BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

402 related articles for article (PubMed ID: 32182809)

  • 1. A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15.
    Casamassa A; Ferrari D; Gelati M; Carella M; Vescovi AL; Rosati J
    Int J Mol Sci; 2020 Mar; 21(5):. PubMed ID: 32182809
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duplication Versus Deletion Through the Lens of 15q13.3: Clinical and Research Implications of Studying Copy Number Variants Associated with Neuropsychiatric Disorders in Induced Pluripotent Stem Cell-Derived Neurons.
    Antony I; Narasimhan M; Shen R; Prakasam R; Kaushik K; Chapman G; Kroll KL
    Stem Cell Rev Rep; 2023 Apr; 19(3):639-650. PubMed ID: 36370261
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity.
    Chen Y; Guo L; Chen J; Zhao X; Zhou W; Zhang C; Wang J; Jin L; Pei D; Zhang F
    BMC Genomics; 2014 Jan; 15():79. PubMed ID: 24472662
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effects of Integrating and Non-Integrating Reprogramming Methods on Copy Number Variation and Genomic Stability of Human Induced Pluripotent Stem Cells.
    Kang X; Yu Q; Huang Y; Song B; Chen Y; Gao X; He W; Sun X; Fan Y
    PLoS One; 2015; 10(7):e0131128. PubMed ID: 26131765
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Passage number is a major contributor to genomic structural variations in mouse iPSCs.
    Liu P; Kaplan A; Yuan B; Hanna JH; Lupski JR; Reiner O
    Stem Cells; 2014 Oct; 32(10):2657-67. PubMed ID: 24965231
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Functional Consequences of CHRNA7 Copy-Number Alterations in Induced Pluripotent Stem Cells and Neural Progenitor Cells.
    Gillentine MA; Yin J; Bajic A; Zhang P; Cummock S; Kim JJ; Schaaf CP
    Am J Hum Genet; 2017 Dec; 101(6):874-887. PubMed ID: 29129316
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Influence of ATM-Mediated DNA Damage Response on Genomic Variation in Human Induced Pluripotent Stem Cells.
    Lu J; Li H; Baccei A; Sasaki T; Gilbert DM; Lerou PH
    Stem Cells Dev; 2016 May; 25(9):740-7. PubMed ID: 26935587
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Altered neuronal physiology, development, and function associated with a common chromosome 15 duplication involving CHRNA7.
    Meganathan K; Prakasam R; Baldridge D; Gontarz P; Zhang B; Urano F; Bonni A; Maloney SE; Turner TN; Huettner JE; Constantino JN; Kroll KL
    BMC Biol; 2021 Jul; 19(1):147. PubMed ID: 34320968
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Factor-induced Reprogramming and Zinc Finger Nuclease-aided Gene Targeting Cause Different Genome Instability in β-Thalassemia Induced Pluripotent Stem Cells (iPSCs).
    Ma N; Shan Y; Liao B; Kong G; Wang C; Huang K; Zhang H; Cai X; Chen S; Pei D; Chen N; Pan G
    J Biol Chem; 2015 May; 290(19):12079-89. PubMed ID: 25795783
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CNV biology in neurodevelopmental disorders.
    Takumi T; Tamada K
    Curr Opin Neurobiol; 2018 Feb; 48():183-192. PubMed ID: 29331932
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.
    Rutkowski TP; Schroeder JP; Gafford GM; Warren ST; Weinshenker D; Caspary T; Mulle JG
    J Neurosci Res; 2017 May; 95(5):1144-1160. PubMed ID: 27859486
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD.
    Drakulic D; Djurovic S; Syed YA; Trattaro S; Caporale N; Falk A; Ofir R; Heine VM; Chawner SJRA; Rodriguez-Moreno A; van den Bree MBM; Testa G; Petrakis S; Harwood AJ
    Mol Autism; 2020 Jun; 11(1):42. PubMed ID: 32487215
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Increased genomic integrity of an improved protein-based mouse induced pluripotent stem cell method compared with current viral-induced strategies.
    Park H; Kim D; Kim CH; Mills RE; Chang MY; Iskow RC; Ko S; Moon JI; Choi HW; Man Yoo PS; Do JT; Han MJ; Lee EG; Jung JK; Zhang C; Lanza R; Kim KS
    Stem Cells Transl Med; 2014 May; 3(5):599-609. PubMed ID: 24763686
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells.
    Abyzov A; Mariani J; Palejev D; Zhang Y; Haney MS; Tomasini L; Ferrandino AF; Rosenberg Belmaker LA; Szekely A; Wilson M; Kocabas A; Calixto NE; Grigorenko EL; Huttner A; Chawarska K; Weissman S; Urban AE; Gerstein M; Vaccarino FM
    Nature; 2012 Dec; 492(7429):438-42. PubMed ID: 23160490
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genomic Instability of iPSCs and Challenges in Their Clinical Applications.
    Yoshihara M; Oguchi A; Murakawa Y
    Adv Exp Med Biol; 2019; 1201():23-47. PubMed ID: 31898780
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Critical reappraisal of mechanistic links of copy number variants to dimensional constructs of neuropsychiatric disorders in mouse models.
    Hiroi N
    Psychiatry Clin Neurosci; 2018 May; 72(5):301-321. PubMed ID: 29369447
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome sequencing of mouse induced pluripotent stem cells reveals retroelement stability and infrequent DNA rearrangement during reprogramming.
    Quinlan AR; Boland MJ; Leibowitz ML; Shumilina S; Pehrson SM; Baldwin KK; Hall IM
    Cell Stem Cell; 2011 Oct; 9(4):366-73. PubMed ID: 21982236
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Great Expectations: Induced pluripotent stem cell technologies in neurodevelopmental impairments.
    Zhang X; Li Z; Liu Y; Gai Z
    Int J Med Sci; 2021; 18(2):459-473. PubMed ID: 33390815
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Copy number variations and human genetic disease.
    Mikhail FM
    Curr Opin Pediatr; 2014 Dec; 26(6):646-52. PubMed ID: 25198053
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.
    Hiroi N; Takahashi T; Hishimoto A; Izumi T; Boku S; Hiramoto T
    Mol Psychiatry; 2013 Nov; 18(11):1153-65. PubMed ID: 23917946
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.