-
1
-
-
38649125625
-
Rumi is a CAP10 domain glycosyltransferase that modifies Notch and is required for Notch signaling
-
Acar, M., Jafar-Nejad, H., Takeuchi, H., Rajan, A., Ibrani, D., Rana, N. A., Pan, H., Haltiwanger, R. S. and Bellen, H. J. (2008). Rumi is a CAP10 domain glycosyltransferase that modifies Notch and is required for Notch signaling. Cell 132, 247-258.
-
(2008)
Cell
, vol.132
, pp. 247-258
-
-
Acar, M.1
Jafar-Nejad, H.2
Takeuchi, H.3
Rajan, A.4
Ibrani, D.5
Rana, N.A.6
Pan, H.7
Haltiwanger, R.S.8
Bellen, H.J.9
-
2
-
-
59049092970
-
Functional UDP-xylose transport across the endoplasmic reticulum/Golgi membrane in a Chinese hamster ovary cell mutant defective in UDP-xylose Synthase
-
Bakker, H., Oka, T., Ashikov, A., Yadav, A., Berger, M., Rana, N. A., Bai, X., Jigami, Y., Haltiwanger, R. S., Esko, J. D. et al. (2009). Functional UDP-xylose transport across the endoplasmic reticulum/Golgi membrane in a Chinese hamster ovary cell mutant defective in UDP-xylose Synthase. J. Biol. Chem. 284, 2576-2583.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 2576-2583
-
-
Bakker, H.1
Oka, T.2
Ashikov, A.3
Yadav, A.4
Berger, M.5
Rana, N.A.6
Bai, X.7
Jigami, Y.8
Haltiwanger, R.S.9
Esko, J.D.10
-
3
-
-
33847660443
-
An optimized transgenesis system for Drosophila using germ-line-specific phiC31 integrases
-
Bischof, J., Maeda, R. K., Hediger, M., Karch, F. and Basler, K. (2007). An optimized transgenesis system for Drosophila using germ-line-specific phiC31 integrases. Proc. Natl. Acad. Sci. USA 104, 3312-3317.
-
(2007)
Proc. Natl. Acad. Sci. USA
, vol.104
, pp. 3312-3317
-
-
Bischof, J.1
Maeda, R.K.2
Hediger, M.3
Karch, F.4
Basler, K.5
-
4
-
-
0034028904
-
Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis
-
Bulman, M. P., Kusumi, K., Frayling, T. M., McKeown, C., Garrett, C., Lander, E. S., Krumlauf, R., Hattersley, A. T., Ellard, S. and Turnpenny, P. D. (2000). Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis. Nat. Genet. 24, 438-441.
-
(2000)
Nat. Genet.
, vol.24
, pp. 438-441
-
-
Bulman, M.P.1
Kusumi, K.2
Frayling, T.M.3
McKeown, C.4
Garrett, C.5
Lander, E.S.6
Krumlauf, R.7
Hattersley, A.T.8
Ellard, S.9
Turnpenny, P.D.10
-
5
-
-
0034607988
-
Involvement of a conserved tryptophan residue in the UDP-glucose binding of large clostridial cytotoxin glycosyltransferases
-
Busch, C., Hofmann, F., Gerhard, R. and Aktories, K. (2000). Involvement of a conserved tryptophan residue in the UDP-glucose binding of large clostridial cytotoxin glycosyltransferases. J. Biol. Chem. 275, 13228-13234.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 13228-13234
-
-
Busch, C.1
Hofmann, F.2
Gerhard, R.3
Aktories, K.4
-
6
-
-
0032836047
-
Isolation, characterization, and localization of a capsule-associated gene, CAP10, of Cryptococcus neoformans
-
Chang, Y. C. and Kwon-Chung, K. J. (1999). Isolation, characterization, and localization of a capsule-associated gene, CAP10, of Cryptococcus neoformans. J. Bacteriol. 181, 5636-5643.
-
(1999)
J. Bacteriol.
, vol.181
, pp. 5636-5643
-
-
Chang, Y.C.1
Kwon-Chung, K.J.2
-
7
-
-
0032728957
-
Mice lacking both presenilin genes exhibit early embryonic patterning defects
-
Donoviel, D. B., Hadjantonakis, A. K., Ikeda, M., Zheng, H., Hyslop, P. S. and Bernstein, A. (1999). Mice lacking both presenilin genes exhibit early embryonic patterning defects. Genes Dev. 13, 2801-2810.
-
(1999)
Genes Dev.
, vol.13
, pp. 2801-2810
-
-
Donoviel, D.B.1
Hadjantonakis, A.K.2
Ikeda, M.3
Zheng, H.4
Hyslop, P.S.5
Bernstein, A.6
-
8
-
-
0035862854
-
Familial tetralogy of Fallot caused by mutation in the jagged1 gene
-
Eldadah, Z. A., Hamosh, A., Biery, N. J., Montgomery, R. A., Duke, M., Elkins, R. and Dietz, H. C. (2001). Familial tetralogy of Fallot caused by mutation in the jagged1 gene. Hum. Mol. Genet. 10, 163-169.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 163-169
-
-
Eldadah, Z.A.1
Hamosh, A.2
Biery, N.J.3
Montgomery, R.A.4
Duke, M.5
Elkins, R.6
Dietz, H.C.7
-
9
-
-
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. and Sklar, J. (1991). TAN-1, the human homolog of the Drosophila notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms. Cell 66, 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
-
10
-
-
0033017848
-
Features of Alagille syndrome in 92 patients: Frequency and relation to prognosis
-
Emerick, K. M., Rand, E. B., Goldmuntz, E., Krantz, I. D., Spinner, N. B. and Piccoli, D. A. (1999). Features of Alagille syndrome in 92 patients: frequency and relation to prognosis. Hepatology 29, 822-829.
-
(1999)
Hepatology
, vol.29
, pp. 822-829
-
-
Emerick, K.M.1
Rand, E.B.2
Goldmuntz, E.3
Krantz, I.D.4
Spinner, N.B.5
Piccoli, D.A.6
-
11
-
-
77249166068
-
A mouse model to dissect progesterone signaling in the female reproductive tract and mammary gland
-
Fernandez-Valdivia, R., Jeong, J., Mukherjee, A., Soyal, S. M., Li, J., Ying, Y., Demayo, F. J. and Lydon, J. P. (2010). A mouse model to dissect progesterone signaling in the female reproductive tract and mammary gland. Genesis 48, 106-113.
-
(2010)
Genesis
, vol.48
, pp. 106-113
-
-
Fernandez-Valdivia, R.1
Jeong, J.2
Mukherjee, A.3
Soyal, S.M.4
Li, J.5
Ying, Y.6
Demayo, F.J.7
Lydon, J.P.8
-
12
-
-
65549121943
-
Notch signaling: The core pathway and its posttranslational regulation
-
Fortini, M. E. (2009). Notch signaling: the core pathway and its posttranslational regulation. Dev. Cell 16, 633-647.
-
(2009)
Dev. Cell
, vol.16
, pp. 633-647
-
-
Fortini, M.E.1
-
13
-
-
0033576646
-
Autonomous and nonautonomous regulation of mammalian neurite development by Notch1 and Delta1
-
Franklin, J. L., Berechid, B. E., Cutting, F. B., Presente, A., Chambers, C. B., Foltz, D. R., Ferreira, A. and Nye, J. S. (1999). Autonomous and nonautonomous regulation of mammalian neurite development by Notch1 and Delta1. Curr. Biol. 9, 1448-1457.
-
(1999)
Curr. Biol.
, vol.9
, pp. 1448-1457
-
-
Franklin, J.L.1
Berechid, B.E.2
Cutting, F.B.3
Presente, A.4
Chambers, C.B.5
Foltz, D.R.6
Ferreira, A.7
Nye, J.S.8
-
14
-
-
24644467759
-
Mutations in NOTCH1 cause aortic valve disease
-
Garg, V., Muth, A. N., Ransom, J. F., Schluterman, M. K., Barnes, R., King, I. N., Grossfeld, P. D. and Srivastava, D. (2005). Mutations in NOTCH1 cause aortic valve disease. Nature 437, 270-274.
-
(2005)
Nature
, vol.437
, pp. 270-274
-
-
Garg, V.1
Muth, A.N.2
Ransom, J.F.3
Schluterman, M.K.4
Barnes, R.5
King, I.N.6
Grossfeld, P.D.7
Srivastava, D.8
-
15
-
-
34547566893
-
Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo
-
Geffers, I., Serth, K., Chapman, G., Jaekel, R., Schuster-Gossler, K., Cordes, R., Sparrow, D. B., Kremmer, E., Dunwoodie, S. L., Klein, T. et al. (2007). Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo. J. Cell Biol. 178, 465-476.
-
(2007)
J. Cell Biol.
, vol.178
, pp. 465-476
-
-
Geffers, I.1
Serth, K.2
Chapman, G.3
Jaekel, R.4
Schuster-Gossler, K.5
Cordes, R.6
Sparrow, D.B.7
Kremmer, E.8
Dunwoodie, S.L.9
Klein, T.10
-
16
-
-
53549114498
-
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells
-
Hansen, G. M., Markesich, D. C., Burnett, M. B., Zhu, Q., Dionne, K. M., Richter, L. J., Finnell, R. H., Sands, A. T., Zambrowicz, B. P. and Abuin, A. (2008). Large-scale gene trapping in C57BL/6N mouse embryonic stem cells. Genome Res. 18, 1670-1679.
-
(2008)
Genome Res.
, vol.18
, pp. 1670-1679
-
-
Hansen, G.M.1
Markesich, D.C.2
Burnett, M.B.3
Zhu, Q.4
Dionne, K.M.5
Richter, L.J.6
Finnell, R.H.7
Sands, A.T.8
Zambrowicz, B.P.9
Abuin, A.10
-
17
-
-
0027205366
-
O-linked fucose and other posttranslational modifications unique to EGF modules
-
Harris, R. J. and Spellman, M. W. (1993). O-linked fucose and other posttranslational modifications unique to EGF modules. Glycobiology 3, 219-224.
-
(1993)
Glycobiology
, vol.3
, pp. 219-224
-
-
Harris, R.J.1
Spellman, M.W.2
-
18
-
-
0024270443
-
A new trisaccharide sugar chain linked to a serine residue in bovine blood coagulation factors VII and IX
-
(Tokyo)
-
Hase, S., Kawabata, S., Nishimura, H., Takeya, H., Sueyoshi, T., Miyata, T., Iwanaga, S., Takao, T., Shimonishi, Y. and Ikenaka, T. (1988). A new trisaccharide sugar chain linked to a serine residue in bovine blood coagulation factors VII and IX. J. Biochem. (Tokyo) 104, 867-868.
-
(1988)
J. Biochem.
, vol.104
, pp. 867-868
-
-
Hase, S.1
Kawabata, S.2
Nishimura, H.3
Takeya, H.4
Sueyoshi, T.5
Miyata, T.6
Iwanaga, S.7
Takao, T.8
Shimonishi, Y.9
Ikenaka, T.10
-
19
-
-
0034253589
-
Fringe differentially modulates Jagged1 and Delta1 signalling through Notch1 and Notch2
-
Hicks, C., Johnston, S. H., diSibio, G., Collazo, A., Vogt, T. F. and Weinmaster, G. (2000). Fringe differentially modulates Jagged1 and Delta1 signalling through Notch1 and Notch2. Nat. Cell Biol. 2, 515-520.
-
(2000)
Nat. Cell Biol.
, vol.2
, pp. 515-520
-
-
Hicks, C.1
Johnston, S.H.2
di Sibio, G.3
Collazo, A.4
Vogt, T.F.5
Weinmaster, G.6
-
20
-
-
17844390391
-
Analysis of Notch function in presomitic mesoderm suggests a gamma-secretaseindependent role for presenilins in somite differentiation
-
Huppert, S. S., Ilagan, M. X., De Strooper, B. and Kopan, R. (2005). Analysis of Notch function in presomitic mesoderm suggests a gamma-secretaseindependent role for presenilins in somite differentiation. Dev. Cell 8, 677-688.
-
(2005)
Dev. Cell
, vol.8
, pp. 677-688
-
-
Huppert, S.S.1
Ilagan, M.X.2
de Strooper, B.3
Kopan, R.4
-
21
-
-
14144255573
-
Notch-1 activation and dendritic atrophy in prion disease
-
Ishikura, N., Clever, J. L., Bouzamondo-Bernstein, E., Samayoa, E., Prusiner, S. B., Huang, E. J. and DeArmond, S. J. (2005). Notch-1 activation and dendritic atrophy in prion disease. Proc. Natl. Acad. Sci. USA 102, 886-891.
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 886-891
-
-
Ishikura, N.1
Clever, J.L.2
Bouzamondo-Bernstein, E.3
Samayoa, E.4
Prusiner, S.B.5
Huang, E.J.6
de Armond, S.J.7
-
22
-
-
77954506026
-
Role of glycans and glycosyltransferases in the regulation of Notch signaling
-
Jafar-Nejad, H., Leonardi, J. and Fernandez-Valdivia, R. (2010). Role of glycans and glycosyltransferases in the regulation of Notch signaling. Glycobiology 20, 931-949.
-
(2010)
Glycobiology
, vol.20
, pp. 931-949
-
-
Jafar-Nejad, H.1
Leonardi, J.2
Fernandez-Valdivia, R.3
-
23
-
-
16044362074
-
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
Joutel, A., Corpechot, C., Ducros, A., Vahedi, K., Chabriat, H., Mouton, P., Alamowitch, S., Domenga, V., Cecillion, M., Marechal, E. et al. (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, H.5
Mouton, P.6
Alamowitch, S.7
Domenga, V.8
Cecillion, M.9
Marechal, E.10
-
24
-
-
0034739801
-
Identification of a novel mammalian endoplasmic reticulumresident KDEL protein using an EST database motif search
-
Kimata, Y., Ooboki, K., Nomura-Furuwatari, C., Hosoda, A., Tsuru, A. and Kohno, K. (2000). Identification of a novel mammalian endoplasmic reticulumresident KDEL protein using an EST database motif search. Gene 261, 321-327.
-
(2000)
Gene
, vol.261
, pp. 321-327
-
-
Kimata, Y.1
Ooboki, K.2
Nomura-Furuwatari, C.3
Hosoda, A.4
Tsuru, A.5
Kohno, K.6
-
25
-
-
64249172203
-
The canonical Notch signaling pathway: Unfolding the activation mechanism
-
Kopan, R. and Ilagan, M. X. (2009). The canonical Notch signaling pathway: unfolding the activation mechanism. Cell 137, 216-233.
-
(2009)
Cell
, vol.137
, pp. 216-233
-
-
Kopan, R.1
Ilagan, M.X.2
-
26
-
-
0034212710
-
Notch signaling is essential for vascular morphogenesis in mice
-
Krebs, L. T., Xue, Y., Norton, C. R., Shutter, J. R., Maguire, M., Sundberg, J. P., Gallahan, D., Closson, V., Kitajewski, J., Callahan, R. et al. (2000). Notch signaling is essential for vascular morphogenesis in mice. Genes Dev. 14, 1343-1352.
-
(2000)
Genes Dev.
, vol.14
, pp. 1343-1352
-
-
Krebs, L.T.1
Xue, Y.2
Norton, C.R.3
Shutter, J.R.4
Maguire, M.5
Sundberg, J.P.6
Gallahan, D.7
Closson, V.8
Kitajewski, J.9
Callahan, R.10
-
27
-
-
20444502607
-
Dosage-dependent requirement for mouse Vezf1 in vascular system development
-
Kuhnert, F., Campagnolo, L., Xiong, J. W., Lemons, D., Fitch, M. J., Zou, Z., Kiosses, W. B., Gardner, H. and Stuhlmann, H. (2005). Dosage-dependent requirement for mouse Vezf1 in vascular system development. Dev. Biol. 283, 140-156.
-
(2005)
Dev. Biol.
, vol.283
, pp. 140-156
-
-
Kuhnert, F.1
Campagnolo, L.2
Xiong, J.W.3
Lemons, D.4
Fitch, M.J.5
Zou, Z.6
Kiosses, W.B.7
Gardner, H.8
Stuhlmann, H.9
-
28
-
-
65349090671
-
Gainof-function mutations and copy number increases of Notch2 in diffuse large Bcell lymphoma
-
Lee, S. Y., Kumano, K., Nakazaki, K., Sanada, M., Matsumoto, A., Yamamoto, G., Nannya, Y., Suzuki, R., Ota, S., Ota, Y. et al. (2009). Gainof-function mutations and copy number increases of Notch2 in diffuse large Bcell lymphoma. Cancer Sci. 100, 920-926.
-
(2009)
Cancer Sci.
, vol.100
, pp. 920-926
-
-
Lee, S.Y.1
Kumano, K.2
Nakazaki, K.3
Sanada, M.4
Matsumoto, A.5
Yamamoto, G.6
Nannya, Y.7
Suzuki, R.8
Ota, S.9
Ota, Y.10
-
29
-
-
0035341376
-
Mosaic analysis with a repressible cell marker (MARCM) for Drosophila neural development
-
Lee, T. and Luo, L. (2001). Mosaic analysis with a repressible cell marker (MARCM) for Drosophila neural development. Trends Neurosci. 24, 251-254.
-
(2001)
Trends Neurosci.
, vol.24
, pp. 251-254
-
-
Lee, T.1
Luo, L.2
-
30
-
-
77956161887
-
O-fucosylation of thrombospondin type 1 repeats
-
Leonhard-Melief, C. and Haltiwanger, R. S. (2010). O-fucosylation of thrombospondin type 1 repeats. Methods Enzymol. 480, 401-416.
-
(2010)
Methods Enzymol.
, vol.480
, pp. 401-416
-
-
Leonhard-Melief, C.1
Haltiwanger, R.S.2
-
31
-
-
0038875342
-
Alagille syndrome is caused by mutations in human Jagged1, 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. et al. (1997). Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. Nat. Genet. 16, 243-251.
-
(1997)
Nat. 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
-
32
-
-
0029997061
-
Constitutively active human Notch1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1-responsive element
-
Lu, F. M. and Lux, S. E. (1996). Constitutively active human Notch1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1-responsive element. Proc. Natl. Acad. Sci. USA 93, 5663-5667.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 5663-5667
-
-
Lu, F.M.1
Lux, S.E.2
-
33
-
-
58149091978
-
O-linked Nacetylglucosamine is present on the extracellular domain of notch receptors
-
Matsuura, A., Ito, M., Sakaidani, Y., Kondo, T., Murakami, K., Furukawa, K., Nadano, D., Matsuda, T. and Okajima, T. (2008). O-linked Nacetylglucosamine is present on the extracellular domain of notch receptors. J. Biol. Chem. 283, 35486-35495.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 35486-35495
-
-
Matsuura, A.1
Ito, M.2
Sakaidani, Y.3
Kondo, T.4
Murakami, K.5
Furukawa, K.6
Nadano, D.7
Matsuda, T.8
Okajima, T.9
-
34
-
-
0035097937
-
Defects in development of the kidney, heart and eye vasculature in mice homozygous for a hypomorphic Notch2 mutation
-
McCright, B., Gao, X., Shen, L., Lozier, J., Lan, Y., Maguire, M., Herzlinger, D., Weinmaster, G., Jiang, R. and Gridley, T. (2001). Defects in development of the kidney, heart and eye vasculature in mice homozygous for a hypomorphic Notch2 mutation. Development 128, 491-502.
-
(2001)
Development
, vol.128
, pp. 491-502
-
-
McCright, B.1
Gao, X.2
Shen, L.3
Lozier, J.4
Lan, Y.5
Maguire, M.6
Herzlinger, D.7
Weinmaster, G.8
Jiang, R.9
Gridley, T.10
-
35
-
-
0036339631
-
A mouse model of Alagille syndrome: Notch2 as a genetic modifier of Jag1 haploinsufficiency
-
McCright, B., Lozier, J. and Gridley, T. (2002). A mouse model of Alagille syndrome: Notch2 as a genetic modifier of Jag1 haploinsufficiency. Development 129, 1075-1082.
-
(2002)
Development
, vol.129
, pp. 1075-1082
-
-
McCright, B.1
Lozier, J.2
Gridley, T.3
-
36
-
-
32344440732
-
Generation of new Notch2 mutant alleles
-
McCright, B., Lozier, J. and Gridley, T. (2006). Generation of new Notch2 mutant alleles. Genesis 44, 29-33.
-
(2006)
Genesis
, vol.44
, pp. 29-33
-
-
McCright, B.1
Lozier, J.2
Gridley, T.3
-
37
-
-
0037191067
-
Down-regulation of Delta by proteolytic processing
-
Mishra-Gorur, K., Rand, M. D., Perez-Villamil, B. and Artavanis-Tsakonas, S. (2002). Down-regulation of Delta by proteolytic processing. J. Cell Biol. 159, 313-324.
-
(2002)
J. Cell Biol.
, vol.159
, pp. 313-324
-
-
Mishra-Gorur, K.1
Rand, M.D.2
Perez-Villamil, B.3
Artavanis-Tsakonas, S.4
-
38
-
-
33646033137
-
A lentiviral RNAi library for human and mouse genes applied to an arrayed viral high-content screen
-
Moffat, J., Grueneberg, D. A., Yang, X., Kim, S. Y., Kloepfer, A. M., Hinkle, G., Piqani, B., Eisenhaure, T. M., Luo, B., Grenier, J. K. et al. (2006). A lentiviral RNAi library for human and mouse genes applied to an arrayed viral high-content screen. Cell 124, 1283-1298.
-
(2006)
Cell
, vol.124
, pp. 1283-1298
-
-
Moffat, J.1
Grueneberg, D.A.2
Yang, X.3
Kim, S.Y.4
Kloepfer, A.M.5
Hinkle, G.6
Piqani, B.7
Eisenhaure, T.M.8
Luo, B.9
Grenier, J.K.10
-
39
-
-
0034737738
-
Mammalian Notch1 is modified with two unusual forms of O-linked glycosylation found on epidermal growth factor-like modules
-
Moloney, D. J., Shair, L. H., Lu, F. M., Xia, J., Locke, R., Matta, K. L. and Haltiwanger, R. S. (2000). Mammalian Notch1 is modified with two unusual forms of O-linked glycosylation found on epidermal growth factor-like modules. J. Biol. Chem. 275, 9604-9611.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 9604-9611
-
-
Moloney, D.J.1
Shair, L.H.2
Lu, F.M.3
Xia, J.4
Locke, R.5
Matta, K.L.6
Haltiwanger, R.S.7
-
40
-
-
0033867521
-
A ligand-induced extracellular cleavage regulates gamma-secretase-like proteolytic activation of Notch1
-
Mumm, J. S., Schroeter, E. H., Saxena, M. T., Griesemer, A., Tian, X., Pan, D. J., Ray, W. J. and Kopan, R. (2000). A ligand-induced extracellular cleavage regulates gamma-secretase-like proteolytic activation of Notch1. Mol. Cell 5, 197-206.
-
(2000)
Mol. Cell
, vol.5
, pp. 197-206
-
-
Mumm, J.S.1
Schroeter, E.H.2
Saxena, M.T.3
Griesemer, A.4
Tian, X.5
Pan, D.J.6
Ray, W.J.7
Kopan, R.8
-
41
-
-
33751342278
-
Methods for analysis of O-linked modifications on epidermal growth factor-like and thrombospondin type 1 repeats
-
Nita-Lazar, A. and Haltiwanger, R. S. (2006). Methods for analysis of O-linked modifications on epidermal growth factor-like and thrombospondin type 1 repeats. Methods Enzymol. 417, 93-111.
-
(2006)
Methods Enzymol.
, vol.417
, pp. 93-111
-
-
Nita-Lazar, A.1
Haltiwanger, R.S.2
-
42
-
-
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. et al. (1997). Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat. Genet. 16, 235-242.
-
(1997)
Nat. 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
-
43
-
-
0028971681
-
Disruption of the mouse RBP-J kappa gene results in early embryonic death
-
Oka, C., Nakano, T., Wakeham, A., de la Pompa, J. L., Mori, C., Sakai, T., Okazaki, S., Kawaichi, M., Shiota, K., Mak, T. W. et al. (1995). Disruption of the mouse RBP-J kappa gene results in early embryonic death. Development 121, 3291-3301.
-
(1995)
Development
, vol.121
, pp. 3291-3301
-
-
Oka, C.1
Nakano, T.2
Wakeham, A.3
de la Pompa, J.L.4
Mori, C.5
Sakai, T.6
Okazaki, S.7
Kawaichi, M.8
Shiota, K.9
Mak, T.W.10
-
44
-
-
0037074006
-
Regulation of notch signaling by o-linked fucose
-
Okajima, T. and Irvine, K. D. (2002). Regulation of notch signaling by o-linked fucose. Cell 111, 893-904.
-
(2002)
Cell
, vol.111
, pp. 893-904
-
-
Okajima, T.1
Irvine, K.D.2
-
45
-
-
25444492595
-
Highly conserved O-fucose sites have distinct effects on Notch1 function
-
Rampal, R., Arboleda-Velasquez, J. F., Nita-Lazar, A., Kosik, K. S. and Haltiwanger, R. S. (2005). Highly conserved O-fucose sites have distinct effects on Notch1 function. J. Biol. Chem. 280, 32133-32140.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 32133-32140
-
-
Rampal, R.1
Arboleda-Velasquez, J.F.2
Nita-Lazar, A.3
Kosik, K.S.4
Haltiwanger, R.S.5
-
46
-
-
35349012675
-
Regulation of vascular morphogenesis by Notch signaling
-
Roca, C. and Adams, R. H. (2007). Regulation of vascular morphogenesis by Notch signaling. Genes Dev. 21, 2511-2524.
-
(2007)
Genes Dev.
, vol.21
, pp. 2511-2524
-
-
Roca, C.1
Adams, R.H.2
-
47
-
-
58149396934
-
Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the Alagille syndrome hepatic phenotype
-
Ryan, M. J., Bales, C., Nelson, A., Gonzalez, D. M., Underkoffler, L., Segalov, M., Wilson-Rawls, J., Cole, S. E., Moran, J. L., Russo, P. et al. (2008). Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the Alagille syndrome hepatic phenotype. Hepatology 48, 1989-1997.
-
(2008)
Hepatology
, vol.48
, pp. 1989-1997
-
-
Ryan, M.J.1
Bales, C.2
Nelson, A.3
Gonzalez, D.M.4
Underkoffler, L.5
Segalov, M.6
Wilson-Rawls, J.7
Cole, S.E.8
Moran, J.L.9
Russo, P.10
-
48
-
-
0141991292
-
Neurotic, a novel maternal neurogenic gene, encodes an O-fucosyltransferase that is essential for Notch-Delta interactions
-
Sasamura, T., Sasaki, N., Miyashita, F., Nakao, S., Ishikawa, H. O., Ito, M., Kitagawa, M., Harigaya, K., Spana, E., Bilder, D. et al. (2003). neurotic, a novel maternal neurogenic gene, encodes an O-fucosyltransferase that is essential for Notch-Delta interactions. Development 130, 4785-4795.
-
(2003)
Development
, vol.130
, pp. 4785-4795
-
-
Sasamura, T.1
Sasaki, N.2
Miyashita, F.3
Nakao, S.4
Ishikawa, H.O.5
Ito, M.6
Kitagawa, M.7
Harigaya, K.8
Spana, E.9
Bilder, D.10
-
49
-
-
0036868766
-
O-glycosylation of EGF repeats: Identification and initial characterization of a UDP-glucose: Protein O-glucosyltransferase
-
Shao, L., Luo, Y., Moloney, D. J. and Haltiwanger, R. (2002). O-glycosylation of EGF repeats: identification and initial characterization of a UDP-glucose: protein O-glucosyltransferase. Glycobiology 12, 763-770.
-
(2002)
Glycobiology
, vol.12
, pp. 763-770
-
-
Shao, L.1
Luo, Y.2
Moloney, D.J.3
Haltiwanger, R.4
-
50
-
-
0037547158
-
Protein O-fucosyltransferase 1 is an essential component of Notch signaling pathways
-
Shi, S. and Stanley, P. (2003). Protein O-fucosyltransferase 1 is an essential component of Notch signaling pathways. Proc. Natl. Acad. Sci. USA 100, 5234-5239.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 5234-5239
-
-
Shi, S.1
Stanley, P.2
-
51
-
-
77950609317
-
Notch signaling regulates formation of the three-dimensional architecture of intrahepatic bile ducts in mice
-
Sparks, E. E., Huppert, K. A., Brown, M. A., Washington, M. K. and Huppert, S. S. (2010). Notch signaling regulates formation of the three-dimensional architecture of intrahepatic bile ducts in mice. Hepatology 51, 1391-1400.
-
(2010)
Hepatology
, vol.51
, pp. 1391-1400
-
-
Sparks, E.E.1
Huppert, K.A.2
Brown, M.A.3
Washington, M.K.4
Huppert, S.S.5
-
52
-
-
44049101200
-
Roles of Pofut1 and O-fucose in mammalian Notch signaling
-
Stahl, M., Uemura, K., Ge, C., Shi, S., Tashima, Y. and Stanley, P. (2008). Roles of Pofut1 and O-fucose in mammalian Notch signaling. J. Biol. Chem. 283, 13638-13651.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 13638-13651
-
-
Stahl, M.1
Uemura, K.2
Ge, C.3
Shi, S.4
Tashima, Y.5
Stanley, P.6
-
53
-
-
33645231142
-
Cloning, expression and characterization of a novel human CAP10-like gene hCLP46 from CD34(+) stem/progenitor cells
-
Teng, Y., Liu, Q., Ma, J., Liu, F., Han, Z., Wang, Y. and Wang, W. (2006). Cloning, expression and characterization of a novel human CAP10-like gene hCLP46 from CD34(+) stem/progenitor cells. Gene 371, 7-15.
-
(2006)
Gene
, vol.371
, pp. 7-15
-
-
Teng, Y.1
Liu, Q.2
Ma, J.3
Liu, F.4
Han, Z.5
Wang, Y.6
Wang, W.7
-
54
-
-
33845698104
-
P[acman]: A BAC transgenic platform for targeted insertion of large DNA fragments in D. melanogaster
-
Venken, K. J., He, Y., Hoskins, R. A. and Bellen, H. J. (2006). P[acman]: a BAC transgenic platform for targeted insertion of large DNA fragments in D. melanogaster. Science 314, 1747-1751.
-
(2006)
Science
, vol.314
, pp. 1747-1751
-
-
Venken, K.J.1
He, Y.2
Hoskins, R.A.3
Bellen, H.J.4
-
55
-
-
33646344977
-
Jagged1 (JAG1) mutations in Alagille syndrome: Increasing the mutation detection rate
-
Warthen, D. M., Moore, E. C., Kamath, B. M., Morrissette, J. J., Sanchez, P., Piccoli, D. A., Krantz, I. D. and Spinner, N. B. (2006). Jagged1 (JAG1) mutations in Alagille syndrome: increasing the mutation detection rate. Hum. Mutat. 27, 436-443.
-
(2006)
Hum. Mutat.
, vol.27
, pp. 436-443
-
-
Warthen, D.M.1
Moore, E.C.2
Kamath, B.M.3
Morrissette, J.J.4
Sanchez, P.5
Piccoli, D.A.6
Krantz, I.D.7
Spinner, N.B.8
-
56
-
-
0019466447
-
Discrete distribution of binding sites for Dolichos biflorus agglutinin (DBA) and for peanut agglutinin (PNA) in mouse organ tissues
-
Watanabe, M., Muramatsu, T., Shirane, H. and Ugai, K. (1981). Discrete distribution of binding sites for Dolichos biflorus agglutinin (DBA) and for peanut agglutinin (PNA) in mouse organ tissues. J. Histochem. Cytochem. 29, 779-780.
-
(1981)
J. Histochem. Cytochem.
, vol.29
, pp. 779-780
-
-
Watanabe, M.1
Muramatsu, T.2
Shirane, H.3
Ugai, K.4
-
57
-
-
77949896358
-
Mammalian Notch is modified by D-Xyl-{alpha}1-3-D-Xyl-{alpha}1-3-D-Glc-{beta}1-O-Ser: Implementation of a method to study O-glucosylation
-
Whitworth, G. E., Zandberg, W. F., Clark, T. and Vocadlo, D. J. (2010). Mammalian Notch is modified by D-Xyl-{alpha}1-3-D-Xyl-{alpha}1-3-D-Glc-{beta}1-O-Ser: implementation of a method to study O-glucosylation. Glycobiology 20, 287-299.
-
(2010)
Glycobiology
, vol.20
, pp. 287-299
-
-
Whitworth, G.E.1
Zandberg, W.F.2
Clark, T.3
Vocadlo, D.J.4
-
58
-
-
0032897080
-
Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1
-
Xue, Y., Gao, X., Lindsell, C. E., Norton, C. R., Chang, B., Hicks, C., Gendron-Maguire, M., Rand, E. B., Weinmaster, G. and Gridley, T. (1999). Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1. Hum. Mol. Genet. 8, 723-730.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 723-730
-
-
Xue, Y.1
Gao, X.2
Lindsell, C.E.3
Norton, C.R.4
Chang, B.5
Hicks, C.6
Gendron-Maguire, M.7
Rand, E.B.8
Weinmaster, G.9
Gridley, T.10
-
59
-
-
12944255642
-
Fringe glycosyltransferases differentially modulate Notch1 proteolysis induced by Delta1 and Jagged1
-
Yang, L. T., Nichols, J. T., Yao, C., Manilay, J. O., Robey, E. A. and Weinmaster, G. (2005). Fringe glycosyltransferases differentially modulate Notch1 proteolysis induced by Delta1 and Jagged1. Mol. Biol. Cell 16, 927-942.
-
(2005)
Mol. Biol. Cell
, vol.16
, pp. 927-942
-
-
Yang, L.T.1
Nichols, J.T.2
Yao, C.3
Manilay, J.O.4
Robey, E.A.5
Weinmaster, G.6
|