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Carpenter, E. M., Goddard, J. M., Chisaka, O., Manley, N. R. and Capecchi, M. R (1993). Loss of Hox-A1 ( Hox-1.6 ) function results in the reorganization of the murine hindbrain. Development 118, 1063-1075.[Abstract]

Chen, F. and Capecchi, M. R (1997). Targeted mutations in Hoxa-9 and Hoxb-9 reveal synergistic interactions. Dev. Biol 181, 186-196.[Medline]

Chisaka, O. and Capecchi, M. R (1991). Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene Hox-1.5. Nature 350, 473-479.[Medline]

Condie, B. G. and Capecchi, M. R (1994). Mice with targeted disruptions in the paralogous genes Hoxa-3 and Hoxd-3 reveal synergistic interactions. Nature 370, 304-307.[Medline]

Davis, A. P. and Capecchi, M. R (1994). Axial homeosis and appendicular skeleton defects in mice with a targeted disruption of Hoxd-11. Development 120, 2187-2198.[Abstract]

Davis, A. P. and Capecchi, M. R (1996). A mutational analysis of the 5 HoxD genes: dissection of genetic interactions during limb development in the mouse. Development 122, 1175-1185.[Abstract]

Davis, A. P., Witte, D. P., Heieh-Li, H. M., Potter, S. S. and Capecchi, M. R (1995). Absence of radius and ulna in mice lacking Hoxa-11 and Hoxd-11. Nature 375, 791-795.[Medline]

Deng, C., Thomas, K. R. and Capecchi, M. R (1993). Location of crossovers during gene targeting with insertion and replacement vectors. Mol. Cell. Biol 13, 2134-2140.[Abstract/Free Full Text]

Detweiler, S. R (1934). An experimental study of spinal nerve segmentation in Amblystoma with reference to the plurisegmental contribution to the brachial plexus. J. Exp. Zool 67, 395-441.

Dolle, P. and Duboule, D (1989). Two gene members of the murine HOX-5 complex show regional and cell-type specific expression in developing limbs and gonads. EMBO J 8, 1507-1515.[Medline]

Dolle, P., Izpis\234a-Belmonte, J.-C., Falkenstein, H., Renucci, A. and Duboule, D (1989). Coordinate expression of the murine Hox-5 complex homeobox-containing genes during limb pattern formation. Nature 342, 767-772.[Medline]

Dolle, P., Dierich, A., LeMeur, M., Schimmang, T., Schuhbaur, B., Chambon, P. and Duboule, D (1993). Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs. Cell 75, 431-441.[Medline]

Duboule, D. and Dolle, P (1989). The structural and functional organization of the murine Hox gene family resembles that of Drosophila homeotic genes. EMBO J 8, 1497-1505.[Medline]

Duboule, D (1991). Patterning in the vertebral limb. Curr. Opin. Genet. Dev 1, 211-216.[Medline]

Duboule, D (1994). Temporal colinearity and the phylotypic progression: a basis for the stability of a vertebrate Bauplan and the evolution of morphologies through heterochrony. Development 1994, 135-142.

Favier, B., LeMeur, M., Chambon, P. and Dolle, P (1995). Axial skeleton homeosis and forelimb malformations in Hoxd11 mutant mice. Proc. Natl. Acad. Sci. USA 92, 310-314.[Abstract/Free Full Text]

Favier, B., Rijli, F. M., Fromental-Ramain, C., Fraulob, V., Chambon, P. and Dolle, P (1996). Functional cooperation between the non-paralogous genes Hoxa-10 and Hoxd-11 in the developing forelimb and axial skeleton. Development 122, 449-460.[Abstract]

Fromental-Ramain, C., Warot, X., Lakkaraju, S., Favier, B., Haack, H., Birling, C., Dierich, A., Dolle, P. and Chambon, P (1996). Specific and redundant functions of the paralogous Hoxa-9 and Hoxd-9 genes in forelimb and axial skeleton patterning. Development 122, 461-472.[Abstract]

Fromental-Ramain, C., Warot, X., Messadecq, N., LeMeur, M., Dolle, P. and Chambon, P (1996). Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopod. Development 122, 2997-3011.[Abstract]

Goddard, J. M., Rossel, M., Manley, N. R. and Capecchi, M. R (1996). Mice with targeted disruption of Hoxb-1 fail to form the motor nucleus of the VIIth nerve. Development 122, 3217-3228.[Abstract]

Graham, A., Papalopulu, N. and Krumlauf, R (1989). The murine and Drosophila homeobox gene complexes have common features of organization and expression. Cell 57, 367-378.[Medline]

Haack, H. and Gruss, P (1993). The establishment of murine Hox-1 expression domains during patterning of the limb. Dev. Biol 157, 410-422.[Medline]

Hamburger, V (1934). The effects of wing bud extirpation on the development of the central nervous system in chick embryos. J. Exp. Zool 68, 449-494.

Hamburger, V (1958). Regression versus peripheral control of differentiation in motor hypoplasia. Am. J. Anat 102, 365-410.[Medline]

Horan, G. S. B., Kov\210cs, E. N., Behringer, R. R. and Featherstone, M. S (1995). Mutations in paralogous Hox genes result in overlapping homeotic transformations of the axial skeleton: Evidence for unique and redundant function. Dev. Biol 169, 359-372.[Medline]

Horan, G. S. B., Ram\222rez-Solis, R., Featherstone, M. S., Wolgemuth, D. J., Bradley, A. and Behringer, R. R (1995). Compound mutants for the paralogous Hoxa-4, Hoxb-4, and Hoxd-4 genes show more complete homeotic transformations and a dose-dependent increase in the number of vertebrae transformed. Genes Dev 9, 1667-1677.[Abstract/Free Full Text]

Izpis\234a-Belmonte, J.-C., Falkenstein, H., Dolle, P., Renucci, A. and Duboule, D (1991). Muringe genes related to the Drosophila AbdB hometic gene are sequentially expressed during development of the posterior part of the body. EMBO J 10, 2279-2289.[Medline]

Keynes, R. J. and Stern, C. D (1984). Segmentation in the vertebrate nervous system. Nature 310, 786-789.[Medline]

Kondo, T., Dolle, P., Z\207k\207ny, J. and Duboule, D (1996). Function of posterior HoxD genes in the morphogenesis of the anal sphincter. Development 122, 2651-2659.[Abstract]

Krumlauf, R (1994). Hox genes in vertebrate development. Cell 78, 191-201.[Medline]

Lance-Jones, C (1982). Motoneuron cell death in the developing lumbar spinal cord of the mouse. Dev. Brain Res 4, 473-479.

Lanser, M. E., Carrington, J. L. and Fallon, J. F (1986). Survival of motoneurons in the brachial lateral motor column of limbless mutant chick embryos depends on the periphery. J. Neurosci 6, 2551-2557.[Abstract]

LeMouellic, H., Lallemand, Y. and Brulet, P (1992). Homeosis in the mouse induced by a null mutation in the Hox-3.1 gene. Cell 69, 251-264.[Medline]

Mansour, S. L., Thomas, K. R. and Capecchi, M. R (1988). Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes. Nature 336, 348-352.[Medline]

Mansour, S. L., Goddard, J. M. and Capecchi, M. R (1993). Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear. Development 117, 13-28.[Abstract]

Mark, M., Lufkin, T., Vonesch, J.-L., Ruberte, E., Olivo, J.-C., Dolle, P., Gorry, P., Lumsden, A. and Chambon, P (1993). Two rhombomeres are altered in Hoxa-1 mutant mice. Development 119, 319-338.[Abstract]

McHanwell, S. and Biscoe, T. J (1981). The localization of motoneurons supplying the hindlimb muscles of the mouse. Phil. Trans. R. Soc. Lond. B 293, 477-508.[Medline]

Nagy, A., Rossant, J., Nagy. R., Abramow-Newerly, W. and Roder, J. C (1993). Derivation of completely cell culture-derived mice from early-passage embryonic stem cell. Proc. Natl. Acad. Sci. USA 90, 8424-8428.[Abstract/Free Full Text]

Oppenheim, R. W., Chu-Wang, I. and Maderdrut, J. L (1978). Cell death ofmotoneurons in the chick embryo spinal cord. III. The differentiation of motoneurons prior to their induced degeneration following limb-bud removal. J. Comp. Neurol 177, 87-112.[Medline]

Phelan, K. A. and Hollyday, M (1990). Axon guidance in muscleless chick wings: the role of muscle cells in motoneuronal pathway selection and muscle nerve formation. J. Neurosci 10, 2699-2716.[Abstract]

Rancourt, D. E., Tsuzuki, T. and Capecchi, M. R (1995). Genetic interaction between Hoxb-5 and Hoxb-6 is revealed by nonallelic noncomplementation. Genes Dev 9, 108-122.[Abstract/Free Full Text]

Renucci, A., Zappavigna, V., Z\207k\207ny, J., Izpis\234a-Belmonte, J. C., Burki, K. and Duboule, D (1992). Comparison of mouse and human HOX-4 complexes defines conserved sequences involved in the regulation of Hox-4.4. EMBO J 11, 1459-1468.[Medline]

Rijli, F. M., Dolle, P., Fraulon, V., LeMeur, M. and Chambon, P (1994). Insertion of a targeting construct in a Hoxd-10 allele can influence the control of Hoxd-9 expression. Dev. Dynamics 201, 366-377.[Medline]

Rijli, F. M., Matyas, R., Pellegrini, M., Dierich, A., Gruss, P., Dolle, P. and Chambon, P (1995). Cryptorchidisn and homeotic transformations of spinal nerves and vertebrae in Hoxa-10 mutant mice. Proc. Natl. Acad. Sci. USA 92, 8185-8189.[Abstract/Free Full Text]

Satokata, I, Benson, G. and Maas, R (1995). Sexually dimorphic sterility phenotypes in Hoxa10 -deficient mice. Nature 374, 460-463.[Medline]

Scott, M. P (1992). Vertebrate homeobox gene nomenclature. Cell 71, 551-553.[Medline]

Small, K. M. and Potter, S. S (1993). Homeotic transformations and limb defects in HoxA-11 mutant mice. Genes Dev 7, 2318-2328.[Abstract/Free Full Text]

Studer, M., Lumsden, A., Ariza-McNaughton, L., Bradley, A. and Krumlauf, R (1996). Altered segmental identity and abnormal migration of motor neurons in mice lacking Hoxb-1. Nature 384, 630-634.[Medline]

Thomas, K. R. and Capecchi, M. R (1987). Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells. Cell 51, 503-512.[Medline]

van der Hoeven, F., Z\207k\207ny, J. and Duboule, D (1996). Gene transpositions in the HoxD complex reveal a hierarchy of regulatory controls. Cell 85, 1025-1035.[Medline]

Z\207k\207ny, J. and Duboule, D (1996). Synpolydactyly in mice with a targeted deficiency in the HoxD complex. Nature 384, 69-71.[Medline]

Z\207k\207ny, J., Gerard, M., Favier., B and Duboule, D (1997). Deletion of a HoxD enhancer induces transcriptional heterochrony leading to transposition of the sacrum. EMBO J 16, 4393-4402.[Medline]




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