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 *

121 related articles for article (PubMed ID: 26477560)

  • 1. Selective chromatid segregation mechanism proposed for the human split hand/foot malformation development by chromosome 2 translocations: A perspective.
    Klar AJ
    Dev Biol; 2015 Dec; 408(1):7-13. PubMed ID: 26477560
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Split hand/foot malformation genetics supports the chromosome 7 copy segregation mechanism for human limb development.
    Klar AJ
    Philos Trans R Soc Lond B Biol Sci; 2016 Dec; 371(1710):. PubMed ID: 27821526
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation.
    Babbs C; Heller R; Everman DB; Crocker M; Twigg SR; Schwartz CE; Giele H; Wilkie AO
    Hum Genet; 2007 Sep; 122(2):191-9. PubMed ID: 17569090
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Absent expression of the osteoblast-specific maternally imprinted genes, DLX5 and DLX6, causes split hand/split foot malformation type I.
    Rattanasopha S; Tongkobpetch S; Srichomthong C; Kitidumrongsook P; Suphapeetiporn K; Shotelersuk V
    J Med Genet; 2014 Dec; 51(12):817-23. PubMed ID: 25332435
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterozygous DLX5 nonsense mutation associated with isolated split-hand/foot malformation with reduced penetrance and variable expressivity in two unrelated families.
    Sowińska-Seidler A; Badura-Stronka M; Latos-Bieleńska A; Stronka M; Jamsheer A
    Birth Defects Res A Clin Mol Teratol; 2014 Oct; 100(10):764-71. PubMed ID: 25196357
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families.
    Aziz A; Irfanullah ; Khan S; Zimri FK; Muhammad N; Rashid S; Ahmad W
    Gene; 2014 Jan; 534(2):265-71. PubMed ID: 24211389
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unbiased segregation of fission yeast chromosome 2 strands to daughter cells.
    Klar AJ; Bonaduce MJ
    Chromosome Res; 2013 May; 21(3):297-309. PubMed ID: 23681661
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Breakpoints around the HOXD cluster result in various limb malformations.
    Dlugaszewska B; Silahtaroglu A; Menzel C; Kübart S; Cohen M; Mundlos S; Tümer Z; Kjaer K; Friedrich U; Ropers HH; Tommerup N; Neitzel H; Kalscheuer VM
    J Med Genet; 2006 Feb; 43(2):111-8. PubMed ID: 15980115
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements.
    Dimitrov BI; de Ravel T; Van Driessche J; de Die-Smulders C; Toutain A; Vermeesch JR; Fryns JP; Devriendt K; Debeer P
    J Med Genet; 2010 Feb; 47(2):103-11. PubMed ID: 19584065
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Support for the selective chromatid segregation hypothesis advanced for the mechanism of left-right body axis development in mice.
    Klar AJ
    Breast Dis; 2008; 29():47-56. PubMed ID: 19029624
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q14.1-q14.2.
    David D; Marques B; Ferreira C; Vieira P; Corona-Rivera A; Ferreira JC; van Bokhoven H
    Eur J Hum Genet; 2009 Aug; 17(8):1024-33. PubMed ID: 19223936
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Selective chromatid segregation mechanism invoked for the human congenital mirror hand movement disorder development by RAD51 mutations: a hypothesis.
    Klar AJ
    Int J Biol Sci; 2014; 10(9):1018-23. PubMed ID: 25210500
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cell type regulates selective segregation of mouse chromosome 7 DNA strands in mitosis.
    Armakolas A; Klar AJ
    Science; 2006 Feb; 311(5764):1146-9. PubMed ID: 16497932
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A genetic mechanism implicates chromosome 11 in schizophrenia and bipolar diseases.
    Klar AJ
    Genetics; 2004 Aug; 167(4):1833-40. PubMed ID: 15342521
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Discovery of the mitotic selective chromatid segregation phenomenon and its implications for vertebrate development.
    Armakolas A; Koutsilieris M; Klar AJ
    Curr Opin Cell Biol; 2010 Feb; 22(1):81-7. PubMed ID: 20022232
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in humans.
    Lango Allen H; Caswell R; Xie W; Xu X; Wragg C; Turnpenny PD; Turner CL; Weedon MN; Ellard S
    J Med Genet; 2014 Apr; 51(4):264-7. PubMed ID: 24459211
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The mechanism of sister chromatid cohesion.
    Uhlmann F
    Exp Cell Res; 2004 May; 296(1):80-5. PubMed ID: 15120997
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster.
    Del Campo M; Jones MC; Veraksa AN; Curry CJ; Jones KL; Mascarello JT; Ali-Kahn-Catts Z; Drumheller T; McGinnis W
    Am J Hum Genet; 1999 Jul; 65(1):104-10. PubMed ID: 10364522
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.
    Scherer SW; Poorkaj P; Allen T; Kim J; Geshuri D; Nunes M; Soder S; Stephens K; Pagon RA; Patton MA
    Am J Hum Genet; 1994 Jul; 55(1):12-20. PubMed ID: 8023840
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion.
    Klopocki E; Lohan S; Doelken SC; Stricker S; Ockeloen CW; Soares Thiele de Aguiar R; Lezirovitz K; Mingroni Netto RC; Jamsheer A; Shah H; Kurth I; Habenicht R; Warman M; Devriendt K; Kordass U; Hempel M; Rajab A; Mäkitie O; Naveed M; Radhakrishna U; Antonarakis SE; Horn D; Mundlos S
    J Med Genet; 2012 Feb; 49(2):119-25. PubMed ID: 22147889
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.