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 *

146 related articles for article (PubMed ID: 16460442)

  • 1. Int22h-related inversions causing hemophilia A: a novel insight into their origin and a new more discriminant PCR test for their detection.
    Bagnall RD; Giannelli F; Green PM
    J Thromb Haemost; 2006 Mar; 4(3):591-8. PubMed ID: 16460442
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A.
    Bagnall RD; Ayres KL; Green PM; Giannelli F
    Genome Res; 2005 Feb; 15(2):214-23. PubMed ID: 15687285
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions.
    Naylor JA; Buck D; Green P; Williamson H; Bentley D; Giannelli F
    Hum Mol Genet; 1995 Jul; 4(7):1217-24. PubMed ID: 8528212
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel DNA inversion causing severe hemophilia A.
    Naylor JA; Nicholson P; Goodeve Anne ; Hassock S; Peake I; Giannelli F
    Blood; 1996 Apr; 87(8):3255-61. PubMed ID: 8605341
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [FVIII intron 22 homologous region mediated recombinations and genotyping methods of hemophilia A].
    Guo ZP; Yang LH
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2014 Jun; 22(3):865-8. PubMed ID: 24989311
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Noninvasive detection of
    Hudecova I; Jiang P; Davies J; Lo YMD; Kadir RA; Chiu RWK
    Blood; 2017 Jul; 130(3):340-347. PubMed ID: 28490568
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A.
    Bagnall RD; Waseem N; Green PM; Giannelli F
    Blood; 2002 Jan; 99(1):168-74. PubMed ID: 11756167
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A possible mechanism for Inv22-related F8 large deletions in severe hemophilia A patients with high responding factor VIII inhibitors.
    Fujita J; Miyawaki Y; Suzuki A; Maki A; Okuyama E; Murata M; Takagi A; Murate T; Suzuki N; Matsushita T; Saito H; Kojima T
    J Thromb Haemost; 2012 Oct; 10(10):2099-107. PubMed ID: 22906111
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of F8 int22h inversions using digital droplet PCR and mile-post assays.
    Manderstedt E; Lind-Halldén C; Ljung R; Astermark J; Halldén C
    J Thromb Haemost; 2020 May; 18(5):1039-1049. PubMed ID: 32031725
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia A.
    Andrikovics H; Klein I; Bors A; Nemes L; Marosi A; Váradi A; Tordai A
    Haematologica; 2003 Jul; 88(7):778-84. PubMed ID: 12857556
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inversions of the factor VIII gene in Japanese patients with severe hemophilia A.
    Fukuda K; Naka H; Morichika S; Shibata M; Tanaka I; Shima M; Yoshioka A
    Int J Hematol; 2004 Apr; 79(3):303-6. PubMed ID: 15168603
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complex recombination with deletion in the F8 and duplication in the TMLHE mediated by int22h copies during early embryogenesis.
    Chen C; Xie X; Wu X; Lu Y; Wang X; Wu W; Hu Y; Ding Q
    Thromb Haemost; 2017 Jul; 117(8):1478-1485. PubMed ID: 28492696
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene.
    Lannoy N; Ravoet M; Grisart B; Fretigny M; Vikkula M; Hermans C
    Thromb Res; 2016 Jan; 137():224-227. PubMed ID: 26653368
    [No Abstract]   [Full Text] [Related]  

  • 14. A Closed-Tube Nested Quantitative PCR Assay for Rapid Detection of Intron 22 Inversions in the Factor VIII Gene.
    Jin S; Shang Q; Jin W; Yang L; Ye Q; Wang X; Zhang T; Hou M; Liu Y; Han J; Ding R; Luan J; Wang X; Jiang M; Ding C
    Clin Chem; 2020 Feb; 66(2):373-378. PubMed ID: 32040575
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inverse shifting PCR based prenatal diagnosis of hemophilia-causative inversions involving int22h and int1h hotspots from chorionic villus samples.
    Radic CP; Rossetti LC; Zuccoli JR; Abelleyro MM; Larripa IB; De Brasi CD
    Prenat Diagn; 2009 Dec; 29(12):1183-5. PubMed ID: 19842127
    [No Abstract]   [Full Text] [Related]  

  • 16. Developing a new generation of tests for genotyping hemophilia-causative rearrangements involving int22h and int1h hotspots in the factor VIII gene.
    Rossetti LC; Radic CP; Larripa IB; De Brasi CD
    J Thromb Haemost; 2008 May; 6(5):830-6. PubMed ID: 18284600
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variant of intron 22 inversions in the factor VIII gene in severe hemophilia A.
    Yamazaki E; Mohri H; Inaba H; Harano H; Kanamori H; Okubo T
    Blood Coagul Fibrinolysis; 1997 Oct; 8(7):445-9. PubMed ID: 9391727
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.
    El-Hattab AW; Fang P; Jin W; Hughes JR; Gibson JB; Patel GS; Grange DK; Manwaring LP; Patel A; Stankiewicz P; Cheung SW
    J Med Genet; 2011 Dec; 48(12):840-50. PubMed ID: 21984752
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counseling.
    Jenkins PV; Collins PW; Goldman E; McCraw A; Riddell A; Lee CA; Pasi KJ
    Blood; 1994 Oct; 84(7):2197-201. PubMed ID: 7919335
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells.
    Rossiter JP; Young M; Kimberland ML; Hutter P; Ketterling RP; Gitschier J; Horst J; Morris MA; Schaid DJ; de Moerloose P
    Hum Mol Genet; 1994 Jul; 3(7):1035-9. PubMed ID: 7981669
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.