-
1
-
-
0000169321
-
The genetic basis of conotruncal cardiac defects: The chromosome 22q11.2 deletion
-
Harvey, R. and Rosenthal, N. (eds), Academic Press, in press
-
Emanuel, B.S., Budarf, M.L. and Scanibler, P.J. (1998) The genetic basis of conotruncal cardiac defects: the chromosome 22q11.2 deletion. In Harvey, R. and Rosenthal, N. (eds), Heart Development. Academic Press, in press.
-
(1998)
Heart Development
-
-
Emanuel, B.S.1
Budarf, M.L.2
Scanibler, P.J.3
-
2
-
-
0021326972
-
Neural crest and normal development: A new perspective
-
Kirby, M.L. and Bockman, D.E. (1984) Neural crest and normal development: a new perspective. Anat. Rec., 209, 1-6.
-
(1984)
Anat. Rec.
, vol.209
, pp. 1-6
-
-
Kirby, M.L.1
Bockman, D.E.2
-
3
-
-
0022939117
-
The DiGeorge anomaly as a developmental field defect
-
Lammer, E.J. and Opitz, J.M. (1986) The DiGeorge anomaly as a developmental field defect. Am. J. Med. Genet., 29, 113-127.
-
(1986)
Am. J. Med. Genet.
, vol.29
, pp. 113-127
-
-
Lammer, E.J.1
Opitz, J.M.2
-
4
-
-
16944364802
-
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
-
Ryan, A.K., Goodship, J.A., Wilson, D.I., Philip, N., Levy, A., Seidel, H., Schuffenhauer, S., Oechlser, H., Belohradsky, B., Prieur, M., Aurias, A., Raymond, F.L., Clayton-Smith, J., Hatchwell, E., McKeown, C., Beemer, F.A., Dallapiccola, B., Novelli, G., Hurst, J.A., Ignatius, J., Green, A.J., Winter, R.M., Brueton, L., Brøndum-Nielsen, K., Stewart, F., Van Essen, T., Patton, M., Paterson, J. and Scambler, P.J. (1997) Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med. Genet., 34, 798-804.
-
(1997)
J Med. Genet.
, vol.34
, pp. 798-804
-
-
Ryan, A.K.1
Goodship, J.A.2
Wilson, D.I.3
Philip, N.4
Levy, A.5
Seidel, H.6
Schuffenhauer, S.7
Oechlser, H.8
Belohradsky, B.9
Prieur, M.10
Aurias, A.11
Raymond, F.L.12
Clayton-Smith, J.13
Hatchwell, E.14
McKeown, C.15
Beemer, F.A.16
Dallapiccola, B.17
Novelli, G.18
Hurst, J.A.19
Ignatius, J.20
Green, A.J.21
Winter, R.M.22
Brueton, L.23
Brøndum-Nielsen, K.24
Stewart, F.25
Van Essen, T.26
Patton, M.27
Paterson, J.28
Scambler, P.J.29
more..
-
5
-
-
0031291657
-
The 22q11.2 deletion: Screening, diagnostic workup and outcome of results; report on 181 patients
-
McDonald-McGinn, D.M., LaRossa, D., Goldmuntz, E., Sullivan, K., Eicher, P., Gerdes, M., Moss, E., Wang, P., Solot, C., Schultz, P., Lynch, D., Bingham, P., Keenan, G., Weinzimer, S., Ming, J.E., Driscoll, D., Clark, B.J., Markowitz, R., Cohen, A., Moshand, T., Pasquariello, P., Randall, P., Emanuel, B.S. and Zackai, E.H. (1997) The 22q11.2 deletion: screening, diagnostic workup and outcome of results; report on 181 patients. Genet. Testing, 1, 99-108.
-
(1997)
Genet. Testing
, vol.1
, pp. 99-108
-
-
McDonald-McGinn, D.M.1
LaRossa, D.2
Goldmuntz, E.3
Sullivan, K.4
Eicher, P.5
Gerdes, M.6
Moss, E.7
Wang, P.8
Solot, C.9
Schultz, P.10
Lynch, D.11
Bingham, P.12
Keenan, G.13
Weinzimer, S.14
Ming, J.E.15
Driscoll, D.16
Clark, B.J.17
Markowitz, R.18
Cohen, A.19
Moshand, T.20
Pasquariello, P.21
Randall, P.22
Emanuel, B.S.23
Zackai, E.H.24
more..
-
6
-
-
0031040868
-
Cloning and developmental expression analysis of chick Hira (Chira). a candidate gene for DiGeorge syndrome
-
Roberts, C., Daw, S.C.M., Halford, S. and Scambler, P.J. (1997) Cloning and developmental expression analysis of chick Hira (Chira). a candidate gene for DiGeorge syndrome. Hum. Mol. Genet., 6, 237-245.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 237-245
-
-
Roberts, C.1
Daw, S.C.M.2
Halford, S.3
Scambler, P.J.4
-
7
-
-
0031058266
-
The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients
-
Wilming, L.G., Snoeren, C.A.S., Van Rijswijk, A., Grosveld, F. and Meijers. C. (1997) The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients. Hum. Mol. Genet., 6, 247-258.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 247-258
-
-
Wilming, L.G.1
Snoeren, C.A.S.2
Van Rijswijk, A.3
Grosveld, F.4
Meijers, C.5
-
8
-
-
0031136322
-
Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein
-
Taylor, C., Wadey, R., O'Donnell, H., Roberts, C., Mattei, M., Kimber, W.L., Wynshaw-Boris, A. and Scambler, P.J. (1997) Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein. Mamm. Genome, 8, 371-375.
-
(1997)
Mamm. Genome
, vol.8
, pp. 371-375
-
-
Taylor, C.1
Wadey, R.2
O'Donnell, H.3
Roberts, C.4
Mattei, M.5
Kimber, W.L.6
Wynshaw-Boris, A.7
Scambler, P.J.8
-
9
-
-
8044247810
-
UFDIL. a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome
-
Pizzutti, A., Novelli, G., Ratti, A., Amati, F., Mari, A., Calabrese, G., Nicolis, S., Silani, V., Marino, B., Scarlato, G., Ottolenghi, S. and Dallapiccola, B. (1997) UFDIL. a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome. Hum. Mol. Genet., 6, 259-265.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 259-265
-
-
Pizzutti, A.1
Novelli, G.2
Ratti, A.3
Amati, F.4
Mari, A.5
Calabrese, G.6
Nicolis, S.7
Silani, V.8
Marino, B.9
Scarlato, G.10
Ottolenghi, S.11
Dallapiccola, B.12
-
10
-
-
0342658137
-
Expression of the T-box family genes, Tbx1-Thx5, during early mouse development
-
Chapman, D.L., Garvey, N., Hancock, S., Alexiou, A., Agulnick, S.I., Gibson-Brown, J.J., Cebra-Thomas, J., Bollag, R.J., Silver, L.M. and Papaioannou, V.E. (1996) Expression of the T-box family genes, Tbx1-Thx5, during early mouse development. Dev. Dyn., 206, 379-390.
-
(1996)
Dev. Dyn.
, vol.206
, pp. 379-390
-
-
Chapman, D.L.1
Garvey, N.2
Hancock, S.3
Alexiou, A.4
Agulnick, S.I.5
Gibson-Brown, J.J.6
Cebra-Thomas, J.7
Bollag, R.J.8
Silver, L.M.9
Papaioannou, V.E.10
-
11
-
-
0031215021
-
Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene
-
Chieffo, C., Garvey, N., Gong, W., Roe, B., Zhang, G., Silver, L., Emanuel, B.S. and Budarf, M.L. (1997) Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene. Genomics, 43, 267-277.
-
(1997)
Genomics
, vol.43
, pp. 267-277
-
-
Chieffo, C.1
Garvey, N.2
Gong, W.3
Roe, B.4
Zhang, G.5
Silver, L.6
Emanuel, B.S.7
Budarf, M.L.8
-
12
-
-
0030940093
-
The DiGeorge syndrome minimal critical region contains a Goosecoid-like homeobox gene that is expressed early in human development
-
Gottlieb, S., Emanuel, B.S., Driscoll, D.S., Sellinger, B., Wang, Z., Roe, B. and Budarf, M.L. (1997) The DiGeorge syndrome minimal critical region contains a Goosecoid-like homeobox gene that is expressed early in human development. Am. J. Hum. Genet., 60, 1194-1201.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1194-1201
-
-
Gottlieb, S.1
Emanuel, B.S.2
Driscoll, D.S.3
Sellinger, B.4
Wang, Z.5
Roe, B.6
Budarf, M.L.7
-
13
-
-
0000071294
-
A comprehensive classification of homeobox genes
-
Duboule, D. (ed.). A Sambrook and Tooze Publication at Oxford University Press
-
Bürglin, T.R. (1994) A comprehensive classification of homeobox genes. In Duboule, D. (ed.). Guidebook to the Homeobox Genes. A Sambrook and Tooze Publication at Oxford University Press, pp. 27-71.
-
(1994)
Guidebook to the Homeobox Genes
, pp. 27-71
-
-
Bürglin, T.R.1
-
14
-
-
0026423012
-
Organizer-specific homeobox genes in Xenopus laevis embryos
-
Blumberg, B., Wright, C.V.E., De Robertis, E.M. and Cho, K.W.Y. (1991) Organizer-specific homeobox genes in Xenopus laevis embryos. Science, 253, 194-196.
-
(1991)
Science
, vol.253
, pp. 194-196
-
-
Blumberg, B.1
Wright, C.V.E.2
De Robertis, E.M.3
Cho, K.W.Y.4
-
15
-
-
0030973366
-
Segregating expression domains of two goosecoid genes during the transition from gastrulation to neurulation in chick embryos
-
Lemaire, L., Roeser, T., Izpisua-Belmonte, J.C. and Kessel, M. (1997) Segregating expression domains of two goosecoid genes during the transition from gastrulation to neurulation in chick embryos. Development. 124, 1443-1452.
-
(1997)
Development
, vol.124
, pp. 1443-1452
-
-
Lemaire, L.1
Roeser, T.2
Izpisua-Belmonte, J.C.3
Kessel, M.4
-
16
-
-
0030008811
-
A functional homologue of goosecoid in Drosophila
-
Goriely, A., Stella, M., Coffinier, C., Kessler, D., Mailhos, C., Dessain, S. and Desplan, C. (1996) A functional homologue of goosecoid in Drosophila. Development, 122, 1641-1660.
-
(1996)
Development
, vol.122
, pp. 1641-1660
-
-
Goriely, A.1
Stella, M.2
Coffinier, C.3
Kessler, D.4
Mailhos, C.5
Dessain, S.6
Desplan, C.7
-
17
-
-
0026649645
-
Gastrulation in the mouse: The role of the homeobox gene goosecoid
-
Blum, M., Gaunt, S.J., Cho, K.W.Y., Steinbeisser, H., Blumberg, B., Bittner, D. and De Robertis, E.M. (1992) Gastrulation in the mouse: the role of the homeobox gene goosecoid. Cell, 69, 1097-1106.
-
(1992)
Cell
, vol.69
, pp. 1097-1106
-
-
Blum, M.1
Gaunt, S.J.2
Cho, K.W.Y.3
Steinbeisser, H.4
Blumberg, B.5
Bittner, D.6
De Robertis, E.M.7
-
18
-
-
0027521087
-
Expression of the mouse goosecoid gene during mid-embryogenesis may mark mesenchymal cell lineages in the developing head, limbs and body wall
-
Gaunt, S.J., Blum, M. and De Robertis, E.M. (1993) Expression of the mouse goosecoid gene during mid-embryogenesis may mark mesenchymal cell lineages in the developing head, limbs and body wall. Development, 117, 769-778.
-
(1993)
Development
, vol.117
, pp. 769-778
-
-
Gaunt, S.J.1
Blum, M.2
De Robertis, E.M.3
-
19
-
-
0029846335
-
A conserved region of engrailed, shared among all en-, gsc-, Nk1-. Nk2- and msh-class homeoproteins, mediates active transcriptional repression in vivo
-
Smith, S.T. and Jaynes, J.B. (1996) A conserved region of engrailed, shared among all en-, gsc-, Nk1-. Nk2- and msh-class homeoproteins, mediates active transcriptional repression in vivo. Development, 122, 3141-3150.
-
(1996)
Development
, vol.122
, pp. 3141-3150
-
-
Smith, S.T.1
Jaynes, J.B.2
-
20
-
-
0031937851
-
Drosophila Goosecoid requires a conserved heptapeptide for repression of Paired-class homeoprotein activators
-
Mailhos, C., André, S., Mollereau, B., Goriely, A., Hemmati-Brivanlou, A. and Desplan, C. (1998) Drosophila Goosecoid requires a conserved heptapeptide for repression of Paired-class homeoprotein activators. Development. 125, 937-947.
-
(1998)
Development
, vol.125
, pp. 937-947
-
-
Mailhos, C.1
André, S.2
Mollereau, B.3
Goriely, A.4
Hemmati-Brivanlou, A.5
Desplan, C.6
-
21
-
-
0026342562
-
Molecular nature of Spemann's organizer: The role of the Xenopus homeobox gene goosecoid
-
Cho, K.W.Y., Blumberg, B., Steinbeisser, H. and De Robertis, E.M. (1991) Molecular nature of Spemann's organizer: the role of the Xenopus homeobox gene goosecoid. Cell, 67, 1111-1120.
-
(1991)
Cell
, vol.67
, pp. 1111-1120
-
-
Cho, K.W.Y.1
Blumberg, B.2
Steinbeisser, H.3
De Robertis, E.M.4
-
22
-
-
15144349175
-
A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region
-
Galili, N., Baldwin, H.S., Lund, J., Reeves, R., Gong, W., Wang, Z., Roe, B.A., Emanuel, B.S., Nayak, S., Mickanin, C., Budarf, M.L. and Buck, C.A. (1997) A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region. Genome Res., 7, 17-26.
-
(1997)
Genome Res.
, vol.7
, pp. 17-26
-
-
Galili, N.1
Baldwin, H.S.2
Lund, J.3
Reeves, R.4
Gong, W.5
Wang, Z.6
Roe, B.A.7
Emanuel, B.S.8
Nayak, S.9
Mickanin, C.10
Budarf, M.L.11
Buck, C.A.12
-
23
-
-
0024320441
-
DNA specificity of the bicoid activator protein is determined by homeodomain recognition helix residue 9
-
Hanes, S. and Brent, R. (1989) DNA specificity of the bicoid activator protein is determined by homeodomain recognition helix residue 9. Cell, 57, 1275-1283.
-
(1989)
Cell
, vol.57
, pp. 1275-1283
-
-
Hanes, S.1
Brent, R.2
-
24
-
-
0026023608
-
A genetic model for interaction of the homeodomain recognition helix with DNA
-
Hanes, S.D. and Brent R. (1991). A genetic model for interaction of the homeodomain recognition helix with DNA. Science, 251, 426-430.
-
(1991)
Science
, vol.251
, pp. 426-430
-
-
Hanes, S.D.1
Brent, R.2
-
25
-
-
0024397687
-
A single amino acid can determine the DNA binding specificity of homeodomain proteins
-
Treisman, J., Gonezy, P., Vashishtha, M., Harris, E. and Desplan, C. (1989) A single amino acid can determine the DNA binding specificity of homeodomain proteins. Cell, 59, 553-562.
-
(1989)
Cell
, vol.59
, pp. 553-562
-
-
Treisman, J.1
Gonezy, P.2
Vashishtha, M.3
Harris, E.4
Desplan, C.5
-
26
-
-
0028108227
-
Differential DNA-binding specificity of the Engrailed homeodomain: The role of residue 50
-
Ades, S.E. and Sauer. R.T. (1994) Differential DNA-binding specificity of the Engrailed homeodomain: the role of residue 50. Biochemistry, 33, 9187-9194.
-
(1994)
Biochemistry
, vol.33
, pp. 9187-9194
-
-
Ades, S.E.1
Sauer, R.T.2
-
27
-
-
0031573850
-
Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/ DGS on 22q11
-
Funke, B., Saint-Jore, B., Puech, A., Sirotkin, H., Edelmann, L., Carlson, C., Raft, S., Pandita, R.K., Kucherlapati, R., Skoultchi, A. and Morrow, B.E. (1997) Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/ DGS on 22q11. Genomics, 46, 364-372.
-
(1997)
Genomics
, vol.46
, pp. 364-372
-
-
Funke, B.1
Saint-Jore, B.2
Puech, A.3
Sirotkin, H.4
Edelmann, L.5
Carlson, C.6
Raft, S.7
Pandita, R.K.8
Kucherlapati, R.9
Skoultchi, A.10
Morrow, B.E.11
-
28
-
-
0027232546
-
Spatially restricted expression of DIx-1, DIx-2 (Tes-1), Gbx-2 and Wnt-3 in the embryonic day 12.5 mouse forebrain defines potential transverse and longitudinal segmental boundaries
-
Bulfone, A., Puelles, L., Porteus, M.H., Frohman, M.A., Martin, G.R. and Rubenstein, J.L.R. (1993) Spatially restricted expression of DIx-1, DIx-2 (Tes-1), Gbx-2 and Wnt-3 in the embryonic day 12.5 mouse forebrain defines potential transverse and longitudinal segmental boundaries. J. Neurol., 13, 3155-3172.
-
(1993)
J. Neurol.
, vol.13
, pp. 3155-3172
-
-
Bulfone, A.1
Puelles, L.2
Porteus, M.H.3
Frohman, M.A.4
Martin, G.R.5
Rubenstein, J.L.R.6
-
29
-
-
0029954503
-
orthodenticle regulation during embryonic head development in Drosophila
-
Gao, Q., Wang, Y. and Finkelstein R. (1996) orthodenticle regulation during embryonic head development in Drosophila. Mech. Dev., 56, 3-15.
-
(1996)
Mech. Dev.
, vol.56
, pp. 3-15
-
-
Gao, Q.1
Wang, Y.2
Finkelstein, R.3
-
30
-
-
0027260743
-
A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo
-
Simeone, A., Acampora, D., Mallamac., A., Stomaiuolo, A., D'Apice, M.R., Nigro, V. and Boncinelli, E. (1993) A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo. EMBO J., 12, 2735-2747.
-
(1993)
EMBO J.
, vol.12
, pp. 2735-2747
-
-
Simeone, A.1
Acampora, D.2
Mallamac, A.3
Stomaiuolo, A.4
D'Apice, M.R.5
Nigro, V.6
Boncinelli, E.7
-
31
-
-
0029939460
-
Ptxl, a bicoid-related homeobox transcription factor involved in transcription of the pro-opiomelanocortin gene
-
Lamonerie, T., Tremblay, J.J., Lanctôt, C., Therrien, M., Gauthier Y. and Drouin J. (1996) Ptxl, a bicoid-related homeobox transcription factor involved in transcription of the pro-opiomelanocortin gene. Genes Dev., 10, 1284-1295.
-
(1996)
Genes Dev.
, vol.10
, pp. 1284-1295
-
-
Lamonerie, T.1
Tremblay, J.J.2
Lanctôt, C.3
Therrien, M.4
Gauthier, Y.5
Drouin, J.6
-
32
-
-
0029821237
-
P-OTX: A PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development
-
Szeto, D.P., Ryan, A.K., O'Connell, S.M. and Rosenfeld, M.G. (1996) P-OTX: a PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development. Proc. Natl Acad. Sci. USA, 93, 7706-7710.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 7706-7710
-
-
Szeto, D.P.1
Ryan, A.K.2
O'Connell, S.M.3
Rosenfeld, M.G.4
-
33
-
-
0028042009
-
Homeobox gene expression during development of the vertebrate brain
-
Rubenstein, J.L.R. and Puelles, L. (1994) Homeobox gene expression during development of the vertebrate brain. Curr. Top. Dev. Biol., 29, 1-63.
-
(1994)
Curr. Top. Dev. Biol.
, vol.29
, pp. 1-63
-
-
Rubenstein, J.L.R.1
Puelles, L.2
-
34
-
-
0031924599
-
ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene
-
Lindsay, E.A., Harvey, E.L., Scambler, P.J. and Baldini, A. (1998) ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene. Hum. Mol. Genet., 7, 629-635.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 629-635
-
-
Lindsay, E.A.1
Harvey, E.L.2
Scambler, P.J.3
Baldini, A.4
-
35
-
-
0020322892
-
An immunohistochemical study of serotonin neuron development in the rat: Ascending pathways and terminal fields
-
Lidov, H.G.W. and Molliver, M.E. (1982) An immunohistochemical study of serotonin neuron development in the rat: ascending pathways and terminal fields. Brain Res. Bull., 9, 389-430.
-
(1982)
Brain Res. Bull.
, vol.9
, pp. 389-430
-
-
Lidov, H.G.W.1
Molliver, M.E.2
-
36
-
-
0020467289
-
Immunohistochemical study of the development of serotonergic neurons in the rat CNS
-
Lidov, H.G.W. and Molliver, M.E. (1982) Immunohistochemical study of the development of serotonergic neurons in the rat CNS. Brain Res. Bull., 9, 559-604.
-
(1982)
Brain Res. Bull.
, vol.9
, pp. 559-604
-
-
Lidov, H.G.W.1
Molliver, M.E.2
-
37
-
-
0031040139
-
Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region
-
Gong, W., Emanuel, B.S., Galili, N., Kim, D.H., Roe, B., Driscoll, D.A. and Budarf, M.L. (1997) Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region. Hum. Mol. Genet., 6, 267-276.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 267-276
-
-
Gong, W.1
Emanuel, B.S.2
Galili, N.3
Kim, D.H.4
Roe, B.5
Driscoll, D.A.6
Budarf, M.L.7
-
38
-
-
0022624762
-
Cytoarchitecture, fiber connections and some histochemical aspects of the interpeduncular nucleus in the rat
-
Groenewegen, H.J., Ahlenius, S., Haber, S.N., Kowall, N.W. and Nauta, WJ.H. (1986) Cytoarchitecture, fiber connections and some histochemical aspects of the interpeduncular nucleus in the rat. J. Comp. Neurol., 249, 65-102.
-
(1986)
J. Comp. Neurol.
, vol.249
, pp. 65-102
-
-
Groenewegen, H.J.1
Ahlenius, S.2
Haber, S.N.3
Kowall, N.W.4
Nauta, W.J.H.5
-
39
-
-
0020024556
-
The dorsal diencephalic conduction system: A review of the anatomy and functions of the habenular complex
-
Sutherland, R.J. (1982) The dorsal diencephalic conduction system: a review of the anatomy and functions of the habenular complex. Neurosci. Biobehav. Rev., 6, 1-13.
-
(1982)
Neurosci. Biobehav. Rev.
, vol.6
, pp. 1-13
-
-
Sutherland, R.J.1
-
40
-
-
0017821181
-
A new syndrome involving cleft palate, cardiac anomalies, typical facies and learning disabilities: Velocardio-facial syndrome
-
Shprintzen, R.J., Goldberg, R.B., Lewin, M.L., Sidoti, E.J., Berkman M.D., Argamaso, R.V. and Young, D.A. (1978) A new syndrome involving cleft palate, cardiac anomalies, typical facies and learning disabilities: velocardio-facial syndrome. Cleft Palate, 15, 56-62.
-
(1978)
Cleft Palate
, vol.15
, pp. 56-62
-
-
Shprintzen, R.J.1
Goldberg, R.B.2
Lewin, M.L.3
Sidoti, E.J.4
Berkman, M.D.5
Argamaso, R.V.6
Young, D.A.7
-
41
-
-
0022391234
-
Velo-cardio-facial syndrome: Language and psychological profiles
-
Golding-Kushner, K.J., Weller, G. and Shprintzen, R.J. (1985) Velo-cardio-facial syndrome: language and psychological profiles. J. Craniofac. Genet., 51, 259-256.
-
(1985)
J. Craniofac. Genet.
, vol.51
, pp. 259-1256
-
-
Golding-Kushner, K.J.1
Weller, G.2
Shprintzen, R.J.3
-
42
-
-
0031009068
-
Intelligence and psychosocial adjustment in velocardiofacial syndrome: A study of 37 children and adolescents with VCFS
-
Swillen, A., Devriendt, K., Legius, E., Durnoulin, M., Gewillig, M. and Fryns, J.P. (1997) Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS. J. Med. Genet., 34, 453-458.
-
(1997)
J. Med. Genet.
, vol.34
, pp. 453-458
-
-
Swillen, A.1
Devriendt, K.2
Legius, E.3
Durnoulin, M.4
Gewillig, M.5
Fryns, J.P.6
-
43
-
-
0032177986
-
Developmental presentation of 22q11.2 deletion (DiGeorge/Velo-cardio-facial syndrome)
-
in press
-
Wang, P.P., Solot, C., Moss, E.M., Gerdes, M., McDonald-McGinn, D.M., Zachai, E.H., Driscoll, D. and Emanuel, B.S. (1998) Developmental presentation of 22q11.2 deletion (DiGeorge/Velo-cardio-facial syndrome). J. Dev. Behev. Ped., in press.
-
(1998)
J. Dev. Behev. Ped.
-
-
Wang, P.P.1
Solot, C.2
Moss, E.M.3
Gerdes, M.4
McDonald-McGinn, D.M.5
Zachai, E.H.6
Driscoll, D.7
Emanuel, B.S.8
-
44
-
-
0027989917
-
Psychotic illness in patients daignosed with Velo-Cardio-Facial Syndrome and their relatives
-
Pulver, A.E., Nestadt, G., Goldberg, R., Sphrintzen, R.J., Lamacz, M., Wolyniec, P.S., Morrow, B., Karayiorgou, M., Antonarakis, S.E., Housman, D. and Kucherlapati, R. (1994) Psychotic illness in patients daignosed with Velo-Cardio-Facial Syndrome and their relatives. J. Nerv. Ment. Dis., 182, 476-478.
-
(1994)
J. Nerv. Ment. Dis.
, vol.182
, pp. 476-478
-
-
Pulver, A.E.1
Nestadt, G.2
Goldberg, R.3
Sphrintzen, R.J.4
Lamacz, M.5
Wolyniec, P.S.6
Morrow, B.7
Karayiorgou, M.8
Antonarakis, S.E.9
Housman, D.10
Kucherlapati, R.11
-
45
-
-
0029102665
-
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
-
Karayiorgou, M., Morris, M.A., Morrow, B., Shprintzen, R.J., Goldberg, R., Borrow, J., Gos, A., Nestadt, G., Wolyniec, P.S., Lasseter, V.K., Eisen, H., Childs, B., Kazazian, H.H., Kucherlapti, R., Antonarakis, S.E., Pulver, A.E. and Housman, D.E. (1995) Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc. Natl Acad. Sci. USA, 92, 7612-7616.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 7612-7616
-
-
Karayiorgou, M.1
Morris, M.A.2
Morrow, B.3
Shprintzen, R.J.4
Goldberg, R.5
Borrow, J.6
Gos, A.7
Nestadt, G.8
Wolyniec, P.S.9
Lasseter, V.K.10
Eisen, H.11
Childs, B.12
Kazazian, H.H.13
Kucherlapti, R.14
Antonarakis, S.E.15
Pulver, A.E.16
Housman, D.E.17
-
46
-
-
0029853761
-
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosme 22q 11 result in bipolar affective disorder?
-
Papolos, D.F., Faedda, G.L., Veit, S., Goldberg, R., Morrow, B., Kucherlapati, R. and Sphrintzen, R.J. (1996) Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosme 22q 11 result in bipolar affective disorder? Am. J. Psychiatry, 153, 1541-1547.
-
(1996)
Am. J. Psychiatry
, vol.153
, pp. 1541-1547
-
-
Papolos, D.F.1
Faedda, G.L.2
Veit, S.3
Goldberg, R.4
Morrow, B.5
Kucherlapati, R.6
Sphrintzen, R.J.7
-
47
-
-
0030910606
-
Molecular analysis of Velo-Cardio-Facial Syndrome patients with psychiatric disorders
-
Carlson, C., Papolos, D., Pandita, R.K., Faedda, G.L., Veit, S., Goldberg, R., Shprintzen, R., Kucherlapati, R. and Morrow, B. (1997) Molecular analysis of Velo-Cardio-Facial Syndrome patients with psychiatric disorders. Am. J. Hum. Genet., 60, 851-859.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 851-859
-
-
Carlson, C.1
Papolos, D.2
Pandita, R.K.3
Faedda, G.L.4
Veit, S.5
Goldberg, R.6
Shprintzen, R.7
Kucherlapati, R.8
Morrow, B.9
-
48
-
-
0024361406
-
Effort and stress influence the effect of lesion of the habenula complex in one-way active avoidance learning
-
Thornton, E. and Bradbury, G.E. (1989) Effort and stress influence the effect of lesion of the habenula complex in one-way active avoidance learning. Physiol. Behav., 45, 929-935.
-
(1989)
Physiol. Behav.
, vol.45
, pp. 929-935
-
-
Thornton, E.1
Bradbury, G.E.2
-
49
-
-
0026711209
-
Habenula and thalamus cell transplants restore normal sleep behaviors disrupted by denervation of the interpeduncular nucleus
-
Haun, F., Eckenrode, T.C. and Murray, M. (1992) Habenula and thalamus cell transplants restore normal sleep behaviors disrupted by denervation of the interpeduncular nucleus. J. Neurosci., 12, 3282-3290.
-
(1992)
J. Neurosci.
, vol.12
, pp. 3282-3290
-
-
Haun, F.1
Eckenrode, T.C.2
Murray, M.3
-
50
-
-
0030297281
-
Lesion of the habenular efferent pathway produces anxiety and locomotor hyperactivity in rats: A comparison of the effects of neonatal and adult lesions
-
Murphy, C.A., DiCamillo, A.M., Haun, F. and Murray, M. (1996) Lesion of the habenular efferent pathway produces anxiety and locomotor hyperactivity in rats: a comparison of the effects of neonatal and adult lesions. Behav. Brain Res., 81, 43-52.
-
(1996)
Behav. Brain Res.
, vol.81
, pp. 43-52
-
-
Murphy, C.A.1
DiCamillo, A.M.2
Haun, F.3
Murray, M.4
-
51
-
-
0028079602
-
Developmental regulation of the orphan receptor COUP-TFII gene in spinal motor neurons
-
Lutz, B.S., Kuratani, S., Cooney, A., Wawersik, S., Tsai, S.Y., Eichele, G. and Tsai, M. (1994) Developmental regulation of the orphan receptor COUP-TFII gene in spinal motor neurons. Development. 120, 25-36.
-
(1994)
Development
, vol.120
, pp. 25-36
-
-
Lutz, B.S.1
Kuratani, S.2
Cooney, A.3
Wawersik, S.4
Tsai, S.Y.5
Eichele, G.6
Tsai, M.7
-
52
-
-
0027437850
-
Cdi1, a human G1 and S phase protein phosphatase that associates with Cdk2
-
Gyuris, J., Golemis, E., Chertkov, H. and Brent, R. (1993) Cdi1, a human G1 and S phase protein phosphatase that associates with Cdk2. Cell, 75, 791-803.
-
(1993)
Cell
, vol.75
, pp. 791-803
-
-
Gyuris, J.1
Golemis, E.2
Chertkov, H.3
Brent, R.4
-
53
-
-
0023649184
-
A new class of yeast transcription activators
-
Ma, J. and Ptashne, M. (1987) A new class of yeast transcription activators. Cell, 51, 113-119.
-
(1987)
Cell
, vol.51
, pp. 113-119
-
-
Ma, J.1
Ptashne, M.2
-
54
-
-
0027240004
-
Fusion of GAL4-VP16 to a steroid-binding domain provides a tool for gratuitous induction of galactose-responsive genes in yeast
-
Louvion, J.-F., Havaux-Copf, B. and Picard, D. (1993) Fusion of GAL4-VP16 to a steroid-binding domain provides a tool for gratuitous induction of galactose-responsive genes in yeast. Gene. 131, 129-34.
-
(1993)
Gene
, vol.131
, pp. 129-134
-
-
Louvion, J.-F.1
Havaux-Copf, B.2
Picard, D.3
-
55
-
-
0021723295
-
Saccharomyces cerevisae GAL1-GAL10 divergent promoter region: Location and function of the upstream activating sequence UASG
-
West, R.W., Yocum, R.R. and Ptashne, M. (1984) Saccharomyces cerevisae GAL1-GAL10 divergent promoter region: location and function of the upstream activating sequence UASG. Mol. Cell. Biol., 4, 2467-2478.
-
(1984)
Mol. Cell. Biol.
, vol.4
, pp. 2467-2478
-
-
West, R.W.1
Yocum, R.R.2
Ptashne, M.3
-
56
-
-
0020529962
-
Transformatin of intact yeast cells treated with alkali cations
-
Ito, H., Fukada, Y., Murata, K. and Kimura, A. (1983) Transformatin of intact yeast cells treated with alkali cations. J. Bacteriol., 53, 163-168.
-
(1983)
J. Bacteriol.
, vol.53
, pp. 163-168
-
-
Ito, H.1
Fukada, Y.2
Murata, K.3
Kimura, A.4
-
57
-
-
0028236069
-
Molecular cloning of the human homeobox gene goosecoid (GSC) and mapping of the gene to human chromosome 14q32.1
-
Blum, M., De Robertis, E.M., Kojis, T., Heinzmann, C., Klisak, I., Geissert, D. and Sparkes, R.S. (1994) Molecular cloning of the human homeobox gene goosecoid (GSC) and mapping of the gene to human chromosome 14q32.1. Genomics, 21, 388-393.
-
(1994)
Genomics
, vol.21
, pp. 388-393
-
-
Blum, M.1
De Robertis, E.M.2
Kojis, T.3
Heinzmann, C.4
Klisak, I.5
Geissert, D.6
Sparkes, R.S.7
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