BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 23708688)

  • 1. Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome.
    Veerappa AM; Padakannaya P; Ramachandra NB
    Funct Integr Genomics; 2013 Aug; 13(3):285-93. PubMed ID: 23708688
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia.
    Veerappa AM; Saldanha M; Padakannaya P; Ramachandra NB
    Am J Med Genet B Neuropsychiatr Genet; 2013 Dec; 162B(8):889-97. PubMed ID: 24591081
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic Diversity on the Human X Chromosome Does Not Support a Strict Pseudoautosomal Boundary.
    Cotter DJ; Brotman SM; Wilson Sayres MA
    Genetics; 2016 May; 203(1):485-92. PubMed ID: 27010023
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pseudoautosomal region 1 length polymorphism in the human population.
    Mensah MA; Hestand MS; Larmuseau MH; Isrie M; Vanderheyden N; Declercq M; Souche EL; Van Houdt J; Stoeva R; Van Esch H; Devriendt K; Voet T; Decorte R; Robinson PN; Vermeesch JR
    PLoS Genet; 2014 Nov; 10(11):e1004578. PubMed ID: 25375121
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function.
    Castro A; Rodríguez F; Flórez M; López P; Curotto B; Martínez D; Maturana A; Lardone MC; Palma C; Mericq V; Ebensperger M; Cassorla F
    Hum Reprod; 2017 Feb; 32(2):465-475. PubMed ID: 28057878
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype.
    Si N; Meng X; Zhao Z; Xia W; Zhang X
    J Transl Med; 2019 Apr; 17(1):138. PubMed ID: 31036090
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Replication profile of PCDH11X and PCDH11Y, a gene pair located in the non-pseudoautosomal homologous region Xq21.3/Yp11.2.
    Wilson ND; Ross LJ; Close J; Mott R; Crow TJ; Volpi EV
    Chromosome Res; 2007; 15(4):485-98. PubMed ID: 17671842
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The horse pseudoautosomal region (PAR): characterization and comparison with the human, chimp and mouse PARs.
    Raudsepp T; Chowdhary BP
    Cytogenet Genome Res; 2008; 121(2):102-9. PubMed ID: 18544933
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recombination hotspots in an extended human pseudoautosomal domain predicted from double-strand break maps and characterized by sperm-based crossover analysis.
    Poriswanish N; Neumann R; Wetton JH; Wagstaff J; Larmuseau MHD; Jobling MA; May CA
    PLoS Genet; 2018 Oct; 14(10):e1007680. PubMed ID: 30296256
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microsatellite variation and evolutionary history of PCDHX/Y gene pair within the Xq21.3/Yp11.2 hominid-specific homology block.
    Lopes AM; Calafell F; Amorim A
    Mol Biol Evol; 2004 Nov; 21(11):2092-101. PubMed ID: 15297598
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dynamic Copy Number Evolution of X- and Y-Linked Ampliconic Genes in Human Populations.
    Lucotte EA; Skov L; Jensen JM; Macià MC; Munch K; Schierup MH
    Genetics; 2018 Jul; 209(3):907-920. PubMed ID: 29769284
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of new susceptibility regions for X;Y translocations in patients with testicular disorder of sex development.
    Beaulieu Bergeron M; Lemyre E; Lemieux N
    Sex Dev; 2011; 5(1):1-6. PubMed ID: 21088380
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The human-specific Yp11.2/Xq21.3 homology block encodes a potentially functional testis-specific TGIF-like retroposon.
    Blanco-Arias P; Sargent CA; Affara NA
    Mamm Genome; 2002 Aug; 13(8):463-8. PubMed ID: 12226713
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy-number gains of HUWE1 due to replication- and recombination-based rearrangements.
    Froyen G; Belet S; Martinez F; Santos-Rebouças CB; Declercq M; Verbeeck J; Donckers L; Berland S; Mayo S; Rosello M; Pimentel MM; Fintelman-Rodrigues N; Hovland R; Rodrigues dos Santos S; Raymond FL; Bose T; Corbett MA; Sheffield L; van Ravenswaaij-Arts CM; Dijkhuizen T; Coutton C; Satre V; Siu V; Marynen P
    Am J Hum Genet; 2012 Aug; 91(2):252-64. PubMed ID: 22840365
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genomic and demographic processes differentially influence genetic variation across the human X chromosome.
    Cotter DJ; Webster TH; Wilson MA
    PLoS One; 2023; 18(11):e0287609. PubMed ID: 37910456
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Role of recombination and faithfulness to partner in sex chromosome degeneration.
    Mackiewicz D; Posacki P; Burdukiewicz M; Błażej P
    Sci Rep; 2018 Jun; 8(1):8978. PubMed ID: 29895905
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification and characterization of an Xp22.33;Yp11.2 translocation causing a triplication of several genes of the pseudoautosomal region 1 in an XX male patient with severe systemic lupus erythematosus.
    Chagnon P; Schneider R; Hébert J; Fortin PR; Provost S; Belisle C; Gingras M; Bolduc V; Perreault C; Silverman E; Busque L
    Arthritis Rheum; 2006 Apr; 54(4):1270-8. PubMed ID: 16575839
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Footprints of X-to-Y gene conversion in recent human evolution.
    Trombetta B; Cruciani F; Underhill PA; Sellitto D; Scozzari R
    Mol Biol Evol; 2010 Mar; 27(3):714-25. PubMed ID: 19812029
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Xq21.31-q21.32 duplication underlies intellectual disability in a large family with five affected males.
    Basit S; Malibari OI; Al-Balawi AM; Afzal S; Eldardear AE; Ramzan K
    Am J Med Genet A; 2016 Jan; 170A(1):87-93. PubMed ID: 26358363
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination.
    Schwartz A; Chan DC; Brown LG; Alagappan R; Pettay D; Disteche C; McGillivray B; de la Chapelle A; Page DC
    Hum Mol Genet; 1998 Jan; 7(1):1-11. PubMed ID: 9384598
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.