-
1
-
-
0023507387
-
Genesis and systematization of cardiovaskular anomalies and analysis of skeletal malformations in murine trisomy 16 and 19
-
Bacchus C, Sterz H, Buselmaier W (1987) Genesis and systematization of cardiovaskular anomalies and analysis of skeletal malformations in murine trisomy 16 and 19. Human Genet 77:12-22
-
(1987)
Human Genet
, vol.77
, pp. 12-22
-
-
Bacchus, C.1
Sterz, H.2
Buselmaier, W.3
-
2
-
-
0024406898
-
Delayed thymocyte maturation in the trisomy 16 mouses
-
Berger CN, Epstein CJ (1989) Delayed thymocyte maturation in the trisomy 16 mouses. J Immunol 143:389-396
-
(1989)
J Immunol
, vol.143
, pp. 389-396
-
-
Berger, C.N.1
Epstein, C.J.2
-
3
-
-
0026307123
-
Genesis and systematization of cardiovascular anomalies in murine trisomy 16
-
Buselmaier W, Bacchus C, Sterz H (1991) Genesis and systematization of cardiovascular anomalies in murine trisomy 16. Prog Clin Biol Res 373:203-214
-
(1991)
Prog Clin Biol Res
, vol.373
, pp. 203-214
-
-
Buselmaier, W.1
Bacchus, C.2
Sterz, H.3
-
4
-
-
0025941664
-
Abnormal production of interleukin-1 by microglia from trisomy 16 mice
-
Colton CA, Yao J, Jaffs RE (1991) Abnormal production of interleukin-1 by microglia from trisomy 16 mice. Neurosci Lett 132:270-274
-
(1991)
Neurosci Lett
, vol.132
, pp. 270-274
-
-
Colton, C.A.1
Yao, J.2
Jaffs, R.E.3
-
5
-
-
13144297482
-
Chromosomal assignment of mouse PRGS: Further evidence for homology between mouse chromosome 16 and human chromosome 21
-
Cox D, Goldblatt D, Epstein CJ (1981) Chromosomal assignment of mouse PRGS: Further evidence for homology between mouse chromosome 16 and human chromosome 21. Am J Hum Genet 33:145
-
(1981)
Am J Hum Genet
, vol.33
, pp. 145
-
-
Cox, D.1
Goldblatt, D.2
Epstein, C.J.3
-
6
-
-
0019734360
-
Functional implications of gene dosage effects in trisomy 21
-
Epstein CJ, Epstein LB, Cox D (1998) Functional implications of gene dosage effects in trisomy 21. Hum Genet 2:155-172
-
(1998)
Hum Genet
, vol.2
, pp. 155-172
-
-
Epstein, C.J.1
Epstein, L.B.2
Cox, D.3
-
7
-
-
0026444321
-
Defects in thymocyte differentiation and thymocyte-stromal interactions in the trisomy 16 mouse
-
Ewart JL, Auerbach R (1992) Defects in thymocyte differentiation and thymocyte-stromal interactions in the trisomy 16 mouse. Dev Immunol 2:215-226
-
(1992)
Dev Immunol
, vol.2
, pp. 215-226
-
-
Ewart, J.L.1
Auerbach, R.2
-
8
-
-
0023177414
-
Influence of mouse trisomy 16 on expression of specific genes
-
Fundele R, Winking H, Jägerbauer EM (1987) Influence of mouse trisomy 16 on expression of specific genes. Dev Genetics 8:35-43
-
(1987)
Dev Genetics
, vol.8
, pp. 35-43
-
-
Fundele, R.1
Winking, H.2
Jägerbauer, E.M.3
-
9
-
-
0022871707
-
Autosomal aneuploidy in mice: Generation and developmental consequences
-
Gearhart JD, Davisson MT, Oster-Granite ML (1986) Autosomal aneuploidy in mice: generation and developmental consequences. Brain Res Bull 16:789-801
-
(1986)
Brain Res Bull
, vol.16
, pp. 789-801
-
-
Gearhart, J.D.1
Davisson, M.T.2
Oster-Granite, M.L.3
-
10
-
-
0026294547
-
Morphogenesis of the brain and craniofacial complex in trisomy 16 mice
-
Grausz H, Richtsmeier JT, Oster-Granite ML (1991) Morphogenesis of the brain and craniofacial complex in trisomy 16 mice. Prog Clin Biol Res 373:169-188
-
(1991)
Prog Clin Biol Res
, vol.373
, pp. 169-188
-
-
Grausz, H.1
Richtsmeier, J.T.2
Oster-Granite, M.L.3
-
11
-
-
0030051077
-
Morphogenetic alterations during endocardial cushon development in the trisomy 16 (Down syndrome) mouse
-
Hiltgen GG, Markwald RR, Litke LL (1996) Morphogenetic alterations during endocardial cushon development in the trisomy 16 (Down syndrome) mouse. Pediatr Cardiol 17:21-30
-
(1996)
Pediatr Cardiol
, vol.17
, pp. 21-30
-
-
Hiltgen, G.G.1
Markwald, R.R.2
Litke, L.L.3
-
13
-
-
0027978518
-
Long-term intracerebral transplants of fetal hippocampus from mouse trisomy 16, a model for Downs syndrome (Trisomy 21), do not exhibit Alzheimer disease neuropathology by ultrastructural criteria
-
Lane NL, Balbo A, Stoll J (1994) Long-term intracerebral transplants of fetal hippocampus from mouse trisomy 16, a model for Downs syndrome (Trisomy 21), do not exhibit Alzheimer disease neuropathology by ultrastructural criteria. Tissue Cell 26:477-488
-
(1994)
Tissue Cell
, vol.26
, pp. 477-488
-
-
Lane, N.L.1
Balbo, A.2
Stoll, J.3
-
14
-
-
0033391115
-
Congenital colonic hypoganglionosis in murine trisomy 16 - An animal model for Down's syndrome
-
Leffler A, Wedel T, Busch LC (1999) Congenital colonic hypoganglionosis in murine trisomy 16 - An animal model for Down's syndrome. Eur J Pediatr Surg 9:381-388
-
(1999)
Eur J Pediatr Surg
, vol.9
, pp. 381-388
-
-
Leffler, A.1
Wedel, T.2
Busch, L.C.3
-
15
-
-
0025007562
-
Examination of the eyelid closure defect in trisomy 16 mice
-
Lipski DA, Bersu ET (1990) Examination of the eyelid closure defect in trisomy 16 mice. Teratology 42:301-308
-
(1990)
Teratology
, vol.42
, pp. 301-308
-
-
Lipski, D.A.1
Bersu, E.T.2
-
16
-
-
0019974174
-
Trisomy 16 in the mouse fetuses associated with generalized edema and cardiovasculae and urinary tract anomalies
-
Miyabara S, Gropp A, Winking H (1982) Trisomy 16 in the mouse fetuses associated with generalized edema and cardiovasculae and urinary tract anomalies. Teratology 25:369-380
-
(1982)
Teratology
, vol.25
, pp. 369-380
-
-
Miyabara, S.1
Gropp, A.2
Winking, H.3
-
17
-
-
0021736639
-
Comparative study of phenotypic expression of mico trisomy 16 by different female strains: Attempt at an animal model for human trisomy 21
-
Miyabara S, Sugihara H, Yonemitsu N (1984) Comparative study of phenotypic expression of mico trisomy 16 by different female strains: attempt at an animal model for human trisomy 21. Congenital Anom 24:283-292
-
(1984)
Congenital Anom
, vol.24
, pp. 283-292
-
-
Miyabara, S.1
Sugihara, H.2
Yonemitsu, N.3
-
18
-
-
0343329753
-
Impaired Ca-signaling in astrocyts from the Ts 16 mouse model of Down syndrome
-
Müller W, Heinemann U, Schuchmann S (1997) Impaired Ca-signaling in astrocyts from the Ts 16 mouse model of Down syndrome. Neurosci Lett 223:81-84
-
(1997)
Neurosci Lett
, vol.223
, pp. 81-84
-
-
Müller, W.1
Heinemann, U.2
Schuchmann, S.3
-
19
-
-
0003584053
-
-
Springer, Berlin Heidelberg New York Tokyo
-
Naumann GOH (1997) Pathologie des Auges. Springer, Berlin Heidelberg New York Tokyo, S 133-134
-
(1997)
Pathologie des Auges
, pp. 133-134
-
-
Naumann, G.O.H.1
-
20
-
-
0030830259
-
Cerebral cortical astroglia from the trisomy 16 mouse, a model for Down syndrome, produce neuronal cholinergic deficits in cell culture
-
Nelson PG, Fitzgerald S, Rapoport SI (1997) Cerebral cortical astroglia from the trisomy 16 mouse, a model for Down syndrome, produce neuronal cholinergic deficits in cell culture. Proc Natl Aca Sci USA 94:12644-12648
-
(1997)
Proc Natl Aca Sci USA
, vol.94
, pp. 12644-12648
-
-
Nelson, P.G.1
Fitzgerald, S.2
Rapoport, S.I.3
-
21
-
-
9844267757
-
Neuroanatomic, ocular and audiovestibular malformations in the trisomy 16 mouse
-
Oster-Granite ML, Baker C, Ozand PT (1983) Neuroanatomic, ocular and audiovestibular malformations in the trisomy 16 mouse. Pediatr Res 17:300
-
(1983)
Pediatr Res
, vol.17
, pp. 300
-
-
Oster-Granite, M.L.1
Baker, C.2
Ozand, P.T.3
-
23
-
-
0015149369
-
Electron microscopic study of the development of the mouse corneal epithelium
-
Pei YF, Thodin JA (1971) Electron microscopic study of the development of the mouse corneal epithelium. Invest Ophthalmol 10:811-825
-
(1971)
Invest Ophthalmol
, vol.10
, pp. 811-825
-
-
Pei, Y.F.1
Thodin, J.A.2
-
24
-
-
0023510775
-
Neurochemical characterization of embryonic brain development in trisomy 19 (Ts 19) mice: Implications of selective deficits observed for abnormal neuron development in aneuploidy
-
Saltarelli MD, Forloni GL, Oster-Granite ML (1987) Neurochemical characterization of embryonic brain development in trisomy 19 (Ts 19) mice: implications of selective deficits observed for abnormal neuron development in aneuploidy. Dev Genet 8:267-279
-
(1987)
Dev Genet
, vol.8
, pp. 267-279
-
-
Saltarelli, M.D.1
Forloni, G.L.2
Oster-Granite, M.L.3
-
25
-
-
0033952295
-
Diminished glutathione levels cause spontaneous and mitochondria-mediated cell death in neurons from trisomy 16 mice: A model of Down's syndrome
-
Schuchmann S, Heinemann U (2000) Diminished glutathione levels cause spontaneous and mitochondria-mediated cell death in neurons from trisomy 16 mice: A model of Down's syndrome. J Neurochem 74:1205-1214
-
(2000)
J Neurochem
, vol.74
, pp. 1205-1214
-
-
Schuchmann, S.1
Heinemann, U.2
-
26
-
-
0032529841
-
Alterated Ca signaling and mitochondrial deficiencies in hippocampal neurons of trisomy 16 mice: A model of Down's syndroma
-
Schuchmann S, Müller W, Heidemann U (1998) Alterated Ca signaling and mitochondrial deficiencies in hippocampal neurons of trisomy 16 mice: a model of Down's syndroma. J Neurosci 18:7216-7231
-
(1998)
J Neurosci
, vol.18
, pp. 7216-7231
-
-
Schuchmann, S.1
Müller, W.2
Heidemann, U.3
-
27
-
-
0021792234
-
The ocular features of Down's syndrome
-
Shapiro MB, France TD (1985) The ocular features of Down's syndrome. Am J Ophthalmol 99:659-663
-
(1985)
Am J Ophthalmol
, vol.99
, pp. 659-663
-
-
Shapiro, M.B.1
France, T.D.2
-
28
-
-
0028815092
-
Capillary gas chromatography combined with ion trap detection for quantitative profiling of polyols in cerebrospinal fluid and plasma
-
Shetty HU, Holloway HW, Rapoport SI (1995) Capillary gas chromatography combined with ion trap detection for quantitative profiling of polyols in cerebrospinal fluid and plasma. Anal Biochem 224:279-285
-
(1995)
Anal Biochem
, vol.224
, pp. 279-285
-
-
Shetty, H.U.1
Holloway, H.W.2
Rapoport, S.I.3
-
29
-
-
0024792006
-
Defects of skeletal morphology, density, and structure in mouse fetuses with trisomy 16
-
Sterz H, Buselmaier W, Bacchus C (1989) Defects of skeletal morphology, density, and structure in mouse fetuses with trisomy 16. Teratology 40:627-639
-
(1989)
Teratology
, vol.40
, pp. 627-639
-
-
Sterz, H.1
Buselmaier, W.2
Bacchus, C.3
-
30
-
-
0024987631
-
Zur Normogenese der Hornhaut und ihrer Beeinflussung durch Cyclophosphamid
-
Tost M, Tost F (1990) Zur Normogenese der Hornhaut und ihrer Beeinflussung durch Cyclophosphamid. Klin Monatsbl Augenheilkd 197:123-127
-
(1990)
Klin Monatsbl Augenheilkd
, vol.197
, pp. 123-127
-
-
Tost, M.1
Tost, F.2
-
31
-
-
0031006692
-
Cardiac morphology at late fetal stages in the mouse with trisomy 16: Consequences for different formation of the atrioventricular junction when compared to humans with trisomy 21
-
Webb S, Brown NA, Anderson RH (1997) Cardiac morphology at late fetal stages in the mouse with trisomy 16: consequences for different formation of the atrioventricular junction when compared to humans with trisomy 21. Cardiovasc Res 34:515-525
-
(1997)
Cardiovasc Res
, vol.34
, pp. 515-525
-
-
Webb, S.1
Brown, N.A.2
Anderson, R.H.3
|