Similar articles for PMID: 7894484

Year	Number of Results
1990	1
1992	2
1993	3
1994	10
1995	5
1996	4
1997	7
1998	5
1999	7
2000	11
2001	8
2002	1
2003	6
2004	8
2005	5
2006	3
2007	5
2008	2
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2010	5
2011	1
2012	1
2013	2
2014	2
2015	2
2017	1
2019	2
2020	2
2021	1
2024	0

1

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

2

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

3

A novel missense mutation in the endoglin gene in hereditary hemorrhagic telangiectasia.

Yamaguchi H, Azuma H, Shigekiyo T, Inoue H, Saito S. Yamaguchi H, et al. Thromb Haemost. 1997 Feb;77(2):243-7. Thromb Haemost. 1997. PMID: 9157574

4

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

5

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.

6

A hereditary haemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1.

Wallace GM, Shovlin CL. Wallace GM, et al. Thorax. 2000 Aug;55(8):685-90. doi: 10.1136/thorax.55.8.685. Thorax. 2000. PMID: 10899246 Free PMC article.

7

Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation.

Lin WD, Wu JY, Hsu HB, Tsai FJ, Lee CC, Tsai CH. Lin WD, et al. J Formos Med Assoc. 2001 Dec;100(12):817-9. J Formos Med Assoc. 2001. PMID: 11802521

8

Molecular defects in rare bleeding disorders: hereditary haemorrhagic telangiectasia.

Shovlin CL. Shovlin CL. Thromb Haemost. 1997 Jul;78(1):145-50. Thromb Haemost. 1997. PMID: 9198145 Review.

9

Genetic and molecular pathogenesis of hereditary hemorrhagic telangiectasia.

Azuma H. Azuma H. J Med Invest. 2000 Aug;47(3-4):81-90. J Med Invest. 2000. PMID: 11019486 Review.

10

Blood outgrowth endothelial cells from Hereditary Haemorrhagic Telangiectasia patients reveal abnormalities compatible with vascular lesions.

Fernandez-L A, Sanz-Rodriguez F, Zarrabeitia R, Pérez-Molino A, Hebbel RP, Nguyen J, Bernabéu C, Botella LM. Fernandez-L A, et al. Cardiovasc Res. 2005 Nov 1;68(2):235-48. doi: 10.1016/j.cardiores.2005.06.009. Epub 2005 Jul 5. Cardiovasc Res. 2005. PMID: 15993872

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