BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 11898846)

  • 1. Homeobox genes and human genetic disorders.
    Zhao Y; Westphal H
    Curr Mol Med; 2002 Feb; 2(1):13-23. PubMed ID: 11898846
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Human HOX gene disorders.
    Quinonez SC; Innis JW
    Mol Genet Metab; 2014 Jan; 111(1):4-15. PubMed ID: 24239177
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homeobox genes and disease.
    Boncinelli E
    Curr Opin Genet Dev; 1997 Jun; 7(3):331-7. PubMed ID: 9229108
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Missense mutations of human homeoboxes: A review.
    D'Elia AV; Tell G; Paron I; Pellizzari L; Lonigro R; Damante G
    Hum Mutat; 2001 Nov; 18(5):361-74. PubMed ID: 11668629
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Modelling genotype-phenotype relationships and human disease with genetic interaction networks.
    Lehner B
    J Exp Biol; 2007 May; 210(Pt 9):1559-66. PubMed ID: 17449820
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Kinase mutations in human disease: interpreting genotype-phenotype relationships.
    Lahiry P; Torkamani A; Schork NJ; Hegele RA
    Nat Rev Genet; 2010 Jan; 11(1):60-74. PubMed ID: 20019687
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ
    Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial diseases: genotype versus phenotype.
    Wallace DC
    Trends Genet; 1993 Apr; 9(4):128-33. PubMed ID: 8516847
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Genetic mutation databases: stakes and perspectives for orphan genetic diseases].
    Humbertclaude V; Tuffery-Giraud S; Bareil C; Thèze C; Paulet D; Desmet FO; Hamroun D; Baux D; Girardet A; Collod-Béroud G; Khau Van Kien P; Roux AF; des Georges M; Béroud C; Claustres M
    Pathol Biol (Paris); 2010 Oct; 58(5):387-95. PubMed ID: 19954899
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Beyond Mendel: an evolving view of human genetic disease transmission.
    Badano JL; Katsanis N
    Nat Rev Genet; 2002 Oct; 3(10):779-89. PubMed ID: 12360236
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heritable collagen disorders: from phenotype to genotype.
    De Paepe A
    Verh K Acad Geneeskd Belg; 1998; 60(5):463-82; discussion 482-4. PubMed ID: 9989335
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Is there a paradigm shift in genetics? Lessons from the study of human diseases.
    Weiss KM
    Mol Phylogenet Evol; 1996 Feb; 5(1):259-65. PubMed ID: 8673294
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ionizing radiation and genetic risks. X. The potential "disease phenotypes" of radiation-induced genetic damage in humans: perspectives from human molecular biology and radiation genetics.
    Sankaranarayanan K
    Mutat Res; 1999 Aug; 429(1):45-83. PubMed ID: 10434024
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome.
    Köchling J; Karbasiyan M; Reis A
    Eur J Hum Genet; 2001 Aug; 9(8):599-605. PubMed ID: 11528505
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular-genetic heterogeneity of hereditary diseases].
    Gaĭtskhoki VS
    Vopr Med Khim; 1997; 43(5):290-300. PubMed ID: 9446319
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.
    Betancur C
    Brain Res; 2011 Mar; 1380():42-77. PubMed ID: 21129364
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genatlas database, genes and development defects.
    Frézal J
    C R Acad Sci III; 1998 Oct; 321(10):805-17. PubMed ID: 9835018
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Modifier genes and oligogenic disease.
    Agarwal S; Moorchung N
    J Nippon Med Sch; 2005 Dec; 72(6):326-34. PubMed ID: 16415512
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Regulation of eye formation by the Rx and pax6 homeobox genes.
    Mathers PH; Jamrich M
    Cell Mol Life Sci; 2000 Feb; 57(2):186-94. PubMed ID: 10766016
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Strategies for elucidating the phenotypic and genetic heterogeneity of a chronic disease with a complex etiology.
    Sing CF; Boerwinkle E; Moll PP
    Prog Clin Biol Res; 1985; 194():39-66. PubMed ID: 3906666
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.