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 *

211 related articles for article (PubMed ID: 24850140)

  • 1. Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome.
    Massingham LJ; Johnson KL; Scholl TM; Slonim DK; Wick HC; Bianchi DW
    Hum Genet; 2014 Sep; 133(9):1075-82. PubMed ID: 24850140
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Amniotic fluid transcriptomics reflects novel disease mechanisms in fetuses with myelomeningocele.
    Tarui T; Kim A; Flake A; McClain L; Stratigis JD; Fried I; Newman R; Slonim DK; Bianchi DW
    Am J Obstet Gynecol; 2017 Nov; 217(5):587.e1-587.e10. PubMed ID: 28735706
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transcriptomic analysis of cell-free fetal RNA suggests a specific molecular phenotype in trisomy 18.
    Koide K; Slonim DK; Johnson KL; Tantravahi U; Cowan JM; Bianchi DW
    Hum Genet; 2011 Mar; 129(3):295-305. PubMed ID: 21152935
    [TBL] [Abstract][Full Text] [Related]  

  • 4. RNA-Seq of amniotic fluid cell-free RNA: a discovery phase study of the pathophysiology of congenital cytomegalovirus infection.
    Hui L; De Catte L; Beard S; Maksimovic J; Vora NL; Oshlack A; Walker SP; Hannan NJ
    Am J Obstet Gynecol; 2022 Oct; 227(4):634.e1-634.e12. PubMed ID: 35609640
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Maternal obesity affects fetal neurodevelopmental and metabolic gene expression: a pilot study.
    Edlow AG; Vora NL; Hui L; Wick HC; Cowan JM; Bianchi DW
    PLoS One; 2014; 9(2):e88661. PubMed ID: 24558408
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Global gene expression changes of amniotic fluid cell free RNA according to fetal development.
    Jang JH; Jung YW; Shim SH; Sin YJ; Lee KJ; Shim SS; Ahn EH; Cha DH
    Eur J Obstet Gynecol Reprod Biol; 2017 Sep; 216():104-110. PubMed ID: 28750298
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bioinformatic Analysis Identifies Potential Key Genes in the Pathogenesis of Turner Syndrome.
    Wang H; Zhu H; Zhu W; Xu Y; Wang N; Han B; Song H; Qiao J
    Front Endocrinol (Lausanne); 2020; 11():104. PubMed ID: 32210915
    [No Abstract]   [Full Text] [Related]  

  • 8. Novel neurodevelopmental information revealed in amniotic fluid supernatant transcripts from fetuses with trisomies 18 and 21.
    Hui L; Slonim DK; Wick HC; Johnson KL; Koide K; Bianchi DW
    Hum Genet; 2012 Nov; 131(11):1751-9. PubMed ID: 22752091
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The amniotic fluid transcriptome: a source of novel information about human fetal development.
    Hui L; Slonim DK; Wick HC; Johnson KL; Bianchi DW
    Obstet Gynecol; 2012 Jan; 119(1):111-8. PubMed ID: 22183218
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epigenetics in Turner syndrome.
    Álvarez-Nava F; Lanes R
    Clin Epigenetics; 2018; 10():45. PubMed ID: 29636833
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microarray analysis of cell-free fetal DNA in amniotic fluid: a prenatal molecular karyotype.
    Larrabee PB; Johnson KL; Pestova E; Lucas M; Wilber K; LeShane ES; Tantravahi U; Cowan JM; Bianchi DW
    Am J Hum Genet; 2004 Sep; 75(3):485-91. PubMed ID: 15252756
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Proteomic analysis of amniotic fluid in pregnancies with Turner syndrome fetuses.
    Mavrou A; Anagnostopoulos AK; Kolialexi A; Vougas K; Papantoniou N; Antsaklis A; Fountoulakis M; Tsangaris GT
    J Proteome Res; 2008 May; 7(5):1862-6. PubMed ID: 18363353
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Epigenetic and transcriptomic consequences of excess X-chromosome material in 47,XXX syndrome-A comparison with Turner syndrome and 46,XX females.
    Nielsen MM; Trolle C; Vang S; Hornshøj H; Skakkebaek A; Hedegaard J; Nordentoft I; Pedersen JS; Gravholt CH
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):279-293. PubMed ID: 32489015
    [TBL] [Abstract][Full Text] [Related]  

  • 14. RNA-Seq and expression microarray highlight different aspects of the fetal amniotic fluid transcriptome.
    Zwemer LM; Hui L; Wick HC; Bianchi DW
    Prenat Diagn; 2014 Oct; 34(10):1006-14. PubMed ID: 24852236
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparative Transcriptome Analysis of Cell-Free Fetal RNA from Amniotic Fluid and RNA from Amniocytes in Uncomplicated Pregnancies.
    Kang JH; Park HJ; Jung YW; Shim SH; Sung SR; Park JE; Cha DH; Ahn EH
    PLoS One; 2015; 10(7):e0132955. PubMed ID: 26181329
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The pathway not taken: understanding 'omics data in the perinatal context.
    Edlow AG; Slonim DK; Wick HC; Hui L; Bianchi DW
    Am J Obstet Gynecol; 2015 Jul; 213(1):59.e1-59.e172. PubMed ID: 25772209
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Integrated functional genomic analyses of Klinefelter and Turner syndromes reveal global network effects of altered X chromosome dosage.
    Zhang X; Hong D; Ma S; Ward T; Ho M; Pattni R; Duren Z; Stankov A; Bade Shrestha S; Hallmayer J; Wong WH; Reiss AL; Urban AE
    Proc Natl Acad Sci U S A; 2020 Mar; 117(9):4864-4873. PubMed ID: 32071206
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mature miR-99a Upregulation in the Amniotic Fluid Samples from Female Fetus Down Syndrome Pregnancies: A Pilot Study.
    Vizitiu AC; Stambouli D; Pavel AG; Muresan MC; Anastasiu DM; Bejinar C; Alexa A; Marian C; Sirbu IO; Sima L
    Medicina (Kaunas); 2019 Nov; 55(11):. PubMed ID: 31703316
    [No Abstract]   [Full Text] [Related]  

  • 19. Global gene expression analysis of the living human fetus using cell-free messenger RNA in amniotic fluid.
    Larrabee PB; Johnson KL; Lai C; Ordovas J; Cowan JM; Tantravahi U; Bianchi DW
    JAMA; 2005 Feb; 293(7):836-42. PubMed ID: 15713773
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Array-CGH analysis of cell-free fetal DNA in 10 mL of amniotic fluid supernatant.
    Lapaire O; Lu XY; Johnson KL; Jarrah Z; Stroh H; Cowan JM; Tantravahi U; Bianchi DW
    Prenat Diagn; 2007 Jul; 27(7):616-21. PubMed ID: 17510923
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.