-
1
-
-
0034101021
-
The transcription factor Lmx1b maintains Wnt1 expression within the isthmic organizer
-
Adams, K. A., Maida, J. M., Golden, J. A. Riddle, R. D. 2000. The transcription factor Lmx1b maintains Wnt1 expression within the isthmic organizer. Development 127, 1857 1867.
-
(2000)
Development
, vol.127
, pp. 1857-1867
-
-
Adams, K.A.1
Maida, J.M.2
Golden, J.A.3
Riddle, R.D.4
-
2
-
-
31044445499
-
Identification of intrinsic determinants of midbrain dopamine neurons
-
Andersson, E., Tryggvason, U., Deng, Q., Friling, S., Alekseenko, Z., Robert, B., Perlmann, T. Ericson, J. 2006. Identification of intrinsic determinants of midbrain dopamine neurons. Cell 124, 393 405.
-
(2006)
Cell
, vol.124
, pp. 393-405
-
-
Andersson, E.1
Tryggvason, U.2
Deng, Q.3
Friling, S.4
Alekseenko, Z.5
Robert, B.6
Perlmann, T.7
Ericson, J.8
-
3
-
-
0036935250
-
CNS expression pattern of Lmx1b and coexpression with ptx genes suggest functional cooperativity in the development of forebrain motor control systems
-
Asbreuk, C. H., Vogelaar, C. F., Hellemons, A., Smidt, M. P. Burbach, J. P. 2002. CNS expression pattern of Lmx1b and coexpression with ptx genes suggest functional cooperativity in the development of forebrain motor control systems. Mol. Cell. Neurosci. 21, 410 420.
-
(2002)
Mol. Cell. Neurosci.
, vol.21
, pp. 410-420
-
-
Asbreuk, C.H.1
Vogelaar, C.F.2
Hellemons, A.3
Smidt, M.P.4
Burbach, J.P.5
-
4
-
-
0014494693
-
Hereditary onycho-osteodysplasia (Nail-Patella syndrome). A report of nine kindreds
-
Beals, R. K. Eckhardt, A. L. 1969. Hereditary onycho-osteodysplasia (Nail-Patella syndrome). A report of nine kindreds. J. Bone Joint. Surg. Am. 51, 505 516.
-
(1969)
J. Bone Joint. Surg. Am.
, vol.51
, pp. 505-516
-
-
Beals, R.K.1
Eckhardt, A.L.2
-
5
-
-
0036957091
-
Nail-patella syndrome. Overview on clinical and molecular findings
-
Bongers, E. M., Gubler, M. C. Knoers, N. V. 2002. Nail-patella syndrome. Overview on clinical and molecular findings. Pediatr. Nephro. 17, 703 712.
-
(2002)
Pediatr. Nephro.
, vol.17
, pp. 703-712
-
-
Bongers, E.M.1
Gubler, M.C.2
Knoers, N.V.3
-
6
-
-
34247106790
-
Sustained interactive Wnt and FGF signaling is required to maintain isthmic identity
-
Canning, C. A., Lee, L., Irving, C., Mason, I. Jones, C. M. 2007. Sustained interactive Wnt and FGF signaling is required to maintain isthmic identity. Dev. Biol. 305, 276 286.
-
(2007)
Dev. Biol.
, vol.305
, pp. 276-286
-
-
Canning, C.A.1
Lee, L.2
Irving, C.3
Mason, I.4
Jones, C.M.5
-
7
-
-
0142091639
-
Patterning cell types in the dorsal spinal cord: What the mouse mutants say
-
Caspary, T. Anderson, K. V. 2003. Patterning cell types in the dorsal spinal cord: what the mouse mutants say. Nat. Rev. Neurosci. 4, 289 297.
-
(2003)
Nat. Rev. Neurosci.
, vol.4
, pp. 289-297
-
-
Caspary, T.1
Anderson, K.V.2
-
9
-
-
0036433896
-
Interactions between dorsal-ventral patterning genes lmx1b, engrailed-1 and wnt-7a in the vertebrate limb
-
Chen, H. Johnson, R. L. 2002. Interactions between dorsal-ventral patterning genes lmx1b, engrailed-1 and wnt-7a in the vertebrate limb. Int. J. Dev. Bio. 46, 937 941.
-
(2002)
Int. J. Dev. Bio.
, vol.46
, pp. 937-941
-
-
Chen, H.1
Johnson, R.L.2
-
10
-
-
0031747153
-
Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome
-
Chen, H., Lun, Y., Ovchinnikov, D., Kokubo, H., Oberg, K. C., Pepicelli, C. V., Gan, L., Lee, B. Johnson, R. L. 1998a. Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome. Nat. Genet. 19, 51 55.
-
(1998)
Nat. Genet.
, vol.19
, pp. 51-55
-
-
Chen, H.1
Lun, Y.2
Ovchinnikov, D.3
Kokubo, H.4
Oberg, K.C.5
Pepicelli, C.V.6
Gan, L.7
Lee, B.8
Johnson, R.L.9
-
11
-
-
0031832048
-
Multiple calvarial defects in lmx1b mutant mice
-
Chen, H., Ovchinnikov, D., Pressman, C. L., Aulehla, A., Lun, Y. Johnson, R. L. 1998b. Multiple calvarial defects in lmx1b mutant mice. Dev. Genet. 22, 314 320.
-
(1998)
Dev. Genet.
, vol.22
, pp. 314-320
-
-
Chen, H.1
Ovchinnikov, D.2
Pressman, C.L.3
Aulehla, A.4
Lun, Y.5
Johnson, R.L.6
-
12
-
-
0034889110
-
The paired homeodomain protein DRG11 is required for the projection of cutaneous sensory afferent fibers to the dorsal spinal cord
-
Chen, Z. F., Rebelo, S., White, F., Malmberg, A. B., Baba, H., Lima, D., Woolf, C. J., Basbaum, A. I. Anderson, D. J. 2001. The paired homeodomain protein DRG11 is required for the projection of cutaneous sensory afferent fibers to the dorsal spinal cord. Neuron 31, 59 73.
-
(2001)
Neuron
, vol.31
, pp. 59-73
-
-
Chen, Z.F.1
Rebelo, S.2
White, F.3
Malmberg, A.B.4
Baba, H.5
Lima, D.6
Woolf, C.J.7
Basbaum, A.I.8
Anderson, D.J.9
-
13
-
-
0242694971
-
Lmx1b, Pet-1, and Nkx2.2 coordinately specify serotonergic neurotransmitter phenotype
-
Cheng, L., Chen, C. L., Luo, P., Tan, M., Qiu, M., Johnson, R. Ma, Q. 2003. Lmx1b, Pet-1, and Nkx2.2 coordinately specify serotonergic neurotransmitter phenotype. J. Neurosci. 23, 9961 9967.
-
(2003)
J. Neurosci.
, vol.23
, pp. 9961-9967
-
-
Cheng, L.1
Chen, C.L.2
Luo, P.3
Tan, M.4
Qiu, M.5
Johnson, R.6
Ma, Q.7
-
14
-
-
11144353684
-
Tlx3 and Tlx1 are post-mitotic selector genes determining glutamatergic over GABAergic cell fates
-
Cheng, L., Arata, A., Mizuguchi, R., Qian, Y., Karunaratne, A., Gray, P. A., Arata, S., Shirasawa, S., Bouchard, M., Luo, P., Chen, C. L., Busslinger, M., Goulding, M., Onimaru, H. Ma, Q. 2004. Tlx3 and Tlx1 are post-mitotic selector genes determining glutamatergic over GABAergic cell fates. Nat. Neurosci. 7, 510 517.
-
(2004)
Nat. Neurosci.
, vol.7
, pp. 510-517
-
-
Cheng, L.1
Arata, A.2
Mizuguchi, R.3
Qian, Y.4
Karunaratne, A.5
Gray, P.A.6
Arata, S.7
Shirasawa, S.8
Bouchard, M.9
Luo, P.10
Chen, C.L.11
Busslinger, M.12
Goulding, M.13
Onimaru, H.14
Ma, Q.15
-
15
-
-
27644445358
-
Lbx1 and Tlx3 are opposing switches in determining GABAergic versus glutamatergic transmitter phenotypes
-
Cheng, L., Samad, O. A., Xu, Y., Mizuguchi, R., Luo, P., Shirasawa, S., Goulding, M. Ma, Q. 2005. Lbx1 and Tlx3 are opposing switches in determining GABAergic versus glutamatergic transmitter phenotypes. Nat. Neurosci. 8, 1510 1515.
-
(2005)
Nat. Neurosci.
, vol.8
, pp. 1510-1515
-
-
Cheng, L.1
Samad, O.A.2
Xu, Y.3
Mizuguchi, R.4
Luo, P.5
Shirasawa, S.6
Goulding, M.7
Ma, Q.8
-
16
-
-
0032763066
-
Restricted distribution of loss-of-function mutations within the LMX1B genes of nail-patella syndrome patients
-
Clough, M. V., Hamlington, J. D. Mcintosh, I. 1999. Restricted distribution of loss-of-function mutations within the LMX1B genes of nail-patella syndrome patients. Hum. Mutat. 14, 459 465.
-
(1999)
Hum. Mutat.
, vol.14
, pp. 459-465
-
-
Clough, M.V.1
Hamlington, J.D.2
McIntosh, I.3
-
17
-
-
0029960330
-
Midbrain development induced by FGF8 in the chick embryo
-
Crossley, P. H., Martinez, S. Martin, G. R. 1996. Midbrain development induced by FGF8 in the chick embryo. Nature 380, 66 68.
-
(1996)
Nature
, vol.380
, pp. 66-68
-
-
Crossley, P.H.1
Martinez, S.2
Martin, G.R.3
-
18
-
-
0031938573
-
DeLIMiting development
-
Curtiss, J. Heilig, J. S. 1998. DeLIMiting development. Bioessays 20, 58 69.
-
(1998)
Bioessays
, vol.20
, pp. 58-69
-
-
Curtiss, J.1
Heilig, J.S.2
-
19
-
-
0031454063
-
Novel regulatory interactions revealed by studies of murine limb pattern in Wnt-7a and En-1 mutants
-
Cygan, J. A., Johnson, R. L. McMahon, A. P. 1997. Novel regulatory interactions revealed by studies of murine limb pattern in Wnt-7a and En-1 mutants. Development 124, 5021 5032.
-
(1997)
Development
, vol.124
, pp. 5021-5032
-
-
Cygan, J.A.1
Johnson, R.L.2
McMahon, A.P.3
-
20
-
-
50149116967
-
Enhanced contextual fear memory in central serotonin-deficient mice
-
Dai, J. X., Han, H. L., Tian, M., Cao, J., Xiu, J. B., Song, N. N., Huang, Y., Xu, T., Ding, Y. Q. Xu, L. 2008a. Enhanced contextual fear memory in central serotonin-deficient mice. Proc. Natl Acad. Sci. USA 105, 11981 11986.
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 11981-11986
-
-
Dai, J.X.1
Han, H.L.2
Tian, M.3
Cao, J.4
Xiu, J.B.5
Song, N.N.6
Huang, Y.7
Xu, T.8
Ding, Y.Q.9
Xu, L.10
-
21
-
-
48249157067
-
Postnatal ontogeny of the transcription factor Lmx1b in the mouse central nervous system
-
Dai, J. X., Hu, Z. L., Shi, M., Guo, C. Ding, Y. Q. 2008b. Postnatal ontogeny of the transcription factor Lmx1b in the mouse central nervous system. J. Comp. Neurol. 509, 341 355.
-
(2008)
J. Comp. Neurol.
, vol.509
, pp. 341-355
-
-
Dai, J.X.1
Hu, Z.L.2
Shi, M.3
Guo, C.4
Ding, Y.Q.5
-
22
-
-
0042360269
-
Lmx1b is essential for the development of serotonergic neurons
-
Ding, Y. Q., Marklund, U., Yuan, W., Yin, J., Wegman, L., Ericson, J., Deneris, E., Johnson, R. L. Chen, Z. F. 2003. Lmx1b is essential for the development of serotonergic neurons. Nat. Neurosci. 6, 933 938.
-
(2003)
Nat. Neurosci.
, vol.6
, pp. 933-938
-
-
Ding, Y.Q.1
Marklund, U.2
Yuan, W.3
Yin, J.4
Wegman, L.5
Ericson, J.6
Deneris, E.7
Johnson, R.L.8
Chen, Z.F.9
-
23
-
-
4444239058
-
Lmx1b controls the differentiation and migration of the superficial dorsal horn neurons of the spinal cord
-
Ding, Y. Q., Yin, J., Kania, A., Zhao, Z. Q., Johnson, R. L. Chen, Z. F. 2004. Lmx1b controls the differentiation and migration of the superficial dorsal horn neurons of the spinal cord. Development 131, 3693 3703.
-
(2004)
Development
, vol.131
, pp. 3693-3703
-
-
Ding, Y.Q.1
Yin, J.2
Kania, A.3
Zhao, Z.Q.4
Johnson, R.L.5
Chen, Z.F.6
-
24
-
-
19744376880
-
Ventral migration of early-born neurons requires Dcc and is essential for the projections of primary afferents in the spinal cord
-
Ding, Y. Q., Kim, J. Y., Xu, Y. S., Rao, Y. Chen, Z. F. 2005. Ventral migration of early-born neurons requires Dcc and is essential for the projections of primary afferents in the spinal cord. Development 132, 2047 2056.
-
(2005)
Development
, vol.132
, pp. 2047-2056
-
-
Ding, Y.Q.1
Kim, J.Y.2
Xu, Y.S.3
Rao, Y.4
Chen, Z.F.5
-
25
-
-
0027477275
-
Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities
-
Dressler, G. R., Wilkinson, J. E., Rothenpieler, U. W., Patterson, L. T., Williams-Simons, L. Westphal, H. 1993. Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities. Nature 362, 65 67.
-
(1993)
Nature
, vol.362
, pp. 65-67
-
-
Dressler, G.R.1
Wilkinson, J.E.2
Rothenpieler, U.W.3
Patterson, L.T.4
Williams-Simons, L.5
Westphal, H.6
-
26
-
-
0031800728
-
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome
-
Dreyer, S. D., Zhou, G., Baldini, A., Winterpacht, A., Zabel, B., Cole, W., Johnson, R. L. Lee, B. 1998. Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome. Nat. Genet. 19, 47 50.
-
(1998)
Nat. Genet.
, vol.19
, pp. 47-50
-
-
Dreyer, S.D.1
Zhou, G.2
Baldini, A.3
Winterpacht, A.4
Zabel, B.5
Cole, W.6
Johnson, R.L.7
Lee, B.8
-
27
-
-
0034639927
-
LMX1B transactivation and expression in nail-patella syndrome
-
Dreyer, S. D., Morello, R., German, M. S., Zabel, B., Winterpacht, A., Lunstrum, G. P., Horton, W. A., Oberg, K. C. Lee, B. 2000. LMX1B transactivation and expression in nail-patella syndrome. Hum. Mol. Genet. 9, 1067 1074.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1067-1074
-
-
Dreyer, S.D.1
Morello, R.2
German, M.S.3
Zabel, B.4
Winterpacht, A.5
Lunstrum, G.P.6
Horton, W.A.7
Oberg, K.C.8
Lee, B.9
-
28
-
-
3843076445
-
The human LMX1B gene: Transcription unit, promoter, and pathogenic mutations
-
Dunston, J. A., Hamlington, J. D., Zaveri, J., Sweeney, E., Sibbring, J., Tran, C., Malbroux, M., O'Neill, J. P., Mountford, R. McIntosh, I. 2004. The human LMX1B gene: transcription unit, promoter, and pathogenic mutations. Genomics 84, 565 576.
-
(2004)
Genomics
, vol.84
, pp. 565-576
-
-
Dunston, J.A.1
Hamlington, J.D.2
Zaveri, J.3
Sweeney, E.4
Sibbring, J.5
Tran, C.6
Malbroux, M.7
O'Neill, J.P.8
Mountford, R.9
McIntosh, I.10
-
29
-
-
14944347438
-
A neurological phenotype in nail patella syndrome (NPS) patients illuminated by studies of murine Lmx1b expression
-
Dunston, J. A., Reimschisel, T., Ding, Y. Q., Sweeney, E., Johnson, R. L., Chen, Z. F. McIntosh, I. 2005. A neurological phenotype in nail patella syndrome (NPS) patients illuminated by studies of murine Lmx1b expression. Eur. J. Hum. Genet. 13, 330 335.
-
(2005)
Eur. J. Hum. Genet.
, vol.13
, pp. 330-335
-
-
Dunston, J.A.1
Reimschisel, T.2
Ding, Y.Q.3
Sweeney, E.4
Johnson, R.L.5
Chen, Z.F.6
McIntosh, I.7
-
30
-
-
0031012353
-
Mutations of the TWIST gene in the Saethre-Chotzen syndrome
-
El Ghouzzi, V., Le Merrer, M., Perrin-Schmitt, F., Lajeunie, E., Benit, P., Renier, D., Bourgeois, P., Bolcato-Bellemin, A. L., Munnich, A. Bonaventure, J. 1997. Mutations of the TWIST gene in the Saethre-Chotzen syndrome. Nat. Genet. 15, 42 46.
-
(1997)
Nat. Genet.
, vol.15
, pp. 42-46
-
-
El Ghouzzi, V.1
Le Merrer, M.2
Perrin-Schmitt, F.3
Lajeunie, E.4
Benit, P.5
Renier, D.6
Bourgeois, P.7
Bolcato-Bellemin, A.L.8
Munnich, A.9
Bonaventure, J.10
-
31
-
-
35848965234
-
Renal phenotype in heterozygous Lmx1b knockout mice (Lmx1b+/-) after unilateral nephrectomy
-
Endele, S., Klein, S., Richter, S., Molter, T., Amann, K., Klanke, B., Witzgall, R., Johnson, R. L., Hilgers, K. F. Winterpacht, A. 2007. Renal phenotype in heterozygous Lmx1b knockout mice (Lmx1b+/-) after unilateral nephrectomy. Transgenic Res. 16, 723 729.
-
(2007)
Transgenic Res.
, vol.16
, pp. 723-729
-
-
Endele, S.1
Klein, S.2
Richter, S.3
Molter, T.4
Amann, K.5
Klanke, B.6
Witzgall, R.7
Johnson, R.L.8
Hilgers, K.F.9
Winterpacht, A.10
-
32
-
-
0035514175
-
Molecular genetics of familial hypercholesterolemia in Spain: Ten novel LDLR mutations and population analysis
-
Garcia-Garcia, A. B., Real, J. T., Puig, O., Cebolla, E., Marin-Garcia, P., Martinez Ferrandis, J. I., Garcia-Sogo, M., Civera, M., Ascaso, J. F., Carmena, R., Armengod, M. E. Chaves, F. J. 2001. Molecular genetics of familial hypercholesterolemia in Spain: ten novel LDLR mutations and population analysis. Hum. Mutat. 18, 458 459.
-
(2001)
Hum. Mutat.
, vol.18
, pp. 458-459
-
-
Garcia-Garcia, A.B.1
Real, J.T.2
Puig, O.3
Cebolla, E.4
Marin-Garcia, P.5
Martinez Ferrandis, J.I.6
Garcia-Sogo, M.7
Civera, M.8
Ascaso, J.F.9
Carmena, R.10
Armengod, M.E.11
Chaves, F.J.12
-
33
-
-
0037118252
-
Lbx1 specifies somatosensory association interneurons in the dorsal spinal cord
-
Gross, M. K., Dottori, M. Goulding, M. 2002. Lbx1 specifies somatosensory association interneurons in the dorsal spinal cord. Neuron 34, 535 549.
-
(2002)
Neuron
, vol.34
, pp. 535-549
-
-
Gross, M.K.1
Dottori, M.2
Goulding, M.3
-
34
-
-
33846983932
-
Lmx1b is essential for Fgf8 and Wnt1 expression in the isthmic organizer during tectum and cerebellum development in mice
-
Guo, C., Qiu, H. Y., Huang, Y., Chen, H., Yang, R. Q., Chen, S. D., Johnson, R. L., Chen, Z. F. Ding, Y. Q. 2007. Lmx1b is essential for Fgf8 and Wnt1 expression in the isthmic organizer during tectum and cerebellum development in mice. Development 134, 317 325.
-
(2007)
Development
, vol.134
, pp. 317-325
-
-
Guo, C.1
Qiu, H.Y.2
Huang, Y.3
Chen, H.4
Yang, R.Q.5
Chen, S.D.6
Johnson, R.L.7
Chen, Z.F.8
Ding, Y.Q.9
-
35
-
-
58149385607
-
Lmx1b-controlled isthmic organizer is essential for development of midbrain dopaminergic neurons
-
Guo, C., Qiu, H., Shi, M., Huang, Y., Johnson, R. L., Rubinstein, M., Chen, S. D. Ding, Y. Q. 2008. Lmx1b-controlled isthmic organizer is essential for development of midbrain dopaminergic neurons. J. Neurosci. 28, 14097 14106.
-
(2008)
J. Neurosci.
, vol.28
, pp. 14097-14106
-
-
Guo, C.1
Qiu, H.2
Shi, M.3
Huang, Y.4
Johnson, R.L.5
Rubinstein, M.6
Chen, S.D.7
Ding, Y.Q.8
-
36
-
-
0035512277
-
Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patients
-
Hamlington, J. D., Jones, C. Mcintosh, I. 2001. Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patients. Hum. Mutat. 18, 458.
-
(2001)
Hum. Mutat.
, vol.18
, pp. 458
-
-
Hamlington, J.D.1
Jones, C.2
McIntosh, I.3
-
37
-
-
0037320689
-
Specification of dorsal spinal cord interneurons
-
Helms, A. W. Johnson, J. E. 2003. Specification of dorsal spinal cord interneurons. Curr. Opin. Neurobiol. 13, 42 49.
-
(2003)
Curr. Opin. Neurobiol.
, vol.13
, pp. 42-49
-
-
Helms, A.W.1
Johnson, J.E.2
-
38
-
-
0032913942
-
The Caenorhabditis elegans lim-6 LIM homeobox gene regulates neurite outgrowth and function of particular GABAergic neurons
-
Hobert, O., Tessmar, K. Ruvkun, G. 1999. The Caenorhabditis elegans lim-6 LIM homeobox gene regulates neurite outgrowth and function of particular GABAergic neurons. Development 126, 1547 1562.
-
(1999)
Development
, vol.126
, pp. 1547-1562
-
-
Hobert, O.1
Tessmar, K.2
Ruvkun, G.3
-
39
-
-
0033041178
-
Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene
-
Hong, H. K., Lass, J. H. Chakravarti, A. 1999. Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum. Mol. Genet. 8, 625 637.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 625-637
-
-
Hong, H.K.1
Lass, J.H.2
Chakravarti, A.3
-
40
-
-
0031021336
-
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome
-
Howard, T. D., Paznekas, W. A., Green, E. D., Chiang, L. C., Ma, N., Ortiz de Luna, R. I., Garcia Delgado, C., Gonzalez-Ramos, M., Kline, A. D. Jabs, E. W. 1997. Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome. Nat. Genet. 15, 36 41.
-
(1997)
Nat. Genet.
, vol.15
, pp. 36-41
-
-
Howard, T.D.1
Paznekas, W.A.2
Green, E.D.3
Chiang, L.C.4
Ma, N.5
Ortiz De Luna, R.I.6
Garcia Delgado, C.7
Gonzalez-Ramos, M.8
Kline, A.D.9
Jabs, E.W.10
-
41
-
-
0034674302
-
Developmental expression of maf-1 messenger ribonucleic acids in rat kidney by in situ hybridization histochemistry
-
Imaki, J., Onodera, H., Tsuchiya, K., Imaki, T., Mochizuki, T., Mishima, T., Yamashita, K., Yoshida, K. Sakai, M. 2000. Developmental expression of maf-1 messenger ribonucleic acids in rat kidney by in situ hybridization histochemistry. Biochem. Biophys. Res. Commun. 272, 777 782.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.272
, pp. 777-782
-
-
Imaki, J.1
Onodera, H.2
Tsuchiya, K.3
Imaki, T.4
Mochizuki, T.5
Mishima, T.6
Yamashita, K.7
Yoshida, K.8
Sakai, M.9
-
42
-
-
0027431005
-
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
-
Jabs, E. W., Muller, U., Li, X., Ma, L., Luo, W., Haworth, I. S., Klisak, I., Sparkes, R., Warman, M. L., Mulliken, J. B., Snead, M. L. Maxson, R. 1993. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 75, 443 450.
-
(1993)
Cell
, vol.75
, pp. 443-450
-
-
Jabs, E.W.1
Muller, U.2
Li, X.3
Ma, L.4
Luo, W.5
Haworth, I.S.6
Klisak, I.7
Sparkes, R.8
Warman, M.L.9
Mulliken, J.B.10
Snead, M.L.11
Maxson, R.12
-
43
-
-
0026515597
-
Structure and function of the brain serotonin system
-
Jacobs, B. L. Azmitia, E. C. 1992. Structure and function of the brain serotonin system. Physiol. Rev. 72, 165 229.
-
(1992)
Physiol. Rev.
, vol.72
, pp. 165-229
-
-
Jacobs, B.L.1
Azmitia, E.C.2
-
44
-
-
0033711978
-
Otx2, Gbx2 and Fgf8 interact to position and maintain a mid-hindbrain organizer
-
Joyner, A. L., Liu, A. Millet, S. 2000. Otx2, Gbx2 and Fgf8 interact to position and maintain a mid-hindbrain organizer. Curr. Opin. Cell Biol. 12, 736 741.
-
(2000)
Curr. Opin. Cell Biol.
, vol.12
, pp. 736-741
-
-
Joyner, A.L.1
Liu, A.2
Millet, S.3
-
45
-
-
0038012646
-
Topographic motor projections in the limb imposed by LIM homeodomain protein regulation of ephrin-A: EphA interactions
-
Kania, A. Jessell, T. M. 2003. Topographic motor projections in the limb imposed by LIM homeodomain protein regulation of ephrin-A: EphA interactions. Neuron 38, 581 596.
-
(2003)
Neuron
, vol.38
, pp. 581-596
-
-
Kania, A.1
Jessell, T.M.2
-
46
-
-
0034697955
-
Coordinate roles for LIM homeobox genes in directing the dorsoventral trajectory of motor axons in the vertebrate limb
-
Kania, A., Johnson, R. L. Jessell, T. M. 2000. Coordinate roles for LIM homeobox genes in directing the dorsoventral trajectory of motor axons in the vertebrate limb. Cell 102, 161 173.
-
(2000)
Cell
, vol.102
, pp. 161-173
-
-
Kania, A.1
Johnson, R.L.2
Jessell, T.M.3
-
47
-
-
0033566179
-
The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye
-
Kidson, S. H., Kume, T., Deng, K., Winfrey, V. Hogan, B. L. 1999. The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye. Dev. Biol. 211, 306 322.
-
(1999)
Dev. Biol.
, vol.211
, pp. 306-322
-
-
Kidson, S.H.1
Kume, T.2
Deng, K.3
Winfrey, V.4
Hogan, B.L.5
-
48
-
-
42149140677
-
Identification of genes controlled by LMX1B in the developing mouse limb bud
-
Krawchuk, D. Kania, A. 2008. Identification of genes controlled by LMX1B in the developing mouse limb bud. Dev. Dyn. 237, 1183 1192.
-
(2008)
Dev. Dyn.
, vol.237
, pp. 1183-1192
-
-
Krawchuk, D.1
Kania, A.2
-
49
-
-
0027182741
-
WT-1 is required for early kidney development
-
Kreidberg, J. A., Sariola, H., Loring, J. M., Maeda, M., Pelletier, J., Housman, D. Jaenisch, R. 1993. WT-1 is required for early kidney development. Cell 74, 679 691.
-
(1993)
Cell
, vol.74
, pp. 679-691
-
-
Kreidberg, J.A.1
Sariola, H.2
Loring, J.M.3
Maeda, M.4
Pelletier, J.5
Housman, D.6
Jaenisch, R.7
-
50
-
-
0033985592
-
Minimal phenotype of mice homozygous for a null mutation in the forkhead/winged helix gene, Mf2
-
Kume, T., Deng, K. Hogan, B. L. 2000. Minimal phenotype of mice homozygous for a null mutation in the forkhead/winged helix gene, Mf2. Mol. Cell. Biol. 20, 1419 1425.
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 1419-1425
-
-
Kume, T.1
Deng, K.2
Hogan, B.L.3
-
51
-
-
0030825171
-
Cosegregation of open-angle glaucoma and the nail-patella syndrome
-
Lichter, P. R., Richards, J. E., Downs, C. A., Stringham, H. M., Boehnke, M. Farley, F. A. 1997. Cosegregation of open-angle glaucoma and the nail-patella syndrome. Am. J. Ophthalmol. 124, 506 515.
-
(1997)
Am. J. Ophthalmol.
, vol.124
, pp. 506-515
-
-
Lichter, P.R.1
Richards, J.E.2
Downs, C.A.3
Stringham, H.M.4
Boehnke, M.5
Farley, F.A.6
-
52
-
-
0028926095
-
DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutations
-
Little, M., Holmes, G., Bickmore, W., Van Heyningen, V., Hastie, N. Wainwright, B. 1995. DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutations. Hum. Mol. Genet. 4, 351 358.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 351-358
-
-
Little, M.1
Holmes, G.2
Bickmore, W.3
Van Heyningen, V.4
Hastie, N.5
Wainwright, B.6
-
53
-
-
0027175810
-
Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion
-
Little, M. H., Williamson, K. A., Mannens, M., Kelsey, A., Gosden, C., Hastie, N. D. van Heyningen, V. 1993. Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion. Hum. Mol. Genet. 2, 259 264.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 259-264
-
-
Little, M.H.1
Williamson, K.A.2
Mannens, M.3
Kelsey, A.4
Gosden, C.5
Hastie, N.D.6
Van Heyningen, V.7
-
54
-
-
0029772359
-
The mouse Engrailed-1 gene and ventral limb patterning
-
Loomis, C. A., Harris, E., Michaud, J., Wurst, W., Hanks, M. Joyner, A. L. 1996. The mouse Engrailed-1 gene and ventral limb patterning. Nature 382, 360 363.
-
(1996)
Nature
, vol.382
, pp. 360-363
-
-
Loomis, C.A.1
Harris, E.2
Michaud, J.3
Wurst, W.4
Hanks, M.5
Joyner, A.L.6
-
55
-
-
0031919712
-
Analysis of the genetic pathway leading to formation of ectopic apical ectodermal ridges in mouse Engrailed-1 mutant limbs
-
Loomis, C. A., Kimmel, R. A., Tong, C. X., Michaud, J. Joyner, A. L. 1998. Analysis of the genetic pathway leading to formation of ectopic apical ectodermal ridges in mouse Engrailed-1 mutant limbs. Development 125, 1137 1148.
-
(1998)
Development
, vol.125
, pp. 1137-1148
-
-
Loomis, C.A.1
Kimmel, R.A.2
Tong, C.X.3
Michaud, J.4
Joyner, A.L.5
-
56
-
-
0032145210
-
The spectrum of behaviors influenced by serotonin
-
Lucki, I. 1998. The spectrum of behaviors influenced by serotonin. Biol. Psychiatry 44, 151 162.
-
(1998)
Biol. Psychiatry
, vol.44
, pp. 151-162
-
-
Lucki, I.1
-
57
-
-
0032908043
-
FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression
-
Martinez, S., Crossley, P. H., Cobos, I., Rubenstein, J. L. Martin, G. R. 1999. FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. Development 126, 1189 1200.
-
(1999)
Development
, vol.126
, pp. 1189-1200
-
-
Martinez, S.1
Crossley, P.H.2
Cobos, I.3
Rubenstein, J.L.4
Martin, G.R.5
-
58
-
-
0036860674
-
Role of Lmx1b and Wnt1 in mesencephalon and metencephalon development
-
Matsunaga, E., Katahira, T. Nakamura, H. 2002. Role of Lmx1b and Wnt1 in mesencephalon and metencephalon development. Development 129, 5269 5277.
-
(2002)
Development
, vol.129
, pp. 5269-5277
-
-
Matsunaga, E.1
Katahira, T.2
Nakamura, H.3
-
59
-
-
0032471924
-
Mutation analysis of LMX1B gene in nail-patella syndrome patients
-
Mcintosh, I., Dreyer, S. D., Clough, M. V., Dunston, J. A., Eyaid, W., Roig, C. M., Montgomery, T., Ala-Mello, S., Kaitila, I., Winterpacht, A., Zabel, B., Frydman, M., Cole, W. G., Francomano, C. A. Lee, B. 1998. Mutation analysis of LMX1B gene in nail-patella syndrome patients. Am. J. Hum. Genet. 63, 1651 1658.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1651-1658
-
-
McIntosh, I.1
Dreyer, S.D.2
Clough, M.V.3
Dunston, J.A.4
Eyaid, W.5
Roig, C.M.6
Montgomery, T.7
Ala-Mello, S.8
Kaitila, I.9
Winterpacht, A.10
Zabel, B.11
Frydman, M.12
Cole, W.G.13
Francomano, C.A.14
Lee, B.15
-
60
-
-
34248183058
-
Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma
-
Milla, E., Hernan, I., Gamundi, M. J., Martinez-Gimeno, M. Carballo, M. 2007. Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma. Mol. Vis. 13, 639 648.
-
(2007)
Mol. Vis.
, vol.13
, pp. 639-648
-
-
Milla, E.1
Hernan, I.2
Gamundi, M.J.3
Martinez-Gimeno, M.4
Carballo, M.5
-
61
-
-
0034677480
-
The mouse dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS
-
Millonig, J. H., Millen, K. J. Hatten, M. E. 2000. The mouse dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS. Nature 403, 764 769.
-
(2000)
Nature
, vol.403
, pp. 764-769
-
-
Millonig, J.H.1
Millen, K.J.2
Hatten, M.E.3
-
62
-
-
33845271685
-
Nail-patella syndrome and its association with glaucoma: A review of eight families
-
Mimiwati, Z., Mackey, D. A., Craig, J. E., Mackinnon, J. R., Rait, J. L., Liebelt, J. E., Ayala-Lugo, R., Vollrath, D. Richards, J. E. 2006. Nail-patella syndrome and its association with glaucoma: a review of eight families. Br. J. Ophthalmol. 90, 1505 1509.
-
(2006)
Br. J. Ophthalmol.
, vol.90
, pp. 1505-1509
-
-
Mimiwati, Z.1
MacKey, D.A.2
Craig, J.E.3
MacKinnon, J.R.4
Rait, J.L.5
Liebelt, J.E.6
Ayala-Lugo, R.7
Vollrath, D.8
Richards, J.E.9
-
63
-
-
24644524228
-
Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome
-
Miyamoto, T., Inoue, H., Sakamoto, Y., Kudo, E., Naito, T., Mikawa, T., Mikawa, Y., Isashiki, Y., Osabe, D., Shinohara, S., Shiota, H. Itakura, M. 2005. Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome. Invest. Ophthalmol. Vis. Sci. 46, 2726 2735.
-
(2005)
Invest. Ophthalmol. Vis. Sci.
, vol.46
, pp. 2726-2735
-
-
Miyamoto, T.1
Inoue, H.2
Sakamoto, Y.3
Kudo, E.4
Naito, T.5
Mikawa, T.6
Mikawa, Y.7
Isashiki, Y.8
Osabe, D.9
Shinohara, S.10
Shiota, H.11
Itakura, M.12
-
64
-
-
0035134740
-
Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome
-
Morello, R., Zhou, G., Dreyer, S. D., Harvey, S. J., Ninomiya, Y., Thorner, P. S., Miner, J. H., Cole, W., Winterpacht, A., Zabel, B., Oberg, K. C. Lee, B. 2001. Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome. Nat. Genet. 27, 205 208.
-
(2001)
Nat. Genet.
, vol.27
, pp. 205-208
-
-
Morello, R.1
Zhou, G.2
Dreyer, S.D.3
Harvey, S.J.4
Ninomiya, Y.5
Thorner, P.S.6
Miner, J.H.7
Cole, W.8
Winterpacht, A.9
Zabel, B.10
Oberg, K.C.11
Lee, B.12
-
65
-
-
0037118260
-
The homeodomain factor lbx1 distinguishes two major programs of neuronal differentiation in the dorsal spinal cord
-
Muller, T., Brohmann, H., Pierani, A., Heppenstall, P. A., Lewin, G. R., Jessell, T. M. Birchmeier, C. 2002. The homeodomain factor lbx1 distinguishes two major programs of neuronal differentiation in the dorsal spinal cord. Neuron 34, 551 562.
-
(2002)
Neuron
, vol.34
, pp. 551-562
-
-
Muller, T.1
Brohmann, H.2
Pierani, A.3
Heppenstall, P.A.4
Lewin, G.R.5
Jessell, T.M.6
Birchmeier, C.7
-
66
-
-
23844467826
-
Isthmus organizer for midbrain and hindbrain development
-
Nakamura, H., Katahira, T., Matsunaga, E. Sato, T. 2005. Isthmus organizer for midbrain and hindbrain development. Brain. Res. Brain. Res. Rev. 49, 120 126.
-
(2005)
Brain. Res. Brain. Res. Rev.
, vol.49
, pp. 120-126
-
-
Nakamura, H.1
Katahira, T.2
Matsunaga, E.3
Sato, T.4
-
67
-
-
44249096162
-
Isthmus organizer for mesencephalon and metencephalon
-
Nakamura, H., Sato, T. Suzuki-Hirano, A. 2008. Isthmus organizer for mesencephalon and metencephalon. Dev. Growth. Differ. 50 (Suppl. 1 S113 S118.
-
(2008)
Dev. Growth. Differ.
, vol.50
, Issue.SUPPL. 1
-
-
Nakamura, H.1
Sato, T.2
Suzuki-Hirano, A.3
-
68
-
-
0033817761
-
A review of the role of serotonin receptors in psychiatric disorders
-
Naughton, M., Mulrooney, J. B. Leonard, B. E. 2000. A review of the role of serotonin receptors in psychiatric disorders. Hum. Psychopharmacol. 15, 397 415.
-
(2000)
Hum. Psychopharmacol.
, vol.15
, pp. 397-415
-
-
Naughton, M.1
Mulrooney, J.B.2
Leonard, B.E.3
-
69
-
-
23844515060
-
Zebrafish Lmx1b.1 and Lmx1b.2 are required for maintenance of the isthmic organizer
-
O'hara, F. P., Beck, E., Barr, L. K., Wong, L. L., Kessler, D. S. Riddle, R. D. 2005. Zebrafish Lmx1b.1 and Lmx1b.2 are required for maintenance of the isthmic organizer. Development 132, 3163 3173.
-
(2005)
Development
, vol.132
, pp. 3163-3173
-
-
O'Hara, F.P.1
Beck, E.2
Barr, L.K.3
Wong, L.L.4
Kessler, D.S.5
Riddle, R.D.6
-
70
-
-
34848896595
-
Differences in neurogenic potential in floor plate cells along an anteroposterior location: Midbrain dopaminergic neurons originate from mesencephalic floor plate cells
-
Ono, Y., Nakatani, T. Sakamoto, Y. 2007. Differences in neurogenic potential in floor plate cells along an anteroposterior location: midbrain dopaminergic neurons originate from mesencephalic floor plate cells. Development 134, 3213 3225.
-
(2007)
Development
, vol.134
, pp. 3213-3225
-
-
Ono, Y.1
Nakatani, T.2
Sakamoto, Y.3
-
71
-
-
0028850292
-
Cranial sutures require tissue interactions with dura mater to resist osseous obliteration in vitro
-
Opperman, L. A., Passarelli, R. W., Morgan, E. P., Reintjes, M. Ogle, R. C. 1995. Cranial sutures require tissue interactions with dura mater to resist osseous obliteration in vitro. J. Bone Miner. Res. 10, 1978 1987.
-
(1995)
J. Bone Miner. Res.
, vol.10
, pp. 1978-1987
-
-
Opperman, L.A.1
Passarelli, R.W.2
Morgan, E.P.3
Reintjes, M.4
Ogle, R.C.5
-
72
-
-
0034090670
-
LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye
-
Pressman, C. L., Chen, H. Johnson, R. L. 2000. LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye. Genesis 26, 15 25.
-
(2000)
Genesis
, vol.26
, pp. 15-25
-
-
Pressman, C.L.1
Chen, H.2
Johnson, R.L.3
-
73
-
-
0033393087
-
The basic-helix-loop-helix protein pod1 is critically important for kidney and lung organogenesis
-
Quaggin, S. E., Schwartz, L., Cui, S., Igarashi, P., Deimling, J., Post, M. Rossant, J. 1999. The basic-helix-loop-helix protein pod1 is critically important for kidney and lung organogenesis. Development 126, 5771 5783.
-
(1999)
Development
, vol.126
, pp. 5771-5783
-
-
Quaggin, S.E.1
Schwartz, L.2
Cui, S.3
Igarashi, P.4
Deimling, J.5
Post, M.6
Rossant, J.7
-
74
-
-
0028848301
-
Induction of the LIM homeobox gene Lmx1 by WNT7a establishes dorsoventral pattern in the vertebrate limb
-
Riddle, R. D., Ensini, M., Nelson, C., Tsuchida, T., Jessell, T. M. Tabin, C. 1995. Induction of the LIM homeobox gene Lmx1 by WNT7a establishes dorsoventral pattern in the vertebrate limb. Cell 83, 631 640.
-
(1995)
Cell
, vol.83
, pp. 631-640
-
-
Riddle, R.D.1
Ensini, M.2
Nelson, C.3
Tsuchida, T.4
Jessell, T.M.5
Tabin, C.6
-
75
-
-
0036117988
-
The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes
-
Rohr, C., Prestel, J., Heidet, L., Hosser, H., Kriz, W., Johnson, R. L., Antignac, C. Witzgall, R. 2002. The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes. J. Clin. Invest. 109, 1073 1082.
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 1073-1082
-
-
Rohr, C.1
Prestel, J.2
Heidet, L.3
Hosser, H.4
Kriz, W.5
Johnson, R.L.6
Antignac, C.7
Witzgall, R.8
-
76
-
-
0027172452
-
Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformations
-
Schneider, S., Wildhardt, G., Ludwig, R. Royer-Pokora, B. 1993. Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformations. Hum. Genet. 91, 599 604.
-
(1993)
Hum. Genet.
, vol.91
, pp. 599-604
-
-
Schneider, S.1
Wildhardt, G.2
Ludwig, R.3
Royer-Pokora, B.4
-
77
-
-
0033192624
-
Identification of LMX1B gene point mutations in Italian patients affected with Nail-Patella syndrome
-
Seri, M., Melchionda, S., Dreyer, S., Marini, M., Carella, M., Cusano, R., Piemontese, M. R., Caroli, F., Silengo, M., Zelante, L., Romeo, G., Ravazzolo, R., Gasparini, P. Lee, B. 1999. Identification of LMX1B gene point mutations in Italian patients affected with Nail-Patella syndrome. Int. J. Mol. Med. 4, 285 290.
-
(1999)
Int. J. Mol. Med.
, vol.4
, pp. 285-290
-
-
Seri, M.1
Melchionda, S.2
Dreyer, S.3
Marini, M.4
Carella, M.5
Cusano, R.6
Piemontese, M.R.7
Caroli, F.8
Silengo, M.9
Zelante, L.10
Romeo, G.11
Ravazzolo, R.12
Gasparini, P.13
Lee, B.14
-
78
-
-
0014108839
-
The Nail-Patella syndrome. Clinical findings and ultrastructural observations in the kidney
-
Silverman, M. E., Goodman, R. M. Cuppage, F. E. 1967. The Nail-Patella syndrome. Clinical findings and ultrastructural observations in the kidney. Arch. Intern. Med. 120, 68 74.
-
(1967)
Arch. Intern. Med.
, vol.120
, pp. 68-74
-
-
Silverman, M.E.1
Goodman, R.M.2
Cuppage, F.E.3
-
79
-
-
0034034739
-
A second independent pathway for development of mesencephalic dopaminergic neurons requires Lmx1b
-
Smidt, M. P., Asbreuk, C. H., Cox, J. J., Chen, H., Johnson, R. L. Burbach, J. P. 2000. A second independent pathway for development of mesencephalic dopaminergic neurons requires Lmx1b. Nat. Neurosci. 3, 337 341.
-
(2000)
Nat. Neurosci.
, vol.3
, pp. 337-341
-
-
Smidt, M.P.1
Asbreuk, C.H.2
Cox, J.J.3
Chen, H.4
Johnson, R.L.5
Burbach, J.P.6
-
80
-
-
34047144364
-
The podocyte-specific inactivation of Lmx1b, Ldb1 and E2a yields new insight into a transcriptional network in podocytes
-
Suleiman, H., Heudobler, D., Raschta, A. S., Zhao, Y., Zhao, Q., Hertting, I., Vitzthum, H., Moeller, M. J., Holzman, L. B., Rachel, R., Johnson, R., Westphal, H., Rascle, A. Witzgall, R. 2007. The podocyte-specific inactivation of Lmx1b, Ldb1 and E2a yields new insight into a transcriptional network in podocytes. Dev. Biol. 304, 701 712.
-
(2007)
Dev. Biol.
, vol.304
, pp. 701-712
-
-
Suleiman, H.1
Heudobler, D.2
Raschta, A.S.3
Zhao, Y.4
Zhao, Q.5
Hertting, I.6
Vitzthum, H.7
Moeller, M.J.8
Holzman, L.B.9
Rachel, R.10
Johnson, R.11
Westphal, H.12
Rascle, A.13
Witzgall, R.14
-
81
-
-
18344407657
-
Inductive tissue interactions, cell signaling, and the control of kidney organogenesis
-
Vainio, S. Muller, U. 1997. Inductive tissue interactions, cell signaling, and the control of kidney organogenesis. Cell 90, 975 978.
-
(1997)
Cell
, vol.90
, pp. 975-978
-
-
Vainio, S.1
Muller, U.2
-
82
-
-
0029563650
-
Dorsal cell fate specified by chick Lmx1 during vertebrate limb development
-
Vogel, A., Rodriguez, C., Warnken, W. Izpisua Belmonte, J. C. 1995. Dorsal cell fate specified by chick Lmx1 during vertebrate limb development. Nature 378, 716 720.
-
(1995)
Nature
, vol.378
, pp. 716-720
-
-
Vogel, A.1
Rodriguez, C.2
Warnken, W.3
Izpisua Belmonte, J.C.4
-
83
-
-
0031750061
-
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome
-
Vollrath, D., Jaramillo-Babb, V. L., Clough, M. V., McIntosh, I., Scott, K. M., Lichter, P. R. Richards, J. E. 1998. Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome. Hum. Mol. Genet. 7, 1091 1098.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1091-1098
-
-
Vollrath, D.1
Jaramillo-Babb, V.L.2
Clough, M.V.3
McIntosh, I.4
Scott, K.M.5
Lichter, P.R.6
Richards, J.E.7
-
84
-
-
0030769180
-
Craniosynostosis: Genes and mechanisms
-
Wilkie, A. O. 1997. Craniosynostosis: genes and mechanisms. Hum. Mol. Genet. 6, 1647 1656.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1647-1656
-
-
Wilkie, A.O.1
-
85
-
-
0035257203
-
Neural plate patterning: Upstream and downstream of the isthmic organizer
-
Wurst, W. Bally-Cuif, L. 2001. Neural plate patterning: upstream and downstream of the isthmic organizer. Nat. Rev. Neurosci. 2, 99 108.
-
(2001)
Nat. Rev. Neurosci.
, vol.2
, pp. 99-108
-
-
Wurst, W.1
Bally-Cuif, L.2
-
86
-
-
33845423914
-
Lmx1b is required for maintenance of central serotonergic neurons and mice lacking central serotonergic system exhibit normal locomotor activity
-
Zhao, Z. Q., Scott, M., Chiechio, S., Wang, J. S., Renner, K. J., Gereau, R. W. th, Johnson, R. L., Deneris, E. S. Chen, Z. F. 2006. Lmx1b is required for maintenance of central serotonergic neurons and mice lacking central serotonergic system exhibit normal locomotor activity. J. Neurosci. 26, 12781 12788.
-
(2006)
J. Neurosci.
, vol.26
, pp. 12781-12788
-
-
Zhao, Z.Q.1
Scott, M.2
Chiechio, S.3
Wang, J.S.4
Renner, K.J.5
Johnson, R.L.6
Deneris, E.S.7
Chen, Z.F.8
-
87
-
-
34249815184
-
Mice lacking central serotonergic neurons show enhanced inflammatory pain and an impaired analgesic response to antidepressant drugs
-
Zhao, Z. Q., Chiechio, S., Sun, Y. G., Zhang, K. H., Zhao, C. S., Scott, M., Johnson, R. L., Deneris, E. S., Renner, K. J., Gereau, R. W. th Chen, Z. F. 2007a. Mice lacking central serotonergic neurons show enhanced inflammatory pain and an impaired analgesic response to antidepressant drugs. J. Neurosci. 27, 6045 6053.
-
(2007)
J. Neurosci.
, vol.27
, pp. 6045-6053
-
-
Zhao, Z.Q.1
Chiechio, S.2
Sun, Y.G.3
Zhang, K.H.4
Zhao, C.S.5
Scott, M.6
Johnson, R.L.7
Deneris, E.S.8
Renner, K.J.9
Chen, Z.F.10
-
88
-
-
35448933250
-
Central serotonergic neurons are differentially required for opioid analgesia but not for morphine tolerance or morphine reward
-
Zhao, Z. Q., Gao, Y. J., Sun, Y. G., Zhao, C. S., Gereau, R. W. th Chen, Z. F. 2007b. Central serotonergic neurons are differentially required for opioid analgesia but not for morphine tolerance or morphine reward. Proc. Natl Acad. Sci. USA 104, 14519 14524.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 14519-14524
-
-
Zhao, Z.Q.1
Gao, Y.J.2
Sun, Y.G.3
Zhao, C.S.4
Chen, Z.F.5
|