Similar articles for PMID: 7782079

Year	Number of Results
1986	1
1987	2
1988	3
1989	4
1990	6
1991	13
1992	5
1993	8
1994	10
1995	10
1996	4
1997	2
1998	1
1999	6
2000	2
2002	1
2003	1
2004	3
2005	3
2006	1
2008	1
2014	1
2015	1
2024	0

1

The murine endoglin gene (Eng) maps to chromosome 2.

Qureshi ST, Gros P, Letarte M, Malo D. Qureshi ST, et al. Genomics. 1995 Mar 1;26(1):165-6. doi: 10.1016/0888-7543(95)80099-8. Genomics. 1995. PMID: 7782079 No abstract available.

2

Assignment of the human endoglin gene (END) to 9q34-->qter.

Fernández-Ruiz E, St-Jacques S, Bellón T, Letarte M, Bernabéu C. Fernández-Ruiz E, et al. Cytogenet Cell Genet. 1993;64(3-4):204-7. doi: 10.1159/000133576. Cytogenet Cell Genet. 1993. PMID: 8404038

3

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.

Vincent P, Plauchu H, Hazan J, Fauré S, Weissenbach J, Godet J. Vincent P, et al. Hum Mol Genet. 1995 May;4(5):945-9. doi: 10.1093/hmg/4.5.945. Hum Mol Genet. 1995. PMID: 7633456

4

Endoglin is not a major susceptibility gene for intracranial aneurysm among Japanese.

Onda H, Kasuya H, Yoneyama T, Hori T, Nakajima T, Inoue I. Onda H, et al. Stroke. 2003 Jul;34(7):1640-4. doi: 10.1161/01.STR.0000075770.70554.99. Epub 2003 May 29. Stroke. 2003. PMID: 12775886

5

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.

McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE, Helmbold EA, Markel DS, McKinnon WC, Murrell J, et al. McAllister KA, et al. Nat Genet. 1994 Dec;8(4):345-51. doi: 10.1038/ng1294-345. Nat Genet. 1994. PMID: 7894484

6

Defective angiogenesis in mice lacking endoglin.

Li DY, Sorensen LK, Brooke BS, Urness LD, Davis EC, Taylor DG, Boak BB, Wendel DP. Li DY, et al. Science. 1999 May 28;284(5419):1534-7. doi: 10.1126/science.284.5419.1534. Science. 1999. PMID: 10348742

7

Cloning and expression of a cDNA encoding mouse endoglin, an endothelial cell TGF-beta ligand.

Ge AZ, Butcher EC. Ge AZ, et al. Gene. 1994 Jan 28;138(1-2):201-6. doi: 10.1016/0378-1119(94)90808-7. Gene. 1994. PMID: 8125301

8

Vascular endothelial growth factor induces abnormal microvasculature in the endoglin heterozygous mouse brain.

Xu B, Wu YQ, Huey M, Arthur HM, Marchuk DA, Hashimoto T, Young WL, Yang GY. Xu B, et al. J Cereb Blood Flow Metab. 2004 Feb;24(2):237-44. doi: 10.1097/01.WCB.0000107730.66603.51. J Cereb Blood Flow Metab. 2004. PMID: 14747750

9

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles.

Gallione CJ, Klaus DJ, Yeh EY, Stenzel TT, Xue Y, Anthony KB, McAllister KA, Baldwin MA, Berg JN, Lux A, Smith JD, Vary CP, Craigen WJ, Westermann CJ, Warner ML, Miller YE, Jackson CE, Guttmacher AE, Marchuk DA. Gallione CJ, et al. Hum Mutat. 1998;11(4):286-94. doi: 10.1002/(SICI)1098-1004(1998)11:4<286::AID-HUMU6>3.0.CO;2-B. Hum Mutat. 1998. PMID: 9554745

10

Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1 suggest a dominant-negative effect of receptor function.

McAllister KA, Baldwin MA, Thukkani AK, Gallione CJ, Berg JN, Porteous ME, Guttmacher AE, Marchuk DA. McAllister KA, et al. Hum Mol Genet. 1995 Oct;4(10):1983-5. doi: 10.1093/hmg/4.10.1983. Hum Mol Genet. 1995. PMID: 8595426 No abstract available.

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