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 *

136 related articles for article (PubMed ID: 28284085)

  • 41. [Chromatin modifications during X-chromosome inactivation in female mammals].
    Shevchenko AI; Pavlova SV; Dement'eva EV; Golubeva DV; Zakiian SM
    Genetika; 2006 Sep; 42(9):1225-34. PubMed ID: 17100090
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome.
    Lopes AM; Burgoyne PS; Ojarikre A; Bauer J; Sargent CA; Amorim A; Affara NA
    BMC Genomics; 2010 Feb; 11():82. PubMed ID: 20122165
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete.
    Zeschnigk M; Martin M; Betzl G; Kalbe A; Sirsch C; Buiting K; Gross S; Fritzilas E; Frey B; Rahmann S; Horsthemke B
    Hum Mol Genet; 2009 Apr; 18(8):1439-48. PubMed ID: 19223391
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Abnormal methylation does not prevent X inactivation in ICF patients.
    Bourc'his D; Miniou P; Jeanpierre M; Molina Gomes D; Dupont J; De Saint-Basile G; Maraschio P; Tiepolo L; Viegas-Péquignot E
    Cytogenet Cell Genet; 1999; 84(3-4):245-52. PubMed ID: 10393442
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome.
    Ko JM; Kim JM; Kim GH; Lee BH; Yoo HW
    Clin Endocrinol (Oxf); 2010 Jul; 73(1):66-71. PubMed ID: 20148908
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Investigation of genomic methylation status using methylation-specific and bisulfite sequencing polymerase chain reaction.
    Carless MA
    Methods Mol Biol; 2015; 1288():193-212. PubMed ID: 25827881
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Quantitative and multiplexed DNA methylation analysis using long-read single-molecule real-time bisulfite sequencing (SMRT-BS).
    Yang Y; Sebra R; Pullman BS; Qiao W; Peter I; Desnick RJ; Geyer CR; DeCoteau JF; Scott SA
    BMC Genomics; 2015 May; 16(1):350. PubMed ID: 25943404
    [TBL] [Abstract][Full Text] [Related]  

  • 48. An atypical Turner syndrome patient with ring X chromosome mosaicism.
    Cantú ES; Jacobs DF; Pai GS
    Ann Clin Lab Sci; 1995; 25(1):60-5. PubMed ID: 7762970
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Parental origin of the X-chromosome does not influence growth hormone treatment effect in Turner syndrome.
    Devernay M; Bolca D; Kerdjana L; Aboura A; Gérard B; Tabet AC; Benzacken B; Ecosse E; Coste J; Carel JC
    J Clin Endocrinol Metab; 2012 Jul; 97(7):E1241-8. PubMed ID: 22593588
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Identification and characterization of marker chromosome in Turner syndrome].
    Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Neonatal detection of Turner syndrome by real-time PCR gene quantification of the ARSE and MAGEH1 genes.
    Corrêa SC; Rocha MN; Richeti F; Kochi C; Silva E Lima LA; Magalhães M; Longui CA
    Genet Mol Res; 2014 Oct; 13(4):9068-76. PubMed ID: 25366798
    [TBL] [Abstract][Full Text] [Related]  

  • 52. DNA Hypermethylation and a Specific Methylation Spectrum on the X Chromosome in Turner Syndrome as Determined by Nanopore Sequencing.
    Fan X; Zhang B; Fan L; Chen J; Su C; Cao B; Wei L; Qin M; Gong C
    J Pers Med; 2022 May; 12(6):. PubMed ID: 35743657
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Applicability of real-time PCR methodology in the neonatal detection of Turner syndrome.
    Rocha MN; Longui CA; Kochi C; Corrêa CS; Faria CD; Richeti F; Melo MR
    Horm Metab Res; 2010 Aug; 42(9):677-81. PubMed ID: 20422505
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
    Liang Y; Luo XP
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities.
    Daggag H; Srour W; El-Khateeb M; Ajlouni K
    Sex Dev; 2013; 7(6):295-302. PubMed ID: 23988405
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Chromosome Xq13.2 Microduplication Involving an X-Inactivation Gene in a Girl with Short Stature, Madelung Deformity, and von Willebrand Disease.
    Nur MM; Yamada M; Tonk V; Wilson GN
    J Pediatr Adolesc Gynecol; 2016 Apr; 29(2):e39-42. PubMed ID: 26639996
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The inactive X chromosome accumulates widespread epigenetic variability with age.
    Liu Y; Sinke L; Jonkman TH; Slieker RC; ; van Zwet EW; Daxinger L; Heijmans BT
    Clin Epigenetics; 2023 Aug; 15(1):135. PubMed ID: 37626340
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females.
    Kubota T; Wakui K; Nakamura T; Ohashi H; Watanabe Y; Yoshino M; Kida T; Okamoto N; Matsumura M; Muroya K; Ogata T; Goto Y; Fukushima Y
    Cytogenet Genome Res; 2002; 99(1-4):276-84. PubMed ID: 12900575
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Rare copy number variants in the genome of Chinese female children and adolescents with Turner syndrome.
    Li L; Li Q; Wang Q; Liu L; Li R; Liu H; He Y; Lash GE
    Biosci Rep; 2019 Jan; 39(1):. PubMed ID: 30530863
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Clinical significance of the parental origin of the X chromosome in turner syndrome.
    Sagi L; Zuckerman-Levin N; Gawlik A; Ghizzoni L; Buyukgebiz A; Rakover Y; Bistritzer T; Admoni O; Vottero A; Baruch O; Fares F; Malecka-Tendera E; Hochberg Z
    J Clin Endocrinol Metab; 2007 Mar; 92(3):846-52. PubMed ID: 17192299
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.