
    Hope KA; McGinn A; Reiter LT
    Sci Rep; 2019 Feb; 9(1):2382. PubMed ID: 30787400
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.