BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

239 related articles for article (PubMed ID: 25128687)

  • 1. Constitutional chromoanasynthesis: description of a rare chromosomal event in a patient.
    Plaisancié J; Kleinfinger P; Cances C; Bazin A; Julia S; Trost D; Lohmann L; Vigouroux A
    Eur J Med Genet; 2014 Oct; 57(10):567-70. PubMed ID: 25128687
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Shattered and stitched chromosomes-chromothripsis and chromoanasynthesis-manifestations of a new chromosome crisis?
    Righolt C; Mai S
    Genes Chromosomes Cancer; 2012 Nov; 51(11):975-81. PubMed ID: 22811041
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromoanasynthesis: another way for the formation of complex chromosomal abnormalities in human reproduction.
    Pellestor F; Gatinois V
    Hum Reprod; 2018 Aug; 33(8):1381-1387. PubMed ID: 30325427
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Cytogenetic-molecular analysis of balanced chromosomal rearrangements in nine patients with intellectual disability, dysmorphic features and congenital abnormalities].
    Borg K; Bocian E; Stankiewicz P; Obersztyn E; Kruczek A; Nowakowska B; Ilnicka A; Mazurczak T
    Med Wieku Rozwoj; 2006; 10(1 Pt 2):227-46. PubMed ID: 17028391
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis.
    Arya P; Hodge JC; Matlock PA; Vance GH; Breman AM
    Cytogenet Genome Res; 2020; 160(11-12):671-679. PubMed ID: 33535208
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Catastrophic cellular events leading to complex chromosomal rearrangements in the germline.
    Fukami M; Shima H; Suzuki E; Ogata T; Matsubara K; Kamimaki T
    Clin Genet; 2017 May; 91(5):653-660. PubMed ID: 27888607
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations.
    Suzuki E; Shima H; Toki M; Hanew K; Matsubara K; Kurahashi H; Narumi S; Ogata T; Kamimaki T; Fukami M
    Cytogenet Genome Res; 2016; 150(2):86-92. PubMed ID: 28099951
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Stable transmission of complex chromosomal rearrangements involving chromosome 1q derived from constitutional chromoanagenesis.
    Gudipati MA; Waters E; Greene C; Goel N; Hoppman NL; Pitel BA; Webley MR; Zou Y
    Mol Cytogenet; 2019; 12():43. PubMed ID: 31695749
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromoanasynthesis as a cause of Jacobsen syndrome.
    Anzick S; Thurm A; Burkett S; Velez D; Cho E; Chlebowski C; Virtaneva K; Bruno D; Martin CB; Lang DM; Brooks B; Martens C; McDermott DH; Murphy PM
    Am J Med Genet A; 2020 Nov; 182(11):2533-2539. PubMed ID: 32841469
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromothripsis: how does such a catastrophic event impact human reproduction?
    Pellestor F
    Hum Reprod; 2014 Mar; 29(3):388-93. PubMed ID: 24452388
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heterogeneity of a Constitutional Complex Chromosomal Rearrangement in 2q.
    Del Rey J; Santos M; González-Meneses A; Milà M; Fuster C
    Cytogenet Genome Res; 2016; 148(2-3):156-64. PubMed ID: 27216161
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms.
    Kloosterman WP; Tavakoli-Yaraki M; van Roosmalen MJ; van Binsbergen E; Renkens I; Duran K; Ballarati L; Vergult S; Giardino D; Hansson K; Ruivenkamp CA; Jager M; van Haeringen A; Ippel EF; Haaf T; Passarge E; Hochstenbach R; Menten B; Larizza L; Guryev V; Poot M; Cuppen E
    Cell Rep; 2012 Jun; 1(6):648-55. PubMed ID: 22813740
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromothripsis: potential origin in gametogenesis and preimplantation cell divisions. A review.
    Pellestor F; Gatinois V; Puechberty J; Geneviève D; Lefort G
    Fertil Steril; 2014 Dec; 102(6):1785-96. PubMed ID: 25439810
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromoanagenesis and cancer: mechanisms and consequences of localized, complex chromosomal rearrangements.
    Holland AJ; Cleveland DW
    Nat Med; 2012 Nov; 18(11):1630-8. PubMed ID: 23135524
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical Consequences of Chromothripsis and Other Catastrophic Cellular Events.
    Fukami M; Kurahashi H
    Methods Mol Biol; 2018; 1769():21-33. PubMed ID: 29564815
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Complex Chromosomal Rearrangements in B-Cell Lymphoma: Evidence of Chromoanagenesis? A Case Report.
    Ortega V; Chaubey A; Mendiola C; Ehman W; Vadlamudi K; Dupont B; Velagaleti G
    Neoplasia; 2016 Apr; 18(4):223-8. PubMed ID: 27108385
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
    Cetin Z; Yakut S; Clark OA; Mihci E; Berker S; Luleci G
    Gene; 2013 Mar; 516(1):176-80. PubMed ID: 23262338
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
    Guilherme RS; Cernach MC; Sfakianakis TE; Takeno SS; Nardozza LM; Rossi C; Bhatt SS; Liehr T; Melaragno MI
    Cytogenet Genome Res; 2013; 141(4):317-23. PubMed ID: 23817307
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic Chaos (Multiple Copy Number Variations and Structural Reorganization) Detected in Two Prenatal Cases.
    Lloveras E; Canellas A; Plaja A; Barranco L; Fernández D; Mendez B; Piqué M; de la Iglesia C; Palau N; Costa M; Herrero M; Yeste D; Auge M; Puig L; Pérez C
    Cytogenet Genome Res; 2021; 161(5):236-242. PubMed ID: 34274931
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.