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Volumn 14, Issue 4, 1996, Pages 392-399

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; TRANSCRIPTION FACTOR;

EID: 10544233785     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1296-392     Document Type: Article
Times cited : (799)

References (72)
  • 1
    • 0029050592 scopus 로고
    • Face facts: Genes, environment, and clefts
    • Murray, J.C. Face facts: genes, environment, and clefts. Am. J. Hum. Genet. 57, 227-232 (1995).
    • (1995) Am. J. Hum. Genet. , vol.57 , pp. 227-232
    • Murray, J.C.1
  • 2
    • 0030031950 scopus 로고    scopus 로고
    • What's in a face?
    • Winter, R. What's in a face? Nature Genet. 12, 124-129 (1996).
    • (1996) Nature Genet. , vol.12 , pp. 124-129
    • Winter, R.1
  • 3
    • 0028907339 scopus 로고
    • Positional cloning moves from perditional to traditional
    • Collins, F.S. Positional cloning moves from perditional to traditional. Nature Genet. 9, 347-360 (1995).
    • (1995) Nature Genet. , vol.9 , pp. 347-360
    • Collins, F.S.1
  • 4
    • 0027953771 scopus 로고
    • Hox genes in vertebrate development
    • Krumlauf, R. Hox genes in vertebrate development. Cell 78, 191-201 (1994).
    • (1994) Cell , vol.78 , pp. 191-201
    • Krumlauf, R.1
  • 5
    • 0028966947 scopus 로고
    • Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies, and vesicoureteral reflux
    • Sanyanusin, P. et al. Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies, and vesicoureteral reflux. Nature Genet. 9, 358-363 (1995).
    • (1995) Nature Genet. , vol.9 , pp. 358-363
    • Sanyanusin, P.1
  • 6
    • 0026584439 scopus 로고
    • An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
    • Baldwin, C.T., Hoth, C.F., Amos, J.A., da-Silva, E.O. & Mtasky, A. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature 355, 637-638 (1992).
    • (1992) Nature , vol.355 , pp. 637-638
    • Baldwin, C.T.1    Hoth, C.F.2    Amos, J.A.3    Da-Silva, E.O.4    Mtasky, A.5
  • 7
    • 0026949405 scopus 로고
    • Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
    • Glaser, T., Walton, D.S. & Maas, R.L. Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene. Nature Genet. 2, 232-238 (1992).
    • (1992) Nature Genet. , vol.2 , pp. 232-238
    • Glaser, T.1    Walton, D.S.2    Maas, R.L.3
  • 8
    • 0027431005 scopus 로고
    • A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
    • Jabs, E.W. et al. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 75, 443-450 (1993).
    • (1993) Cell , vol.75 , pp. 443-450
    • Jabs, E.W.1
  • 9
  • 10
    • 0029871929 scopus 로고    scopus 로고
    • Altered growth and branching patterns in synpotydactyly caused by mutations in HOXD13
    • Muragaki, Y., Mundlos S., Upton J. & Olsen B.J. Altered growth and branching patterns in synpotydactyly caused by mutations in HOXD13. Science 272, 548-551 (1996).
    • (1996) Science , vol.272 , pp. 548-551
    • Muragaki, Y.1    Mundlos, S.2    Upton, J.3    Olsen, B.J.4
  • 11
    • 0030065606 scopus 로고    scopus 로고
    • Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
    • Brunelli, S. et al. Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly. Nature Genet. 12, 94-96 (1996).
    • (1996) Nature Genet. , vol.12 , pp. 94-96
    • Brunelli, S.1
  • 12
    • 0026667857 scopus 로고
    • Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia
    • Pfäffle, R.W. et al. Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia. Science 257, 1118-1121 (1992).
    • (1992) Science , vol.257 , pp. 1118-1121
    • Pfäffle, R.W.1
  • 13
    • 0343800497 scopus 로고
    • Kongenitale anomalien der iris
    • Vossius, A. Kongenitale anomalien der iris. Klin. Mbl. Augenheilk 21, 233-237 (1883).
    • (1883) Klin. Mbl. Augenheilk , vol.21 , pp. 233-237
    • Vossius, A.1
  • 15
    • 0001558614 scopus 로고
    • Dysgenesis mesodermalis coreneal et iridis
    • Rieger, H. Dysgenesis mesodermalis coreneal et iridis. Z. Augenheilk 86, 333 (1935).
    • (1935) Z. Augenheilk , vol.86 , pp. 333
    • Rieger, H.1
  • 16
    • 0026920886 scopus 로고
    • Linkage of Rieger syndrome to the region of the epidermal growth factor on chromosome 4
    • Murray, J.C. et al. Linkage of Rieger syndrome to the region of the epidermal growth factor on chromosome 4. Nature Genet. 2, 46-49 (1992).
    • (1992) Nature Genet. , vol.2 , pp. 46-49
    • Murray, J.C.1
  • 17
    • 0029762015 scopus 로고    scopus 로고
    • A second locus for Rieger syndrome maps to chromosome 13q14
    • Phillips, J.C. et al. A second locus for Rieger syndrome maps to chromosome 13q14. Am J. Hum. Genet. 59, 613-619 (1996).
    • (1996) Am J. Hum. Genet. , vol.59 , pp. 613-619
    • Phillips, J.C.1
  • 18
    • 0027527696 scopus 로고
    • Rieger syndrome revisited: Experimental approaches using pharmacologic and antisense strategies to abrogate EGF and TGF-a functions resulting in dysmorphogenesis during embryonic mouse crantofacial morphogenesis
    • Slavkin, H.C. Rieger syndrome revisited: experimental approaches using pharmacologic and antisense strategies to abrogate EGF and TGF-a functions resulting in dysmorphogenesis during embryonic mouse crantofacial morphogenesis. Am. J. Med. Genet. 47, 689-697 (1993).
    • (1993) Am. J. Med. Genet. , vol.47 , pp. 689-697
    • Slavkin, H.C.1
  • 19
    • 19244364120 scopus 로고    scopus 로고
    • Closing in on the Rieger syndrome gene on 4q25: Mapping translocation breakpoints within a 50-kb region
    • in the press
    • Datson, N. et al. Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region. Am. J. Hum. Genet. (in the press).
    • Am. J. Hum. Genet.
    • Datson, N.1
  • 20
    • 19244364500 scopus 로고    scopus 로고
    • Exclusion of epidermal growth factor (EGF) and high-resolution physical mapping across the Rieger syndrome locus
    • in the press
    • Semina, E. et al. Exclusion of epidermal growth factor (EGF) and high-resolution physical mapping across the Rieger syndrome locus. Am. J. Hum. Genet. (in the press).
    • Am. J. Hum. Genet.
    • Semina, E.1
  • 21
    • 0026922430 scopus 로고
    • Characterizatton of the human HOX7 cDNA and identification of polymorphic markers
    • Padanilam, B.J. et al. Characterizatton of the human HOX7 cDNA and identification of polymorphic markers. Hum. Mol. Genet. 1, 407-410 (1992).
    • (1992) Hum. Mol. Genet. , vol.1 , pp. 407-410
    • Padanilam, B.J.1
  • 22
    • 0030213227 scopus 로고    scopus 로고
    • Interpreting cDNA sequences: Some insights from studies on translation
    • Kozak, M. Interpreting cDNA sequences: some insights from studies on translation. Mamm. Genome 7, 563-574 (1996).
    • (1996) Mamm. Genome , vol.7 , pp. 563-574
    • Kozak, M.1
  • 23
    • 0029939460 scopus 로고    scopus 로고
    • Ptx1, a bicoid-related homeo box transcription factor involved in transcription of the pro-opiomelanocortin gene
    • Lamonerie, T. et al. Ptx1, a bicoid-related homeo box transcription factor involved in transcription of the pro-opiomelanocortin gene. Genes Dev. 10, 1284-1295 (1996).
    • (1996) Genes Dev. , vol.10 , pp. 1284-1295
    • Lamonerie, T.1
  • 24
    • 0029821237 scopus 로고    scopus 로고
    • P-OTX: A PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development
    • Szeto D.P., Ryan A.K., O'Connell S.M. & Rosenfeld M.G. P-OTX: A PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development. Proc. Natl. Acad. Sci. USA 93, 7706-7710 (1996).
    • (1996) Proc. Natl. Acad. Sci. USA , vol.93 , pp. 7706-7710
    • Szeto, D.P.1    Ryan, A.K.2    O'Connell, S.M.3    Rosenfeld, M.G.4
  • 25
    • 0024320441 scopus 로고
    • DNA specificity of the bicoid activator protein is determined by homeodomain recognition helix residue 9
    • Hanes, S.D. & Brent, R. DNA specificity of the bicoid activator protein is determined by homeodomain recognition helix residue 9. Cell 57, 1275-1283 (1989).
    • (1989) Cell , vol.57 , pp. 1275-1283
    • Hanes, S.D.1    Brent, R.2
  • 26
    • 0028568659 scopus 로고
    • Control of type-D GABAergic neuron differentiation by C. elegans UNC-30 homeodomain protein
    • Jin, Y., Hoskins, R. & Horvitz, H.R. Control of type-D GABAergic neuron differentiation by C. elegans UNC-30 homeodomain protein. Nature 372, 780-783 (1994).
    • (1994) Nature , vol.372 , pp. 780-783
    • Jin, Y.1    Hoskins, R.2    Horvitz, H.R.3
  • 27
    • 0027260743 scopus 로고
    • A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo
    • Simeone, A. et al. A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo. EMBO J. 12, 2735-2747 (1993).
    • (1993) EMBO J. , vol.12 , pp. 2735-2747
    • Simeone, A.1
  • 28
    • 0028206856 scopus 로고
    • Specific DNA recognition and intersite spacing are critical for action of the bicoid morphogen
    • Hanes, S.D., Riddihough, G., Ish-Horowicz, D. & Brent, R. Specific DNA recognition and intersite spacing are critical for action of the bicoid morphogen. Mol. Cell Biol. 14, 3364-3375 (1994).
    • (1994) Mol. Cell Biol. , vol.14 , pp. 3364-3375
    • Hanes, S.D.1    Riddihough, G.2    Ish-Horowicz, D.3    Brent, R.4
  • 29
    • 0027249822 scopus 로고
    • A chicken homeobox gene related to Drosophile paired is predominantly expressed in the developing limb
    • Nohno, T. et al. A chicken homeobox gene related to Drosophile paired is predominantly expressed in the developing limb. Dev. Biol. 158, 254-264 (1993).
    • (1993) Dev. Biol. , vol.158 , pp. 254-264
    • Nohno, T.1
  • 30
    • 0029086672 scopus 로고
    • Expression patterns of the paired-related homeobox genes Mhox/Prx1 and S8/Prx2 suggest roles in development of the heart and forebrain
    • Leussink, B. et al. Expression patterns of the paired-related homeobox genes Mhox/Prx1 and S8/Prx2 suggest roles in development of the heart and forebrain. Mech. Dev. 52, 51-64 (1995).
    • (1995) Mech. Dev. , vol.52 , pp. 51-64
    • Leussink, B.1
  • 31
    • 0027973640 scopus 로고
    • The gene for the homeodomajn-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development
    • Zhao, G.Q, Eberspaecher, H., Seldin, M.F. & de Crombrugghe, B. The gene for the homeodomajn-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development. Mech. Dev. 48, 245-254 (1994).
    • (1994) Mech. Dev. , vol.48 , pp. 245-254
    • Zhao, G.Q.1    Eberspaecher, H.2    Seldin, M.F.3    De Crombrugghe, B.4
  • 32
    • 0027417887 scopus 로고
    • Molecular genetics of aristaless, a prd-type homeo box gene involved in the morphogenesis of proximal and distal pattern elements in a subset of appendages in Drosophila
    • Schneitz, K., Spielmann, P. & Noll, M. Molecular genetics of aristaless, a prd-type homeo box gene involved in the morphogenesis of proximal and distal pattern elements in a subset of appendages in Drosophila. Genes Dev. 7, 114-129 (1993).
    • (1993) Genes Dev. , vol.7 , pp. 114-129
    • Schneitz, K.1    Spielmann, P.2    Noll, M.3
  • 33
    • 0029150732 scopus 로고
    • Identification by differential RT-PCR of a novel paired homeodomain protein specifically expressed in sensory neurons and a subset of their CNS targets
    • Saito, T., Greenwood, A., Sun, Q. & Anderson, D.J. Identification by differential RT-PCR of a novel paired homeodomain protein specifically expressed in sensory neurons and a subset of their CNS targets. Mol. Cell. Neurosci. 6, 280-292 (1995).
    • (1995) Mol. Cell. Neurosci. , vol.6 , pp. 280-292
    • Saito, T.1    Greenwood, A.2    Sun, Q.3    Anderson, D.J.4
  • 34
    • 0028048848 scopus 로고
    • Developmental expression of a novel murine homeobox gene (Chx10): Evidence for roles in determination of the neuroretina and inner nuclear layer
    • Liu, I.S. et al. Developmental expression of a novel murine homeobox gene (Chx10): evidence for roles in determination of the neuroretina and inner nuclear layer. Neuron 13, 377-393 (1994).
    • (1994) Neuron , vol.13 , pp. 377-393
    • Liu, I.S.1
  • 35
    • 0027991262 scopus 로고
    • Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila
    • Simeone, A. et al. Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila. Neuron 13, 81-101 (1994).
    • (1994) Neuron , vol.13 , pp. 81-101
    • Simeone, A.1
  • 36
    • 0023651307 scopus 로고
    • RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression
    • Shapiro, M.B. RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression. Nucl. Acids Res. 15, 7155-7174 (1987).
    • (1987) Nucl. Acids Res. , vol.15 , pp. 7155-7174
    • Shapiro, M.B.1
  • 37
    • 0024808994 scopus 로고
    • The organization of 3′ splice-site sequences in mammalian introns
    • Reed, R. The organization of 3′ splice-site sequences in mammalian introns. Genes Dev. 3, 2113-2123 (1989).
    • (1989) Genes Dev. , vol.3 , pp. 2113-2123
    • Reed, R.1
  • 39
    • 0024022215 scopus 로고
    • The role of localization of bicoid RNA in organizing the anterior pattern of the Drosophila embryo
    • Berleth, T. et al. The role of localization of bicoid RNA in organizing the anterior pattern of the Drosophila embryo. EMBO J. 7, 1749-56 (1988).
    • (1988) EMBO J. , vol.7 , pp. 1749-1756
    • Berleth, T.1
  • 40
    • 0025286831 scopus 로고
    • Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors
    • Simmons, D.M. et al. Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors. Genes Dev. 4, 695-711 (1990).
    • (1990) Genes Dev. , vol.4 , pp. 695-711
    • Simmons, D.M.1
  • 42
    • 0016162989 scopus 로고
    • Autosomal dominant transmission of isolated growth hormone deficiency in ins-dental dysplasia (Rieger's syndrome)
    • Sadeghi-Nejad, A. & Senior, B. Autosomal dominant transmission of isolated growth hormone deficiency in ins-dental dysplasia (Rieger's syndrome). J. Pediatr. 85, 644-648 (1974).
    • (1974) J. Pediatr. , vol.85 , pp. 644-648
    • Sadeghi-Nejad, A.1    Senior, B.2
  • 43
    • 0026824439 scopus 로고
    • The homeodomain: A new face for the helix-turn-helix?
    • Treisman, J., Harris, E., Wilson, D. & Desplan, C. The homeodomain: a new face for the helix-turn-helix? BioEssays 14, 145-150 (1992).
    • (1992) BioEssays , vol.14 , pp. 145-150
    • Treisman, J.1    Harris, E.2    Wilson, D.3    Desplan, C.4
  • 45
    • 0029053016 scopus 로고
    • Degradation of mRNA in eukaryotes
    • Beelman, C.A. & Parker, R. Degradation of mRNA in eukaryotes. Cell 81, 179-183 (1995).
    • (1995) Cell , vol.81 , pp. 179-183
    • Beelman, C.A.1    Parker, R.2
  • 46
    • 0030059840 scopus 로고    scopus 로고
    • RNA recognition and translational regulation by a homeodomain protein
    • Dubnau, J. & Struhl, G. RNA recognition and translational regulation by a homeodomain protein. Nature 379, 694-699 (1996).
    • (1996) Nature , vol.379 , pp. 694-699
    • Dubnau, J.1    Struhl, G.2
  • 47
    • 0029091048 scopus 로고
    • Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)
    • Héon, E. et al. Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25). Hum. Mol. Genet. 4, 1435-1439 (1995).
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 1435-1439
    • Héon, E.1
  • 49
    • 0026762590 scopus 로고
    • Expression patterns of the homeobox gene, Hox-8, in the mouse embryo suggest a role in specifying tooth initiation and shape
    • MacKenzie, A., Ferguson, M.W.J. & Sharpe, P.T. Expression patterns of the homeobox gene, Hox-8, in the mouse embryo suggest a role in specifying tooth initiation and shape. Development 115, 403-420 (1992).
    • (1992) Development , vol.115 , pp. 403-420
    • MacKenzie, A.1    Ferguson, M.W.J.2    Sharpe, P.T.3
  • 50
    • 0018363465 scopus 로고
    • Rieger's syndrome associated with a large Meckel's diverticulum
    • Krespi, Y. P. & Pertsemlidis, D. Rieger's syndrome associated with a large Meckel's diverticulum. Am. J. Gastroenter. 71, 608-610 (1979).
    • (1979) Am. J. Gastroenter. , vol.71 , pp. 608-610
    • Krespi, Y.P.1    Pertsemlidis, D.2
  • 52
    • 0014103798 scopus 로고
    • Iris dysgenesis with other anomalies
    • Crawford, R.A.D. Iris dysgenesis with other anomalies. Brit. J. Ophthalmol. 51, 438-440 (1967).
    • (1967) Brit. J. Ophthalmol. , vol.51 , pp. 438-440
    • Crawford, R.A.D.1
  • 53
    • 0017806488 scopus 로고
    • The Axenfeld syndrome and the Rieger syndrome
    • Fitch, N. & Kaback, M. The Axenfeld syndrome and the Rieger syndrome. J. Med. Genet. 15, 30-34 (1978).
    • (1978) J. Med. Genet. , vol.15 , pp. 30-34
    • Fitch, N.1    Kaback, M.2
  • 54
    • 0023176710 scopus 로고
    • Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6
    • Eiberg, H., Bixler, B., Nielsen, L.S., Coneally, P.M. & Mohr, J. Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6. Clin. Genet. 32, 129-132 (1987).
    • (1987) Clin. Genet. , vol.32 , pp. 129-132
    • Eiberg, H.1    Bixler, B.2    Nielsen, L.S.3    Coneally, P.M.4    Mohr, J.5
  • 55
    • 0023275513 scopus 로고
    • Linkage of an X-chromosome cleft palate gene
    • Moore, G. E. et al. Linkage of an X-chromosome cleft palate gene. Nature 326, 91-92 (1987).
    • (1987) Nature , vol.326 , pp. 91-92
    • Moore, G.E.1
  • 56
    • 11944262571 scopus 로고
    • Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome 1q
    • Murray, J.C. et al. Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome 1q. Am. J. Hum. Genet. 46, 486-191 (1990).
    • (1990) Am. J. Hum. Genet. , vol.46 , pp. 486-1191
    • Murray, J.C.1
  • 57
    • 0028023154 scopus 로고
    • Linkage of human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity
    • Muenke, M. et al. Linkage of human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity. Proc. Nat. Acad. Sci. USA 91, 8102-8106 (1994).
    • (1994) Proc. Nat. Acad. Sci. USA , vol.91 , pp. 8102-8106
    • Muenke, M.1
  • 58
    • 0026602124 scopus 로고
    • Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
    • Tassabehji, M. et al. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature 355, 635-636 (1992).
    • (1992) Nature , vol.355 , pp. 635-636
    • Tassabehji, M.1
  • 59
    • 0030070052 scopus 로고    scopus 로고
    • Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome
    • Dixon, J. et al. Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. Nature Genet. 12, 130-136 (1996).
    • (1996) Nature Genet. , vol.12 , pp. 130-136
    • Dixon, J.1
  • 60
    • 0029883637 scopus 로고    scopus 로고
    • Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome
    • Slaney, S.F. et al. Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome. Am. J. Hum. Genet. 58, 923-932 (1996).
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 923-932
    • Slaney, S.F.1
  • 61
    • 0028126564 scopus 로고
    • Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative Rho/Rac guanine nucleotide exchange factor
    • Pasteris, N.G. et al. Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor. Cell 79, 669-678 (1994).
    • (1994) Cell , vol.79 , pp. 669-678
    • Pasteris, N.G.1
  • 62
    • 0026320812 scopus 로고
    • Restriction fragment length polymorphisms, glucccorticoid receptors, and phenytoin-induced cleft palate in congenic strains of mice with serious susceptibility differences
    • Gasser, D.L., Goldner-Sauve, A., Katsuma, M. & Goldman, A.S. Restriction fragment length polymorphisms, glucccorticoid receptors, and phenytoin-induced cleft palate in congenic strains of mice with serious susceptibility differences. J. Craniofac. Genet. Dev. Bio. 11, 366-371 (1991).
    • (1991) J. Craniofac. Genet. Dev. Bio. , vol.11 , pp. 366-371
    • Gasser, D.L.1    Goldner-Sauve, A.2    Katsuma, M.3    Goldman, A.S.4
  • 63
    • 0027419349 scopus 로고
    • A region of the mouse genome homologous to human chromosome 1q21 affects facial clefting
    • Karolyi, J. & Erickson, R. P. A region of the mouse genome homologous to human chromosome 1q21 affects facial clefting. J. Craniofac. Genet. Dev. Bio. 13, 1-5 (1993).
    • (1993) J. Craniofac. Genet. Dev. Bio. , vol.13 , pp. 1-5
    • Karolyi, J.1    Erickson, R.P.2
  • 64
    • 0028292605 scopus 로고
    • Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
    • Satokata, I. & Maas, R. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nature Genet. 6, 348-356 (1994).
    • (1994) Nature Genet. , vol.6 , pp. 348-356
    • Satokata, I.1    Maas, R.2
  • 65
    • 0029240543 scopus 로고
    • The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11
    • Juriloff, D. M. & Mah, D. G. The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11. Mamm. Genome 6, 63-69 (1995).
    • (1995) Mamm. Genome , vol.6 , pp. 63-69
    • Juriloff, D.M.1    Mah, D.G.2
  • 66
    • 0028806184 scopus 로고
    • Abnormal lung development and cleft palate in mice lacking TGF-β3 indicates defects of epithelial-mesenchymal interaction
    • Kaartinen, V. et al. Abnormal lung development and cleft palate in mice lacking TGF-β3 indicates defects of epithelial-mesenchymal interaction. Nature Genet. 11, 415-421 (1995).
    • (1995) Nature Genet. , vol.11 , pp. 415-421
    • Kaartinen, V.1
  • 67
    • 0028972869 scopus 로고
    • Transforming growlh factor-β3 is required for secondary palate fusion
    • Proetzel, G. et al. Transforming growlh factor-β3 is required for secondary palate fusion. Nature Genet. 11, 409-414 (1995).
    • (1995) Nature Genet. , vol.11 , pp. 409-414
    • Proetzel, G.1
  • 68
    • 0028808204 scopus 로고
    • Null mutation of DIx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain
    • Qiu, M. et al. Null mutation of DIx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain. Genes Dev. 9, 2523-2538 (1995).
    • (1995) Genes Dev. , vol.9 , pp. 2523-2538
    • Qiu, M.1
  • 69
    • 0023181267 scopus 로고
    • Use of restriction enzymes to detect potential gene sequences in mammalian DNA
    • Lindsay, S. & Bird, A.P. Use of restriction enzymes to detect potential gene sequences in mammalian DNA. Nature 327, 336-338 (1987).
    • (1987) Nature , vol.327 , pp. 336-338
    • Lindsay, S.1    Bird, A.P.2
  • 71
    • 0027501673 scopus 로고
    • Detection of messenger RNA by in situ hybridization
    • Sassoon, D. & Rosenthal, N. Detection of messenger RNA by in situ hybridization. Meth. Enzymol. 225, 384-404 (1993).
    • (1993) Meth. Enzymol. , vol.225 , pp. 384-404
    • Sassoon, D.1    Rosenthal, N.2
  • 72
    • 0026285616 scopus 로고
    • In situ hybridization: An improved whole-mount method for Xenopus embryos
    • Appendix G
    • Harland & Richard, M.H. In situ hybridization: an improved whole-mount method for Xenopus embryos. Meth. Cell Biol. 36, 685-695, Appendix G (1991).
    • (1991) Meth. Cell Biol. , vol.36 , pp. 685-695
    • Harland1    Richard, M.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.