-
1
-
-
0028639196
-
Targeted and natural (piebaldlethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice
-
Hosoda K, Hammer RE, Richardson JA, Baynash AG, Cheung JC, Giaid A, Yanagisawa M (1994) Targeted and natural (piebaldlethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice. Cell 79: 1267-1276
-
(1994)
Cell
, vol.79
, pp. 1267-1276
-
-
Hosoda, K.1
Hammer, R.E.2
Richardson, J.A.3
Baynash, A.G.4
Cheung, J.C.5
Giaid, A.6
Yanagisawa, M.7
-
2
-
-
0028609612
-
Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons
-
Baynash AG, Hosoda K, Giaid A, Richardson JA, Emoto N, Hammer RE, Yanagisawa M (1994) Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons. Cell 79: 1277-1285
-
(1994)
Cell
, vol.79
, pp. 1277-1285
-
-
Baynash, A.G.1
Hosoda, K.2
Giaid, A.3
Richardson, J.A.4
Emoto, N.5
Hammer, R.E.6
Yanagisawa, M.7
-
3
-
-
0028618372
-
A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease
-
Puffenberger EG, Hosoda K, Washington SS, Nakao K, deWit D, Yanagisawa M, Chakravarti A (1994) A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease. Cell 79: 1257-1266
-
(1994)
Cell
, vol.79
, pp. 1257-1266
-
-
Puffenberger, E.G.1
Hosoda, K.2
Washington, S.S.3
Nakao, K.4
Dewit, D.5
Yanagisawa, M.6
Chakravarti, A.7
-
4
-
-
0024358095
-
Association of 13q deletion and Hirschsprung's disease
-
Kiss P, Osztovics M (1989) Association of 13q deletion and Hirschsprung's disease. J Med Genet 26: 793-794
-
(1989)
J Med Genet
, vol.26
, pp. 793-794
-
-
Kiss, P.1
Osztovics, M.2
-
5
-
-
0024576097
-
Interstitial deletion of distal 13q associated with Hirschsprung's disease
-
Lamont MA, Fitchett M, Dennis NR (1989) Interstitial deletion of distal 13q associated with Hirschsprung's disease. J Med Genet 26: 100-104
-
(1989)
J Med Genet
, vol.26
, pp. 100-104
-
-
Lamont, M.A.1
Fitchett, M.2
Dennis, N.R.3
-
6
-
-
0025944896
-
A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): Potential mapping of one disease locus
-
Bottani A, Xie Y, Binkert F (1991) A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus. Hum Genet 87: 748-750
-
(1991)
Hum Genet
, vol.87
, pp. 748-750
-
-
Bottani, A.1
Xie, Y.2
Binkert, F.3
-
7
-
-
0027499701
-
The human endothelin-B receptor gene: Structural organization and chromosomal assignment
-
Arai H, Nakao K, Takaya K, Hosoda K, Ogawa Y, Nakanishi S, Imura H (1993) The human endothelin-B receptor gene: structural organization and chromosomal assignment. J Biol Chem 268: 3463-3470
-
(1993)
J Biol Chem
, vol.268
, pp. 3463-3470
-
-
Arai, H.1
Nakao, K.2
Takaya, K.3
Hosoda, K.4
Ogawa, Y.5
Nakanishi, S.6
Imura, H.7
-
8
-
-
0028069130
-
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22
-
Puffenberger EG, Kauffman ER, Bolk S, Matise TC, Washington SS, Angrist M, Weissenbach J, Garver KL, Mascari M, Ladda T (1994) Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. Hum Mol Genet 3: 1217-1225
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1217-1225
-
-
Puffenberger, E.G.1
Kauffman, E.R.2
Bolk, S.3
Matise, T.C.4
Washington, S.S.5
Angrist, M.6
Weissenbach, J.7
Garver, K.L.8
Mascari, M.9
Ladda, T.10
-
9
-
-
0028844260
-
Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (si) rat
-
Ceccherini I, Zhang AL, Matera I, Yang G, Devoto M, Romeo G, Cass DT (1995) Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (si) rat. Hum Mol Genet 4: 2089-2096
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2089-2096
-
-
Ceccherini, I.1
Zhang, A.L.2
Matera, I.3
Yang, G.4
Devoto, M.5
Romeo, G.6
Cass, D.T.7
-
10
-
-
0030033185
-
Null mutation of endothelin receptor type B in spotting lethal rats causes aganglionic megacolon and white coat color
-
Gariepy CE, Cass DT, Yanagisawa M (1996) Null mutation of endothelin receptor type B in spotting lethal rats causes aganglionic megacolon and white coat color. Proc Natl Acad Sci USA 93: 867-872
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 867-872
-
-
Gariepy, C.E.1
Cass, D.T.2
Yanagisawa, M.3
-
11
-
-
0013543367
-
The human endothelin family: Three structurally and pharmacologically distinct isopeptides predicted by three separate genes
-
Inoue A, Yanagisawa M, Kimura S, Kasuya Y, Miyauchi T, Goto K, Masaki T (1989) The human endothelin family: three structurally and pharmacologically distinct isopeptides predicted by three separate genes. Proc Natl Acad Sci U S A 86: 2863-2867
-
(1989)
Proc Natl Acad Sci U S A
, vol.86
, pp. 2863-2867
-
-
Inoue, A.1
Yanagisawa, M.2
Kimura, S.3
Kasuya, Y.4
Miyauchi, T.5
Goto, K.6
Masaki, T.7
-
12
-
-
0023859136
-
A novel potent vasoconstrictor peptide produced by vascular endothelial cells
-
Yanagisawa M, Kurihara H, Kimura S, Tomobe Y, Kobayashi M, Mitsui Y, Yazaki Y, Goto K, Masaki T (1988) A novel potent vasoconstrictor peptide produced by vascular endothelial cells. Nature 332: 411-415
-
(1988)
Nature
, vol.332
, pp. 411-415
-
-
Yanagisawa, M.1
Kurihara, H.2
Kimura, S.3
Tomobe, Y.4
Kobayashi, M.5
Mitsui, Y.6
Yazaki, Y.7
Goto, K.8
Masaki, T.9
-
13
-
-
0024465081
-
Molecular biology and biochemistry of the endothelins
-
Yanagisawa M, Masaki T (1989) Molecular biology and biochemistry of the endothelins. TIBS 10: 374-378
-
(1989)
TIBS
, vol.10
, pp. 374-378
-
-
Yanagisawa, M.1
Masaki, T.2
-
14
-
-
0027724236
-
Presence of furin mRNA in cultured bovine endothelial cells and possible involvement of furin in the processing of the endothelin precursor
-
Laporte S, Denault JB, D'Orleans-Juste P, Leduc R (1993) Presence of furin mRNA in cultured bovine endothelial cells and possible involvement of furin in the processing of the endothelin precursor. J Cardiovasc Pharmacol 22 [suppl 8]: S7-S10
-
(1993)
J Cardiovasc Pharmacol
, vol.22
, Issue.8 SUPPL.
-
-
Laporte, S.1
Denault, J.B.2
D'Orleans-Juste, P.3
Leduc, R.4
-
15
-
-
0028916603
-
Processing of proendothelin-1 by human furin convertase
-
Denault JB, Claing A, D'Orleans-Juste P, Sawamura T, Kido T, Masaki T, Leduc R (1995) Processing of proendothelin-1 by human furin convertase. FEBS Lett 362: 276-280
-
(1995)
FEBS Lett
, vol.362
, pp. 276-280
-
-
Denault, J.B.1
Claing, A.2
D'Orleans-Juste, P.3
Sawamura, T.4
Kido, T.5
Masaki, T.6
Leduc, R.7
-
16
-
-
0027992642
-
ECE-1: A membrane-bound metalloprotease that catalyzes the proteolytic activation of big endothelin-1
-
Xu D, Emoto N, Giaid A, Slaughter C, Kaw S, deWit D, Yanagisawa M (1994) ECE-1: a membrane-bound metalloprotease that catalyzes the proteolytic activation of big endothelin-1. Cell 78: 473-485
-
(1994)
Cell
, vol.78
, pp. 473-485
-
-
Xu, D.1
Emoto, N.2
Giaid, A.3
Slaughter, C.4
Kaw, S.5
DeWit, D.6
Yanagisawa, M.7
-
17
-
-
0025605345
-
Cloning and expression of a cDNA encoding an endothelin receptor
-
Arai H, Hori S, Aramori I, Ohkubo H, Nakanishi S (1990) Cloning and expression of a cDNA encoding an endothelin receptor. Nature 348: 730-732
-
(1990)
Nature
, vol.348
, pp. 730-732
-
-
Arai, H.1
Hori, S.2
Aramori, I.3
Ohkubo, H.4
Nakanishi, S.5
-
18
-
-
0025605930
-
Cloning of a cDNA encoding a non-isopeptide-selective subtype of the endothelin receptor
-
Sakurai T, Yanagisawa MYT, Miyazaki H, Kimura S, Goto K, Masaki T (1990) Cloning of a cDNA encoding a non-isopeptide-selective subtype of the endothelin receptor. Nature 348: 732-735
-
(1990)
Nature
, vol.348
, pp. 732-735
-
-
Sakurai, T.1
Yanagisawa, M.Y.T.2
Miyazaki, H.3
Kimura, S.4
Goto, K.5
Masaki, T.6
-
19
-
-
0026667386
-
Organization, structure, chromosomal assignment, and expression of the gene encoding the human endothelin-A receptor
-
Hosoda K, Nakao K, Tamura N, Arai H, Ogawa Y, Suga S, Nakanishi S, Imura H (1992) Organization, structure, chromosomal assignment, and expression of the gene encoding the human endothelin-A receptor. J Biol Chem 267: 18797-18804
-
(1992)
J Biol Chem
, vol.267
, pp. 18797-18804
-
-
Hosoda, K.1
Nakao, K.2
Tamura, N.3
Arai, H.4
Ogawa, Y.5
Suga, S.6
Nakanishi, S.7
Imura, H.8
-
21
-
-
0028212006
-
The endothelin system: A new target for therapeutic intervention
-
Yanagisawa M (1994) The endothelin system: a new target for therapeutic intervention. Circulation 89: 1320-1322
-
(1994)
Circulation
, vol.89
, pp. 1320-1322
-
-
Yanagisawa, M.1
-
22
-
-
0028074215
-
Molecular and functional characterization of the non-isopeptide-selective ETB receptor in endothelial cells: Receptor coupling to nitric oxide synthase
-
Tsukahara H, Ende H, Magazine HI, Bahou WF, Gologorsky MS (1994) Molecular and functional characterization of the non-isopeptide-selective ETB receptor in endothelial cells: receptor coupling to nitric oxide synthase. J Biol Chem 269: 21 778-21 785
-
(1994)
J Biol Chem
, vol.269
, pp. 21778-21785
-
-
Tsukahara, H.1
Ende, H.2
Magazine, H.I.3
Bahou, W.F.4
Gologorsky, M.S.5
-
23
-
-
0029077731
-
Differentiation of embryonal carcinoma cells to a neural or cardiomyocyte lineage is associated with selective expression of endothelin receptors
-
Monge JC, Stewart DJ, Cernacek P (1995) Differentiation of embryonal carcinoma cells to a neural or cardiomyocyte lineage is associated with selective expression of endothelin receptors. J Biol Chem 270: 15 385-15 390
-
(1995)
J Biol Chem
, vol.270
, pp. 15385-15390
-
-
Monge, J.C.1
Stewart, D.J.2
Cernacek, P.3
-
24
-
-
0345230340
-
A receptor gene in mice results in developmental defects in brachial region
-
A receptor gene in mice results in developmental defects in brachial region. Circulation 90: 634
-
(1994)
Circulation
, vol.90
, pp. 634
-
-
Hosoda, K.1
Hammer, R.2
Yanagisawa, M.3
-
25
-
-
0028360062
-
Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1
-
Kurihara Y, Kurihara H, Suzuku H, Kodama T, Maemura K, Nagai R, Oda H, Kuwaki T, Cao WH, Kamada N (1994) Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1. Nature 368: 703-710
-
(1994)
Nature
, vol.368
, pp. 703-710
-
-
Kurihara, Y.1
Kurihara, H.2
Suzuku, H.3
Kodama, T.4
Maemura, K.5
Nagai, R.6
Oda, H.7
Kuwaki, T.8
Cao, W.H.9
Kamada, N.10
-
26
-
-
0029092767
-
Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1
-
Kurihara Y, Kurihara H, Oda H, Maemura K, Nagai R, Ishikawa T, Yazaki Y (1995) Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1. J Clin Invest 96: 293-300
-
(1995)
J Clin Invest
, vol.96
, pp. 293-300
-
-
Kurihara, Y.1
Kurihara, H.2
Oda, H.3
Maemura, K.4
Nagai, R.5
Ishikawa, T.6
Yazaki, Y.7
-
28
-
-
0024433980
-
A novel peptide, vasoactive intestinal contractor, of a new (endothelin) peptide family: Molecular cloning, expression, and biological activity
-
Saida K, Mitsui Y, Ishida N (1989) A novel peptide, vasoactive intestinal contractor, of a new (endothelin) peptide family: molecular cloning, expression, and biological activity. J Biol Chem 264: 14 613-14 616
-
(1989)
J Biol Chem
, vol.264
, pp. 14613-14616
-
-
Saida, K.1
Mitsui, Y.2
Ishida, N.3
-
29
-
-
0025847317
-
cDNA cloning and chromosomal assignment of the endothelin 2 gene: Vasoactive intestinal contractor peptide is rat endothelin 2
-
Bloch KD, Hong CC, Eddy RL, Shows TB, Quertermous T (1991) cDNA cloning and chromosomal assignment of the endothelin 2 gene: vasoactive intestinal contractor peptide is rat endothelin 2. Genomics 10: 236-242
-
(1991)
Genomics
, vol.10
, pp. 236-242
-
-
Bloch, K.D.1
Hong, C.C.2
Eddy, R.L.3
Shows, T.B.4
Quertermous, T.5
-
30
-
-
0030022843
-
Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease
-
Kusafuka T, Wang Y, Puri P (1996) Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease. Hum Mol Genet 5: 347-349
-
(1996)
Hum Mol Genet
, vol.5
, pp. 347-349
-
-
Kusafuka, T.1
Wang, Y.2
Puri, P.3
-
31
-
-
0030962660
-
Mutation analysis of the RET, the endothelin-B receptor and the endothelin-3 genes in sporadic patients with Hirschsprung's disease
-
in press
-
Kusafuka T, Wang Y, Puri P (in press) Mutation analysis of the RET, the endothelin-B receptor and the endothelin-3 genes in sporadic patients with Hirschsprung's disease. J Pediatr Surg
-
J Pediatr Surg
-
-
Kusafuka, T.1
Wang, Y.2
Puri, P.3
-
32
-
-
0028862473
-
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease
-
Attie T, Till M, Pelet A, Amiel J, Edery P, Boutrand L, Munnich A, Lyonnet S (1995) Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease. Hum Mol Genet 4: 2407-2409
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2407-2409
-
-
Attie, T.1
Till, M.2
Pelet, A.3
Amiel, J.4
Edery, P.5
Boutrand, L.6
Munnich, A.7
Lyonnet, S.8
-
33
-
-
0030070810
-
Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population
-
Auricchio A, Casari G, Staiano A, Ballabio A (1996) Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population. Hum Mol Genet 5: 351-354
-
(1996)
Hum Mol Genet
, vol.5
, pp. 351-354
-
-
Auricchio, A.1
Casari, G.2
Staiano, A.3
Ballabio, A.4
-
34
-
-
9044220230
-
Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease
-
Amiel J, Attie T, Jan D, Pelet A, Edery P, Bidaud C, Lacombe D, Tam P, Simeoni J, Flori E (1996) Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease. Hum Mol Genet 5: 355-357
-
(1996)
Hum Mol Genet
, vol.5
, pp. 355-357
-
-
Amiel, J.1
Attie, T.2
Jan, D.3
Pelet, A.4
Edery, P.5
Bidaud, C.6
Lacombe, D.7
Tam, P.8
Simeoni, J.9
Flori, E.10
-
35
-
-
0009675716
-
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)
-
Hofstra RMW, Osinga J, Tan-Sindhunata G, Wu Y, Kamsteeg EJ, Stulp RP, Ravenswaaij-Arts C v, Majoor-Krakauer D, Angrist M, Chakravarti A (1996) A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome). Nat Genet 12: 445-447
-
(1996)
Nat Genet
, vol.12
, pp. 445-447
-
-
Hofstra, R.M.W.1
Osinga, J.2
Tan-Sindhunata, G.3
Wu, Y.4
Kamsteeg, E.J.5
Stulp, R.P.6
Ravenswaaij-Arts, C.V.7
Majoor-Krakauer, D.8
Angrist, M.9
Chakravarti, A.10
-
36
-
-
0006457459
-
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
-
Edery P, Attie T, Amiel J, Pelet A, Eng C, Hofstra RMW, Martelh H, Bidaud C, Munnich A, Lyonnet S (1996) Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome). Nat Genet 12: 442-444
-
(1996)
Nat Genet
, vol.12
, pp. 442-444
-
-
Edery, P.1
Attie, T.2
Amiel, J.3
Pelet, A.4
Eng, C.5
Hofstra, R.M.W.6
Martelh, H.7
Bidaud, C.8
Munnich, A.9
Lyonnet, S.10
-
37
-
-
0021348864
-
Interstitial deletion of long arm of chromosome 13
-
Paris
-
Carnevale A, Frias S, Alcantar R (1984) Interstitial deletion of long arm of chromosome 13. Ann Genet (Paris) 27: 49-52
-
(1984)
Ann Genet
, vol.27
, pp. 49-52
-
-
Carnevale, A.1
Frias, S.2
Alcantar, R.3
-
38
-
-
0030029691
-
Endothelin receptor-mediated signaling in Hirschsprung disease
-
Chakravarti A (1996) Endothelin receptor-mediated signaling in Hirschsprung disease. Hum Mol Genet 5: 303-307
-
(1996)
Hum Mol Genet
, vol.5
, pp. 303-307
-
-
Chakravarti, A.1
|