-
1
-
-
77957553895
-
Principal component analysis
-
Computational Statistics 2
-
Abdi H., Williams L.J. Principal component analysis. WIREs 2010, Computational Statistics 2.
-
(2010)
WIREs
-
-
Abdi, H.1
Williams, L.J.2
-
2
-
-
19944433119
-
Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays
-
Arima K., Shiotsugu J., Niu R., Khandpur R., Martinez M., Shin Y., Koide T., Cho K.W., Kitayama A., Ueno N., Chandraratna R.A., Blumberg B. Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays. Dev. Dyn. 2005, 232:414-431.
-
(2005)
Dev. Dyn.
, vol.232
, pp. 414-431
-
-
Arima, K.1
Shiotsugu, J.2
Niu, R.3
Khandpur, R.4
Martinez, M.5
Shin, Y.6
Koide, T.7
Cho, K.W.8
Kitayama, A.9
Ueno, N.10
Chandraratna, R.A.11
Blumberg, B.12
-
3
-
-
84867894480
-
Williams syndrome transcription factor is critical for neural crest cell function in Xenopus laevis
-
Barnett C., Yazgan O., Kuo H.C., Malakar S., Thomas T., Fitzgerald A., Harbour W., Henry J.J., Krebs J.E. Williams syndrome transcription factor is critical for neural crest cell function in Xenopus laevis. Mech. Dev. 2012, 129:324-338.
-
(2012)
Mech. Dev.
, vol.129
, pp. 324-338
-
-
Barnett, C.1
Yazgan, O.2
Kuo, H.C.3
Malakar, S.4
Thomas, T.5
Fitzgerald, A.6
Harbour, W.7
Henry, J.J.8
Krebs, J.E.9
-
4
-
-
17744388353
-
Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome
-
Bi W.M., Ohyama T., Nakamura H., Yan J., Visvanathan J., Justice M.J., Lupski J.R. Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome. Hum. Mol. Genet. 2005, 14:983-995.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 983-995
-
-
Bi, W.M.1
Ohyama, T.2
Nakamura, H.3
Yan, J.4
Visvanathan, J.5
Justice, M.J.6
Lupski, J.R.7
-
5
-
-
17744388353
-
Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome
-
Bi W., Ohyama T., Nakamura H., Yan J., Visvanathan J., Justice M.J., Lupski J.R. Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome. Hum. Mol. Genet. 2005, 14:983-995.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 983-995
-
-
Bi, W.1
Ohyama, T.2
Nakamura, H.3
Yan, J.4
Visvanathan, J.5
Justice, M.J.6
Lupski, J.R.7
-
6
-
-
33750575898
-
RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome
-
Bi W., Saifi G.M., Girirajan S., Shi X., Szomju B., Firth H., Magenis R.E., Potocki L., Elsea S.H., Lupski J.R. RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome. Am. J. Med. Genet. A 2006, 140:2454-2463.
-
(2006)
Am. J. Med. Genet. A
, vol.140
, pp. 2454-2463
-
-
Bi, W.1
Saifi, G.M.2
Girirajan, S.3
Shi, X.4
Szomju, B.5
Firth, H.6
Magenis, R.E.7
Potocki, L.8
Elsea, S.H.9
Lupski, J.R.10
-
7
-
-
34547851814
-
Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes
-
Bi W., Yan J., Shi X., Yuva-Paylor L.A., Antalffy B.A., Goldman A., Yoo J.W., Noebels J.L., Armstrong D.L., Paylor R., Lupski J.R. Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. Hum. Mol. Genet. 2007, 16:1802-1813.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 1802-1813
-
-
Bi, W.1
Yan, J.2
Shi, X.3
Yuva-Paylor, L.A.4
Antalffy, B.A.5
Goldman, A.6
Yoo, J.W.7
Noebels, J.L.8
Armstrong, D.L.9
Paylor, R.10
Lupski, J.R.11
-
8
-
-
77957743861
-
Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome
-
Burns B., Schmidt K., Williams S.R., Kim S., Girirajan S., Elsea S.H. Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome. Hum. Mol. Genet. 2010, 19:4026-4042.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 4026-4042
-
-
Burns, B.1
Schmidt, K.2
Williams, S.R.3
Kim, S.4
Girirajan, S.5
Elsea, S.H.6
-
9
-
-
84908197173
-
Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memory
-
Cao L., Molina J., Abad C., Carmona-Mora P., Cardenas Oyarzo A., Young J.I., Walz K. Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memory. Hum. Mol. Genet. 2013.
-
(2013)
Hum. Mol. Genet.
-
-
Cao, L.1
Molina, J.2
Abad, C.3
Carmona-Mora, P.4
Cardenas Oyarzo, A.5
Young, J.I.6
Walz, K.7
-
10
-
-
78650001399
-
Retinoic acid induced 1, RAI1: a dosage sensitive gene related to neurobehavioral alterations including autistic behavior
-
Carmona-Mora P., Walz K. Retinoic acid induced 1, RAI1: a dosage sensitive gene related to neurobehavioral alterations including autistic behavior. Curr. Genomics 2010, 11:607-617.
-
(2010)
Curr. Genomics
, vol.11
, pp. 607-617
-
-
Carmona-Mora, P.1
Walz, K.2
-
11
-
-
77955781545
-
Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis syndrome
-
Carmona-Mora P., Encina C.A., Canales C.P., Cao L., Molina J., Kairath P., Young J.I., Walz K. Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis syndrome. BMC Mol. Biol. 2010, 11.
-
(2010)
BMC Mol. Biol.
, vol.11
-
-
Carmona-Mora, P.1
Encina, C.A.2
Canales, C.P.3
Cao, L.4
Molina, J.5
Kairath, P.6
Young, J.I.7
Walz, K.8
-
12
-
-
78349307637
-
Analysis of messenger RNA expression by in situ hybridization using RNA probes synthesized via in vitro transcription
-
Carter B.S., Fletcher J.S., Thompson R.C. Analysis of messenger RNA expression by in situ hybridization using RNA probes synthesized via in vitro transcription. Methods 2010, 52:322-331.
-
(2010)
Methods
, vol.52
, pp. 322-331
-
-
Carter, B.S.1
Fletcher, J.S.2
Thompson, R.C.3
-
14
-
-
0035117914
-
Increased XRALDH2 activity has a posteriorizing effect on the central nervous system of Xenopus embryos
-
Chen Y., Pollet N., Niehrs C., Pieler T. Increased XRALDH2 activity has a posteriorizing effect on the central nervous system of Xenopus embryos. Mech. Dev. 2001, 101:91-103.
-
(2001)
Mech. Dev.
, vol.101
, pp. 91-103
-
-
Chen, Y.1
Pollet, N.2
Niehrs, C.3
Pieler, T.4
-
15
-
-
20144385350
-
Discovery-based science education: functional genomic dissection in Drosophila by undergraduate researchers
-
Chen J., Call G.B., Beyer E., Bui C., Cespedes A., Chan A., Chan J., Chan S., Chhabra A., Dang P., Deravanesian A., Hermogeno B., Jen J., Kim E., Lee E., Lewis G., Marshall J., Regalia K., Shadpour F., Shemmassian A., Spivey K., Wells M., Wu J., Yamauchi Y., Yavari A., Abrams A., Abramson A., Amado L., Anderson J., Bashour K., Bibikova E., Bookatz A., Brewer S., Buu N., Calvillo S., Cao J., Chang A., Chang D., Chang Y., Chen Y., Choi J., Chou J., Datta S., Davarifar A., Desai P., Fabrikant J., Farnad S., Fu K., Garcia E., Garrone N., Gasparyan S., Gayda P., Goffstein C., Gonzalez C., Guirguis M., Hassid R., Hong A., Hong J., Hovestreydt L., Hu C., Jamshidian F., Kahen K., Kao L., Kelley M., Kho T., Kim S., Kim Y., Kirkpatrick B., Kohan E., Kwak R., Langenbacher A., Laxamana S., Lee C., Lee J., Lee S.Y., Lee T.H., Lee T., Lezcano S., Lin H., Lin P., Luu J., Luu T., Marrs W., Marsh E., Min S., Minasian T., Misra A., Morimoto M., Moshfegh Y., Murray J., Nguyen C., Nguyen K., Nodado E., O'Donahue A., Onugha N., Orjiakor N., Padhiar B., Pavel-Dinu M., Pavlenko A., Paz E., et al. Discovery-based science education: functional genomic dissection in Drosophila by undergraduate researchers. PLoS Biol. 2005, 3:e59.
-
(2005)
PLoS Biol.
, vol.3
, pp. e59
-
-
Chen, J.1
Call, G.B.2
Beyer, E.3
Bui, C.4
Cespedes, A.5
Chan, A.6
Chan, J.7
Chan, S.8
Chhabra, A.9
Dang, P.10
Deravanesian, A.11
Hermogeno, B.12
Jen, J.13
Kim, E.14
Lee, E.15
Lewis, G.16
Marshall, J.17
Regalia, K.18
Shadpour, F.19
Shemmassian, A.20
Spivey, K.21
Wells, M.22
Wu, J.23
Yamauchi, Y.24
Yavari, A.25
Abrams, A.26
Abramson, A.27
Amado, L.28
Anderson, J.29
Bashour, K.30
Bibikova, E.31
Bookatz, A.32
Brewer, S.33
Buu, N.34
Calvillo, S.35
Cao, J.36
Chang, A.37
Chang, D.38
Chang, Y.39
Chen, Y.40
Choi, J.41
Chou, J.42
Datta, S.43
Davarifar, A.44
Desai, P.45
Fabrikant, J.46
Farnad, S.47
Fu, K.48
Garcia, E.49
Garrone, N.50
Gasparyan, S.51
Gayda, P.52
Goffstein, C.53
Gonzalez, C.54
Guirguis, M.55
Hassid, R.56
Hong, A.57
Hong, J.58
Hovestreydt, L.59
Hu, C.60
Jamshidian, F.61
Kahen, K.62
Kao, L.63
Kelley, M.64
Kho, T.65
Kim, S.66
Kim, Y.67
Kirkpatrick, B.68
Kohan, E.69
Kwak, R.70
Langenbacher, A.71
Laxamana, S.72
Lee, C.73
Lee, J.74
Lee, S.Y.75
Lee, T.H.76
Lee, T.77
Lezcano, S.78
Lin, H.79
Lin, P.80
Luu, J.81
Luu, T.82
Marrs, W.83
Marsh, E.84
Min, S.85
Minasian, T.86
Misra, A.87
Morimoto, M.88
Moshfegh, Y.89
Murray, J.90
Nguyen, C.91
Nguyen, K.92
Nodado, E.93
O'Donahue, A.94
Onugha, N.95
Orjiakor, N.96
Padhiar, B.97
Pavel-Dinu, M.98
Pavlenko, A.99
more..
-
16
-
-
0030759543
-
Neurotrophin regulation of the developing nervous system: analyses of knockout mice
-
Conover J.C., Yancopoulos G.D. Neurotrophin regulation of the developing nervous system: analyses of knockout mice. Rev. Neurosci. 1997, 8:13-27.
-
(1997)
Rev. Neurosci.
, vol.8
, pp. 13-27
-
-
Conover, J.C.1
Yancopoulos, G.D.2
-
17
-
-
84885737397
-
A phylogenetic study of SPBP and RAI1: evolutionary conservation of chromatin binding modules
-
Darvekar S., Rekdal C., Johansen T., Sjottem E. A phylogenetic study of SPBP and RAI1: evolutionary conservation of chromatin binding modules. PLoS One 2013, 8:e78907.
-
(2013)
PLoS One
, vol.8
, pp. e78907
-
-
Darvekar, S.1
Rekdal, C.2
Johansen, T.3
Sjottem, E.4
-
18
-
-
78651073326
-
Reiterative AP2a activity controls sequential steps in the neural crest gene regulatory network
-
de Croze N., Maczkowiak F., Monsoro-Burq A.H. Reiterative AP2a activity controls sequential steps in the neural crest gene regulatory network. Proc. Natl. Acad. Sci. U.S.A. 2011, 108:155-160.
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
, pp. 155-160
-
-
de Croze, N.1
Maczkowiak, F.2
Monsoro-Burq, A.H.3
-
19
-
-
33745236662
-
Development of the primary mouth in Xenopus laevis
-
Dickinson A.J., Sive H. Development of the primary mouth in Xenopus laevis. Dev. Biol. 2006, 295:700-713.
-
(2006)
Dev. Biol.
, vol.295
, pp. 700-713
-
-
Dickinson, A.J.1
Sive, H.2
-
20
-
-
67449113924
-
The Wnt antagonists Frzb-1 and crescent locally regulate basement membrane dissolution in the developing primary mouth
-
Dickinson A.J., Sive H.L. The Wnt antagonists Frzb-1 and crescent locally regulate basement membrane dissolution in the developing primary mouth. Development 2009, 136:1071-1081.
-
(2009)
Development
, vol.136
, pp. 1071-1081
-
-
Dickinson, A.J.1
Sive, H.L.2
-
21
-
-
0037314551
-
Comparison of immunohistochemistry for activated caspase-3 and cleaved cytokeratin 18 with the TUNEL method for quantification of apoptosis in histological sections of PC-3 subcutaneous xenografts
-
Duan W.R., Garner D.S., Williams S.D., Funckes-Shippy C.L., Spath I.S., Blomme E.A. Comparison of immunohistochemistry for activated caspase-3 and cleaved cytokeratin 18 with the TUNEL method for quantification of apoptosis in histological sections of PC-3 subcutaneous xenografts. J. Pathol. 2003, 199:221-228.
-
(2003)
J. Pathol.
, vol.199
, pp. 221-228
-
-
Duan, W.R.1
Garner, D.S.2
Williams, S.D.3
Funckes-Shippy, C.L.4
Spath, I.S.5
Blomme, E.A.6
-
22
-
-
49949086671
-
Controlling morpholino experiments: do not stop making antisense
-
Eisen J.S., Smith J.C. Controlling morpholino experiments: do not stop making antisense. Development 2008, 135:1735-1743.
-
(2008)
Development
, vol.135
, pp. 1735-1743
-
-
Eisen, J.S.1
Smith, J.C.2
-
24
-
-
0031429540
-
Definition of the critical interval for Smith-Magenis syndrome
-
Elsea S.H., Purandare S.M., Adell R.A., Juyal R.C., Davis J.G., Finucane B., Magenis R.E., Patel P.I. Definition of the critical interval for Smith-Magenis syndrome. Cytogenet. Cell Genet. 1997, 79:276-281.
-
(1997)
Cytogenet. Cell Genet.
, vol.79
, pp. 276-281
-
-
Elsea, S.H.1
Purandare, S.M.2
Adell, R.A.3
Juyal, R.C.4
Davis, J.G.5
Finucane, B.6
Magenis, R.E.7
Patel, P.I.8
-
25
-
-
81855176220
-
Aquatic animal models of human disease: selected papers from the 5th conference preface
-
Fieber L.A., Tanguay R.L., Walter R.B., Williams D.E. Aquatic animal models of human disease: selected papers from the 5th conference preface. Comp. Biochem. Physiol. C-Toxicol. Pharmacol. 2012, 155:9-10.
-
(2012)
Comp. Biochem. Physiol. C-Toxicol. Pharmacol.
, vol.155
, pp. 9-10
-
-
Fieber, L.A.1
Tanguay, R.L.2
Walter, R.B.3
Williams, D.E.4
-
26
-
-
60549090775
-
Why the embryo still matters: CSF and the neuroepithelium as interdependent regulators of embryonic brain growth, morphogenesis and histiogenesis
-
Gato A., Desmond M.E. Why the embryo still matters: CSF and the neuroepithelium as interdependent regulators of embryonic brain growth, morphogenesis and histiogenesis. Dev. Biol. 2009, 327:263-272.
-
(2009)
Dev. Biol.
, vol.327
, pp. 263-272
-
-
Gato, A.1
Desmond, M.E.2
-
27
-
-
64949140303
-
Abnormal maternal behavior, altered sociability, and impaired serotonin metabolism in Rai1-transgenic mice
-
Girirajan S., Elsea S.H. Abnormal maternal behavior, altered sociability, and impaired serotonin metabolism in Rai1-transgenic mice. Mamm. Genome 2009, 20:247-255.
-
(2009)
Mamm. Genome
, vol.20
, pp. 247-255
-
-
Girirajan, S.1
Elsea, S.H.2
-
28
-
-
33748130455
-
Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum
-
Girirajan S., Vlangos C.N., Szomju B.B., Edelman E., Trevors C.D., Dupuis L., Nezarati M., Bunyan D.J., Elsea S.H. Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum. Genet. Med. 2006, 8:417-427.
-
(2006)
Genet. Med.
, vol.8
, pp. 417-427
-
-
Girirajan, S.1
Vlangos, C.N.2
Szomju, B.B.3
Edelman, E.4
Trevors, C.D.5
Dupuis, L.6
Nezarati, M.7
Bunyan, D.J.8
Elsea, S.H.9
-
31
-
-
77951823093
-
The genome of the Western clawed frog Xenopus tropicalis
-
Hellsten U., Harland R.M., Gilchrist M.J., Hendrix D., Jurka J., Kapitonov V., Ovcharenko I., Putnam N.H., Shu S.Q., Taher L., Blitz I.L., Blumberg B., Dichmann D.S., Dubchak I., Amaya E., Detter J.C., Fletcher R., Gerhard D.S., Goodstein D., Graves T., Grigoriev I.V., Grimwood J., Kawashima T., Lindquist E., Lucas S.M., Mead P.E., Mitros T., Ogino H., Ohta Y., Poliakov A.V., Pollet N., Robert J., Salamov A., Sater A.K., Schmutz J., Terry A., Vize P.D., Warren W.C., Wells D., Wills A., Wilson R.K., Zimmerman L.B., Zorn A.M., Grainger R., Grammer T., Khokha M.K., Richardson P.M., Rokhsar D.S. The genome of the Western clawed frog Xenopus tropicalis. Science 2010, 328:633-636.
-
(2010)
Science
, vol.328
, pp. 633-636
-
-
Hellsten, U.1
Harland, R.M.2
Gilchrist, M.J.3
Hendrix, D.4
Jurka, J.5
Kapitonov, V.6
Ovcharenko, I.7
Putnam, N.H.8
Shu, S.Q.9
Taher, L.10
Blitz, I.L.11
Blumberg, B.12
Dichmann, D.S.13
Dubchak, I.14
Amaya, E.15
Detter, J.C.16
Fletcher, R.17
Gerhard, D.S.18
Goodstein, D.19
Graves, T.20
Grigoriev, I.V.21
Grimwood, J.22
Kawashima, T.23
Lindquist, E.24
Lucas, S.M.25
Mead, P.E.26
Mitros, T.27
Ogino, H.28
Ohta, Y.29
Poliakov, A.V.30
Pollet, N.31
Robert, J.32
Salamov, A.33
Sater, A.K.34
Schmutz, J.35
Terry, A.36
Vize, P.D.37
Warren, W.C.38
Wells, D.39
Wills, A.40
Wilson, R.K.41
Zimmerman, L.B.42
Zorn, A.M.43
Grainger, R.44
Grammer, T.45
Khokha, M.K.46
Richardson, P.M.47
Rokhsar, D.S.48
more..
-
32
-
-
0019966525
-
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome
-
Hittner H.M., King R.A., Riccardi V.M., Ledbetter D.H., Borda R.P., Ferrell R.E., Kretzer F.L. Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome. Am. J. Ophthalmol. 1982, 94:328-337.
-
(1982)
Am. J. Ophthalmol.
, vol.94
, pp. 328-337
-
-
Hittner, H.M.1
King, R.A.2
Riccardi, V.M.3
Ledbetter, D.H.4
Borda, R.P.5
Ferrell, R.E.6
Kretzer, F.L.7
-
33
-
-
35848938945
-
The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha
-
Hu C.J., Sataur A., Wang L., Chen H., Simon M.C. The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha. Mol. Biol. Cell 2007, 18:4528-4542.
-
(2007)
Mol. Biol. Cell
, vol.18
, pp. 4528-4542
-
-
Hu, C.J.1
Sataur, A.2
Wang, L.3
Chen, H.4
Simon, M.C.5
-
34
-
-
34250863291
-
BDNF promotes target innervation of Xenopus mandibular trigeminal axons in vivo
-
Huang J.K., Dorey K., Ishibashi S., Amaya E. BDNF promotes target innervation of Xenopus mandibular trigeminal axons in vivo. BMC Dev. Biol. 2007, 7:59.
-
(2007)
BMC Dev. Biol.
, vol.7
, pp. 59
-
-
Huang, J.K.1
Dorey, K.2
Ishibashi, S.3
Amaya, E.4
-
36
-
-
0029078225
-
Cloning of a retinoic acid-induced gene, Gt1, in the embryonal carcinoma cell-line P19 - neuron-specific expression in the mouse-brain
-
Imai Y., Suzuki Y., Matsui T., Tohyama M., Wanaka A., Takagi T. Cloning of a retinoic acid-induced gene, Gt1, in the embryonal carcinoma cell-line P19 - neuron-specific expression in the mouse-brain. Mol. Brain Res. 1995, 31:1-9.
-
(1995)
Mol. Brain Res.
, vol.31
, pp. 1-9
-
-
Imai, Y.1
Suzuki, Y.2
Matsui, T.3
Tohyama, M.4
Wanaka, A.5
Takagi, T.6
-
37
-
-
0025260871
-
Anomalous brain morphology on magnetic-resonance images in Williams syndrome and down syndrome
-
Jernigan T.L., Bellugi U. Anomalous brain morphology on magnetic-resonance images in Williams syndrome and down syndrome. Arch. Neurol. 1990, 47:529-533.
-
(1990)
Arch. Neurol.
, vol.47
, pp. 529-533
-
-
Jernigan, T.L.1
Bellugi, U.2
-
38
-
-
0029978246
-
Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients
-
Juyal R.C., Figuera L.E., Hauge X., Elsea S.H., Lupski J.R., Greenberg F., Baldini A., Patel P.I. Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients. Am. J. Hum. Genet. 1996, 58:998-1007.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 998-1007
-
-
Juyal, R.C.1
Figuera, L.E.2
Hauge, X.3
Elsea, S.H.4
Lupski, J.R.5
Greenberg, F.6
Baldini, A.7
Patel, P.I.8
-
39
-
-
79958172223
-
Xenopus: an emerging model for studying congenital heart disease
-
Kaltenbrun E., Tandon P., Amin N.M., Waldron L., Showell C., Conlon F.L. Xenopus: an emerging model for studying congenital heart disease. Birth Defects Res. Part a-Clin. Mol. Teratol. 2011, 91:495-510.
-
(2011)
Birth Defects Res. Part a-Clin. Mol. Teratol.
, vol.91
, pp. 495-510
-
-
Kaltenbrun, E.1
Tandon, P.2
Amin, N.M.3
Waldron, L.4
Showell, C.5
Conlon, F.L.6
-
40
-
-
84859436519
-
Median facial clefts in Xenopus laevis: roles of retinoic acid signaling and homeobox genes
-
Kennedy A.E., Dickinson A.J. Median facial clefts in Xenopus laevis: roles of retinoic acid signaling and homeobox genes. Dev. Biol. 2012, 365:229-240.
-
(2012)
Dev. Biol.
, vol.365
, pp. 229-240
-
-
Kennedy, A.E.1
Dickinson, A.J.2
-
41
-
-
84899471544
-
Quantitative analysis of orofacial development and median clefts in Xenopus laevis
-
Kennedy A.E., Dickinson A.J. Quantitative analysis of orofacial development and median clefts in Xenopus laevis. Anat. Rec. (Hoboken) 2014, 297:834-855.
-
(2014)
Anat. Rec. (Hoboken)
, vol.297
, pp. 834-855
-
-
Kennedy, A.E.1
Dickinson, A.J.2
-
42
-
-
84858000785
-
Xenopus white papers and resources: folding functional genomics and genetics into the frog
-
Khokha M.K. Xenopus white papers and resources: folding functional genomics and genetics into the frog. Genesis 2012, 50:133-142.
-
(2012)
Genesis
, vol.50
, pp. 133-142
-
-
Khokha, M.K.1
-
43
-
-
78650839801
-
MorphoJ: an integrated software package for geometric morphometrics
-
Klingenberg C.P. MorphoJ: an integrated software package for geometric morphometrics. Mol. Ecol. Resour. 2011, 11:353-357.
-
(2011)
Mol. Ecol. Resour.
, vol.11
, pp. 353-357
-
-
Klingenberg, C.P.1
-
44
-
-
78649633356
-
Prenatal alcohol exposure alters the patterns of facial asymmetry
-
Klingenberg C.P., Wetherill L., Rogers J., Moore E., Ward R., Autti-Ramo I., Fagerlund A., Jacobson S.W., Robinson L.K., Hoyme H.E., Mattson S.N., Li T.K., Riley E.P., Foroud T. Prenatal alcohol exposure alters the patterns of facial asymmetry. Alcohol 2010, 44:649-657.
-
(2010)
Alcohol
, vol.44
, pp. 649-657
-
-
Klingenberg, C.P.1
Wetherill, L.2
Rogers, J.3
Moore, E.4
Ward, R.5
Autti-Ramo, I.6
Fagerlund, A.7
Jacobson, S.W.8
Robinson, L.K.9
Hoyme, H.E.10
Mattson, S.N.11
Li, T.K.12
Riley, E.P.13
Foroud, T.14
-
45
-
-
0036429169
-
The role of neural crest during cardiac development in a mouse model of DiGeorge syndrome
-
Kochilas L., Merscher-Gomez S., Lu M.M., Potluri V., Liao J., Kucherlapati R., Morrow B., Epstein J.A. The role of neural crest during cardiac development in a mouse model of DiGeorge syndrome. Dev. Biol. 2002, 251:157-166.
-
(2002)
Dev. Biol.
, vol.251
, pp. 157-166
-
-
Kochilas, L.1
Merscher-Gomez, S.2
Lu, M.M.3
Potluri, V.4
Liao, J.5
Kucherlapati, R.6
Morrow, B.7
Epstein, J.A.8
-
46
-
-
78049410034
-
Autism spectrum features in Smith-Magenis syndrome
-
Laje G., Morse R., Richter W., Ball J., Pao M., Smith A.C. Autism spectrum features in Smith-Magenis syndrome. Am. J. Med. Genet. C Semin. Med. Genet. 2010, 154C:456-462.
-
(2010)
Am. J. Med. Genet. C Semin. Med. Genet.
, vol.154 C
, pp. 456-462
-
-
Laje, G.1
Morse, R.2
Richter, W.3
Ball, J.4
Pao, M.5
Smith, A.C.6
-
47
-
-
29044436565
-
Developmental expression of Xenopus fragile X mental retardation-1 gene
-
Lim J.H., Luo T., Sargent T.D., Fallon J.R. Developmental expression of Xenopus fragile X mental retardation-1 gene. Int. J. Dev. Biol. 2005, 49:981-984.
-
(2005)
Int. J. Dev. Biol.
, vol.49
, pp. 981-984
-
-
Lim, J.H.1
Luo, T.2
Sargent, T.D.3
Fallon, J.R.4
-
48
-
-
0030605486
-
Role of neurotrophins and trk receptors in the development and maintenance of sensory neurons: an overview
-
Lindsay R.M. Role of neurotrophins and trk receptors in the development and maintenance of sensory neurons: an overview. Philos. Trans. R. Soc. Lond. B Biol. Sci. 1996, 351:365-373.
-
(1996)
Philos. Trans. R. Soc. Lond. B Biol. Sci.
, vol.351
, pp. 365-373
-
-
Lindsay, R.M.1
-
49
-
-
65449152953
-
Totally tubular: the mystery behind function and origin of the brain ventricular system
-
Lowery L.A., Sive H. Totally tubular: the mystery behind function and origin of the brain ventricular system. BioEssays 2009, 31:446-458.
-
(2009)
BioEssays
, vol.31
, pp. 446-458
-
-
Lowery, L.A.1
Sive, H.2
-
50
-
-
5444261739
-
Retinoic acid signalling in the development of branchial arches
-
Mark M., Ghyselinck N.B., Chambon P. Retinoic acid signalling in the development of branchial arches. Curr. Opin. Genet. Dev. 2004, 14:591-598.
-
(2004)
Curr. Opin. Genet. Dev.
, vol.14
, pp. 591-598
-
-
Mark, M.1
Ghyselinck, N.B.2
Chambon, P.3
-
51
-
-
80052594360
-
FGF and retinoic acid activity gradients control the timing of neural crest cell emigration in the trunk
-
Martinez-Morales P.L., del Corral R.D., Olivera-Martinez I., Quiroga A.C., Das R.M., Barbas J.A., Storey K.G., Morales A.V. FGF and retinoic acid activity gradients control the timing of neural crest cell emigration in the trunk. J. Cell Biol. 2011, 194:489-503.
-
(2011)
J. Cell Biol.
, vol.194
, pp. 489-503
-
-
Martinez-Morales, P.L.1
del Corral, R.D.2
Olivera-Martinez, I.3
Quiroga, A.C.4
Das, R.M.5
Barbas, J.A.6
Storey, K.G.7
Morales, A.V.8
-
52
-
-
75749129110
-
PHD fingers epigenetic effectors and potential drug targets
-
Musselman C.A., Kutateladze T.G. PHD fingers epigenetic effectors and potential drug targets. Mol. Interventions 2009, 9:314-323.
-
(2009)
Mol. Interventions
, vol.9
, pp. 314-323
-
-
Musselman, C.A.1
Kutateladze, T.G.2
-
54
-
-
84883860621
-
Modeling human neurodevelopmental disorders in the Xenopus tadpole: from mechanisms to therapeutic targets
-
Pratt K.G., Khakhalin A.S. Modeling human neurodevelopmental disorders in the Xenopus tadpole: from mechanisms to therapeutic targets. Dis. Models Mech. 2013, 6:1057-1065.
-
(2013)
Dis. Models Mech.
, vol.6
, pp. 1057-1065
-
-
Pratt, K.G.1
Khakhalin, A.S.2
-
55
-
-
84908197172
-
Hypertelorism
-
In: Bentz, M.L. (Ed.), McGraw-Hill Professional, New York.
-
Renato Ocampo, J. and Persing, J.A. 1997. Hypertelorism. In: Bentz, M.L. (Ed.), Pediatric Plastic Surgery, McGraw-Hill Professional, New York.
-
(1997)
Pediatric Plastic Surgery
-
-
Renato Ocampo, J.1
Persing, J.A.2
-
56
-
-
59849119800
-
A neural crest deficit in down syndrome mice is associated with deficient mitotic response to Sonic hedgehog
-
Roper R.J., VanHorn J.F., Cain C.C., Reeves R.H. A neural crest deficit in down syndrome mice is associated with deficient mitotic response to Sonic hedgehog. Mech. Dev. 2009, 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
-
57
-
-
84863557893
-
Hooked! modeling human disease in zebrafish
-
Santoriello C., Zon L.I. Hooked! modeling human disease in zebrafish. J. Clin. Invest. 2012, 122:2337-2343.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 2337-2343
-
-
Santoriello, C.1
Zon, L.I.2
-
58
-
-
0034936509
-
Evidence for apoptosis in the fetal down syndrome brain
-
Seidl R., Bidmon B., Bajo M., Yoo B.C., Cairns N., LaCasse E.C., Lubec G. Evidence for apoptosis in the fetal down syndrome brain. J. Child Neurol. 2001, 16:438-442.
-
(2001)
J. Child Neurol.
, vol.16
, pp. 438-442
-
-
Seidl, R.1
Bidmon, B.2
Bajo, M.3
Yoo, B.C.4
Cairns, N.5
LaCasse, E.C.6
Lubec, G.7
-
59
-
-
34347355313
-
Decoding development in Xenopus tropicalis
-
Showell C., Conlon F.L. Decoding development in Xenopus tropicalis. Genesis 2007, 45:418-426.
-
(2007)
Genesis
, vol.45
, pp. 418-426
-
-
Showell, C.1
Conlon, F.L.2
-
60
-
-
79952352259
-
'Model' or 'tool'? New definitions for translational research
-
Sive H. 'Model' or 'tool'? New definitions for translational research. Dis. Models Mech. 2011, 4:137-138.
-
(2011)
Dis. Models Mech.
, vol.4
, pp. 137-138
-
-
Sive, H.1
-
62
-
-
0344177207
-
Mutations in RAI1 associated with Smith-Magenis syndrome
-
Slager R.E., Newton T.L., Vlangos C.N., Finucane B., Elsea S.H. Mutations in RAI1 associated with Smith-Magenis syndrome. Nat. Genet. 2003, 33:466-468.
-
(2003)
Nat. Genet.
, vol.33
, pp. 466-468
-
-
Slager, R.E.1
Newton, T.L.2
Vlangos, C.N.3
Finucane, B.4
Elsea, S.H.5
-
63
-
-
34247566116
-
Morpholino, siRNA, and S-DNA compared: impact of structure and mechanism of action on off-target effects and sequence specificity
-
Summerton J.E. Morpholino, siRNA, and S-DNA compared: impact of structure and mechanism of action on off-target effects and sequence specificity. Curr. Top. Med. Chem. 2007, 7:651-660.
-
(2007)
Curr. Top. Med. Chem.
, vol.7
, pp. 651-660
-
-
Summerton, J.E.1
-
64
-
-
15444363122
-
Neuritic beading induced by activated microglia is an early feature of neuronal dysfunction toward neuronal death by inhibition of mitochondrial respiration and axonal transport
-
Takeuchi H., Mizuno T., Zhang G.Q., Wang J.Y., Kawanokuchi J., Kuno R., Suzumura A. Neuritic beading induced by activated microglia is an early feature of neuronal dysfunction toward neuronal death by inhibition of mitochondrial respiration and axonal transport. J. Biol. Chem. 2005, 280:10444-10454.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 10444-10454
-
-
Takeuchi, H.1
Mizuno, T.2
Zhang, G.Q.3
Wang, J.Y.4
Kawanokuchi, J.5
Kuno, R.6
Suzumura, A.7
-
65
-
-
84856255728
-
Morpholino injection in Xenopus
-
Tandon P., Showell C., Christine K., Conlon F.L. Morpholino injection in Xenopus. Methods Mol. Biol. 2012, 843:29-46.
-
(2012)
Methods Mol. Biol.
, vol.843
, pp. 29-46
-
-
Tandon, P.1
Showell, C.2
Christine, K.3
Conlon, F.L.4
-
66
-
-
0000529717
-
Revised procedures for staining and clearing small fishes and other vertebrates for bone and cartilage study
-
Taylor W. Revised procedures for staining and clearing small fishes and other vertebrates for bone and cartilage study. Cybium 1985, 9:107-119.
-
(1985)
Cybium
, vol.9
, pp. 107-119
-
-
Taylor, W.1
-
67
-
-
0242291084
-
Can zebrafish be used as a model to study the neurodevelopmental causes of autism?
-
Tropepe V., Sive H.L. Can zebrafish be used as a model to study the neurodevelopmental causes of autism?. Genes Brain Behav 2003, 2:268-281.
-
(2003)
Genes Brain Behav
, vol.2
, pp. 268-281
-
-
Tropepe, V.1
Sive, H.L.2
-
68
-
-
84863012284
-
Axon degeneration: molecular mechanisms of a self-destruction pathway
-
Wang J.T., Medress Z.A., Barres B.A. Axon degeneration: molecular mechanisms of a self-destruction pathway. J. Cell Biol. 2012, 196:7-18.
-
(2012)
J. Cell Biol.
, vol.196
, pp. 7-18
-
-
Wang, J.T.1
Medress, Z.A.2
Barres, B.A.3
-
69
-
-
84885399548
-
Zebrafish models of human liver development and disease
-
Wilkins B.J., Pack M. Zebrafish models of human liver development and disease. Compr. Physiol. 2013, 3:1213-1230.
-
(2013)
Compr. Physiol.
, vol.3
, pp. 1213-1230
-
-
Wilkins, B.J.1
Pack, M.2
-
70
-
-
0025895658
-
Developmental regulation of transcription factor AP-2 during Xenopus laevis embryogenesis
-
Winning R.S., Shea L.J., Marcus S.J., Sargent T.D. Developmental regulation of transcription factor AP-2 during Xenopus laevis embryogenesis. Nucleic Acids Res. 1991, 19:3709-3714.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 3709-3714
-
-
Winning, R.S.1
Shea, L.J.2
Marcus, S.J.3
Sargent, T.D.4
-
71
-
-
14644418529
-
Inactivation of TGFbeta signaling in neural crest stem cells leads to multiple defects reminiscent of DiGeorge syndrome
-
Wurdak H., Ittner L.M., Lang K.S., Leveen P., Suter U., Fischer J.A., Karlsson S., Born W., Sommer L. Inactivation of TGFbeta signaling in neural crest stem cells leads to multiple defects reminiscent of DiGeorge syndrome. Genes Dev. 2005, 19:530-535.
-
(2005)
Genes Dev.
, vol.19
, pp. 530-535
-
-
Wurdak, H.1
Ittner, L.M.2
Lang, K.S.3
Leveen, P.4
Suter, U.5
Fischer, J.A.6
Karlsson, S.7
Born, W.8
Sommer, L.9
-
72
-
-
33748419822
-
Brain developmental abnormalities in Prader-Willi syndrome detected by diffusion tensor imaging
-
Yamada K., Matsuzawa H., Uchiyama M., Kwee I.L., Nakada T. Brain developmental abnormalities in Prader-Willi syndrome detected by diffusion tensor imaging. Pediatrics 2006, 118:E442-E448.
-
(2006)
Pediatrics
, vol.118
, pp. E442-E448
-
-
Yamada, K.1
Matsuzawa, H.2
Uchiyama, M.3
Kwee, I.L.4
Nakada, T.5
-
73
-
-
33847191389
-
Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike
-
Yan J., Bi W., Lupski J.R. Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike. Am. J. Hum. Genet. 2007, 80:518-525.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 518-525
-
-
Yan, J.1
Bi, W.2
Lupski, J.R.3
-
74
-
-
0033052683
-
Zebrafish: a new model for human disease
-
Zon L.I. Zebrafish: a new model for human disease. Genome Res. 1999, 9:99-100.
-
(1999)
Genome Res.
, vol.9
, pp. 99-100
-
-
Zon, L.I.1
|