메뉴 건너뛰기




Volumn 80, Issue 6, 2002, Pages 593-600

Genetic and comparative mapping of genes dysregulated in mouse hearts lacking the Hand2 transcription factor gene

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; COMPLEMENTARY DNA; HELIX LOOP HELIX PROTEIN; NEBULETTE; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR HAND2; UNCLASSIFIED DRUG;

EID: 12244273279     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2002.7009     Document Type: Article
Times cited : (22)

References (34)
  • 1
    • 0029549692 scopus 로고
    • A subclass of bHLH proteins required for cardiac morphogenesis
    • Srivastava, D., Cserjesi, P., and Olson, E. N. (1995). A subclass of bHLH proteins required for cardiac morphogenesis. Science 270: 1995-1999.
    • (1995) Science , vol.270 , pp. 1995-1999
    • Srivastava, D.1    Cserjesi, P.2    Olson, E.N.3
  • 2
    • 0030903857 scopus 로고    scopus 로고
    • Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND
    • Published erratum appears in Nat. Genet., 1997, 16: 410
    • Srivastava, D., et al. (1997). Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND. Nat. Genet. 16: 154-160. [Published erratum appears in Nat. Genet., 1997, 16: 410]
    • (1997) Nat. Genet. , vol.16 , pp. 154-160
    • Srivastava, D.1
  • 3
    • 0034130648 scopus 로고    scopus 로고
    • Role of dHAND in the anterior-posterior polarization of the limb bud: Implications for the Sonic hedgehog pathway
    • Fernandez-Teran, M., et al. (2000). Role of dHAND in the anterior-posterior polarization of the limb bud: Implications for the Sonic hedgehog pathway. Development 127: 2133-2142.
    • (2000) Development , vol.127 , pp. 2133-2142
    • Fernandez-Teran, M.1
  • 4
    • 0031695316 scopus 로고    scopus 로고
    • A signaling cascade involving endothelin-1, dHAND and msx1 regulates development of neural-crest-derived branchial arch mesenchyme
    • Thomas, T., et al. (1998). A signaling cascade involving endothelin-1, dHAND and msx1 regulates development of neural-crest-derived branchial arch mesenchyme. Development 125: 3005-3014.
    • (1998) Development , vol.125 , pp. 3005-3014
    • Thomas, T.1
  • 5
    • 0024992614 scopus 로고
    • Role of neural crest in congenital heart disease
    • Kirby, M. L., and Waldo, K. L. (1990). Role of neural crest in congenital heart disease. Circulation 82: 332-340.
    • (1990) Circulation , vol.82 , pp. 332-340
    • Kirby, M.L.1    Waldo, K.L.2
  • 6
    • 0033968447 scopus 로고    scopus 로고
    • The basic helix-loop-helix transcription factor, dHAND, is required for vascular development
    • Yamagishi, H., Olson, E. N., and Srivastava, D. (2000). The basic helix-loop-helix transcription factor, dHAND, is required for vascular development. J. Clin. Invest. 105: 261-270.
    • (2000) J. Clin. Invest. , vol.105 , pp. 261-270
    • Yamagishi, H.1    Olson, E.N.2    Srivastava, D.3
  • 7
    • 0035098436 scopus 로고    scopus 로고
    • Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome
    • Guris, D. L., Fantes, J., Tara, D., Druker, B. J., and Imamoto, A. (2001). Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome. Nat. Genet. 27: 293-298.
    • (2001) Nat. Genet. , vol.27 , pp. 293-298
    • Guris, D.L.1    Fantes, J.2    Tara, D.3    Druker, B.J.4    Imamoto, A.5
  • 8
    • 0035263599 scopus 로고    scopus 로고
    • Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
    • Lindsay, E. A., et al. (2001). Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice. Nature 410: 97-101.
    • (2001) Nature , vol.410 , pp. 97-101
    • Lindsay, E.A.1
  • 9
    • 17744395906 scopus 로고    scopus 로고
    • TBX1 is responsible for cardiovascular defects in velo-cardiofacial/DiGeorge syndrome
    • Merscher, S., et al. (2001). TBX1 is responsible for cardiovascular defects in velo-cardiofacial/DiGeorge syndrome. Cell 104: 619-629.
    • (2001) Cell , vol.104 , pp. 619-629
    • Merscher, S.1
  • 10
    • 0035098557 scopus 로고    scopus 로고
    • DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
    • Jerome, L. A., and Papaioannou, V. E. (2001). DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1. Nat. Genet. 27: 286-291.
    • (2001) Nat. Genet. , vol.27 , pp. 286-291
    • Jerome, L.A.1    Papaioannou, V.E.2
  • 11
    • 0033582626 scopus 로고    scopus 로고
    • A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects
    • Yamagishi, H., Garg, V., Matsuoka, R., Thomas, T., and Srivastava, D. (1999). A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects. Science 283: 1158-1161.
    • (1999) Science , vol.283 , pp. 1158-1161
    • Yamagishi, H.1    Garg, V.2    Matsuoka, R.3    Thomas, T.4    Srivastava, D.5
  • 12
    • 0029119522 scopus 로고
    • A proteolytic pathway that recognizes ubiquitin as a degradation signal
    • Johnson, E. S., Ma, P. C., Ota, I. M., and Varshavsky, A. (1995). A proteolytic pathway that recognizes ubiquitin as a degradation signal. J. Biol. Chem. 270: 17442-17456.
    • (1995) J. Biol. Chem. , vol.270 , pp. 17442-17456
    • Johnson, E.S.1    Ma, P.C.2    Ota, I.M.3    Varshavsky, A.4
  • 13
    • 0035825662 scopus 로고    scopus 로고
    • Functional annotation of a full-length mouse cDNA collection
    • Kawai, J., et al. (2001). Functional annotation of a full-length mouse cDNA collection. Nature 409: 685-690.
    • (2001) Nature , vol.409 , pp. 685-690
    • Kawai, J.1
  • 14
    • 15844403609 scopus 로고    scopus 로고
    • A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
    • Daw, S. C., et al. (1996). A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Nat. Genet. 13: 458-460.
    • (1996) Nat. Genet. , vol.13 , pp. 458-460
    • Daw, S.C.1
  • 15
    • 13144252168 scopus 로고    scopus 로고
    • Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)
    • Schuffenhauer, S., et al. (1998). Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2). Eur. J. Hum. Genet. 6: 213-225
    • (1998) Eur. J. Hum. Genet. , vol.6 , pp. 213-225
    • Schuffenhauer, S.1
  • 16
    • 0028784365 scopus 로고
    • Nebulette: A 107 kD nebulin-like protein in cardiac muscle
    • Moncman, C. L., and Wang, K. (1995). Nebulette: A 107 kD nebulin-like protein in cardiac muscle. Cell Motil. Cytoskeleton 32: 205-225.
    • (1995) Cell Motil. Cytoskeleton , vol.32 , pp. 205-225
    • Moncman, C.L.1    Wang, K.2
  • 17
    • 0032860929 scopus 로고    scopus 로고
    • Functional dissection of nebulette demonstrates actin binding of nebulin-like repeats and Z-line targeting of SH3 and linker domains
    • Moncman, C. L., and Wang, K. (1999). Functional dissection of nebulette demonstrates actin binding of nebulin-like repeats and Z-line targeting of SH3 and linker domains. Cell Motil. Cytoskeleton 44: 1-22.
    • (1999) Cell Motil. Cytoskeleton , vol.44 , pp. 1-22
    • Moncman, C.L.1    Wang, K.2
  • 18
    • 0032508463 scopus 로고    scopus 로고
    • Characterization of nebulette and nebulin and emerging concepts of their roles for vertebrate Z-discs
    • Millevoi, S., et al. (1998). Characterization of nebulette and nebulin and emerging concepts of their roles for vertebrate Z-discs. J. Mol. Biol. 282: 111-123.
    • (1998) J. Mol. Biol. , vol.282 , pp. 111-123
    • Millevoi, S.1
  • 19
    • 0031912717 scopus 로고    scopus 로고
    • Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype
    • Gottlieb, S., et al. (1998). Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype. Am. J. Hum. Genet. 62: 495-498.
    • (1998) Am. J. Hum. Genet. , vol.62 , pp. 495-498
    • Gottlieb, S.1
  • 20
    • 0032568790 scopus 로고    scopus 로고
    • Targeted disruption of mouse conventional kinesin heavy chain, kif5B, results in abnormal perinuclear clustering of mitochondria
    • Tanaka, Y., et al. (1998). Targeted disruption of mouse conventional kinesin heavy chain, kif5B, results in abnormal perinuclear clustering of mitochondria. Cell 93: 1147-1158.
    • (1998) Cell , vol.93 , pp. 1147-1158
    • Tanaka, Y.1
  • 21
    • 0034852125 scopus 로고    scopus 로고
    • Divergent expression of delayed rectifier K(+) channel subunits during mouse heart development
    • Franco, D., et al. (2001). Divergent expression of delayed rectifier K(+) channel subunits during mouse heart development. Cardiovasc. Res. 52: 65-75.
    • (2001) Cardiovasc. Res. , vol.52 , pp. 65-75
    • Franco, D.1
  • 22
    • 0030588594 scopus 로고    scopus 로고
    • Cloning and characterization of mouse ACF7, a novel member of the dystonin subfamily of actin binding proteins
    • Bernier, G., Mathieu, M., De Repentigny, Y., Vidal, S. M., and Kothary, R. (1996). Cloning and characterization of mouse ACF7, a novel member of the dystonin subfamily of actin binding proteins. Genomics 38: 19-29.
    • (1996) Genomics , vol.38 , pp. 19-29
    • Bernier, G.1    Mathieu, M.2    De Repentigny, Y.3    Vidal, S.M.4    Kothary, R.5
  • 23
    • 0030833392 scopus 로고    scopus 로고
    • Characterization of mutations in the myotubularin gene in twenty six patients with X-linked myotubular myopathy
    • de Gouyon, B. M., et al. (1997). Characterization of mutations in the myotubularin gene in twenty six patients with X-linked myotubular myopathy. Hum. Mol. Genet. 6: 1499-1504.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 1499-1504
    • De Gouyon, B.M.1
  • 24
    • 9844265393 scopus 로고    scopus 로고
    • Mutations in the MTM1 gene implicated in X-linked myotubular myopathy
    • ENMC International Consortium on Myotubular Myopathy, European Neuro-Muscular Center
    • Laporte, J., et al. (1997). Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy, European Neuro-Muscular Center. Hum. Mol. Genet. 6: 1505-1511.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 1505-1511
    • Laporte, J.1
  • 25
    • 0033033506 scopus 로고    scopus 로고
    • Characterization of 34 novel and six known MTM1 gene mutations in 47 unrelated X-linked myotubular myopathy patients
    • Tanner, S. M., et al. (1999). Characterization of 34 novel and six known MTM1 gene mutations in 47 unrelated X-linked myotubular myopathy patients. Neuromusc. Disord. 9: 41-49.
    • (1999) Neuromusc. Disord. , vol.9 , pp. 41-49
    • Tanner, S.M.1
  • 26
    • 0035693730 scopus 로고    scopus 로고
    • Linkage and mutation analysis in two Taiwanese families with long QT syndrome
    • Ko, Y. L., et al. (2001). Linkage and mutation analysis in two Taiwanese families with long QT syndrome. J. Formosan Med. Assoc. 100: 767-771.
    • (2001) J. Formosan Med. Assoc. , vol.100 , pp. 767-771
    • Ko, Y.L.1
  • 27
    • 0035193284 scopus 로고    scopus 로고
    • Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias
    • Kubota, T., et al. (2001). Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias. J. Cardiovasc. Electrophysiol. 12: 1223-1229.
    • (2001) J. Cardiovasc. Electrophysiol. , vol.12 , pp. 1223-1229
    • Kubota, T.1
  • 28
    • 0034141999 scopus 로고    scopus 로고
    • A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly
    • Schmitt, N., et al. (2000). A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly. EMBO J. 19: 332-340.
    • (2000) EMBO J. , vol.19 , pp. 332-340
    • Schmitt, N.1
  • 29
    • 0033966954 scopus 로고    scopus 로고
    • 2+-ATPase 2 (SERCA2) isoforms
    • 2+-ATPase 2 (SERCA2) isoforms. Mamm. Genome 11: 159-163.
    • (2000) Mamm. Genome , vol.11 , pp. 159-163
    • Ver Heyen, M.1
  • 30
    • 0028355162 scopus 로고
    • Sarcoplasmic reticulum gene expression in cardiac hypertrophy and heart failure
    • Arai, M., Matsui, H., and Periasamy, M. (1994). Sarcoplasmic reticulum gene expression in cardiac hypertrophy and heart failure. Circ. Res. 74: 555-564.
    • (1994) Circ. Res. , vol.74 , pp. 555-564
    • Arai, M.1    Matsui, H.2    Periasamy, M.3
  • 31
    • 1642602480 scopus 로고    scopus 로고
    • An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14
    • Lichtner, P., et al. (2000). An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14. J. Med. Genet. 37: 33-37.
    • (2000) J. Med. Genet. , vol.37 , pp. 33-37
    • Lichtner, P.1
  • 32
    • 0033582626 scopus 로고    scopus 로고
    • A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects
    • Yamagishi, H., Garg, V., Matsuoka, R., Thomas, T., and Srivastava, D. (1999). A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects. Science 283: 1158-1161.
    • (1999) Science , vol.283 , pp. 1158-1161
    • Yamagishi, H.1    Garg, V.2    Matsuoka, R.3    Thomas, T.4    Srivastava, D.5
  • 33
    • 0033358665 scopus 로고    scopus 로고
    • Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families
    • Shaikh, T. H., Budarf, M. L., Celle, L., Zackai, E. H., and Emanuel, B. S. (1999). Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families. Am. J. Hum. Genet. 65: 1595-1607.
    • (1999) Am. J. Hum. Genet. , vol.65 , pp. 1595-1607
    • Shaikh, T.H.1    Budarf, M.L.2    Celle, L.3    Zackai, E.H.4    Emanuel, B.S.5
  • 34
    • 0023692635 scopus 로고
    • Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries
    • Lichter, P., Cremer, T., Borden, J., Manuelidis, L., and Ward, D. C. (1988). Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum. Genet. 80: 224-234.
    • (1988) Hum. Genet. , vol.80 , pp. 224-234
    • Lichter, P.1    Cremer, T.2    Borden, J.3    Manuelidis, L.4    Ward, D.C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.