메뉴 건너뛰기




Volumn 4, Issue 3, 2009, Pages

Characterization of the Drosophila ortholog of the human Usher syndrome type 1G protein sans

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; CADHERIN 99C; CRINKLED; MYOSIN VIIA; PROTEIN SANS; PROTEIN USH1G; SCAFFOLD PROTEIN; SYNTAXIN; SYNTAXIN AVALANCHE; UNCLASSIFIED DRUG; ANKYRIN; CRINKLED PROTEIN, DROSOPHILA; DROSOPHILA PROTEIN; MYOSIN; NERVE PROTEIN; USH1G PROTEIN, HUMAN;

EID: 62749177524     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0004753     Document Type: Article
Times cited : (12)

References (51)
  • 2
    • 0043244878 scopus 로고    scopus 로고
    • The molecular genetics of Usher syndrome
    • Ahmed ZM, Riazuddin S, Wilcox ER (2003) The molecular genetics of Usher syndrome. Clin Genet 63: 431-444.
    • (2003) Clin Genet , vol.63 , pp. 431-444
    • Ahmed, Z.M.1    Riazuddin, S.2    Wilcox, E.R.3
  • 3
    • 27844517356 scopus 로고    scopus 로고
    • Usher I syndrome: Unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells
    • El-Amraoui A, Petit C (2005) Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells. J Cell Sci 118: 4593-4603.
    • (2005) J Cell Sci , vol.118 , pp. 4593-4603
    • El-Amraoui, A.1    Petit, C.2
  • 4
    • 33646856845 scopus 로고    scopus 로고
    • Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease
    • Reiners J, Nagel-Wolfrum K, Jurgens K, Marker T, Wolfrum U (2006) Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease. Exp Eye Res 83: 97-119.
    • (2006) Exp Eye Res , vol.83 , pp. 97-119
    • Reiners, J.1    Nagel-Wolfrum, K.2    Jurgens, K.3    Marker, T.4    Wolfrum, U.5
  • 5
    • 0028815440 scopus 로고
    • Defective myosin VIIA gene responsible for Usher syndrome type 1B
    • Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, et al. (1995) Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374: 60-61.
    • (1995) Nature , vol.374 , pp. 60-61
    • Weil, D.1    Blanchard, S.2    Kaplan, J.3    Guilford, P.4    Gibson, F.5
  • 6
    • 0034968358 scopus 로고    scopus 로고
    • Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
    • Ahmed ZM, Riazuddin S, Bernstein SL, Ahmed Z, Khan S, et al. (2001) Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am J Hum Genet 69: 25-34.
    • (2001) Am J Hum Genet , vol.69 , pp. 25-34
    • Ahmed, Z.M.1    Riazuddin, S.2    Bernstein, S.L.3    Ahmed, Z.4    Khan, S.5
  • 7
    • 0035159856 scopus 로고    scopus 로고
    • The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
    • Alagramam KN, Murcia CL, Kwon HY, Pawlowski KS, Wright CG, et al. (2001) The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene. Nat Genet 27: 99-102.
    • (2001) Nat Genet , vol.27 , pp. 99-102
    • Alagramam, K.N.1    Murcia, C.L.2    Kwon, H.Y.3    Pawlowski, K.S.4    Wright, C.G.5
  • 8
    • 0035158639 scopus 로고    scopus 로고
    • Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
    • Bolz H, von Brederlow B, Ramirez A, Bryda EC, Kutsche K, et al. (2001) Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nat Genet 27: 108-112.
    • (2001) Nat Genet , vol.27 , pp. 108-112
    • Bolz, H.1    von Brederlow, B.2    Ramirez, A.3    Bryda, E.C.4    Kutsche, K.5
  • 9
    • 0035168168 scopus 로고    scopus 로고
    • Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
    • Bork JM, Peters LM, Riazuddin S, Bernstein SL, Ahmed ZM, et al. (2001) Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet 68: 26-37.
    • (2001) Am J Hum Genet , vol.68 , pp. 26-37
    • Bork, J.M.1    Peters, L.M.2    Riazuddin, S.3    Bernstein, S.L.4    Ahmed, Z.M.5
  • 10
    • 0037341463 scopus 로고    scopus 로고
    • Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin
    • Weil D, El-Amraoui A, Masmoudi S, Mustapha M, Kikkawa Y, et al. (2003) Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin. Hum Mol Genet 12: 463-471.
    • (2003) Hum Mol Genet , vol.12 , pp. 463-471
    • Weil, D.1    El-Amraoui, A.2    Masmoudi, S.3    Mustapha, M.4    Kikkawa, Y.5
  • 11
    • 0034627754 scopus 로고    scopus 로고
    • F-actin bundles are derivatives of microvilli: What does this tell us about how bundles might form?
    • DeRosier DJ, Tilney LG (2000) F-actin bundles are derivatives of microvilli: What does this tell us about how bundles might form? J Cell Biol 148: 1-6.
    • (2000) J Cell Biol , vol.148 , pp. 1-6
    • DeRosier, D.J.1    Tilney, L.G.2
  • 13
    • 12244277402 scopus 로고    scopus 로고
    • Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle
    • Boeda B, El-Amraoui A, Bahloul A, Goodyear R, Daviet L, et al. (2002) Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle. Embo J 21: 6689-6699.
    • (2002) Embo J , vol.21 , pp. 6689-6699
    • Boeda, B.1    El-Amraoui, A.2    Bahloul, A.3    Goodyear, R.4    Daviet, L.5
  • 14
    • 25444448312 scopus 로고    scopus 로고
    • Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C)
    • Reiners J, Marker T, Jurgens K, Reidel B, Wolfrum U (2005) Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C). Mol Vis 11: 347-355.
    • (2005) Mol Vis , vol.11 , pp. 347-355
    • Reiners, J.1    Marker, T.2    Jurgens, K.3    Reidel, B.4    Wolfrum, U.5
  • 15
    • 0037069346 scopus 로고    scopus 로고
    • The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions
    • Siemens J, Kazmierczak P, Reynolds A, Sticker M, Littlewood-Evans A, et al. (2002) The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions. Proc Natl Acad Sci U S A 99: 14946-14951.
    • (2002) Proc Natl Acad Sci U S A , vol.99 , pp. 14946-14951
    • Siemens, J.1    Kazmierczak, P.2    Reynolds, A.3    Sticker, M.4    Littlewood-Evans, A.5
  • 16
    • 33644537736 scopus 로고    scopus 로고
    • Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells
    • Senften M, Schwander M, Kazmierczak P, Lillo C, Shin JB, et al. (2006) Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells. J Neurosci 26: 2060-2071.
    • (2006) J Neurosci , vol.26 , pp. 2060-2071
    • Senften, M.1    Schwander, M.2    Kazmierczak, P.3    Lillo, C.4    Shin, J.B.5
  • 17
    • 0348013128 scopus 로고    scopus 로고
    • PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
    • Ahmed ZM, Riazuddin S, Ahmad J, Bernstein SL, Guo Y, et al. (2003) PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Hum Mol Genet 12: 3215-3223.
    • (2003) Hum Mol Genet , vol.12 , pp. 3215-3223
    • Ahmed, Z.M.1    Riazuddin, S.2    Ahmad, J.3    Bernstein, S.L.4    Guo, Y.5
  • 18
    • 44449102085 scopus 로고    scopus 로고
    • A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth
    • Lefevre G, Michel V, Weil D, Lepelletier L, Bizard E, et al. (2008) A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Development 135: 1427-1437.
    • (2008) Development , vol.135 , pp. 1427-1437
    • Lefevre, G.1    Michel, V.2    Weil, D.3    Lepelletier, L.4    Bizard, E.5
  • 19
    • 34548509448 scopus 로고    scopus 로고
    • Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells
    • Kazmierczak P, Sakaguchi H, Tokita J, Wilson-Kubalek EM, Milligan RA, et al. (2007) Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells. Nature 449: 87-91.
    • (2007) Nature , vol.449 , pp. 87-91
    • Kazmierczak, P.1    Sakaguchi, H.2    Tokita, J.3    Wilson-Kubalek, E.M.4    Milligan, R.A.5
  • 20
    • 2342421512 scopus 로고    scopus 로고
    • Cadherin 23 is a component of the tip link in hair-cell stereocilia
    • Siemens J, Lillo C, Dumont RA, Reynolds A, Williams DS, et al. (2004) Cadherin 23 is a component of the tip link in hair-cell stereocilia. Nature 428: 950-955.
    • (2004) Nature , vol.428 , pp. 950-955
    • Siemens, J.1    Lillo, C.2    Dumont, R.A.3    Reynolds, A.4    Williams, D.S.5
  • 21
    • 0035168151 scopus 로고    scopus 로고
    • Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
    • Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, et al. (2001) Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nat Genet 27: 103-107.
    • (2001) Nat Genet , vol.27 , pp. 103-107
    • Di Palma, F.1    Holme, R.H.2    Bryda, E.C.3    Belyantseva, I.A.4    Pellegrino, R.5
  • 22
    • 0028860302 scopus 로고
    • A type VII myosin encoded by the mouse deafness gene shaker-1
    • Gibson F, Walsh J, Mburu P, Varela A, Brown KA, et al. (1995) A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374: 62-64.
    • (1995) Nature , vol.374 , pp. 62-64
    • Gibson, F.1    Walsh, J.2    Mburu, P.3    Varela, A.4    Brown, K.A.5
  • 23
    • 0345530996 scopus 로고    scopus 로고
    • Mouse models of USH1C and DFNB18: Phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene
    • Johnson KR, Gagnon LH, Webb LS, Peters LL, Hawes NL, et al. (2003) Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene. Hum Mol Genet 12: 3075-3086.
    • (2003) Hum Mol Genet , vol.12 , pp. 3075-3086
    • Johnson, K.R.1    Gagnon, L.H.2    Webb, L.S.3    Peters, L.L.4    Hawes, N.L.5
  • 25
    • 0037337023 scopus 로고    scopus 로고
    • Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice
    • Kikkawa Y, Shitara H, Wakana S, Kohara Y, Takada T, et al. (2003) Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice. Hum Mol Genet 12: 453-461.
    • (2003) Hum Mol Genet , vol.12 , pp. 453-461
    • Kikkawa, Y.1    Shitara, H.2    Wakana, S.3    Kohara, Y.4    Takada, T.5
  • 26
    • 0034284683 scopus 로고    scopus 로고
    • Mariner is defective in myosin VIIA: A zebrafish model for human hereditary deafness
    • Ernest S, Rauch GJ, Haffter P, Geisler R, Petit C, et al. (2000) Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness. Hum Mol Genet 9: 2189-2196.
    • (2000) Hum Mol Genet , vol.9 , pp. 2189-2196
    • Ernest, S.1    Rauch, G.J.2    Haffter, P.3    Geisler, R.4    Petit, C.5
  • 27
    • 14044258529 scopus 로고    scopus 로고
    • Duplicated genes with split functions: Independent roles of protocadherin 15 orthologues in zebrafish hearing and vision
    • Seiler C, Finger-Baier KC, Rinner O, Makhankov YV, Schwarz H, et al. (2005) Duplicated genes with split functions: independent roles of protocadherin 15 orthologues in zebrafish hearing and vision. Development 132: 615-623.
    • (2005) Development , vol.132 , pp. 615-623
    • Seiler, C.1    Finger-Baier, K.C.2    Rinner, O.3    Makhankov, Y.V.4    Schwarz, H.5
  • 28
    • 84905556082 scopus 로고    scopus 로고
    • Sollner C, Rauch GJ, Siemens J, Geisler R, Schuster SC, et al. (2004) Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells. Nature 428: 955-959.
    • Sollner C, Rauch GJ, Siemens J, Geisler R, Schuster SC, et al. (2004) Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells. Nature 428: 955-959.
  • 29
    • 10844264543 scopus 로고    scopus 로고
    • Drosophila crinkled, mutations of which disrupt morphogenesis and cause lethality, encodes fly myosin VIIA
    • Kiehart DP, Franke JD, Chee MK, Montague RA, Chen TL, et al. (2004) Drosophila crinkled, mutations of which disrupt morphogenesis and cause lethality, encodes fly myosin VIIA. Genetics 168: 1337-1352.
    • (2004) Genetics , vol.168 , pp. 1337-1352
    • Kiehart, D.P.1    Franke, J.D.2    Chee, M.K.3    Montague, R.A.4    Chen, T.L.5
  • 30
    • 18944408058 scopus 로고    scopus 로고
    • Myosin VIIA defects, which underlie the Usher 1B syndrome in humans, lead to deafness in Drosophila
    • Todi SV, Franke JD, Kiehart DP, Eberl DF (2005) Myosin VIIA defects, which underlie the Usher 1B syndrome in humans, lead to deafness in Drosophila. Curr Biol 15: 862-868.
    • (2005) Curr Biol , vol.15 , pp. 862-868
    • Todi, S.V.1    Franke, J.D.2    Kiehart, D.P.3    Eberl, D.F.4
  • 32
    • 27744493562 scopus 로고    scopus 로고
    • Drosophila melanogaster Cad99C, the orthologue of human Usher cadherin PCDH15, regulates the length of microvilli
    • D'Alterio C, Tran DD, Yeung MW, Hwang MS, Li MA, et al. (2005) Drosophila melanogaster Cad99C, the orthologue of human Usher cadherin PCDH15, regulates the length of microvilli. J Cell Biol 171: 549-558.
    • (2005) J Cell Biol , vol.171 , pp. 549-558
    • D'Alterio, C.1    Tran, D.D.2    Yeung, M.W.3    Hwang, M.S.4    Li, M.A.5
  • 33
    • 33645736042 scopus 로고    scopus 로고
    • Cadherin Cad99C is required for normal microvilli morphology in Drosophila follicle cells
    • Schlichting K, Wilsch-Brauninger M, Demontis F, Dahmann C (2006) Cadherin Cad99C is required for normal microvilli morphology in Drosophila follicle cells. J Cell Sci 119: 1184-1195.
    • (2006) J Cell Sci , vol.119 , pp. 1184-1195
    • Schlichting, K.1    Wilsch-Brauninger, M.2    Demontis, F.3    Dahmann, C.4
  • 34
    • 0002031074 scopus 로고
    • Developmental Genetics of Oogenesis
    • Bate M, Martinez Arias A, eds, New York: Cold Spring Harbor Laboratory Press. pp
    • Spradling AC (1993) Developmental Genetics of Oogenesis. In: Bate M, Martinez Arias A, eds. The Development of Drosophila melanogaster. New York: Cold Spring Harbor Laboratory Press. pp 1-70.
    • (1993) The Development of Drosophila melanogaster , pp. 1-70
    • Spradling, A.C.1
  • 35
    • 38749124706 scopus 로고    scopus 로고
    • Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy
    • Williams DS (2008) Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy. Vision Res 48: 433-441.
    • (2008) Vision Res , vol.48 , pp. 433-441
    • Williams, D.S.1
  • 37
    • 28544438939 scopus 로고    scopus 로고
    • Endocytic control of epithelial polarity and proliferation in Drosophila
    • Lu H, Bilder D (2005) Endocytic control of epithelial polarity and proliferation in Drosophila. Nat Cell Biol 7: 1232-1239.
    • (2005) Nat Cell Biol , vol.7 , pp. 1232-1239
    • Lu, H.1    Bilder, D.2
  • 38
    • 38049094318 scopus 로고    scopus 로고
    • Expression profile of the cadherin family in the developing Drosophila brain
    • Fung S,Wang F, Chase M, Godt D, Hartenstein V (2008) Expression profile of the cadherin family in the developing Drosophila brain. J Comp Neurol 506: 469-488.
    • (2008) J Comp Neurol , vol.506 , pp. 469-488
    • Fung, S.1    Wang, F.2    Chase, M.3    Godt, D.4    Hartenstein, V.5
  • 40
    • 0030801002 scopus 로고    scopus 로고
    • Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
    • Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, et al. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25: 3389-3402.
    • (1997) Nucleic Acids Res , vol.25 , pp. 3389-3402
    • Altschul, S.F.1    Madden, T.L.2    Schaffer, A.A.3    Zhang, J.4    Zhang, Z.5
  • 41
    • 0032568655 scopus 로고    scopus 로고
    • SMART, a simple modular architecture research tool: Identification of signaling domains
    • Schultz J, Milpetz F, Bork P, Ponting CP (1998) SMART, a simple modular architecture research tool: identification of signaling domains. Proc Natl Acad Sci U S A 95: 5857-5864.
    • (1998) Proc Natl Acad Sci U S A , vol.95 , pp. 5857-5864
    • Schultz, J.1    Milpetz, F.2    Bork, P.3    Ponting, C.P.4
  • 42
    • 13544271823 scopus 로고    scopus 로고
    • Cadherin Cad99C is regulated by Hedgehog signaling in Drosophila
    • Schlichting K, Demontis F, Dahmann C (2005) Cadherin Cad99C is regulated by Hedgehog signaling in Drosophila. Dev Biol 279: 142-154.
    • (2005) Dev Biol , vol.279 , pp. 142-154
    • Schlichting, K.1    Demontis, F.2    Dahmann, C.3
  • 43
    • 5644274022 scopus 로고    scopus 로고
    • Harp (harmonin-interacting, ankyrin repeat-containing protein), a novel protein that interacts with harmonin in epithelial tissues
    • Johnston AM, Naselli G, Niwa H, Brodnicki T, Harrison LC, et al. (2004) Harp (harmonin-interacting, ankyrin repeat-containing protein), a novel protein that interacts with harmonin in epithelial tissues. Genes Cells 9: 967-982.
    • (2004) Genes Cells , vol.9 , pp. 967-982
    • Johnston, A.M.1    Naselli, G.2    Niwa, H.3    Brodnicki, T.4    Harrison, L.C.5
  • 44
    • 0023664018 scopus 로고
    • Comparison of the consensus sequence flanking translational start sites in Drosophila and vertebrates
    • Cavener DR (1987) Comparison of the consensus sequence flanking translational start sites in Drosophila and vertebrates. Nucleic Acids Res 15: 1353-1361.
    • (1987) Nucleic Acids Res , vol.15 , pp. 1353-1361
    • Cavener, D.R.1
  • 45
    • 0027160708 scopus 로고
    • Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
    • Brand AH, Perrimon N (1993) Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 118: 401-415.
    • (1993) Development , vol.118 , pp. 401-415
    • Brand, A.H.1    Perrimon, N.2
  • 46
    • 0029861146 scopus 로고    scopus 로고
    • A modular misexpression screen in Drosophila detecting tissue-specific phenotypes
    • Rorth P (1996) A modular misexpression screen in Drosophila detecting tissue-specific phenotypes. Proc Natl Acad Sci U S A 93: 12418-12422.
    • (1996) Proc Natl Acad Sci U S A , vol.93 , pp. 12418-12422
    • Rorth, P.1
  • 47
    • 0025834782 scopus 로고
    • Isolation and characterization of Drosophila multidrug resistance gene homologs
    • Wu CT, Budding M, Griffin MS, Croop JM (1991) Isolation and characterization of Drosophila multidrug resistance gene homologs. Mol Cell Biol 11: 3940-3948.
    • (1991) Mol Cell Biol , vol.11 , pp. 3940-3948
    • Wu, C.T.1    Budding, M.2    Griffin, M.S.3    Croop, J.M.4
  • 48
    • 0024102419 scopus 로고
    • Studies of the genetic organization of the vestigial microregion of Drosophila melanogaster
    • Lasko PF, Pardue ML (1988) Studies of the genetic organization of the vestigial microregion of Drosophila melanogaster. Genetics 120: 495-502.
    • (1988) Genetics , vol.120 , pp. 495-502
    • Lasko, P.F.1    Pardue, M.L.2
  • 49
    • 0031040449 scopus 로고    scopus 로고
    • Induction of Drosophila eye development by decapentaplegic
    • Pignoni F, Zipursky SL (1997) Induction of Drosophila eye development by decapentaplegic. Development 124: 271-278.
    • (1997) Development , vol.124 , pp. 271-278
    • Pignoni, F.1    Zipursky, S.L.2
  • 50
    • 0036795371 scopus 로고    scopus 로고
    • Drosophila crumbs is required to inhibit light-induced photoreceptor degeneration
    • Johnson K, Grawe F, Grzeschik N, Knust E (2002) Drosophila crumbs is required to inhibit light-induced photoreceptor degeneration. Curr Biol 12: 1675-1680.
    • (2002) Curr Biol , vol.12 , pp. 1675-1680
    • Johnson, K.1    Grawe, F.2    Grzeschik, N.3    Knust, E.4
  • 51
    • 0028033098 scopus 로고
    • A Drosophila homolog of cadherin associated with armadillo and essential for embryonic cell-cell adhesion
    • Oda H, Uemura T, Harada Y, Iwai Y, Takeichi M (1994) A Drosophila homolog of cadherin associated with armadillo and essential for embryonic cell-cell adhesion. Dev Biol 165: 716-726.
    • (1994) Dev Biol , vol.165 , pp. 716-726
    • Oda, H.1    Uemura, T.2    Harada, Y.3    Iwai, Y.4    Takeichi, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.