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 *

274 related articles for article (PubMed ID: 38424476)

  • 21. X chromosome regulation: diverse patterns in development, tissues and disease.
    Deng X; Berletch JB; Nguyen DK; Disteche CM
    Nat Rev Genet; 2014 Jun; 15(6):367-78. PubMed ID: 24733023
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Aneuploid rescue precedes X-chromosome inactivation and increases the incidence of its skewness by reducing the size of the embryonic progenitor cell pool.
    Yoshida T; Miyado M; Mikami M; Suzuki E; Kinjo K; Matsubara K; Ogata T; Akutsu H; Kagami M; Fukami M
    Hum Reprod; 2019 Sep; 34(9):1762-1769. PubMed ID: 31398259
    [TBL] [Abstract][Full Text] [Related]  

  • 23. X-inactivation and human disease: X-linked dominant male-lethal disorders.
    Franco B; Ballabio A
    Curr Opin Genet Dev; 2006 Jun; 16(3):254-9. PubMed ID: 16650755
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial skewed X-chromosome inactivation linked to a component of the cohesin complex, SA2.
    Renault NK; Renault MP; Copeland E; Howell RE; Greer WL
    J Hum Genet; 2011 May; 56(5):390-7. PubMed ID: 21412246
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern.
    Fieremans N; Van Esch H; Holvoet M; Van Goethem G; Devriendt K; Rosello M; Mayo S; Martinez F; Jhangiani S; Muzny DM; Gibbs RA; Lupski JR; Vermeesch JR; Marynen P; Froyen G
    Hum Mutat; 2016 Aug; 37(8):804-11. PubMed ID: 27159028
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dosage Compensation in Females with X-Linked Metabolic Disorders.
    Juchniewicz P; Piotrowska E; Kloska A; Podlacha M; Mantej J; Węgrzyn G; Tukaj S; Jakóbkiewicz-Banecka J
    Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33925963
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes.
    Giorgio E; Brussino A; Biamino E; Belligni EF; Bruselles A; Ciolfi A; Caputo V; Pizzi S; Calcia A; Di Gregorio E; Cavalieri S; Mancini C; Pozzi E; Ferrero M; Riberi E; Borelli I; Amoroso A; Ferrero GB; Tartaglia M; Brusco A
    Eur J Paediatr Neurol; 2017 May; 21(3):475-484. PubMed ID: 28027854
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel phenotype characterized by digital abnormalities, intellectual disability, and short stature in a Mexican family maps to Xp11.4-p11.21.
    Barboza-Cerda MC; Campos-Acevedo LD; Rangel R; Martínez-de-Villarreal LE; Déctor MA
    Am J Med Genet A; 2013 Feb; 161A(2):237-43. PubMed ID: 23307567
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The pathogenicity of genomic/genetic variant of X-chromosomal genes in males with intellectual disability.
    Peng JP; Liu F; Xie H; Chen XL
    Yi Chuan; 2017 Jun; 39(6):455-468. PubMed ID: 28903905
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Female X-chromosome mosaicism for gp91phox expression diversifies leukocyte responses during endotoxemia.
    Chandra R; Federici S; Haskó G; Deitch EA; Spolarics Z
    Crit Care Med; 2010 Oct; 38(10):2003-10. PubMed ID: 20657276
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome.
    Wimplinger I; Rauch A; Orth U; Schwarzer U; Trautmann U; Kutsche K
    Eur J Med Genet; 2007; 50(6):421-31. PubMed ID: 17845869
    [TBL] [Abstract][Full Text] [Related]  

  • 32. X-linked intellectual disability: Phenotypic expression in carrier females.
    Ziats CA; Schwartz CE; Gecz J; Shaw M; Field MJ; Stevenson RE; Neri G
    Clin Genet; 2020 Mar; 97(3):418-425. PubMed ID: 31705537
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A Novel and Mosaic WDR45 Nonsense Variant Causes Beta-Propeller Protein-Associated Neurodegeneration Identified Through Whole Exome Sequencing and X chromosome Heterozygosity Analysis.
    Akçakaya NH; Salman B; Görmez Z; Tarkan Argüden Y; Çırakoğlu A; Çakmur R; Dönmez Çolakoğlu B; Hacıhanefioğlu S; Özbek U; Yapıcı Z; Uğur İşeri SA
    Neuromolecular Med; 2019 Mar; 21(1):54-59. PubMed ID: 30612247
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular signatures of X chromosome inactivation and associations with clinical outcomes in epithelial ovarian cancer.
    Winham SJ; Larson NB; Armasu SM; Fogarty ZC; Larson MC; McCauley BM; Wang C; Lawrenson K; Gayther S; Cunningham JM; Fridley BL; Goode EL
    Hum Mol Genet; 2019 Apr; 28(8):1331-1342. PubMed ID: 30576442
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Developmental regulation of X-chromosome inactivation.
    Payer B
    Semin Cell Dev Biol; 2016 Aug; 56():88-99. PubMed ID: 27112543
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. X-chromosome inactivation: implications in human disease.
    Pereira G; Dória S
    J Genet; 2021; 100():. PubMed ID: 34553695
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The Role of X-Chromosome Inactivation in Retinal Development and Disease.
    Fahim AT; Daiger SP
    Adv Exp Med Biol; 2016; 854():325-31. PubMed ID: 26427428
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Next-generation sequencing in X-linked intellectual disability.
    Tzschach A; Grasshoff U; Beck-Woedl S; Dufke C; Bauer C; Kehrer M; Evers C; Moog U; Oehl-Jaschkowitz B; Di Donato N; Maiwald R; Jung C; Kuechler A; Schulz S; Meinecke P; Spranger S; Kohlhase J; Seidel J; Reif S; Rieger M; Riess A; Sturm M; Bickmann J; Schroeder C; Dufke A; Riess O; Bauer P
    Eur J Hum Genet; 2015 Nov; 23(11):1513-8. PubMed ID: 25649377
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Heritability of skewed X-inactivation in female twins is tissue-specific and associated with age.
    Zito A; Davies MN; Tsai PC; Roberts S; Andres-Ejarque R; Nardone S; Bell JT; Wong CCY; Small KS
    Nat Commun; 2019 Nov; 10(1):5339. PubMed ID: 31767861
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.