-
2
-
-
0028674212
-
Functional analysis of theTAN-1Notch
-
Aster J., Pear W., Hasserjian R., Erba H., Davi F., Luo B., Scott M., Baltimore D., Sklar J. Functional analysis of theTAN-1Notch. Cold Spring Harb. Symp. Quant. Biol. 59:1994;125-136.
-
(1994)
Cold Spring Harb. Symp. Quant. Biol.
, vol.59
, pp. 125-136
-
-
Aster, J.1
Pear, W.2
Hasserjian, R.3
Erba, H.4
Davi, F.5
Luo, B.6
Scott, M.7
Baltimore, D.8
Sklar, J.9
-
3
-
-
0028822543
-
Vertebrate retinal ganglion cells are selected from competent progenitors by the action ofNotch
-
Austin C. P., Feldman D. E., Ida J. A. Jr., Cepko C. L. Vertebrate retinal ganglion cells are selected from competent progenitors by the action ofNotch. Development. 121:1995;3637-3650.
-
(1995)
Development
, vol.121
, pp. 3637-3650
-
-
Austin, C.P.1
Feldman, D.E.2
Ida J.A., Jr.3
Cepko, C.L.4
-
4
-
-
0029023204
-
Transient and restricted expression during mouse embryogenesis ofDll1,Delta
-
Bettenhausen B., Hrabe de Angelis M., Simon D., Guenet J.-L., Gossler A. Transient and restricted expression during mouse embryogenesis ofDll1,Delta. Development. 121:1995;2407-2418.
-
(1995)
Development
, vol.121
, pp. 2407-2418
-
-
Bettenhausen, B.1
Hrabe De Angelis, M.2
Simon, D.3
Guenet, J.-L.4
Gossler, A.5
-
5
-
-
0029089247
-
Clinical spectrum of CADASIL: A study of 7 families
-
Chabriat H., Vahedi K., Iba-Zizen M. T., Joutel A. Clinical spectrum of CADASIL: A study of 7 families. Lancet. 346:1995;934-939.
-
(1995)
Lancet
, vol.346
, pp. 934-939
-
-
Chabriat, H.1
Vahedi, K.2
Iba-Zizen, M.T.3
Joutel, A.4
-
6
-
-
0029061491
-
Primary neurogenesis in Xenopus embryos regulated by a holologue of the Drosophila neurogenic geneDelta
-
Chitnis A., Henrique D., Lewis J., Ish-Horowicz D., Kintner C. Primary neurogenesis in Xenopus embryos regulated by a holologue of the Drosophila neurogenic geneDelta. Nature. 375:1995;761-766.
-
(1995)
Nature
, vol.375
, pp. 761-766
-
-
Chitnis, A.1
Henrique, D.2
Lewis, J.3
Ish-Horowicz, D.4
Kintner, C.5
-
7
-
-
0027300294
-
Expression of an extracellular deletion of Xotch diverts cell fate in Xenopus embryos
-
Coffman C., Skoglund P., Harris W. A., Kintner C. Expression of an extracellular deletion of Xotch diverts cell fate in Xenopus embryos. Cell. 73:1993;659-671.
-
(1993)
Cell
, vol.73
, pp. 659-671
-
-
Coffman, C.1
Skoglund, P.2
Harris, W.A.3
Kintner, C.4
-
8
-
-
0028989016
-
Notch1 is required for the coordinate segmentation of somites
-
Conlon R. A., Reaume A. G., Rossant J. Notch1 is required for the coordinate segmentation of somites. Development. 121:1995;1533-1545.
-
(1995)
Development
, vol.121
, pp. 1533-1545
-
-
Conlon, R.A.1
Reaume, A.G.2
Rossant, J.3
-
9
-
-
0028082218
-
Modifications of the notch function by Abruptex mutations in Drosophila melanogaster
-
de Celis J. F., Garcia-Bellido A. Modifications of the notch function by Abruptex mutations in Drosophila melanogaster. Genetics. 136:1994;183-194.
-
(1994)
Genetics
, vol.136
, pp. 183-194
-
-
De Celis, J.F.1
Garcia-Bellido, A.2
-
10
-
-
0030933977
-
Conservation of the Notch signalling pathway in mammalian neurogenesis
-
de la Pompa J. L., Wakeham A., Correia K. M., Samper E., Brown S., Aguilera R. J., Nakano T., Honjo T., Mak T. W., Rossant J., Conlon R. A. Conservation of the Notch signalling pathway in mammalian neurogenesis. Development. 124:1997;1139-1148.
-
(1997)
Development
, vol.124
, pp. 1139-1148
-
-
De La Pompa, J.L.1
Wakeham, A.2
Correia, K.M.3
Samper, E.4
Brown, S.5
Aguilera, R.J.6
Nakano, T.7
Honjo, T.8
Mak, T.W.9
Rossant, J.10
Conlon, R.A.11
-
12
-
-
0029655609
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval
-
Ducros A., Nagy T., Alamowitch S., Nibbio A. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval. Am. J. Hum. Genet. 58:1996;171-181.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 171-181
-
-
Ducros, A.1
Nagy, T.2
Alamowitch, S.3
Nibbio, A.4
-
13
-
-
0025856717
-
TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms
-
Ellisen L. W., Bird J., West D. C., Soreng A. L., Reynolds T. C., Smith S. D., Sklar J. TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms. Cell. 66:1991;649-661.
-
(1991)
Cell
, vol.66
, pp. 649-661
-
-
Ellisen, L.W.1
Bird, J.2
West, D.C.3
Soreng, A.L.4
Reynolds, T.C.5
Smith, S.D.6
Sklar, J.7
-
14
-
-
0026670590
-
Expression ofMotch,Drosophila Notch
-
Franco del Amo F., Smith D. E., Swiatek P. J., Gendron-Maguire M., Greenspan R. J., McMahon A. P., Gridley T. Expression ofMotch,Drosophila Notch, Development. 115:1992;737-745.
-
(1992)
Development
, vol.115
, pp. 737-745
-
-
Franco Del Amo, F.1
Smith, D.E.2
Swiatek, P.J.3
Gendron-Maguire, M.4
Greenspan, R.J.5
McMahon, A.P.6
Gridley, T.7
-
15
-
-
0029871104
-
Expression of a truncated Int3 gene in developing secretory mammary epithelium specifically retards lobular differentiation resulting in tumorigenesis
-
Gallahan D., Jhappan C., Robinson G., Hennighausen L., Sharp R., Kordon E., Callahan R., Merlino G., Smith G. H. Expression of a truncated Int3 gene in developing secretory mammary epithelium specifically retards lobular differentiation resulting in tumorigenesis. Cancer Res. 56:1996;1775-1785.
-
(1996)
Cancer Res.
, vol.56
, pp. 1775-1785
-
-
Gallahan, D.1
Jhappan, C.2
Robinson, G.3
Hennighausen, L.4
Sharp, R.5
Kordon, E.6
Callahan, R.7
Merlino, G.8
Smith, G.H.9
-
16
-
-
0027536121
-
Altered epidermal growth factor-like sequences provide evidence for a role of Notch as a receptor in cell fate decisions
-
Heitzler P., Simpson P. Altered epidermal growth factor-like sequences provide evidence for a role of Notch as a receptor in cell fate decisions. Development. 117:1993;1113-1123.
-
(1993)
Development
, vol.117
, pp. 1113-1123
-
-
Heitzler, P.1
Simpson, P.2
-
17
-
-
0029062934
-
Expression of aDelta
-
Henrique D., Adam J., Myat A., Chitnis A., Lewis J., Ish-Horowicz D. Expression of aDelta. Nature. 375:1995;787-790.
-
(1995)
Nature
, vol.375
, pp. 787-790
-
-
Henrique, D.1
Adam, J.2
Myat, A.3
Chitnis, A.4
Lewis, J.5
Ish-Horowicz, D.6
-
18
-
-
0030976083
-
Maintenance of somite borders in mice requires theDeltaDll1
-
Hrabé de Angelis M., McIntyre II J., Gossler A. Maintenance of somite borders in mice requires theDeltaDll1. Nature. 386:1997;717-721.
-
(1997)
Nature
, vol.386
, pp. 717-721
-
-
Hrabé De Angelis, M.1
McIntyre J. II2
Gossler, A.3
-
19
-
-
0030938788
-
The Notch ligand, X-Delta-2, mediates segmentation of the paraxial mesoderm in Xenopus embryos
-
Jen W.-C., Wettstein D., Turner D., Chitnis A., Kintner C. The Notch ligand, X-Delta-2, mediates segmentation of the paraxial mesoderm in Xenopus embryos. Development. 124:1997;1169-1178.
-
(1997)
Development
, vol.124
, pp. 1169-1178
-
-
Jen, W.-C.1
Wettstein, D.2
Turner, D.3
Chitnis, A.4
Kintner, C.5
-
20
-
-
0026517312
-
Expression of an activatedNotchint-3
-
Jhappan C., Gallahan D., Stahle C., Chu E., Smith G. H., Merlino G., Callahan R. Expression of an activatedNotchint-3. Genes Dev. 6:1992;345-355.
-
(1992)
Genes Dev.
, vol.6
, pp. 345-355
-
-
Jhappan, C.1
Gallahan, D.2
Stahle, C.3
Chu, E.4
Smith, G.H.5
Merlino, G.6
Callahan, R.7
-
21
-
-
16044362074
-
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
Joutel A., Corpechot C., Ducros A., Vahedi K. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature. 383:1996;707-710.
-
(1996)
Nature
, vol.383
, pp. 707-710
-
-
Joutel, A.1
Corpechot, C.2
Ducros, A.3
Vahedi, K.4
-
22
-
-
0029096518
-
Cerebral autosomal dominant arteriopathy with subcortical linfarcts and leukoencephalopathy: A clinicopathological and genetic study of a Swiss family
-
Jung H. H., Bassetti C., Tournier-Lasserve E., Vahedi K., Arnaboldi M., Arifi V. B., Gurgunder J. M. Cerebral autosomal dominant arteriopathy with subcortical linfarcts and leukoencephalopathy: A clinicopathological and genetic study of a Swiss family. J. Neurol. Neurosurg. Psychiatry. 59:1995;138-143.
-
(1995)
J. Neurol. Neurosurg. Psychiatry
, vol.59
, pp. 138-143
-
-
Jung, H.H.1
Bassetti, C.2
Tournier-Lasserve, E.3
Vahedi, K.4
Arnaboldi, M.5
Arifi, V.B.6
Gurgunder, J.M.7
-
23
-
-
0023762877
-
Mechanisms of vertebrate segmentation
-
Keynes R. J., Stern C. D. Mechanisms of vertebrate segmentation. Development. 103:1988;413-429.
-
(1988)
Development
, vol.103
, pp. 413-429
-
-
Keynes, R.J.1
Stern, C.D.2
-
24
-
-
0028605515
-
The human NOTCH1,2 and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation
-
Larsson C., Lardelli M., White I., Lendahl U. The human NOTCH1,2 and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation. Genomics. 24:1994;253-258.
-
(1994)
Genomics
, vol.24
, pp. 253-258
-
-
Larsson, C.1
Lardelli, M.2
White, I.3
Lendahl, U.4
-
27
-
-
0026319187
-
Localization of a nervous system-specific class II beta-tubulin gene in Xenopus laevis embryos by whole-mount in situ hybridization
-
Oschwald R., Richter K., Grunz H. Localization of a nervous system-specific class II beta-tubulin gene in Xenopus laevis embryos by whole-mount in situ hybridization. Int. J. Dev. Biol. 35:1991;399-405.
-
(1991)
Int. J. Dev. Biol.
, vol.35
, pp. 399-405
-
-
Oschwald, R.1
Richter, K.2
Grunz, H.3
-
28
-
-
0029942842
-
Exclusive development of T cell neoplasms in mice transplanted with bone marrow expressing activatedNotch
-
Pear W. S., Aster J. C., Scott M. L., Hasserjian R. P., Soffer B., Sklar J., Baltimore D. Exclusive development of T cell neoplasms in mice transplanted with bone marrow expressing activatedNotch. J. Exp. Med. 183:1996;2283-2291.
-
(1996)
J. Exp. Med.
, vol.183
, pp. 2283-2291
-
-
Pear, W.S.1
Aster, J.C.2
Scott, M.L.3
Hasserjian, R.P.4
Soffer, B.5
Sklar, J.6
Baltimore, D.7
-
29
-
-
0029092525
-
An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
-
Ragno M., Tournier-Lasserve E., Fiori M. G., Manca A. An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Ann. Neurol. 38:1995;231-236.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 231-236
-
-
Ragno, M.1
Tournier-Lasserve, E.2
Fiori, M.G.3
Manca, A.4
-
30
-
-
0026462702
-
Expression analysis of aNotch
-
Reaume A. G., Conlon R. A., Zirngibl R., Yamaguchi T. P., Rossant J. Expression analysis of aNotch. Dev. Biol. 154:1992;377-387.
-
(1992)
Dev. Biol.
, vol.154
, pp. 377-387
-
-
Reaume, A.G.1
Conlon, R.A.2
Zirngibl, R.3
Yamaguchi, T.P.4
Rossant, J.5
-
31
-
-
0030297895
-
An activated form of Notch influences the choice between CD4 and CD8 T cell lineages
-
Robey E., Chang D., Itano A., Cado D., Alexander H., Lans D., Weinmaster G., Salmon P. An activated form of Notch influences the choice between CD4 and CD8 T cell lineages. Cell. 87:1996;483-492.
-
(1996)
Cell
, vol.87
, pp. 483-492
-
-
Robey, E.1
Chang, D.2
Itano, A.3
Cado, D.4
Alexander, H.5
Lans, D.6
Weinmaster, G.7
Salmon, P.8
-
33
-
-
0030475857
-
Viral genetic variation, AIDS, and the multistep nature of carcinogenesis: The feline leukemia virus model
-
Rohn J. L., Gwynn S. R., Lauring A. S., Linenberger M. L., Overbaugh J. Viral genetic variation, AIDS, and the multistep nature of carcinogenesis: The feline leukemia virus model. Leukemia. 10:1996a;1867-1869.
-
(1996)
Leukemia
, vol.10
, pp. 1867-1869
-
-
Rohn, J.L.1
Gwynn, S.R.2
Lauring, A.S.3
Linenberger, M.L.4
Overbaugh, J.5
-
35
-
-
0029050447
-
Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Ruchoux M. M., Guerouaou D., Vandenhaute B., Pruvo J. P., Vermersch P., Leys D. Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Acta Neuropathol. 89:1995;500-512.
-
(1995)
Acta Neuropathol.
, vol.89
, pp. 500-512
-
-
Ruchoux, M.M.1
Guerouaou, D.2
Vandenhaute, B.3
Pruvo, J.P.4
Vermersch, P.5
Leys, D.6
-
36
-
-
0028216808
-
Notch1
-
Swiatek P. J., Lindsell C. E., Franco del Amo F., Weinmaster G., Gridley T. Notch1. Genes Dev. 8:1994;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
-
37
-
-
0027479304
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
-
Tournier-Lasserve E., Joutel A., Melki J., Weissenbach J. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nature Genet. 3:1993;256-259.
-
(1993)
Nature Genet.
, vol.3
, pp. 256-259
-
-
Tournier-Lasserve, E.1
Joutel, A.2
Melki, J.3
Weissenbach, J.4
-
38
-
-
0030054646
-
Notch4/int-3, a mammary proto-oncogene, is an endothelial cell-specific mammalian Notch gene
-
Uyttendaele H., Marazzi G., Wu G., Yan Q., Sassoon D., Kitajewski J. Notch4/int-3, a mammary proto-oncogene, is an endothelial cell-specific mammalian Notch gene. Development. 122:1996;2251-2259.
-
(1996)
Development
, vol.122
, pp. 2251-2259
-
-
Uyttendaele, H.1
Marazzi, G.2
Wu, G.3
Yan, Q.4
Sassoon, D.5
Kitajewski, J.6
-
39
-
-
0031001247
-
Notch activity influences the αβ vs. γδ T cell lineage decision
-
Washburn T., Schweighoffer E., Gridley T., Chang D., Fowlkes B., Cado D., Salmon P., Robey E. Notch activity influences the αβ vs. γδ T cell lineage decision. Cell. 88:1997;833-843.
-
(1997)
Cell
, vol.88
, pp. 833-843
-
-
Washburn, T.1
Schweighoffer, E.2
Gridley, T.3
Chang, D.4
Fowlkes, B.5
Cado, D.6
Salmon, P.7
Robey, E.8
-
41
-
-
0343452617
-
TheXenopusDrosophila Suppressor of Hairless
-
Wettstein D. A., Turner D. L., Kintner C. TheXenopusDrosophila Suppressor of Hairless. Development. 124:1997;3693-3702.
-
(1997)
Development
, vol.124
, pp. 3693-3702
-
-
Wettstein, D.A.1
Turner, D.L.2
Kintner, C.3
-
42
-
-
0028844121
-
Complementary and combinatorial patterns ofNotch
-
Williams R., Lendahl U., Lardelli M. Complementary and combinatorial patterns ofNotch. Mech. Dev. 53:1995;357-368.
-
(1995)
Mech. Dev.
, vol.53
, pp. 357-368
-
-
Williams, R.1
Lendahl, U.2
Lardelli, M.3
-
43
-
-
0029078323
-
Alterations in Notch signaling in neoplastic lesions of the human cervix
-
Zagouras P., Stifani S., Blaumueller C. M., Carcangiu M. L., Artavanis-Tsakonas S. Alterations in Notch signaling in neoplastic lesions of the human cervix. Proc. Natl. Acad. Sci. USA. 92:1995;6414-6418.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 6414-6418
-
-
Zagouras, P.1
Stifani, S.2
Blaumueller, C.M.3
Carcangiu, M.L.4
Artavanis-Tsakonas, S.5
|