BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 34128148)

  • 1. X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay.
    Rossanti R; Nozu K; Fukunaga A; Nagano C; Horinouchi T; Yamamura T; Sakakibara N; Minamikawa S; Ishiko S; Aoto Y; Okada E; Ninchoji T; Kato N; Maruyama S; Kono K; Nishi S; Iijima K; Fujii H
    Clin Exp Nephrol; 2021 Nov; 25(11):1224-1230. PubMed ID: 34128148
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Female Fabry disease patients and X-chromosome inactivation.
    Juchniewicz P; Kloska A; Tylki-Szymańska A; Jakóbkiewicz-Banecka J; Węgrzyn G; Moskot M; Gabig-Cimińska M; Piotrowska E
    Gene; 2018 Jan; 641():259-264. PubMed ID: 29079200
    [TBL] [Abstract][Full Text] [Related]  

  • 3. X-chromosome inactivation in female patients with Fabry disease.
    Echevarria L; Benistan K; Toussaint A; Dubourg O; Hagege AA; Eladari D; Jabbour F; Beldjord C; De Mazancourt P; Germain DP
    Clin Genet; 2016 Jan; 89(1):44-54. PubMed ID: 25974833
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disease manifestations and X inactivation in heterozygous females with Fabry disease.
    Maier EM; Osterrieder S; Whybra C; Ries M; Gal A; Beck M; Roscher AA; Muntau AC
    Acta Paediatr Suppl; 2006 Apr; 95(451):30-8. PubMed ID: 16720462
    [TBL] [Abstract][Full Text] [Related]  

  • 5. X-inactivation in Fabry disease.
    Elstein D; Schachamorov E; Beeri R; Altarescu G
    Gene; 2012 Sep; 505(2):266-8. PubMed ID: 22710134
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-chromosomal inactivation patterns in women with Fabry disease.
    Wagenhäuser L; Rickert V; Sommer C; Wanner C; Nordbeck P; Rost S; Üçeyler N
    Mol Genet Genomic Med; 2022 Sep; 10(9):e2029. PubMed ID: 35971858
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pitfalls of X-chromosome inactivation testing in females with Fabry disease.
    Řeboun M; Sikora J; Magner M; Wiederlechnerová H; Černá A; Poupětová H; Štorkánova G; Mušálková D; Dostálová G; Goláň L; Linhart A; Dvořáková L
    Am J Med Genet A; 2022 Jul; 188(7):1979-1989. PubMed ID: 35338595
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease.
    Minamikawa S; Nozu K; Nozu Y; Yamamura T; Taniguchi-Ikeda M; Nakanishi K; Fujimura J; Horinouchi T; Shima Y; Nakanishi K; Hattori M; Kanda K; Tanaka R; Morisada N; Nagano C; Sakakibara N; Nagase H; Morioka I; Kaito H; Iijima K
    J Hum Genet; 2018 May; 63(5):589-595. PubMed ID: 29459630
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X Chromosome Inactivation in Carriers of Fabry Disease: Review and Meta-Analysis.
    Viggiano E; Politano L
    Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34299283
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Relationship between X-inactivation and clinical involvement in Fabry heterozygotes. Eleven novel mutations in the alpha-galactosidase A gene in the Czech and Slovak population.
    Dobrovolny R; Dvorakova L; Ledvinova J; Magage S; Bultas J; Lubanda JC; Elleder M; Karetova D; Pavlikova M; Hrebicek M
    J Mol Med (Berl); 2005 Aug; 83(8):647-54. PubMed ID: 15806320
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA methylation impact on Fabry disease.
    Di Risi T; Vinciguerra R; Cuomo M; Della Monica R; Riccio E; Cocozza S; Imbriaco M; Duro G; Pisani A; Chiariotti L
    Clin Epigenetics; 2021 Feb; 13(1):24. PubMed ID: 33531072
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ultra-Deep DNA Methylation Analysis of X-Linked Genes:
    De Riso G; Cuomo M; Di Risi T; Della Monica R; Buonaiuto M; Costabile D; Pisani A; Cocozza S; Chiariotti L
    Genes (Basel); 2020 Jun; 11(6):. PubMed ID: 32512878
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Correlation of X chromosome inactivation with clinical presentation of Fabry disease in a case report.
    Rodríguez Doyágüez P; Furlano M; Ars Criach E; Arce Y; Guirado L; Torra Balcells R
    Nefrologia (Engl Ed); 2023 Dec; 43 Suppl 2():91-95. PubMed ID: 38278716
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A new sex-specific underlying mechanism for female schizophrenia: accelerated skewed X chromosome inactivation.
    Zhang X; Li Y; Ma L; Zhang G; Liu M; Wang C; Zheng Y; Li R
    Biol Sex Differ; 2020 Jul; 11(1):39. PubMed ID: 32680558
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Future clinical and biochemical predictions of Fabry disease in females by methylation studies of the
    Hossain MA; Wu C; Yanagisawa H; Miyajima T; Akiyama K; Eto Y
    Mol Genet Metab Rep; 2019 Sep; 20():100497. PubMed ID: 31372342
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].
    Jiang SL; Bao XH; Song FY; Pan H; Li MR; Wu XR
    Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):648-52. PubMed ID: 17217653
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome.
    Hossain MA; Yanagisawa H; Miyajima T; Wu C; Takamura A; Akiyama K; Itagaki R; Eto K; Iwamoto T; Yokoi T; Kurosawa K; Numabe H; Eto Y
    Mol Genet Metab; 2017 Mar; 120(3):173-179. PubMed ID: 28087245
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease.
    Hasholt L; Ballegaard M; Bundgaard H; Christiansen M; Law I; Lund AM; Norremolle A; Krogh Rasmussen A; Ravn K; Tumer Z; Wibrand F; Feldt-Rasmussen U
    Scand J Clin Lab Invest; 2017 Dec; 77(8):617-621. PubMed ID: 29037082
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene.
    Redonnet-Vernhet I; Ploos van Amstel JK; Jansen RP; Wevers RA; Salvayre R; Levade T
    J Med Genet; 1996 Aug; 33(8):682-8. PubMed ID: 8863162
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.