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 *

186 related articles for article (PubMed ID: 37205408)

  • 1. Epigenomic signature of major congenital heart defects in newborns with Down syndrome.
    Mouat JS; Li S; Myint SS; Laufer BI; Lupo PJ; Schraw JM; Woodhouse JP; de Smith AJ; LaSalle JM
    medRxiv; 2023 May; ():. PubMed ID: 37205408
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epigenomic signature of major congenital heart defects in newborns with Down syndrome.
    Mouat JS; Li S; Myint SS; Laufer BI; Lupo PJ; Schraw JM; Woodhouse JP; de Smith AJ; LaSalle JM
    Hum Genomics; 2023 Oct; 17(1):92. PubMed ID: 37803336
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Low-pass whole genome bisulfite sequencing of neonatal dried blood spots identifies a role for RUNX1 in Down syndrome DNA methylation profiles.
    Laufer BI; Hwang H; Jianu JM; Mordaunt CE; Korf IF; Hertz-Picciotto I; LaSalle JM
    Hum Mol Genet; 2021 Jan; 29(21):3465-3476. PubMed ID: 33001180
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole genome bisulfite sequencing of Down syndrome brain reveals regional DNA hypermethylation and novel disorder insights.
    Laufer BI; Hwang H; Vogel Ciernia A; Mordaunt CE; LaSalle JM
    Epigenetics; 2019 Jul; 14(7):672-684. PubMed ID: 31010359
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes.
    Mordaunt CE; Jianu JM; Laufer BI; Zhu Y; Hwang H; Dunaway KW; Bakulski KM; Feinberg JI; Volk HE; Lyall K; Croen LA; Newschaffer CJ; Ozonoff S; Hertz-Picciotto I; Fallin MD; Schmidt RJ; LaSalle JM
    Genome Med; 2020 Oct; 12(1):88. PubMed ID: 33054850
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Stable DNMT3L overexpression in SH-SY5Y neurons recreates a facet of the genome-wide Down syndrome DNA methylation signature.
    Laufer BI; Gomez JA; Jianu JM; LaSalle JM
    Epigenetics Chromatin; 2021 Mar; 14(1):13. PubMed ID: 33750431
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide methylation analysis reveals differentially methylated CpG sites and altered expression of heart development-associated genes in fetuses with cardiac defects.
    Zhou J; Xiong Y; Dong X; Wang H; Qian Y; Ma D; Li X
    Exp Ther Med; 2021 Sep; 22(3):1032. PubMed ID: 34373718
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sex differences for major congenital heart defects in Down Syndrome: A population based study.
    Santoro M; Coi A; Spadoni I; Bianchi F; Pierini A
    Eur J Med Genet; 2018 Sep; 61(9):546-550. PubMed ID: 29753092
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypomethylation coordinates antagonistically with hypermethylation in cancer development: a case study of leukemia.
    Kushwaha G; Dozmorov M; Wren JD; Qiu J; Shi H; Xu D
    Hum Genomics; 2016 Jul; 10 Suppl 2(Suppl 2):18. PubMed ID: 27461342
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epigenome-wide base-resolution profiling of DNA methylation in chorionic villi of fetuses with Down syndrome by methyl-capture sequencing.
    Lim JH; Kang YJ; Lee BY; Han YJ; Chung JH; Kim MY; Kim MH; Kim JW; Cho YH; Ryu HM
    Clin Epigenetics; 2019 Dec; 11(1):180. PubMed ID: 31801612
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancers.
    Mordaunt CE; Kieffer DA; Shibata NM; Członkowska A; Litwin T; Weiss KH; Zhu Y; Bowlus CL; Sarkar S; Cooper S; Wan YY; Ali MR; LaSalle JM; Medici V
    Epigenetics Chromatin; 2019 Feb; 12(1):10. PubMed ID: 30709419
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates.
    Henneman P; Bouman A; Mul A; Knegt L; van der Kevie-Kersemaekers AM; Zwaveling-Soonawala N; Meijers-Heijboer HEJ; van Trotsenburg ASP; Mannens MM
    PLoS One; 2018; 13(3):e0194938. PubMed ID: 29601581
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Effects of Developmental Lead and Phthalate Exposures on DNA Methylation in Adult Mouse Blood, Brain, and Liver Identifies Tissue- and Sex-Specific Changes with Implications for Genomic Imprinting.
    Morgan RK; Wang K; Svoboda LK; Rygiel CA; Lalancette C; Cavalcante R; Bartolomei MS; Prasasya R; Neier K; Perera BPU; Jones TR; Colacino JA; Sartor MA; Dolinoy DC
    bioRxiv; 2023 Oct; ():. PubMed ID: 37873115
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide survey reveals dynamic widespread tissue-specific changes in DNA methylation during development.
    Liang P; Song F; Ghosh S; Morien E; Qin M; Mahmood S; Fujiwara K; Igarashi J; Nagase H; Held WA
    BMC Genomics; 2011 May; 12(1):231. PubMed ID: 21569359
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternal LINE-1 DNA Methylation and Congenital Heart Defects in Down Syndrome.
    Babić Božović I; Stanković A; Živković M; Vraneković J; Mahulja-Stamenković V; Brajenović-Milić B
    Front Genet; 2019; 10():41. PubMed ID: 30787943
    [No Abstract]   [Full Text] [Related]  

  • 16. Comparative genome-wide DNA methylation analysis in myocardial tissue from donors with and without Down syndrome.
    Cejas RB; Wang J; Hageman-Blair R; Liu S; Blanco JG
    Gene; 2021 Jan; 764():145099. PubMed ID: 32861879
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A methylome-wide study of aging using massively parallel sequencing of the methyl-CpG-enriched genomic fraction from blood in over 700 subjects.
    McClay JL; Aberg KA; Clark SL; Nerella S; Kumar G; Xie LY; Hudson AD; Harada A; Hultman CM; Magnusson PK; Sullivan PF; Van Den Oord EJ
    Hum Mol Genet; 2014 Mar; 23(5):1175-85. PubMed ID: 24135035
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole-Genome Bisulfite Sequencing of Human Pancreatic Islets Reveals Novel Differentially Methylated Regions in Type 2 Diabetes Pathogenesis.
    Volkov P; Bacos K; Ofori JK; Esguerra JL; Eliasson L; Rönn T; Ling C
    Diabetes; 2017 Apr; 66(4):1074-1085. PubMed ID: 28052964
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Meta-Analysis of DNA Methylation Datasets Shows Aberrant DNA Methylation of Thyroid Development or Function Genes in Down Syndrome.
    Lauffer P; Zwaveling-Soonawala N; Li S; Bacalini MG; Naumova OY; Wiemels J; Boelen A; Henneman P; de Smith AJ; van Trotsenburg ASP
    Thyroid; 2023 Jan; 33(1):53-62. PubMed ID: 36326208
    [No Abstract]   [Full Text] [Related]  

  • 20. Epigenetic markers for newborn congenital heart defect (CHD).
    Bahado-Singh RO; Zaffra R; Albayarak S; Chelliah A; Bolinjkar R; Turkoglu O; Radhakrishna U
    J Matern Fetal Neonatal Med; 2016; 29(12):1881-7. PubMed ID: 26429603
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.