-
1
-
-
34548264230
-
Classification of human chromosome 21 gene-expression variations in Down syndrome: Impact on disease phenotypes
-
Ait Yahya-Graison E, Aubert J, Dauphinot L, Rivals I, Prieur M, Golfier G, Rossier J, Personnaz L, Creau N, Blehaut H, Robin S, Delabar JM, Potier MC. 2007. Classification of human chromosome 21 gene-expression variations in Down syndrome: Impact on disease phenotypes. Am J Hum Genet 81:475-491.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 475-491
-
-
Ait Yahya-Graison, E.1
Aubert, J.2
Dauphinot, L.3
Rivals, I.4
Prieur, M.5
Golfier, G.6
Rossier, J.7
Personnaz, L.8
Creau, N.9
Blehaut, H.10
Robin, S.11
Delabar, J.M.12
Potier, M.C.13
-
2
-
-
2442514340
-
Interactions between Sox9 and beta-catenin control chondrocyte differentiation
-
Akiyama H, Lyons JP, Mori-Akiyama Y, Yang X, Zhang R, Zhang Z, Deng JM, Taketo MM, Nakamura T, Behringer RR, McCrea PD, de Crombrugghe B. 2004. Interactions between Sox9 and beta-catenin control chondrocyte differentiation. Genes Dev 18:1072-1087.
-
(2004)
Genes Dev
, vol.18
, pp. 1072-1087
-
-
Akiyama, H.1
Lyons, J.P.2
Mori-Akiyama, Y.3
Yang, X.4
Zhang, R.5
Zhang, Z.6
Deng, J.M.7
Taketo, M.M.8
Nakamura, T.9
Behringer, R.R.10
McCrea, P.D.11
de Crombrugghe, B.12
-
4
-
-
33646171446
-
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21
-
Arron JR, Winslow MM, Polleri A, Chang CP, Wu H, Gao X, Neilson JR, Chen L, Heit JJ, Kim SK, Yamasaki N, Miyakawa T, Francke U, Graef IA, Crabtree GR. 2006. NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21. Nature 441:595-600.
-
(2006)
Nature
, vol.441
, pp. 595-600
-
-
Arron, J.R.1
Winslow, M.M.2
Polleri, A.3
Chang, C.P.4
Wu, H.5
Gao, X.6
Neilson, J.R.7
Chen, L.8
Heit, J.J.9
Kim, S.K.10
Yamasaki, N.11
Miyakawa, T.12
Francke, U.13
Graef, I.A.14
Crabtree, G.R.15
-
5
-
-
0030481054
-
Targeted disruption of the Hoxb-2 locus in mice interferes with expression of Hoxb-1 and Hoxb-4
-
Barrow JR, Capecchi MR. 1996. Targeted disruption of the Hoxb-2 locus in mice interferes with expression of Hoxb-1 and Hoxb-4. Development 122:3817-3828.
-
(1996)
Development
, vol.122
, pp. 3817-3828
-
-
Barrow, J.R.1
Capecchi, M.R.2
-
6
-
-
0033978891
-
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
-
7
-
-
9644278035
-
Synaptic structural abnormalities in the Ts65Dn mouse model of Down syndrome
-
Belichenko PV, Masliah E, Kleschevnikov AM, Villar AJ, Epstein CJ, Salehi A, Mobley WC. 2004. Synaptic structural abnormalities in the Ts65Dn mouse model of Down syndrome. J Comp Neurol 480:281-298.
-
(2004)
J Comp Neurol
, vol.480
, pp. 281-298
-
-
Belichenko, P.V.1
Masliah, E.2
Kleschevnikov, A.M.3
Villar, A.J.4
Epstein, C.J.5
Salehi, A.6
Mobley, W.C.7
-
8
-
-
0001677717
-
Controlling for false discovery rate: A practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y. 1995. Controlling for false discovery rate: A practical and powerful approach to multiple testing. J R Stat Soc Ser B 57:289-300.
-
(1995)
J R Stat Soc Ser B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
9
-
-
77952719225
-
Embryonic and not maternal trisomy causes developmental attenuation in the Ts65Dn mouse model for Down syndrome
-
Blazek JD, Billingsley CN, Newbauer A, Roper RJ. 2010. Embryonic and not maternal trisomy causes developmental attenuation in the Ts65Dn mouse model for Down syndrome. Dev Dyn 239:1645-1653.
-
(2010)
Dev Dyn
, vol.239
, pp. 1645-1653
-
-
Blazek, J.D.1
Billingsley, C.N.2
Newbauer, A.3
Roper, R.J.4
-
10
-
-
35548970343
-
Defects in embryonic neurogenesis and initial synapse formation in the forebrain of the Ts65Dn mouse model of Down syndrome
-
Chakrabarti L, Galdzicki Z, Haydar TF. 2007. Defects in embryonic neurogenesis and initial synapse formation in the forebrain of the Ts65Dn mouse model of Down syndrome. J Neurosci 27:11483-11495.
-
(2007)
J Neurosci
, vol.27
, pp. 11483-11495
-
-
Chakrabarti, L.1
Galdzicki, Z.2
Haydar, T.F.3
-
11
-
-
34548565802
-
HOXA5 acts directly downstream of retinoic acid receptor beta and contributes to retinoic acid-induced apoptosis and growth inhibition
-
Chen H, Zhang H, Lee J, Liang X, Wu X, Zhu T, Lo PK, Zhang X, Sukumar S. 2007. HOXA5 acts directly downstream of retinoic acid receptor beta and contributes to retinoic acid-induced apoptosis and growth inhibition. Cancer Res 67:8007-8013.
-
(2007)
Cancer Res
, vol.67
, pp. 8007-8013
-
-
Chen, H.1
Zhang, H.2
Lee, J.3
Liang, X.4
Wu, X.5
Zhu, T.6
Lo, P.K.7
Zhang, X.8
Sukumar, S.9
-
12
-
-
77949518398
-
PathGen: A transitive gene pathway generator
-
Clement K, Gustafson N, Berbert A, Carroll H, Merris C, Olsen A, Clement M, Snell Q, Allen J, Roper RJ. 2010. PathGen: A transitive gene pathway generator. Bioinformatics 26:423-425.
-
(2010)
Bioinformatics
, vol.26
, pp. 423-425
-
-
Clement, K.1
Gustafson, N.2
Berbert, A.3
Carroll, H.4
Merris, C.5
Olsen, A.6
Clement, M.7
Snell, Q.8
Allen, J.9
Roper, R.J.10
-
13
-
-
13544259937
-
The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome
-
Dauphinot L, Lyle R, Rivals I, Dang MT, Moldrich RX, Golfier G, Ettwiller L, Toyama K, Rossier J, Personnaz L, Antonarakis SE, Epstein CJ, Sinet PM, Potier MC. 2005. The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome. Hum Mol Genet 14:373-384.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 373-384
-
-
Dauphinot, L.1
Lyle, R.2
Rivals, I.3
Dang, M.T.4
Moldrich, R.X.5
Golfier, G.6
Ettwiller, L.7
Toyama, K.8
Rossier, J.9
Personnaz, L.10
Antonarakis, S.E.11
Epstein, C.J.12
Sinet, P.M.13
Potier, M.C.14
-
14
-
-
31644437052
-
The homeoprotein engrailed 1 has pleiotropic functions in calvarial intramembranous bone formation and remodeling
-
Deckelbaum RA, Majithia A, Booker T, Henderson JE, Loomis CA. 2006. The homeoprotein engrailed 1 has pleiotropic functions in calvarial intramembranous bone formation and remodeling. Development 133:63-74.
-
(2006)
Development
, vol.133
, pp. 63-74
-
-
Deckelbaum, R.A.1
Majithia, A.2
Booker, T.3
Henderson, J.E.4
Loomis, C.A.5
-
15
-
-
0036166918
-
Cellular and cis-regulation of En-2 expression in the mandibular arch
-
Degenhardt K, Rentschler S, Fishman G, Sassoon DA. 2002. Cellular and cis-regulation of En-2 expression in the mandibular arch. Mech Dev 111:125-136.
-
(2002)
Mech Dev
, vol.111
, pp. 125-136
-
-
Degenhardt, K.1
Rentschler, S.2
Fishman, G.3
Sassoon, D.A.4
-
16
-
-
83455197218
-
Trisomic and allelic differences influence phenotypic variability during development of Down syndrome mice
-
Deitz SL, Roper RJ. 2011. Trisomic and allelic differences influence phenotypic variability during development of Down syndrome mice. Genetics 189:1487-1495.
-
(2011)
Genetics
, vol.189
, pp. 1487-1495
-
-
Deitz, S.L.1
Roper, R.J.2
-
17
-
-
0038005018
-
DAVID: Database for Annotation, Visualization, and Integrated Discovery
-
Dennis G Jr, Sherman BT, Hosack DA, Yang J, Gao W, Lane HC, Lempicki RA. 2003. DAVID: Database for Annotation, Visualization, and Integrated Discovery. Genome Biol 4:P3.
-
(2003)
Genome Biol
, vol.4
-
-
Dennis Jr, G.1
Sherman, B.T.2
Hosack, D.A.3
Yang, J.4
Gao, W.5
Lane, H.C.6
Lempicki, R.A.7
-
18
-
-
0000089059
-
Down syndrome (trisomy 21)
-
Scriver CR, Beaudet AL, Sly WS, Valle D, editors. New York: McGraw-Hill.
-
Epstein CJ. 2001. Down syndrome (trisomy 21). In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill. pp 1223-1256.
-
(2001)
The metabolic and molecular bases of inherited disease
, pp. 1223-1256
-
-
Epstein, C.J.1
-
19
-
-
54049141273
-
Masticatory dysfunction in persons with Down's syndrome. Part 1: Aetiology and incidence
-
Faulks D, Collado V, Mazille MN, Veyrune JL, Hennequin M. 2008. Masticatory dysfunction in persons with Down's syndrome. Part 1: Aetiology and incidence. J Oral Rehabil 35:854-862.
-
(2008)
J Oral Rehabil
, vol.35
, pp. 854-862
-
-
Faulks, D.1
Collado, V.2
Mazille, M.N.3
Veyrune, J.L.4
Hennequin, M.5
-
20
-
-
33644820338
-
Biometry of face and brain in fetuses with trisomy 21
-
Guihard-Costa AM, Khung S, Delbecque K, Menez F, Delezoide AL. 2006. Biometry of face and brain in fetuses with trisomy 21. Pediatr Res 59:33-38.
-
(2006)
Pediatr Res
, vol.59
, pp. 33-38
-
-
Guihard-Costa, A.M.1
Khung, S.2
Delbecque, K.3
Menez, F.4
Delezoide, A.L.5
-
21
-
-
51649097590
-
Relative rather than absolute macroglossia in patients with Down syndrome: Implications for treatment of obstructive sleep apnea
-
Guimaraes CV, Donnelly LF, Shott SR, Amin RS, Kalra M. 2008. Relative rather than absolute macroglossia in patients with Down syndrome: Implications for treatment of obstructive sleep apnea. Pediatr Radiol 38:1062-1067.
-
(2008)
Pediatr Radiol
, vol.38
, pp. 1062-1067
-
-
Guimaraes, C.V.1
Donnelly, L.F.2
Shott, S.R.3
Amin, R.S.4
Kalra, M.5
-
22
-
-
34347263383
-
Multiplex ligation-dependent probe amplification (MLPA) genotyping assay for mouse models of Down syndrome
-
Hewitt CA, Carmichael CL, Wilkins EJ, Cannon PZ, Pritchard MA, Scott HS. 2007. Multiplex ligation-dependent probe amplification (MLPA) genotyping assay for mouse models of Down syndrome. Front Biosci 12:3010-3016.
-
(2007)
Front Biosci
, vol.12
, pp. 3010-3016
-
-
Hewitt, C.A.1
Carmichael, C.L.2
Wilkins, E.J.3
Cannon, P.Z.4
Pritchard, M.A.5
Scott, H.S.6
-
23
-
-
34147113358
-
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
-
24
-
-
0002294347
-
A simple sequentially rejective multiple test procedure
-
Holm S. 1979. A simple sequentially rejective multiple test procedure. Scand J Stat 6:65-70.
-
(1979)
Scand J Stat
, vol.6
, pp. 65-70
-
-
Holm, S.1
-
25
-
-
61449172037
-
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
-
Huang da W, Sherman BT, Lempicki RA. 2009. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc 4:44-57.
-
(2009)
Nat Protoc
, vol.4
, pp. 44-57
-
-
Huang da, W.1
Sherman, B.T.2
Lempicki, R.A.3
-
26
-
-
0027070676
-
Dominant mutation of the murine Hox-2.2 gene results in developmental abnormalities
-
Kaur S, Singh G, Stock JL, Schreiner CM, Kier AB, Yager KL, Mucenski ML, Scott WJ Jr, Potter SS. 1992. Dominant mutation of the murine Hox-2.2 gene results in developmental abnormalities. J Exp Zool 264:323-336.
-
(1992)
J Exp Zool
, vol.264
, pp. 323-336
-
-
Kaur, S.1
Singh, G.2
Stock, J.L.3
Schreiner, C.M.4
Kier, A.B.5
Yager, K.L.6
Mucenski, M.L.7
Scott Jr, W.J.8
Potter, S.S.9
-
27
-
-
0030774258
-
Cis-acting elements conserved between mouse and pufferfish Otx2 genes govern the expression in mesencephalic neural crest cells
-
Kimura C, Takeda N, Suzuki M, Oshimura M, Aizawa S, Matsuo I. 1997. Cis-acting elements conserved between mouse and pufferfish Otx2 genes govern the expression in mesencephalic neural crest cells. Development 124:3929-3941.
-
(1997)
Development
, vol.124
, pp. 3929-3941
-
-
Kimura, C.1
Takeda, N.2
Suzuki, M.3
Oshimura, M.4
Aizawa, S.5
Matsuo, I.6
-
28
-
-
21844447818
-
Quantitative immunohistochemistry of fluorescence labelled probes using low-cost software
-
Kirkeby S, Thomsen CE. 2005. Quantitative immunohistochemistry of fluorescence labelled probes using low-cost software. J Immunol Methods 301:102-113.
-
(2005)
J Immunol Methods
, vol.301
, pp. 102-113
-
-
Kirkeby, S.1
Thomsen, C.E.2
-
29
-
-
84934437775
-
Cranial neural crest and development of the head skeleton
-
Knight RD, Schilling TF. 2006. Cranial neural crest and development of the head skeleton. Adv Exp Med Biol 589:120-133.
-
(2006)
Adv Exp Med Biol
, vol.589
, pp. 120-133
-
-
Knight, R.D.1
Schilling, T.F.2
-
30
-
-
65549148290
-
Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development
-
Laffaire J, Rivals I, Dauphinot L, Pasteau F, Wehrle R, Larrat B, Vitalis T, Moldrich RX, Rossier J, Sinkus R, Herault Y, Dusart I, Potier MC. 2009. Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development. BMC Genomics 10:138.
-
(2009)
BMC Genomics
, vol.10
, pp. 138
-
-
Laffaire, J.1
Rivals, I.2
Dauphinot, L.3
Pasteau, F.4
Wehrle, R.5
Larrat, B.6
Vitalis, T.7
Moldrich, R.X.8
Rossier, J.9
Sinkus, R.10
Herault, Y.11
Dusart, I.12
Potier, M.C.13
-
32
-
-
80054764764
-
Genetic analysis of Down syndrome-associated heart defects in mice
-
Liu C, Morishima M, Yu T, Matsui S, Zhang L, Fu D, Pao A, Costa AC, Gardiner KJ, Cowell JK, Nowak NJ, Parmacek MS, Liang P, Baldini A, Yu YE. 2011. Genetic analysis of Down syndrome-associated heart defects in mice. Hum Genet 130:623-632.
-
(2011)
Hum Genet
, vol.130
, pp. 623-632
-
-
Liu, C.1
Morishima, M.2
Yu, T.3
Matsui, S.4
Zhang, L.5
Fu, D.6
Pao, A.7
Costa, A.C.8
Gardiner, K.J.9
Cowell, J.K.10
Nowak, N.J.11
Parmacek, M.S.12
Liang, P.13
Baldini, A.14
Yu, Y.E.15
-
33
-
-
0034000849
-
Quantitative immunohistochemistry by measuring cumulative signal strength using commercially available software photoshop and matlab
-
Matkowskyj KA, Schonfeld D, Benya RV. 2000. Quantitative immunohistochemistry by measuring cumulative signal strength using commercially available software photoshop and matlab. J Histochem Cytochem 48:303-312.
-
(2000)
J Histochem Cytochem
, vol.48
, pp. 303-312
-
-
Matkowskyj, K.A.1
Schonfeld, D.2
Benya, R.V.3
-
34
-
-
0028895055
-
Mouse Otx2 functions in the formation and patterning of rostral head
-
Matsuo I, Kuratani S, Kimura C, Takeda N, Aizawa S. 1995. Mouse Otx2 functions in the formation and patterning of rostral head. Genes Dev 9:2646-2658.
-
(1995)
Genes Dev
, vol.9
, pp. 2646-2658
-
-
Matsuo, I.1
Kuratani, S.2
Kimura, C.3
Takeda, N.4
Aizawa, S.5
-
35
-
-
0041923688
-
Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest
-
Mori-Akiyama Y, Akiyama H, Rowitch DH, de Crombrugghe B. 2003. Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest. Proc Natl Acad Sci USA 100:9360-9365.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 9360-9365
-
-
Mori-Akiyama, Y.1
Akiyama, H.2
Rowitch, D.H.3
de Crombrugghe, B.4
-
37
-
-
78650206677
-
Updated National Birth Prevalence estimates for selected birth defects in the United States, 2004-2006
-
Parker SE, Mai CT, Canfield MA, Rickard R, Wang Y, Meyer RE, Anderson P, Mason CA, Collins JS, Kirby RS, Correa A. 2010. Updated National Birth Prevalence estimates for selected birth defects in the United States, 2004-2006. Birth Defects Res A Clin Mol Teratol 88:1008-1016.
-
(2010)
Birth Defects Res A Clin Mol Teratol
, vol.88
, pp. 1008-1016
-
-
Parker, S.E.1
Mai, C.T.2
Canfield, M.A.3
Rickard, R.4
Wang, Y.5
Meyer, R.E.6
Anderson, P.7
Mason, C.A.8
Collins, J.S.9
Kirby, R.S.10
Correa, A.11
-
38
-
-
0041565066
-
The growth and morphogenesis of the early mouse mandible: A quantitative analysis
-
Ramaesh T, Bard JB. 2003. The growth and morphogenesis of the early mouse mandible: A quantitative analysis. J Anat 203:213-222.
-
(2003)
J Anat
, vol.203
, pp. 213-222
-
-
Ramaesh, T.1
Bard, J.B.2
-
39
-
-
0029114706
-
A mouse model for Down syndrome exhibits learning and behaviour deficits
-
Reeves RH, Irving NG, Moran TH, Wohn A, Kitt C, Sisodia SS, Schmidt C, Bronson RT, Davisson MT. 1995. A mouse model for Down syndrome exhibits learning and behaviour deficits. Nat Genet 11:177-184.
-
(1995)
Nat Genet
, vol.11
, pp. 177-184
-
-
Reeves, R.H.1
Irving, N.G.2
Moran, T.H.3
Wohn, A.4
Kitt, C.5
Sisodia, S.S.6
Schmidt, C.7
Bronson, R.T.8
Davisson, M.T.9
-
40
-
-
0033980511
-
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
-
41
-
-
31944432753
-
Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice
-
Roper RJ, Baxter LL, Saran NG, Klinedinst DK, Beachy PA, Reeves RH. 2006a. Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice. Proc Natl Acad Sci USA 103:1452-1456.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 1452-1456
-
-
Roper, R.J.1
Baxter, L.L.2
Saran, N.G.3
Klinedinst, D.K.4
Beachy, P.A.5
Reeves, R.H.6
-
42
-
-
33644781665
-
Perinatal loss of Ts65Dn Down syndrome mice
-
Roper RJ, St John HK, Philip J, Lawler A, Reeves RH. 2006b. Perinatal loss of Ts65Dn Down syndrome mice. Genetics 172:437-443.
-
(2006)
Genetics
, vol.172
, pp. 437-443
-
-
Roper, R.J.1
St John, H.K.2
Philip, J.3
Lawler, A.4
Reeves, R.H.5
-
43
-
-
59849119800
-
A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehog
-
Roper RJ, VanHorn JF, Cain CC, Reeves RH. 2009. A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehog. Mech Dev 126:212-219.
-
(2009)
Mech Dev
, vol.126
, pp. 212-219
-
-
Roper, R.J.1
VanHorn, J.F.2
Cain, C.C.3
Reeves, R.H.4
-
44
-
-
34548084502
-
Genome-wide expression analysis of cultured trophoblast with trisomy 21 karyotype
-
Rozovski U, Jonish-Grossman A, Bar-Shira A, Ochshorn Y, Goldstein M, Yaron Y. 2007. Genome-wide expression analysis of cultured trophoblast with trisomy 21 karyotype. Hum Reprod 22:2538-2545.
-
(2007)
Hum Reprod
, vol.22
, pp. 2538-2545
-
-
Rozovski, U.1
Jonish-Grossman, A.2
Bar-Shira, A.3
Ochshorn, Y.4
Goldstein, M.5
Yaron, Y.6
-
45
-
-
0142215398
-
Cranial neural crest and the building of the vertebrate head
-
Santagati F, Rijli FM. 2003. Cranial neural crest and the building of the vertebrate head. Nat Rev Neurosci 4:806-818.
-
(2003)
Nat Rev Neurosci
, vol.4
, pp. 806-818
-
-
Santagati, F.1
Rijli, F.M.2
-
46
-
-
28844479695
-
Temporal requirement of Hoxa2 in cranial neural crest skeletal morphogenesis
-
Santagati F, Minoux M, Ren SY, Rijli FM. 2005. Temporal requirement of Hoxa2 in cranial neural crest skeletal morphogenesis. Development 132:4927-4936.
-
(2005)
Development
, vol.132
, pp. 4927-4936
-
-
Santagati, F.1
Minoux, M.2
Ren, S.Y.3
Rijli, F.M.4
-
47
-
-
0042420452
-
Global disruption of the cerebellar transcriptome in a Down syndrome mouse model
-
Saran NG, Pletcher MT, Natale JE, Cheng Y, Reeves RH. 2003. Global disruption of the cerebellar transcriptome in a Down syndrome mouse model. Hum Mol Genet 12:2013-2019.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2013-2019
-
-
Saran, N.G.1
Pletcher, M.T.2
Natale, J.E.3
Cheng, Y.4
Reeves, R.H.5
-
48
-
-
33748073121
-
Down syndrome: Common otolaryngologic manifestations
-
Shott SR. 2006. Down syndrome: Common otolaryngologic manifestations. Am J Med Genet Part C Semin Med Genet 142C:131-140.
-
(2006)
Am J Med Genet Part C Semin Med Genet
, vol.142 C
, pp. 131-140
-
-
Shott, S.R.1
-
50
-
-
80051549592
-
Transcript catalogs of human chromosome 21 and orthologous chimpanzee and mouse regions
-
Sturgeon X, Gardiner KJ. 2011. Transcript catalogs of human chromosome 21 and orthologous chimpanzee and mouse regions. Mamm Genome 22:261-271.
-
(2011)
Mamm Genome
, vol.22
, pp. 261-271
-
-
Sturgeon, X.1
Gardiner, K.J.2
-
51
-
-
39749134383
-
Characterization of the cardiac phenotype in neonatal Ts65Dn mice
-
Williams AD, Mjaatvedt CH, Moore CS. 2008. Characterization of the cardiac phenotype in neonatal Ts65Dn mice. Dev Dyn 237:426-435.
-
(2008)
Dev Dyn
, vol.237
, pp. 426-435
-
-
Williams, A.D.1
Mjaatvedt, C.H.2
Moore, C.S.3
-
53
-
-
24944575365
-
HoxB2 binds mutant SOD1 and is altered in transgenic model of ALS
-
Zhai J, Lin H, Canete-Soler R, Schlaepfer WW. 2005. HoxB2 binds mutant SOD1 and is altered in transgenic model of ALS. Hum Mol Genet 14:2629-2640.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 2629-2640
-
-
Zhai, J.1
Lin, H.2
Canete-Soler, R.3
Schlaepfer, W.W.4
-
54
-
-
77949568224
-
Dynamic expression and heterogeneous intracellular location of En-1 during late mouse embryonic development
-
Zhong SC, Chen XS, Cai QY, Luo X, Chen XH, Liu J, Yao ZX. 2010. Dynamic expression and heterogeneous intracellular location of En-1 during late mouse embryonic development. Cells Tissues Organs 191:289-300.
-
(2010)
Cells Tissues Organs
, vol.191
, pp. 289-300
-
-
Zhong, S.C.1
Chen, X.S.2
Cai, Q.Y.3
Luo, X.4
Chen, X.H.5
Liu, J.6
Yao, Z.X.7
|