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Journal Abstract Search

118 related items for PubMed ID: 12217321

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  • 5. Hox genes maintain critical roles in the adult skeleton.
    Song JY, Pineault KM, Dones JM, Raines RT, Wellik DM.
    Proc Natl Acad Sci U S A; 2020 Mar 31; 117(13):7296-7304. PubMed ID: 32170021
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  • 6. Hox10 and Hox11 genes are required to globally pattern the mammalian skeleton.
    Wellik DM, Capecchi MR.
    Science; 2003 Jul 18; 301(5631):363-7. PubMed ID: 12869760
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  • 8. Targeted disruption of Hoxd9 and Hoxd10 alters locomotor behavior, vertebral identity, and peripheral nervous system development.
    de la Cruz CC, Der-Avakian A, Spyropoulos DD, Tieu DD, Carpenter EM.
    Dev Biol; 1999 Dec 15; 216(2):595-610. PubMed ID: 10642795
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  • 10. Mutations in paralogous Hox genes result in overlapping homeotic transformations of the axial skeleton: evidence for unique and redundant function.
    Horan GS, Kovàcs EN, Behringer RR, Featherstone MS.
    Dev Biol; 1995 May 15; 169(1):359-72. PubMed ID: 7750651
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  • 11. A mutational analysis of the 5' HoxD genes: dissection of genetic interactions during limb development in the mouse.
    Davis AP, Capecchi MR.
    Development; 1996 Apr 15; 122(4):1175-85. PubMed ID: 8620844
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  • 12. Functional cooperation between the non-paralogous genes Hoxa-10 and Hoxd-11 in the developing forelimb and axial skeleton.
    Favier B, Rijli FM, Fromental-Ramain C, Fraulob V, Chambon P, Dollé P.
    Development; 1996 Feb 15; 122(2):449-60. PubMed ID: 8625796
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  • 13. Restricted patterns of Hoxd10 and Hoxd11 set segmental differences in motoneuron subtype complement in the lumbosacral spinal cord.
    Misra M, Shah V, Carpenter E, McCaffery P, Lance-Jones C.
    Dev Biol; 2009 Jun 01; 330(1):54-72. PubMed ID: 19306865
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  • 14. Axial homeosis and appendicular skeleton defects in mice with a targeted disruption of hoxd-11.
    Davis AP, Capecchi MR.
    Development; 1994 Aug 01; 120(8):2187-98. PubMed ID: 7925020
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  • 15. Timed deletion of Twist1 in the limb bud reveals age-specific impacts on autopod and zeugopod patterning.
    Loebel DA, Hor AC, Bildsoe HK, Tam PP.
    PLoS One; 2014 Aug 01; 9(6):e98945. PubMed ID: 24893291
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  • 16. Regulation of endometrial receptivity by the highly expressed HOXA9, HOXA11 and HOXD10 HOX-class homeobox genes.
    Xu B, Geerts D, Bu Z, Ai J, Jin L, Li Y, Zhang H, Zhu G.
    Hum Reprod; 2014 Apr 01; 29(4):781-90. PubMed ID: 24549215
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  • 17. A dual role for Hox genes in limb anterior-posterior asymmetry.
    Zákány J, Kmita M, Duboule D.
    Science; 2004 Jun 11; 304(5677):1669-72. PubMed ID: 15192229
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  • 18. The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes.
    Bruneau S, Johnson KR, Yamamoto M, Kuroiwa A, Duboule D.
    Dev Biol; 2001 Sep 15; 237(2):345-53. PubMed ID: 11543619
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  • 19. Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11.
    Davis AP, Witte DP, Hsieh-Li HM, Potter SS, Capecchi MR.
    Nature; 1995 Jun 29; 375(6534):791-5. PubMed ID: 7596412
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  • 20. Hoxa13 regulates expression of common Hox target genes involved in cartilage development to coordinate the expansion of the autopodal anlage.
    Yamamoto S, Uchida Y, Ohtani T, Nozaki E, Yin C, Gotoh Y, Yakushiji-Kaminatsui N, Higashiyama T, Suzuki T, Takemoto T, Shiraishi YI, Kuroiwa A.
    Dev Growth Differ; 2019 Apr 29; 61(3):228-251. PubMed ID: 30895612
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