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 *

172 related articles for article (PubMed ID: 16859890)

  • 1. Identification of a doublet missense substitution in the bovine LRP4 gene as a candidate causal mutation for syndactyly in Holstein cattle.
    Duchesne A; Gautier M; Chadi S; Grohs C; Floriot S; Gallard Y; Caste G; Ducos A; Eggen A
    Genomics; 2006 Nov; 88(5):610-21. PubMed ID: 16859890
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4).
    Drögemüller C; Leeb T; Harlizius B; Tammen I; Distl O; Höltershinken M; Gentile A; Duchesne A; Eggen A
    BMC Genet; 2007 Feb; 8():5. PubMed ID: 17319939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The bovine aristaless-like homeobox 4 (ALX4) as a candidate gene for syndactyly.
    Wöhlke A; Kuiper H; Distl O; Drögemüller C
    Cytogenet Genome Res; 2006; 115(2):123-8. PubMed ID: 17065792
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Defective splicing of Megf7/Lrp4, a regulator of distal limb development, in autosomal recessive mulefoot disease.
    Johnson EB; Steffen DJ; Lynch KW; Herz J
    Genomics; 2006 Nov; 88(5):600-9. PubMed ID: 16963222
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic analysis of syndactyly in German Holstein cattle.
    Drögemüller C; Distl O
    Vet J; 2006 Jan; 171(1):120-5. PubMed ID: 16427589
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Case report: Syndactyly in German Holstein calves].
    Bähr C; Drögemüller C; Distl O
    Dtsch Tierarztl Wochenschr; 2004 Dec; 111(12):473-6. PubMed ID: 15648617
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The locus for bovine dilated cardiomyopathy maps to chromosome 18.
    Guziewicz KE; Owczarek-Lipska M; Küffer J; Schelling C; Tontis A; Denis C; Eggen A; Leeb T; Dolf G; Braunschweig MH
    Anim Genet; 2007 Jun; 38(3):265-9. PubMed ID: 17433012
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Progeny testing for bovine syndactyly.
    Johnson JL; Leipold HW; Snider GW; Baker RD
    J Am Vet Med Assoc; 1980 Mar; 176(6):549-50. PubMed ID: 6245051
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cenani-Lenz syndrome restricted to limb and kidney anomalies associated with a novel LRP4 missense mutation.
    Khan TN; Klar J; Ali Z; Khan F; Baig SM; Dahl N
    Eur J Med Genet; 2013 Jul; 56(7):371-4. PubMed ID: 23664847
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identity-by-descent mapping of recessive traits in livestock: application to map the bovine syndactyly locus to chromosome 15.
    Charlier C; Farnir F; Berzi P; Vanmanshoven P; Brouwers B; Vromans H; Georges M
    Genome Res; 1996 Jul; 6(7):580-9. PubMed ID: 8796345
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage mapping of the locus responsible for forelimb-girdle muscular anomaly of Japanese black cattle on bovine chromosome 26.
    Masoudi AA; Uchida K; Yokouchi K; Ohwada K; Abbasi AR; Tsuji T; Watanabe T; Hirano T; Sugimoto Y; Kunieda T
    Anim Genet; 2008 Feb; 39(1):46-50. PubMed ID: 18254734
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Serrate2 is disrupted in the mouse limb-development mutant syndactylism.
    Sidow A; Bulotsky MS; Kerrebrock AW; Bronson RT; Daly MJ; Reeve MP; Hawkins TL; Birren BW; Jaenisch R; Lander ES
    Nature; 1997 Oct; 389(6652):722-5. PubMed ID: 9338782
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A deletion of the paracellin-1 gene is responsible for renal tubular dysplasia in cattle.
    Ohba Y; Kitagawa H; Kitoh K; Sasaki Y; Takami M; Shinkai Y; Kunieda T
    Genomics; 2000 Sep; 68(3):229-36. PubMed ID: 10995564
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic effects on coat colour in cattle: dilution of eumelanin and phaeomelanin pigments in an F2-Backcross Charolais x Holstein population.
    Gutiérrez-Gil B; Wiener P; Williams JL
    BMC Genet; 2007 Aug; 8():56. PubMed ID: 17705851
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An integrated radiation hybrid map of bovine chromosome 18 that refines a critical region associated with multiple ocular defects in cattle.
    Abbasi AR; Geriletoya ; Ihara N; Khalaj M; Sugimoto Y; Kunieda T
    Anim Genet; 2006 Feb; 37(1):58-61. PubMed ID: 16441298
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a mutation associated with factor XI deficiency in Holstein cattle.
    Marron BM; Robinson JL; Gentry PA; Beever JE
    Anim Genet; 2004 Dec; 35(6):454-6. PubMed ID: 15566468
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Positional cloning of the gene LIMBIN responsible for bovine chondrodysplastic dwarfism.
    Takeda H; Takami M; Oguni T; Tsuji T; Yoneda K; Sato H; Ihara N; Itoh T; Kata SR; Mishina Y; Womack JE; Moritomo Y; Sugimoto Y; Kunieda T
    Proc Natl Acad Sci U S A; 2002 Aug; 99(16):10549-54. PubMed ID: 12136126
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7.
    Shiels A; Bennett TM; Prince JB; Tychsen L
    Mol Vis; 2007 Nov; 13():2233-41. PubMed ID: 18087240
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Toll-like receptors TLR1, TLR2 and TLR4 gene mutations and natural resistance to Mycobacterium avium subsp. paratuberculosis infection in cattle.
    Mucha R; Bhide MR; Chakurkar EB; Novak M; Mikula I
    Vet Immunol Immunopathol; 2009 Apr; 128(4):381-8. PubMed ID: 19131114
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.
    Drögemüller C; Drögemüller M; Leeb T; Mascarello F; Testoni S; Rossi M; Gentile A; Damiani E; Sacchetto R
    Genomics; 2008 Dec; 92(6):474-7. PubMed ID: 18786632
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.