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 *

154 related articles for article (PubMed ID: 25919240)

  • 1. Genetic Evaluation of Copy Number Variations, Loss of Heterozygosity, and Single-Nucleotide Variant Levels in Human Embryonic Stem Cells With or Without Skewed X Chromosome Inactivation.
    Liu WQ; Li JL; Wang J; He WY; Va L; Sheng XM; Wu BL; Sun XF
    Stem Cells Dev; 2015 Aug; 24(15):1779-92. PubMed ID: 25919240
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High-resolution chromosomal microarray analysis of early-stage human embryonic stem cells reveals an association between X chromosome instability and skewed X inactivation.
    Luo Y; Li J; Zhu D; Fan Y; Li S; Sun X
    Cell Biosci; 2014; 4(1):74. PubMed ID: 25506417
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Skewed X chromosome inactivation in diploid and triploid female human embryonic stem cells.
    Liu W; Sun X
    Hum Reprod; 2009 Aug; 24(8):1834-43. PubMed ID: 19429659
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Variations of X chromosome inactivation occur in early passages of female human embryonic stem cells.
    Dvash T; Lavon N; Fan G
    PLoS One; 2010 Jun; 5(6):e11330. PubMed ID: 20593031
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Higher copy number variation and diverse X chromosome inactivation in parthenote-derived human embryonic stem cells.
    Liu W; Guo L; He W; Li Q; Sun X
    J Reprod Dev; 2012; 58(6):642-8. PubMed ID: 22813599
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing.
    Szelinger S; Malenica I; Corneveaux JJ; Siniard AL; Kurdoglu AA; Ramsey KM; Schrauwen I; Trent JM; Narayanan V; Huentelman MJ; Craig DW
    PLoS One; 2014; 9(12):e113036. PubMed ID: 25503791
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The dynamic changes of X chromosome inactivation during early culture of human embryonic stem cells.
    Xie P; Ouyang Q; Leng L; Hu L; Cheng D; Tan Y; Lu G; Lin G
    Stem Cell Res; 2016 Jul; 17(1):84-92. PubMed ID: 27262949
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epigenetic regulation of X-inactivation in human embryonic stem cells.
    Dvash T; Fan G
    Epigenetics; 2009 Jan; 4(1):19-22. PubMed ID: 19106643
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Meta-analysis of the heterogeneity of X chromosome inactivation in human pluripotent stem cells.
    Bruck T; Benvenisty N
    Stem Cell Res; 2011 Mar; 6(2):187-93. PubMed ID: 21276761
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Female human pluripotent stem cells rapidly lose X chromosome inactivation marks and progress to a skewed methylation pattern during culture.
    Geens M; Seriola A; Barbé L; Santalo J; Veiga A; Dée K; Van Haute L; Sermon K; Spits C
    Mol Hum Reprod; 2016 Apr; 22(4):285-98. PubMed ID: 26786180
    [TBL] [Abstract][Full Text] [Related]  

  • 11. X-inactivation in female human embryonic stem cells is in a nonrandom pattern and prone to epigenetic alterations.
    Shen Y; Matsuno Y; Fouse SD; Rao N; Root S; Xu R; Pellegrini M; Riggs AD; Fan G
    Proc Natl Acad Sci U S A; 2008 Mar; 105(12):4709-14. PubMed ID: 18339804
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity.
    Närvä E; Autio R; Rahkonen N; Kong L; Harrison N; Kitsberg D; Borghese L; Itskovitz-Eldor J; Rasool O; Dvorak P; Hovatta O; Otonkoski T; Tuuri T; Cui W; Brüstle O; Baker D; Maltby E; Moore HD; Benvenisty N; Andrews PW; Yli-Harja O; Lahesmaa R
    Nat Biotechnol; 2010 Apr; 28(4):371-7. PubMed ID: 20351689
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.
    Žilina O; Koltšina M; Raid R; Kurg A; Tõnisson N; Salumets A
    BMC Genomics; 2015 Sep; 16(1):703. PubMed ID: 26376747
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The State of Skewed X Chromosome Inactivation is Retained in the Induced Pluripotent Stem Cells from a Female with Hemophilia B.
    Lyu C; Shen J; Zhang J; Xue F; Liu X; Liu W; Fu R; Zhang L; Li H; Zhang D; Zhang X; Cheng T; Yang R; Zhang L
    Stem Cells Dev; 2017 Jul; 26(13):1003-1011. PubMed ID: 28401797
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X chromosome inactivation in human parthenogenetic embryonic stem cells following prolonged passaging.
    Qi Q; Ding C; Hong P; Yang G; Xie Y; Wang J; Huang S; He K; Zhou C
    Int J Mol Med; 2015 Mar; 35(3):569-78. PubMed ID: 25524499
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular Mechanisms of Skewed X-Chromosome Inactivation in Female Hemophilia Patients-Lessons from Wide Genome Analyses.
    Dardik R; Avishai E; Lalezari S; Barg AA; Levy-Mendelovich S; Budnik I; Barel O; Khavkin Y; Kenet G; Livnat T
    Int J Mol Sci; 2021 Aug; 22(16):. PubMed ID: 34445777
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Aberrant patterns of X chromosome inactivation in a new line of human embryonic stem cells established in physiological oxygen concentrations.
    de Oliveira Georges JA; Vergani N; Fonseca SA; Fraga AM; de Mello JC; Albuquerque MC; Fujihara LS; Pereira LV
    Stem Cell Rev Rep; 2014 Aug; 10(4):472-9. PubMed ID: 24633531
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation.
    Wang J; Yu R; Shete S
    Genet Epidemiol; 2014 Sep; 38(6):483-93. PubMed ID: 25043884
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes.
    Giovenino C; Trajkova S; Pavinato L; Cardaropoli S; Pullano V; Ferrero E; Sukarova-Angelovska E; Carestiato S; Salmin P; Rinninella A; Battaglia A; Bertoli L; Fadda A; Palermo F; Carli D; Mussa A; Dimartino P; Bruselles A; Froukh T; Mandrile G; Pasini B; De Rubeis S; Buxbaum JD; Pippucci T; Tartaglia M; Rossato M; Delledonne M; Ferrero GB; Brusco A
    Eur J Hum Genet; 2023 Nov; 31(11):1228-1236. PubMed ID: 36879111
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease.
    Fadra N; Schultz-Rogers LE; Chanana P; Cousin MA; Macke EL; Ferrer A; Pinto E Vairo F; Olson RJ; Oliver GR; Mulvihill LA; Jenkinson G; Klee EW
    BMC Genomics; 2024 Apr; 25(1):371. PubMed ID: 38627676
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.