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Volumn 164, Issue 8, 2014, Pages 1981-1990

Overlapping trisomies for human chromosome 21 orthologs produce similar effects on skull and brain morphology of Dp(16)1Yey and Ts65Dn mice

Author keywords

Brain morphology; Craniofacial morphogenesis; Down syndrome; Gene dosage imbalance; Trisomy 21

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CELL DENSITY; CELL GRANULE; CEREBELLUM; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; CRANIOFACIAL MORPHOLOGY; DOWN SYNDROME; GENE DOSAGE; GENE LOCATION; GENETIC ANALYSIS; MICRO-COMPUTED TOMOGRAPHY; MORPHOLOGY; MOUSE; NEUROANATOMY; NONHUMAN; OPEN READING FRAME; ORTHOLOGY; PHENOTYPE; PRIORITY JOURNAL; PURKINJE CELL; QUANTITATIVE ANALYSIS; ANIMAL; BRAIN; DISEASE MODEL; GENETICS; HUMAN; METABOLISM; PATHOLOGY; SKULL;

EID: 84904382695     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36594     Document Type: Article
Times cited : (37)

References (42)
  • 1
    • 0027520384 scopus 로고
    • Anthropometric craniofacial pattern profiles in Down syndrome
    • Allanson JE, O'Hara P, Farkas LG, Nair RC. 1993. Anthropometric craniofacial pattern profiles in Down syndrome. Am J Med Genet 47:748-752.
    • (1993) Am J Med Genet , vol.47 , pp. 748-752
    • Allanson, J.E.1    O'Hara, P.2    Farkas, L.G.3    Nair, R.C.4
  • 4
    • 0033978891 scopus 로고    scopus 로고
    • Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse
    • Baxter LL, Moran TH, Richtsmeier JT, Troncoso J, Reeves RH. 2000. Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse. Hum Mol Genet 9:195-202.
    • (2000) Hum Mol Genet , vol.9 , pp. 195-202
    • Baxter, L.L.1    Moran, T.H.2    Richtsmeier, J.T.3    Troncoso, J.4    Reeves, R.H.5
  • 5
    • 78650997057 scopus 로고    scopus 로고
    • Disruption of bone development and homeostasis by trisomy in Ts65Dn Down syndrome mice
    • Blazek JD, Gaddy A, Meyer R, Roper RJ, Li J. 2011. Disruption of bone development and homeostasis by trisomy in Ts65Dn Down syndrome mice. Bone 48:275-280.
    • (2011) Bone , vol.48 , pp. 275-280
    • Blazek, J.D.1    Gaddy, A.2    Meyer, R.3    Roper, R.J.4    Li, J.5
  • 6
    • 12344250141 scopus 로고    scopus 로고
    • MIBoot Windows-based software for bootstrapbased comparison of morphological integration patterns
    • Richtsmeier Lab. Available at: Accessed on 20 December, 2013.
    • Cole T III. 2002. MIBoot Windows-based software for bootstrapbased comparison of morphological integration patterns. Richtsmeier Lab. Available at: http://getahead.psu.edu. Accessed on 20 December, 2013.
    • (2002)
    • Cole III, T.1
  • 7
    • 10044294000 scopus 로고    scopus 로고
    • GATA1 mutations in Down syndrome: implications for biology and diagnosis of children with transient myeloproliferative disorder and acute megakaryoblastic leukemia
    • Crispino JD. 2005. GATA1 mutations in Down syndrome: implications for biology and diagnosis of children with transient myeloproliferative disorder and acute megakaryoblastic leukemia. Pediatr Blood Cancer 44:40-44.
    • (2005) Pediatr Blood Cancer , vol.44 , pp. 40-44
    • Crispino, J.D.1
  • 8
    • 80052298841 scopus 로고    scopus 로고
    • The use of mouse models to understand and improve cognitive deficits in Down syndrome
    • Das I, Reeves RH. 2011. The use of mouse models to understand and improve cognitive deficits in Down syndrome. Dis Model Mech 4:596-606.
    • (2011) Dis Model Mech , vol.4 , pp. 596-606
    • Das, I.1    Reeves, R.H.2
  • 11
    • 84655161322 scopus 로고    scopus 로고
    • Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: Relevance for modeling down syndrome
    • Duchon A, Raveau M, Chevalier C, Nalesso V, Sharp AJ, Herault Y. 2011. Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: Relevance for modeling down syndrome. Mamm Genome 22:674-684.
    • (2011) Mamm Genome , vol.22 , pp. 674-684
    • Duchon, A.1    Raveau, M.2    Chevalier, C.3    Nalesso, V.4    Sharp, A.J.5    Herault, Y.6
  • 12
    • 0022271552 scopus 로고
    • Mouse trisomy 16: An animal model of human trisomy 21 (Down syndrome)
    • Epstein CJ, Cox DR, Epstein LB. 1985. Mouse trisomy 16: An animal model of human trisomy 21 (Down syndrome). Ann N Y Acad Sci 450:157-168.
    • (1985) Ann N Y Acad Sci , vol.450 , pp. 157-168
    • Epstein, C.J.1    Cox, D.R.2    Epstein, L.B.3
  • 13
    • 0016499748 scopus 로고
    • A quantative study of the face in Down's syndrome
    • Fink GB, Madaus WK, Walker GF. 1975. A quantative study of the face in Down's syndrome. Am J Orthod 67:540-553.
    • (1975) Am J Orthod , vol.67 , pp. 540-553
    • Fink, G.B.1    Madaus, W.K.2    Walker, G.F.3
  • 14
    • 0015095827 scopus 로고
    • Craniofacial complex in the trisomy 21 syndrome (Down's syndrome)
    • Frostad WA, Cleall JF, Melosky LC. 1971. Craniofacial complex in the trisomy 21 syndrome (Down's syndrome). Archs Oral Biol 16:707-722.
    • (1971) Archs Oral Biol , vol.16 , pp. 707-722
    • Frostad, W.A.1    Cleall, J.F.2    Melosky, L.C.3
  • 15
    • 75149166144 scopus 로고    scopus 로고
    • Molecular basis of pharmacotherapies for cognition in Down syndrome
    • Gardiner KJ. 2010. Molecular basis of pharmacotherapies for cognition in Down syndrome. Trends Pharmacol Sci 31:66-73.
    • (2010) Trends Pharmacol Sci , vol.31 , pp. 66-73
    • Gardiner, K.J.1
  • 16
    • 0242348738 scopus 로고    scopus 로고
    • Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions
    • Gardiner K, Fortna A, Bechtel L, Davisson MT. 2003. Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions. Gene 318:137-147.
    • (2003) Gene , vol.318 , pp. 137-147
    • Gardiner, K.1    Fortna, A.2    Bechtel, L.3    Davisson, M.T.4
  • 19
    • 34147113358 scopus 로고    scopus 로고
    • Effects of aneuploidy on skull growth in a mouse model of Down syndrome
    • Hill CA, Reeves RH, Richtsmeier JT. 2007. Effects of aneuploidy on skull growth in a mouse model of Down syndrome. J Anat 210:394-405.
    • (2007) J Anat , vol.210 , pp. 394-405
    • Hill, C.A.1    Reeves, R.H.2    Richtsmeier, J.T.3
  • 21
    • 0026050115 scopus 로고
    • Euclidean distance matrix analysis: a coordinate-free approach for comparing biological shapes using landmark data
    • Lele S, Richtsmeier JT. 1991. Euclidean distance matrix analysis: a coordinate-free approach for comparing biological shapes using landmark data. Am J Phys Anthropol 86:415-427.
    • (1991) Am J Phys Anthropol , vol.86 , pp. 415-427
    • Lele, S.1    Richtsmeier, J.T.2
  • 23
    • 34447331007 scopus 로고    scopus 로고
    • Duplication of the entire 22.9Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities
    • Li Z, Yu T, Morishima M, Pao A, LaDuca J, Conroy J, Nowak N, Matsui S, Shiraishi I, Yu YE. 2007. Duplication of the entire 22.9Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities. Hum Mol Genet 16:1359-1366.
    • (2007) Hum Mol Genet , vol.16 , pp. 1359-1366
    • Li, Z.1    Yu, T.2    Morishima, M.3    Pao, A.4    LaDuca, J.5    Conroy, J.6    Nowak, N.7    Matsui, S.8    Shiraishi, I.9    Yu, Y.E.10
  • 26
    • 3042612213 scopus 로고    scopus 로고
    • Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes
    • Olson LE, Roper RJ, Baxter LL, Carlson EJ, Epstein CJ, Reeves RH. 2004. Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes. Dev Dyn 230:581-589.
    • (2004) Dev Dyn , vol.230 , pp. 581-589
    • Olson, L.E.1    Roper, R.J.2    Baxter, L.L.3    Carlson, E.J.4    Epstein, C.J.5    Reeves, R.H.6
  • 27
    • 0018019004 scopus 로고
    • Dimensional and proportional characteristics of the face in Down's syndrome
    • O'Riordan MW, Walker GF. 1979. Dimensional and proportional characteristics of the face in Down's syndrome. J Dent Handicap 4:6-9.
    • (1979) J Dent Handicap , vol.4 , pp. 6-9
    • O'Riordan, M.W.1    Walker, G.F.2
  • 29
    • 0038687498 scopus 로고    scopus 로고
    • The neuropsychology of Down syndrome: Evidence for hippocampal dysfunction
    • Pennington BF, Moon J, Edgin J, Stedron J, Nadel L. 2003. The neuropsychology of Down syndrome: Evidence for hippocampal dysfunction. Child Dev 74:75-93.
    • (2003) Child Dev , vol.74 , pp. 75-93
    • Pennington, B.F.1    Moon, J.2    Edgin, J.3    Stedron, J.4    Nadel, L.5
  • 33
    • 0033980511 scopus 로고    scopus 로고
    • Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice
    • Richtsmeier JT, Baxter LL, Reeves RH. 2000. Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice. Dev Dyn 217:137-145.
    • (2000) Dev Dyn , vol.217 , pp. 137-145
    • Richtsmeier, J.T.1    Baxter, L.L.2    Reeves, R.H.3
  • 36
    • 84862333723 scopus 로고    scopus 로고
    • Mouse models of Down syndrome as a tool to unravel the causes of mental disabilities
    • Epub PMID: 22685678.
    • Rueda N, Florez J, Martinez-Cue C. 2012. Mouse models of Down syndrome as a tool to unravel the causes of mental disabilities. Neural Plast Epub PMID: 22685678.
    • (2012) Neural Plast
    • Rueda, N.1    Florez, J.2    Martinez-Cue, C.3
  • 38
    • 0025071591 scopus 로고
    • Brain growth in Down syndrome subjects 15 to 22 weeks of gestational age and birth to 60 months
    • Schmidt-Sidor B, Wisniewski KE, Shepard TH, Sersen EA. 1990. Brain growth in Down syndrome subjects 15 to 22 weeks of gestational age and birth to 60 months. Clin Neuropathol 9:181-190.
    • (1990) Clin Neuropathol , vol.9 , pp. 181-190
    • Schmidt-Sidor, B.1    Wisniewski, K.E.2    Shepard, T.H.3    Sersen, E.A.4
  • 39
    • 0016741618 scopus 로고
    • Amplified developmental instability in Down's syndrome
    • Shapiro B. 1975. Amplified developmental instability in Down's syndrome. Ann Hum Genet, London 38:429-437.
    • (1975) Ann Hum Genet, London , vol.38 , pp. 429-437
    • Shapiro, B.1
  • 40
    • 0020661091 scopus 로고
    • Down syndrome-A disruption of homeostasis
    • Shapiro B. 1983. Down syndrome-A disruption of homeostasis. Am J Med Genet 14:241-269.
    • (1983) Am J Med Genet , vol.14 , pp. 241-269
    • Shapiro, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.