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Journal Abstract Search

502 related items for PubMed ID: 10945466

  • 1. A novel candidate gene for mouse and human preaxial polydactyly with altered expression in limbs of Hemimelic extra-toes mutant mice.
    Clark RM, Marker PC, Kingsley DM.
    Genomics; 2000 Jul 01; 67(1):19-27. PubMed ID: 10945466
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  • 2. Single nucleotide polymorphisms in the chicken Lmbr1 gene are associated with chicken polydactyly.
    Huang YQ, Deng XM, Du ZQ, Qiu X, Du X, Chen W, Morisson M, Leroux S, Ponce de Léon FA, Da Y, Li N.
    Gene; 2006 Jun 07; 374():10-8. PubMed ID: 16650944
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  • 3. The Hemimelic extra toes mouse mutant: Historical perspective on unraveling mechanisms of dysmorphogenesis.
    Knudsen TB, Kochhar DM.
    Birth Defects Res C Embryo Today; 2010 Jun 07; 90(2):155-62. PubMed ID: 20544697
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  • 4. Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly.
    Lettice LA, Horikoshi T, Heaney SJ, van Baren MJ, van der Linde HC, Breedveld GJ, Joosse M, Akarsu N, Oostra BA, Endo N, Shibata M, Suzuki M, Takahashi E, Shinka T, Nakahori Y, Ayusawa D, Nakabayashi K, Scherer SW, Heutink P, Hill RE, Noji S.
    Proc Natl Acad Sci U S A; 2002 May 28; 99(11):7548-53. PubMed ID: 12032320
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  • 6. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.
    Tsukurov O, Boehmer A, Flynn J, Nicolai JP, Hamel BC, Traill S, Zaleske D, Mankin HJ, Yeon H, Ho C.
    Nat Genet; 1994 Mar 28; 6(3):282-6. PubMed ID: 8012391
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  • 8. Polydactyly in the Strong's luxoid mouse is suppressed by limb deformity alleles.
    Vogt TF, Leder P.
    Dev Genet; 1996 Mar 28; 19(1):33-42. PubMed ID: 8792607
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  • 9. Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1.
    Clark RM, Marker PC, Roessler E, Dutra A, Schimenti JC, Muenke M, Kingsley DM.
    Genetics; 2001 Oct 28; 159(2):715-26. PubMed ID: 11606546
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  • 10. Isolation of the chicken Lmbr1 coding sequence and characterization of its role during chick limb development.
    Maas SA, Fallon JF.
    Dev Dyn; 2004 Mar 28; 229(3):520-8. PubMed ID: 14991708
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  • 11. Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.
    Mohlke KL, Purkayastha AA, Westrick RJ, Ginsburg D.
    Genomics; 1998 Nov 15; 54(1):19-30. PubMed ID: 9806826
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  • 12. A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35.
    Hayes C, Rump A, Cadman MR, Harrison M, Evans EP, Lyon MF, Morriss-Kay GM, Rosenthal A, Brown SD.
    Genomics; 2001 Dec 15; 78(3):197-205. PubMed ID: 11735226
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  • 13. A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36.
    Heus HC, Hing A, van Baren MJ, Joosse M, Breedveld GJ, Wang JC, Burgess A, Donnis-Keller H, Berglund C, Zguricas J, Scherer SW, Rommens JM, Oostra BA, Heutink P.
    Genomics; 1999 May 01; 57(3):342-51. PubMed ID: 10329000
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  • 14. A series of ENU-induced single-base substitutions in a long-range cis-element altering Sonic hedgehog expression in the developing mouse limb bud.
    Masuya H, Sezutsu H, Sakuraba Y, Sagai T, Hosoya M, Kaneda H, Miura I, Kobayashi K, Sumiyama K, Shimizu A, Nagano J, Yokoyama H, Kaneko S, Sakurai N, Okagaki Y, Noda T, Wakana S, Gondo Y, Shiroishi T.
    Genomics; 2007 Feb 01; 89(2):207-14. PubMed ID: 17049204
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  • 15. High-resolution genetic, physical, and transcript map of the mnd2 region of mouse chromosome 6.
    Weber JS, Jang W, Simin K, Lu W, Yu J, Meisler MH.
    Genomics; 1998 Nov 15; 54(1):107-15. PubMed ID: 9806835
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  • 16. The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23.
    Gorman SW, Haider NB, Grieshammer U, Swiderski RE, Kim E, Welch JW, Searby C, Leng S, Carmi R, Sheffield VC, Duhl DM.
    Genomics; 1999 Jul 15; 59(2):150-60. PubMed ID: 10409426
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  • 20. Physical and transcriptional map of a 3-Mb region of mouse chromosome 1 containing the gene for the neural tube defect mutant loop-tail (Lp).
    Eddleston J, Murdoch JN, Copp AJ, Stanier P.
    Genomics; 1999 Mar 01; 56(2):149-59. PubMed ID: 10051400
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