메뉴 건너뛰기




Volumn 18, Issue 6, 1998, Pages 3466-3474

Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster

Author keywords

[No Author keywords available]

Indexed keywords

DNA METHYLTRANSFERASE; RNA;

EID: 0031844688     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.18.6.3466     Document Type: Article
Times cited : (220)

References (65)
  • 1
    • 0019023345 scopus 로고
    • Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA
    • Auffray, C., and F. Rougeon. 1980. Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA. Eur. J. Biochem. 107:303-314.
    • (1980) Eur. J. Biochem. , vol.107 , pp. 303-314
    • Auffray, C.1    Rougeon, F.2
  • 3
    • 0030670449 scopus 로고    scopus 로고
    • Competition - A common motif for the imprinting mechanism?
    • Barlow, D. P. 1997. Competition - a common motif for the imprinting mechanism? EMBO J. 16:6899-6905.
    • (1997) EMBO J. , vol.16 , pp. 6899-6905
    • Barlow, D.P.1
  • 5
    • 0027203606 scopus 로고
    • Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
    • Bartolomei, M. S., A. L. Webber, M. E. Brunkow, and S. M. Tilghman. 1993. Epigenetic mechanisms underlying the imprinting of the mouse H19 gene. Genes Dev. 7:1663-1673.
    • (1993) Genes Dev. , vol.7 , pp. 1663-1673
    • Bartolomei, M.S.1    Webber, A.L.2    Brunkow, M.E.3    Tilghman, S.M.4
  • 6
    • 0025809321 scopus 로고
    • Parental imprinting of the mouse H19 gene
    • Bartolomei, M. S., S. Zemel, and S. M. Tilghman. 1991. Parental imprinting of the mouse H19 gene. Nature 351:153-155.
    • (1991) Nature , vol.351 , pp. 153-155
    • Bartolomei, M.S.1    Zemel, S.2    Tilghman, S.M.3
  • 7
    • 0029806141 scopus 로고    scopus 로고
    • Imprinting mutation in the Beckwith-Wiedemann syndrome leads to hiallelic IGF2 expression through an H19-independent pathway
    • Brown, K. W., A. J. Villar, W. Bickmore, J. Clayton-Smith, D. Catchpole, E. R. Maher, and W. Reik. 1996. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to hiallelic IGF2 expression through an H19-independent pathway. Hum. Mol. Genet. 5:2027-2032.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 2027-2032
    • Brown, K.W.1    Villar, A.J.2    Bickmore, W.3    Clayton-Smith, J.4    Catchpole, D.5    Maher, E.R.6    Reik, W.7
  • 8
    • 0028939902 scopus 로고
    • Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
    • Buiting, K., S. Saitoh, S. Gross, B. Dittrich, S. Schwartz, R. D. Nicholls, and B. Horsthemke. 1995. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat. Genet. 9:395-400.
    • (1995) Nat. Genet. , vol.9 , pp. 395-400
    • Buiting, K.1    Saitoh, S.2    Gross, S.3    Dittrich, B.4    Schwartz, S.5    Nicholls, R.D.6    Horsthemke, B.7
  • 10
    • 0029847299 scopus 로고    scopus 로고
    • Chromosome 11p15.5 regional imprinting: Comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors
    • Chung, W.-Y., L. Yuan, L. Feng, T. Hensle, and B. Tycko. 1996. Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors. Hum. Mol. Genet. 5:1101-1108.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1101-1108
    • Chung, W.-Y.1    Yuan, L.2    Feng, L.3    Hensle, T.4    Tycko, B.5
  • 13
    • 0022377642 scopus 로고
    • Cell-specific expression of the rat insulin gene: Evidence for role of two distinct 5′ flanking elements
    • Edlund, T., M. D. Walker, P. J. Barr, and W. J. Rutter. 1985. Cell-specific expression of the rat insulin gene: evidence for role of two distinct 5′ flanking elements. Science 230:912-916.
    • (1985) Science , vol.230 , pp. 912-916
    • Edlund, T.1    Walker, M.D.2    Barr, P.J.3    Rutter, W.J.4
  • 14
    • 0030660180 scopus 로고    scopus 로고
    • Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes
    • Eggenschwiler, J., T. Ludwig, P. Fisher, P. A. Leighton, S. M. Tilghman, and A. Efstratiadis. 1997. Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes. Genes Dev. 11:3128-3142.
    • (1997) Genes Dev. , vol.11 , pp. 3128-3142
    • Eggenschwiler, J.1    Ludwig, T.2    Fisher, P.3    Leighton, P.A.4    Tilghman, S.M.5    Efstratiadis, A.6
  • 15
    • 0027172684 scopus 로고
    • Parental-origin-specific epigenetic modifications of the mouse H19 gene
    • Ferguson-Smith, A. C., H. Sasaki, B. M. Cattanach, and M. A. Surani. 1993. Parental-origin-specific epigenetic modifications of the mouse H19 gene. Nature 362:751-755.
    • (1993) Nature , vol.362 , pp. 751-755
    • Ferguson-Smith, A.C.1    Sasaki, H.2    Cattanach, B.M.3    Surani, M.A.4
  • 16
    • 0028365598 scopus 로고
    • Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting
    • Giddings, S. J., C. D. King, K. W. Harman, J. F. Flood, and L. R. Carnaghi. 1994. Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting. Nat. Genet. 6:310-313.
    • (1994) Nat. Genet. , vol.6 , pp. 310-313
    • Giddings, S.J.1    King, C.D.2    Harman, K.W.3    Flood, J.F.4    Carnaghi, L.R.5
  • 17
    • 0031114837 scopus 로고    scopus 로고
    • Genomic imprinting: Potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes
    • Glenn, C. C., D. J. Driscoll, P. Yang, and R. D. Nicholls. 1997. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes. Mol. Hum. Reprod. 3:321-332.
    • (1997) Mol. Hum. Reprod. , vol.3 , pp. 321-332
    • Glenn, C.C.1    Driscoll, D.J.2    Yang, P.3    Nicholls, R.D.4
  • 19
    • 0027941535 scopus 로고
    • Essential role of Mash-2 in extraembryonic development
    • Guillemot, F., A. Nagy, A. Auerbach, J. Rossant, and A. L. Joyner. 1994. Essential role of Mash-2 in extraembryonic development. Nature 371:333-336.
    • (1994) Nature , vol.371 , pp. 333-336
    • Guillemot, F.1    Nagy, A.2    Auerbach, A.3    Rossant, J.4    Joyner, A.L.5
  • 20
    • 0028933627 scopus 로고
    • Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region
    • Gunaratne, P. H., M. Nakao, D. H. Ledbetter, J. S. Sutcliffe, and A. C. Chinault. 1995. Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region. Genes Dev. 9:808-820.
    • (1995) Genes Dev. , vol.9 , pp. 808-820
    • Gunaratne, P.H.1    Nakao, M.2    Ledbetter, D.H.3    Sutcliffe, J.S.4    Chinault, A.C.5
  • 21
    • 0028980026 scopus 로고
    • Genomic imprinting of p57/KIP2, a cyclin-dependent kinase inhibitor, in mouse
    • Hatada, I., and T. Mukai. 1995. Genomic imprinting of p57/KIP2, a cyclin-dependent kinase inhibitor, in mouse. Nat. Genet. 11:204-206.
    • (1995) Nat. Genet. , vol.11 , pp. 204-206
    • Hatada, I.1    Mukai, T.2
  • 23
    • 0029807080 scopus 로고    scopus 로고
    • A novel human homologue of yeast nucleosome assembly protein. 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues
    • Hu, R.-J., M. P. Lee, L. A. Johnson, and A. P. Feinberg. 1996. A novel human homologue of yeast nucleosome assembly protein. 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues. Hum. Mol. Genet. 5:1743-1748.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1743-1748
    • Hu, R.-J.1    Lee, M.P.2    Johnson, L.A.3    Feinberg, A.P.4
  • 24
    • 0027450207 scopus 로고
    • Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation
    • Kay, G. F., G. D. Penny, D. Patel, A. Ashworth, N. Brockdorff, and S. Rastan. 1993. Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation. Cell 72:171-182.
    • (1993) Cell , vol.72 , pp. 171-182
    • Kay, G.F.1    Penny, G.D.2    Patel, D.3    Ashworth, A.4    Brockdorff, N.5    Rastan, S.6
  • 25
    • 0031012849 scopus 로고    scopus 로고
    • UBE3A/E6-AP mutations cause Angelman syndrome
    • Kishino, T., M. Lalande, and J. Wagstaff. 1997. UBE3A/E6-AP mutations cause Angelman syndrome. Nat. Genet. 15:70-73.
    • (1997) Nat. Genet. , vol.15 , pp. 70-73
    • Kishino, T.1    Lalande, M.2    Wagstaff, J.3
  • 27
    • 0028260642 scopus 로고
    • Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region
    • Knoll, J. H., S. D. Cheng, and M. Lalande. 1994. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region. Nat. Genet. 6:41-40.
    • (1994) Nat. Genet. , vol.6 , pp. 41-140
    • Knoll, J.H.1    Cheng, S.D.2    Lalande, M.3
  • 28
    • 0030458551 scopus 로고    scopus 로고
    • Parental imprinting and disease
    • Lalande, M. 1996. Parental imprinting and disease. Annu. Rev. Genet. 30:173-195.
    • (1996) Annu. Rev. Genet. , vol.30 , pp. 173-195
    • Lalande, M.1
  • 30
    • 0031046285 scopus 로고    scopus 로고
    • Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
    • Lee, M. P., R. Hu, L. A. Johnson, and A. P. Feinberg. 1997. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nat. Genet. 15:181-185.
    • (1997) Nat. Genet. , vol.15 , pp. 181-185
    • Lee, M.P.1    Hu, R.2    Johnson, L.A.3    Feinberg, A.P.4
  • 31
    • 0027018063 scopus 로고
    • Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region
    • Leff, S. E., C. I. Brannan, M. L. Reed, T. Ozcelik, U. Francke, N. G. Copeland, and N. A. Jenkins. 1992. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nat. Genet. 2:259-264.
    • (1992) Nat. Genet. , vol.2 , pp. 259-264
    • Leff, S.E.1    Brannan, C.I.2    Reed, M.L.3    Ozcelik, T.4    Francke, U.5    Copeland, N.G.6    Jenkins, N.A.7
  • 34
    • 0027378582 scopus 로고
    • The role of DNA methylation in genomic imprinting
    • Li, E., C. Beard, and R. Jaenisch. 1993. The role of DNA methylation in genomic imprinting. Nature 366:362-365.
    • (1993) Nature , vol.366 , pp. 362-365
    • Li, E.1    Beard, C.2    Jaenisch, R.3
  • 35
    • 0026708177 scopus 로고
    • Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
    • Li, E., T. H. Bester, and R. Jaenisch. 1992. Targeted mutation of the DNA methyltransferase gene results in embryonic lethality. Cell 69:915-926.
    • (1992) Cell , vol.69 , pp. 915-926
    • Li, E.1    Bester, T.H.2    Jaenisch, R.3
  • 36
    • 0027200763 scopus 로고
    • Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of the DNa spanning the insulin gene and associated VNTR
    • Lucassen, A. M., C. Julier, J. P. Beressi, C. Boitard, P. Froguel, M. Lathrop, and J. I. Bell. 1993. Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of the DNA spanning the insulin gene and associated VNTR. Nat. Genet. 4:305-310.
    • (1993) Nat. Genet. , vol.4 , pp. 305-310
    • Lucassen, A.M.1    Julier, C.2    Beressi, J.P.3    Boitard, C.4    Froguel, P.5    Lathrop, M.6    Bell, J.I.7
  • 37
    • 0030948267 scopus 로고    scopus 로고
    • Normal lymphocyte development but delayed humoral immune response in CD81-null mice
    • Maecker, H. T., and S. Levy. 1997. Normal lymphocyte development but delayed humoral immune response in CD81-null mice. J. Exp. Med. 185: 1505-1510.
    • (1997) J. Exp. Med. , vol.185 , pp. 1505-1510
    • Maecker, H.T.1    Levy, S.2
  • 38
    • 0031044166 scopus 로고    scopus 로고
    • Xist-deficient mice are defective in dosage compensation but not spermatogenesis
    • Marahrens, Y., B. Panning, J. Dausman, W. Strauss, and R. Jaenisch. 1997. Xist-deficient mice are defective in dosage compensation but not spermatogenesis. Genes Dev. 11:156-166.
    • (1997) Genes Dev. , vol.11 , pp. 156-166
    • Marahrens, Y.1    Panning, B.2    Dausman, J.3    Strauss, W.4    Jaenisch, R.5
  • 40
    • 0030610260 scopus 로고    scopus 로고
    • Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors
    • O'Keefe, D., D. Dao, L. Zhao, R. Sanderson, D. Warburton, L. Weiss, K. Anyane-Yeboa, and B. Tycko. 1997. Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors. Am. J. Hum. Genet. 61:295-303.
    • (1997) Am. J. Hum. Genet. , vol.61 , pp. 295-303
    • O'Keefe, D.1    Dao, D.2    Zhao, L.3    Sanderson, R.4    Warburton, D.5    Weiss, L.6    Anyane-Yeboa, K.7    Tycko, B.8
  • 41
    • 0029360421 scopus 로고
    • Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies
    • Paldi, A., G. Gyapay, and J. Jami. 1995. Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies. Curr. Biol. 5:1030-1035.
    • (1995) Curr. Biol. , vol.5 , pp. 1030-1035
    • Paldi, A.1    Gyapay, G.2    Jami, J.3
  • 43
    • 9844265406 scopus 로고    scopus 로고
    • The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis
    • Qian, N., D. Frank, D. O'Keefe, D. Dao, L. Zhao, L. Yuan, Q. Wang, M. Keating, C. Walsh, and B. Tycko. 1997. The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. Hum. Mol. Genet. 6:2021-2029.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 2021-2029
    • Qian, N.1    Frank, D.2    O'Keefe, D.3    Dao, D.4    Zhao, L.5    Yuan, L.6    Wang, Q.7    Keating, M.8    Walsh, C.9    Tycko, B.10
  • 45
    • 0030856668 scopus 로고    scopus 로고
    • Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome
    • Reik, W., and E. R. Maher. 1997. Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome. Trends Genet. 13:330-334.
    • (1997) Trends Genet. , vol.13 , pp. 330-334
    • Reik, W.1    Maher, E.R.2
  • 46
    • 0030993133 scopus 로고    scopus 로고
    • Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
    • Ripoche, M.-A., C. Kress, F. Poirier, and L. Dandolo. 1997. Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element. Genes Dev. 11:1596-1604.
    • (1997) Genes Dev. , vol.11 , pp. 1596-1604
    • Ripoche, M.-A.1    Kress, C.2    Poirier, F.3    Dandolo, L.4
  • 48
    • 0030886796 scopus 로고    scopus 로고
    • Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
    • Shemer, R., Y. Birger, A. D. Riggs, and A. Razin. 1997. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Proc. Natl. Acad. Sci. USA 94:10267-10272.
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , pp. 10267-10272
    • Shemer, R.1    Birger, Y.2    Riggs, A.D.3    Razin, A.4
  • 50
    • 0030735169 scopus 로고    scopus 로고
    • Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome
    • Sun, F.-L., W. Dean, G. Kelsey, N. D. Allen, and W. Reik. 1997. Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. Nature 389:809-815.
    • (1997) Nature , vol.389 , pp. 809-815
    • Sun, F.-L.1    Dean, W.2    Kelsey, G.3    Allen, N.D.4    Reik, W.5
  • 51
  • 52
    • 0016692463 scopus 로고
    • Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse
    • Takagi, N., and M. Sasaki. 1975. Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse. Nature 256:640-642.
    • (1975) Nature , vol.256 , pp. 640-642
    • Takagi, N.1    Sasaki, M.2
  • 53
    • 0028968205 scopus 로고
    • A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
    • Tremblay, K. D., J. R. Saam, R. S. Ingram, S. M. Tilghman, and M. S. Bartolomei. 1995. A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nat. Genet. 9:407-413.
    • (1995) Nat. Genet. , vol.9 , pp. 407-413
    • Tremblay, K.D.1    Saam, J.R.2    Ingram, R.S.3    Tilghman, S.M.4    Bartolomei, M.S.5
  • 56
    • 0032509990 scopus 로고    scopus 로고
    • Location of enhancers is essential for imprinting of H19 and Igf2
    • Webber, A., R. I. Ingram, J. Levorse, and S. M. Tilghman. 1998. Location of enhancers is essential for imprinting of H19 and Igf2. Nature 391:711-715.
    • (1998) Nature , vol.391 , pp. 711-715
    • Webber, A.1    Ingram, R.I.2    Levorse, J.3    Tilghman, S.M.4
  • 57
    • 0027420362 scopus 로고
    • Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
    • Weksberg, R., D. R. Shen, Y. L. Fei, Q. L. Song, and J. Squire. 1993. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nat. Genet. 5:143-150.
    • (1993) Nat. Genet. , vol.5 , pp. 143-150
    • Weksberg, R.1    Shen, D.R.2    Fei, Y.L.3    Song, Q.L.4    Squire, J.5
  • 58
    • 0028124726 scopus 로고
    • Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
    • Wevrick, R., J. A. Kerns, and U. Francke. 1994. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum. Mol. Genet. 3:1877-1882.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1877-1882
    • Wevrick, R.1    Kerns, J.A.2    Francke, U.3
  • 59
    • 0027860527 scopus 로고
    • Epigenetic and chromosomal control of gene expression: Molecular and genetic analysis of X chromosome inactivation
    • Willard, H. F., C. J. Brown, L. Carrel, B. Hendrich, and A. P. Miller. 1993. Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation. Cold Spring Harbor Symp. Quant. Biol. 58:315-322.
    • (1993) Cold Spring Harbor Symp. Quant. Biol. , vol.58 , pp. 315-322
    • Willard, H.F.1    Brown, C.J.2    Carrel, L.3    Hendrich, B.4    Miller, A.P.5
  • 61
    • 0027716060 scopus 로고
    • Functional polymorphism in the parental imprinting of the human ICF2R gene
    • Xu, Y., C. G. Goodyer, C. Deal, and C. Polychronakos. 1993. Functional polymorphism in the parental imprinting of the human ICF2R gene. Biochem. Biophys. Res. Commun. 197:747-754.
    • (1993) Biochem. Biophys. Res. Commun. , vol.197 , pp. 747-754
    • Xu, Y.1    Goodyer, C.G.2    Deal, C.3    Polychronakos, C.4
  • 62
    • 0030955563 scopus 로고    scopus 로고
    • Ablation of the CDK inhibitor p57KIP2 results in increased apoptosis and delayed differentiation during mouse development
    • Van, Y., J. Frisén, M.-H. Lee, J. Massagué, and M. Barbacid. 1997. Ablation of the CDK inhibitor p57KIP2 results in increased apoptosis and delayed differentiation during mouse development. Genes Dev. 11:973-983.
    • (1997) Genes Dev. , vol.11 , pp. 973-983
    • Van, Y.1    Frisén, J.2    Lee, M.-H.3    Massagué, J.4    Barbacid, M.5
  • 63
    • 0026922595 scopus 로고
    • Physical linkage of two mammalian imprinted genes
    • Zemel, S., M. S. Bartolomei, and S. M. Tilghman. 1992. Physical linkage of two mammalian imprinted genes. Nat. Genet. 2:61-65.
    • (1992) Nat. Genet. , vol.2 , pp. 61-65
    • Zemel, S.1    Bartolomei, M.S.2    Tilghman, S.M.3
  • 65
    • 0028912476 scopus 로고
    • Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development
    • Zhou, Q.-Y., C. J. Quaife, and R. D. Palmiter. 1995. Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development. Nature 374:640-643.
    • (1995) Nature , vol.374 , pp. 640-643
    • Zhou, Q.-Y.1    Quaife, C.J.2    Palmiter, R.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.