-
1
-
-
0028943243
-
Notch signaling
-
Artavanis-Tsakonas, S., Matsuno, K. and Fortini, M.E. (1995) Notch signaling. Science, 268, 225-232.
-
(1995)
Science
, vol.268
, pp. 225-232
-
-
Artavanis-Tsakonas, S.1
Matsuno, K.2
Fortini, M.E.3
-
2
-
-
0030748716
-
The ins and outs of Notch signaling
-
Weinmaster, G. (1997) The ins and outs of Notch signaling. Mol. Cell. Neurosci., 9, 91-102.
-
(1997)
Mol. Cell. Neurosci.
, vol.9
, pp. 91-102
-
-
Weinmaster, G.1
-
3
-
-
0030807094
-
Notch signaling in vertebrate development and disease
-
Gridley, T. (1997) Notch signaling in vertebrate development and disease. Mol. Cell. Neurosci., 9, 103-108.
-
(1997)
Mol. Cell. Neurosci.
, vol.9
, pp. 103-108
-
-
Gridley, T.1
-
4
-
-
16044362074
-
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
Joutel, A., Corpechot, C., Ducros, A., Vahedi, K., Chabriat, K.H., Mouton, P., Alamowitch, S., Domenga, V., Cécillion, M., Maréchal, E., Maciazek, J., Vayssiére, C., Cruaud, C., Cabanis, E.-A., Ruchoux, M.M., Weissenbach, J., Bach, J.F., Bousser, M.G. and Tournier-Lasserve, E. (1996) Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature, 383, 707-710.
-
(1996)
Nature
, vol.383
, pp. 707-710
-
-
Joutel, A.1
Corpechot, C.2
Ducros, A.3
Vahedi, K.4
Chabriat, K.H.5
Mouton, P.6
Alamowitch, S.7
Domenga, V.8
Cécillion, M.9
Maréchal, E.10
Maciazek, J.11
Vayssiére, C.12
Cruaud, C.13
Cabanis, E.-A.14
Ruchoux, M.M.15
Weissenbach, J.16
Bach, J.F.17
Bousser, M.G.18
Tournier-Lasserve, E.19
-
5
-
-
0028950732
-
Jagged: A mammalian ligand that activates Notch1
-
Lindsell, C.E., Shawber, C.J., Boulter, J. and Weinmaster, G. (1995)Jagged: a mammalian ligand that activates Notch1. Cell, 80, 909-917.
-
(1995)
Cell
, vol.80
, pp. 909-917
-
-
Lindsell, C.E.1
Shawber, C.J.2
Boulter, J.3
Weinmaster, G.4
-
6
-
-
0038875342
-
Alagille syndrome is caused by mutations in human Jaggedl. which encodes a ligand for Notch1
-
Li, L., Krantz, I.D., Deng, Y., Genin, A., Banta, A.B., Collins, C.C., Qi, M., Trask, B.J., Kuo, W.L., Cochran, J., Costa, T., Pierpont, M.E., Rand, E.B., Piccoli, D.A., Hood, L. and Spinner, N.B. (1997) Alagille syndrome is caused by mutations in human Jaggedl. which encodes a ligand for Notch1. Nature Genet., 16, 243-251.
-
(1997)
Nature Genet.
, vol.16
, pp. 243-251
-
-
Li, L.1
Krantz, I.D.2
Deng, Y.3
Genin, A.4
Banta, A.B.5
Collins, C.C.6
Qi, M.7
Trask, B.J.8
Kuo, W.L.9
Cochran, J.10
Costa, T.11
Pierpont, M.E.12
Rand, E.B.13
Piccoli, D.A.14
Hood, L.15
Spinner, N.B.16
-
7
-
-
0030914459
-
Mutations in the human Jagged1 gene are responsible for Alagille syndrome
-
Oda, T., Elkahloun, A.G., Pike, B.L., Okajima, K., Krantz, I.D., Genin, A., Piccoli, D.A., Meltzer, P.S., Spinner, N.B., Collins, F.S. and Chandrasekharappa, S.C. (1997) Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nature Genet., 16, 235-242.
-
(1997)
Nature Genet.
, vol.16
, pp. 235-242
-
-
Oda, T.1
Elkahloun, A.G.2
Pike, B.L.3
Okajima, K.4
Krantz, I.D.5
Genin, A.6
Piccoli, D.A.7
Meltzer, P.S.8
Spinner, N.B.9
Collins, F.S.10
Chandrasekharappa, S.C.11
-
8
-
-
0031048131
-
Alagille syndrome
-
Krantz, I.D., Piccoli, D.A. and Spinner, N.B. (1997) Alagille syndrome. J. Med. Genet., 34, 152-157.
-
(1997)
J. Med. Genet.
, vol.34
, pp. 152-157
-
-
Krantz, I.D.1
Piccoli, D.A.2
Spinner, N.B.3
-
9
-
-
0031778069
-
Spectrum and frequency of Jagged1 (JAG1) mutations in Alagille syndrome patients and their families
-
Krantz, I.D., Colliton, R.P., Genin, A., Rand, E.B., Li, L., Piccoli, D.A. and Spinner, N.B. (1998) Spectrum and frequency of Jagged1 (JAG1) mutations in Alagille syndrome patients and their families. Am. J. Hum. Genet., 62, 1361-1369.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 1361-1369
-
-
Krantz, I.D.1
Colliton, R.P.2
Genin, A.3
Rand, E.B.4
Li, L.5
Piccoli, D.A.6
Spinner, N.B.7
-
10
-
-
0031705770
-
Mutational analysis of the Jagged1 gene in Alagille syndrome families
-
Yuan, Z.-R., Kohsaka, T., Ikegaya, T., Suzuki, T., Okano, S., Abe, J., Kobayashi, N. and Yamada, M. (1998) Mutational analysis of the Jagged1 gene in Alagille syndrome families. Hum. Mol. Genet., 7, 1363-1369.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1363-1369
-
-
Yuan, Z.-R.1
Kohsaka, T.2
Ikegaya, T.3
Suzuki, T.4
Okano, S.5
Abe, J.6
Kobayashi, N.7
Yamada, M.8
-
11
-
-
0028670620
-
Delta-Notch signaling and Drosophila cell fate choice
-
Muskavitch, M.A.T. (1994) Delta-Notch signaling and Drosophila cell fate choice. Dev. Biol., 166, 415-430.
-
(1994)
Dev. Biol.
, vol.166
, pp. 415-430
-
-
Muskavitch, M.A.T.1
-
12
-
-
0027938406
-
Platelet endothelial cell adhesion molecule-1 (PECAM-1/CD31): Alternatively spliced, functionally distinct isoforms expressed during mammalian cardiovascular development
-
Baldwin, H.S., Shen, H.M., Yan, H.C., De Lisser, H.M., Chung, A., Mickanin, C., Trask, T., Kirschbaum, N.E., Newman, P.J., Albeda, S.M. and Buck, C.A. (1994) Platelet endothelial cell adhesion molecule-1 (PECAM-1/CD31): alternatively spliced, functionally distinct isoforms expressed during mammalian cardiovascular development. Development, 120, 2539-2553.
-
(1994)
Development
, vol.120
, pp. 2539-2553
-
-
Baldwin, H.S.1
Shen, H.M.2
Yan, H.C.3
De Lisser, H.M.4
Chung, A.5
Mickanin, C.6
Trask, T.7
Kirschbaum, N.E.8
Newman, P.J.9
Albeda, S.M.10
Buck, C.A.11
-
13
-
-
0030956814
-
Mouse Serrate-1 (Jagged1): Expression in the developing tooth is regulated by epithelial-mesenchymal interactions and fibroblast growth factor-4
-
Mitsiadis, T.A., Henrique, D., Thesleff, I. and Lendahl, U. (1997) Mouse Serrate-1 (Jagged1): expression in the developing tooth is regulated by epithelial-mesenchymal interactions and fibroblast growth factor-4. Development, 124, 1473-1483.
-
(1997)
Development
, vol.124
, pp. 1473-1483
-
-
Mitsiadis, T.A.1
Henrique, D.2
Thesleff, I.3
Lendahl, U.4
-
14
-
-
0029925224
-
A chick homologue of Serrate and its relationship with Notch and Delta homologues during central neurogenesis
-
Myat, A., Henrique, D., Ish-Horowicz, D. and Lewis, J. (1996) A chick homologue of Serrate and its relationship with Notch and Delta homologues during central neurogenesis. Dev. Biol., 174, 233-247.
-
(1996)
Dev. Biol.
, vol.174
, pp. 233-247
-
-
Myat, A.1
Henrique, D.2
Ish-Horowicz, D.3
Lewis, J.4
-
15
-
-
0031728570
-
Expression patterns of Notch1, Serrate1, Serrate2 and Delta1 in tissues of the developing chick limb
-
Vargesson, N., Patel, K., Lewis, J. and Tickle, C. (1998) Expression patterns of Notch1, Serrate1, Serrate2 and Delta1 in tissues of the developing chick limb. Mech. Dev., 77, 197-200.
-
(1998)
Mech. Dev.
, vol.77
, pp. 197-200
-
-
Vargesson, N.1
Patel, K.2
Lewis, J.3
Tickle, C.4
-
16
-
-
0028216808
-
Notch1 is essential for postimplantation development in mice
-
Swiatek, P.J., Lindsell, C.E., Franco del Amo, F., Weinmaster, G. and Gridley, T. (1994) Notch1 is essential for postimplantation development in mice. Genes Dev., 8, 707-719.
-
(1994)
Genes Dev.
, vol.8
, pp. 707-719
-
-
Swiatek, P.J.1
Lindsell, C.E.2
Franco Del Amo, F.3
Weinmaster, G.4
Gridley, T.5
-
17
-
-
0028989016
-
Notch1 is required for the coordinate segmentation of somites
-
Conlon, R.A., Reaume, A.G. and Rossant, J. (1995) Notch1 is required for the coordinate segmentation of somites. Development, 121, 1533-1545.
-
(1995)
Development
, vol.121
, pp. 1533-1545
-
-
Conlon, R.A.1
Reaume, A.G.2
Rossant, J.3
-
18
-
-
0030976083
-
Maintenance of somite borders in mice requires the Delta homologue D111
-
Hrabé de Angelis, M., McIntyre, J. and Gossler, A. (1997) Maintenance of somite borders in mice requires the Delta homologue D111. Nature, 386, 717-721.
-
(1997)
Nature
, vol.386
, pp. 717-721
-
-
Hrabé De Angelis, M.1
McIntyre, J.2
Gossler, A.3
-
19
-
-
17344368196
-
The mouse pudgy mutation disrupts Delta homologue D113 and initiation of early somite boundaries
-
Kusumi, K., Sun, E., Kerrebrock, A.W., Bronson, R.T., Chi, D.-C., Bulotsky, M.S., Spencer, J.B., Birren, B.W., Frankel, W.N. and Lander, E.S. (1998) The mouse pudgy mutation disrupts Delta homologue D113 and initiation of early somite boundaries. Nature Genet., 19, 274-278.
-
(1998)
Nature Genet.
, vol.19
, pp. 274-278
-
-
Kusumi, K.1
Sun, E.2
Kerrebrock, A.W.3
Bronson, R.T.4
Chi, D.-C.5
Bulotsky, M.S.6
Spencer, J.B.7
Birren, B.W.8
Frankel, W.N.9
Lander, E.S.10
-
20
-
-
0032560814
-
Lunatic fringe is an essential mediator of somite segmentation and patterning
-
Evrard, Y.A., Lun, Y., Aulehla, A., Gan, L. and Johnson, R.L. (1998) Lunatic fringe is an essential mediator of somite segmentation and patterning. Nature, 394, 377-381.
-
(1998)
Nature
, vol.394
, pp. 377-381
-
-
Evrard, Y.A.1
Lun, Y.2
Aulehla, A.3
Gan, L.4
Johnson, R.L.5
-
21
-
-
0032560766
-
Defects in somite formation in Lunatic fringe deficient mice
-
Zhang, N. and Gridley, T. (1998) Defects in somite formation in Lunatic fringe deficient mice. Nature, 394, 374-377.
-
(1998)
Nature
, vol.394
, pp. 374-377
-
-
Zhang, N.1
Gridley, T.2
-
22
-
-
0030981168
-
Fringe boundaries coincide with Notch-dependent patterning centres in mammals and alter Notch-dependent development in Drosophila
-
Cohen, B., Bashirullah, A., Dagnino, L., Campbell, C., Fisher, W.W., Leow, C.C., Whiting, E., Ryan, D., Zinyk, D., Boulianne, G., Hui, C.-C., Gallie, B., Phillips, R.A., Lipshitz, H.D. and Egan, S.E. (1997) Fringe boundaries coincide with Notch-dependent patterning centres in mammals and alter Notch-dependent development in Drosophila. Nature Genet., 16, 283-288.
-
(1997)
Nature Genet.
, vol.16
, pp. 283-288
-
-
Cohen, B.1
Bashirullah, A.2
Dagnino, L.3
Campbell, C.4
Fisher, W.W.5
Leow, C.C.6
Whiting, E.7
Ryan, D.8
Zinyk, D.9
Boulianne, G.10
Hui, C.-C.11
Gallie, B.12
Phillips, R.A.13
Lipshitz, H.D.14
Egan, S.E.15
-
23
-
-
0029023204
-
Transient and restricted expression during mouse embryogenesis of D111, a murine gene closely related to Drosophila Delta
-
Bettenhausen, B., Hrabé de Angelis, M., Simon, D., Guenet, J.-L. and Gossler, A. (1995) Transient and restricted expression during mouse embryogenesis of D111, a murine gene closely related to Drosophila Delta. Development, 121, 2407-2418.
-
(1995)
Development
, vol.121
, pp. 2407-2418
-
-
Bettenhausen, B.1
Hrabé De Angelis, M.2
Simon, D.3
Guenet, J.-L.4
Gossler, A.5
-
24
-
-
0030961091
-
Mouse D113: A novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo
-
Dunwoodie, S.L., Henrique, D., Harrison, S.M. and Beddington, R.S. (1997) Mouse D113: a novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo. Development, 124, 3065-3076.
-
(1997)
Development
, vol.124
, pp. 3065-3076
-
-
Dunwoodie, S.L.1
Henrique, D.2
Harrison, S.M.3
Beddington, R.S.4
-
25
-
-
0030668283
-
A mouse gene of the paired-related homeobox class expressed in the caudal somite compartment and in the developing vertebral column, kidney and nervous system
-
Neidhardt, L.M., Kispert, A. and Hermann, B.G. (1997) A mouse gene of the paired-related homeobox class expressed in the caudal somite compartment and in the developing vertebral column, kidney and nervous system. Dev. Genes Evol., 207, 330-339.
-
(1997)
Dev. Genes Evol.
, vol.207
, pp. 330-339
-
-
Neidhardt, L.M.1
Kispert, A.2
Hermann, B.G.3
-
26
-
-
0028340242
-
Deletion map of the coloboma (Cm) locus on mouse Chromosome 2
-
Hess, E.J., Collins, K.A., Copeland, N.G., Jenkins, N.A. and Wilson, M.C. (1994) Deletion map of the coloboma (Cm) locus on mouse Chromosome 2. Genomics, 21, 257-261.
-
(1994)
Genomics
, vol.21
, pp. 257-261
-
-
Hess, E.J.1
Collins, K.A.2
Copeland, N.G.3
Jenkins, N.A.4
Wilson, M.C.5
-
27
-
-
0029947330
-
Mouse model of hyperkinesis implicates SNAP-25 in behavioral regulation
-
Hess, E.J., Collins, K.A. and Wilson, M.C. (1996) Mouse model of hyperkinesis implicates SNAP-25 in behavioral regulation. J. Neurosci., 16, 3104-3111.
-
(1996)
J. Neurosci.
, vol.16
, pp. 3104-3111
-
-
Hess, E.J.1
Collins, K.A.2
Wilson, M.C.3
-
28
-
-
0019518811
-
Development of coloboma (Cm/+), a mutation with anterior lens adhesion
-
Theiler, K. and Vamum, D.S. (1981) Development of coloboma (Cm/+), a mutation with anterior lens adhesion. Anat. Embryol., 162, 121-126.
-
(1981)
Anat. Embryol.
, vol.162
, pp. 121-126
-
-
Theiler, K.1
Vamum, D.S.2
-
29
-
-
0030851764
-
Signaling vascular morphogenesis and maintenance
-
Hanahan, D. (1997) Signaling vascular morphogenesis and maintenance. Science, 277, 48-50.
-
(1997)
Science
, vol.277
, pp. 48-50
-
-
Hanahan, D.1
-
30
-
-
0030952289
-
Mechanisms of angiogenesis
-
Risau, W. (1997) Mechanisms of angiogenesis. Nature, 386, 671-674.
-
(1997)
Nature
, vol.386
, pp. 671-674
-
-
Risau, W.1
-
31
-
-
0343661701
-
An antisense oligonucleotide to the notch ligand jagged enhances fibroblast growth factor-induced angiogenesis in vitro
-
Zimrin, A.B., Pepper, M.S., McMahon, G.A., Nguyen, F., Montesano, R. and Maciag, T. (1996) An antisense oligonucleotide to the notch ligand jagged enhances fibroblast growth factor-induced angiogenesis in vitro. J. Biol. Chem., 271, 32499-32502.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 32499-32502
-
-
Zimrin, A.B.1
Pepper, M.S.2
McMahon, G.A.3
Nguyen, F.4
Montesano, R.5
Maciag, T.6
-
32
-
-
0030744231
-
A family of mammalian Fringe genes implicated in boundary determination and the Notch pathway
-
Johnston, S.H., Rauskolb, C., Wilson, R., Prabhakaran, B., Irvine, K.D. and Vogt, T.F. (1997) A family of mammalian Fringe genes implicated in boundary determination and the Notch pathway. Development, 124, 2245-2254.
-
(1997)
Development
, vol.124
, pp. 2245-2254
-
-
Johnston, S.H.1
Rauskolb, C.2
Wilson, R.3
Prabhakaran, B.4
Irvine, K.D.5
Vogt, T.F.6
-
33
-
-
0032054238
-
Defects in limb, craniofacial and thymic development in Jagged2 mutant mice
-
Jiang, R., Lan, Y., Chapman, H.D., Shawber, C., Norton, C.R., Serreze, D.V., Weinmaster, G. and Gridley, T. (1998) Defects in limb, craniofacial and thymic development in Jagged2 mutant mice. Genes Dev., 12, 1046-1057.
-
(1998)
Genes Dev.
, vol.12
, pp. 1046-1057
-
-
Jiang, R.1
Lan, Y.2
Chapman, H.D.3
Shawber, C.4
Norton, C.R.5
Serreze, D.V.6
Weinmaster, G.7
Gridley, T.8
-
35
-
-
0030199830
-
Expression patterns of Jagged, Delta1, Notch1, Notch2 and Notch3 genes identify ligand-receptor pairs that may function in neural development
-
Lindsell, C.E., Boulter, J., diSibio, G., Gossler, A. and Weinmaster, G. (1996) Expression patterns of Jagged, Delta1, Notch1, Notch2 and Notch3 genes identify ligand-receptor pairs that may function in neural development. Mol. Cell. Neurosci., 8, 14-27.
-
(1996)
Mol. Cell. Neurosci.
, vol.8
, pp. 14-27
-
-
Lindsell, C.E.1
Boulter, J.2
DiSibio, G.3
Gossler, A.4
Weinmaster, G.5
-
36
-
-
0031033948
-
The expression and function of Notch pathway genes in the developing rat eye
-
Bao, Z.Z. and Cepko, C.L. (1997) The expression and function of Notch pathway genes in the developing rat eye. J. Neurosci., 17, 1425-1434.
-
(1997)
J. Neurosci.
, vol.17
, pp. 1425-1434
-
-
Bao, Z.Z.1
Cepko, C.L.2
-
37
-
-
0025838674
-
The Notch locus and the cell biology of neuroblast segregation
-
Artavanis-Tsakonas, S., Delidakis, C. and Fehon, R.G. (1991) The Notch locus and the cell biology of neuroblast segregation. Annu. Rev. Cell Biol., 7, 427-452.
-
(1991)
Annu. Rev. Cell Biol.
, vol.7
, pp. 427-452
-
-
Artavanis-Tsakonas, S.1
Delidakis, C.2
Fehon, R.G.3
-
38
-
-
0008237260
-
Deletions and other structural abnormalities of the autosomes
-
Rimoin, D.L., Connor, J.M. and Pyeritz, R.E. (eds). Churchill Livingstone, New York, NY
-
Spinner, N.B. and Emanuel, B.S. (1996) Deletions and other structural abnormalities of the autosomes. In Rimoin, D.L., Connor, J.M. and Pyeritz, R.E. (eds), Emery and Rimoin's Principles and Practice of Medical Genetics, 3rd Edn. Churchill Livingstone, New York, NY, pp. 999-1025.
-
(1996)
Emery and Rimoin's Principles and Practice of Medical Genetics, 3rd Edn.
, pp. 999-1025
-
-
Spinner, N.B.1
Emanuel, B.S.2
-
39
-
-
0026023289
-
Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
-
Soriano, P., Montgomery, C., Geske, R. and Bradley, A. (1991) Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice. Cell, 64, 693-702.
-
(1991)
Cell
, vol.64
, pp. 693-702
-
-
Soriano, P.1
Montgomery, C.2
Geske, R.3
Bradley, A.4
-
40
-
-
0024296027
-
Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: A general strategy for targeting mutations to non-selectable genes
-
Mansour, S.L., Thomas, K.R. and Capecchi, M.R. (1988) Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes. Nature, 336, 348-352.
-
(1988)
Nature
, vol.336
, pp. 348-352
-
-
Mansour, S.L.1
Thomas, K.R.2
Capecchi, M.R.3
-
41
-
-
0027484361
-
Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20
-
Swiatek, P. and Gridley, T. (1993) Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20. Genes Dev., 7, 2071-2084.
-
(1993)
Genes Dev.
, vol.7
, pp. 2071-2084
-
-
Swiatek, P.1
Gridley, T.2
-
42
-
-
0032054763
-
Assignment of the murine Notch2 and Notch3 genes to chromosomes 3 and 17
-
Gao, X., Copeland, N.G., Gilbert, D.J., Jenkins, N.A. and Gridley, T. (1998) Assignment of the murine Notch2 and Notch3 genes to chromosomes 3 and 17. Genomics, 49, 160-161.
-
(1998)
Genomics
, vol.49
, pp. 160-161
-
-
Gao, X.1
Copeland, N.G.2
Gilbert, D.J.3
Jenkins, N.A.4
Gridley, T.5
-
43
-
-
0028430196
-
Maps from two interspecific backcross DNA panels available as a community genetic mapping resource
-
Rowe, L.B., Nadeau, J.H., Turner, R., Frankel, W.N., Letts, V.A., Eppig, J.T., Ko, M.S., Thurston, S.J. and Birkenmeier, E.H. (1994) Maps from two interspecific backcross DNA panels available as a community genetic mapping resource. Mamm. Genome, 5, 253-274.
-
(1994)
Mamm. Genome
, vol.5
, pp. 253-274
-
-
Rowe, L.B.1
Nadeau, J.H.2
Turner, R.3
Frankel, W.N.4
Letts, V.A.5
Eppig, J.T.6
Ko, M.S.7
Thurston, S.J.8
Birkenmeier, E.H.9
|