PubMed (OMIM) for id: 324960

Year	Number of Results
1972	1
1993	2
1994	5
1995	2
1996	1
1997	1
1998	1
1999	1
2000	3
2001	3
2003	7
2004	2
2005	1
2024	0

1

Human retroviral gag- and gag-pol-like proteins interact with the transforming growth factor-beta receptor activin receptor-like kinase 1.

Lux A, Beil C, Majety M, Barron S, Gallione CJ, Kuhn HM, Berg JN, Kioschis P, Marchuk DA, Hafner M. Lux A, et al. J Biol Chem. 2005 Mar 4;280(9):8482-93. doi: 10.1074/jbc.M409197200. Epub 2004 Dec 16. J Biol Chem. 2005. PMID: 15611116 Free article.

2

Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France.

Lesca G, Plauchu H, Coulet F, Lefebvre S, Plessis G, Odent S, Rivière S, Leheup B, Goizet C, Carette MF, Cordier JF, Pinson S, Soubrier F, Calender A, Giraud S; French Rendu-Osler Network. Lesca G, et al. Hum Mutat. 2004 Apr;23(4):289-99. doi: 10.1002/humu.20017. Hum Mutat. 2004. PMID: 15024723

3

Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia.

Harrison RE, Flanagan JA, Sankelo M, Abdalla SA, Rowell J, Machado RD, Elliott CG, Robbins IM, Olschewski H, McLaughlin V, Gruenig E, Kermeen F, Halme M, Räisänen-Sokolowski A, Laitinen T, Morrell NW, Trembath RC. Harrison RE, et al. J Med Genet. 2003 Dec;40(12):865-71. doi: 10.1136/jmg.40.12.865. J Med Genet. 2003. PMID: 14684682 Free PMC article.

4

Arterial endothelium-specific activin receptor-like kinase 1 expression suggests its role in arterialization and vascular remodeling.

Seki T, Yun J, Oh SP. Seki T, et al. Circ Res. 2003 Oct 3;93(7):682-9. doi: 10.1161/01.RES.0000095246.40391.3B. Epub 2003 Sep 11. Circ Res. 2003. PMID: 12970115

5

Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.

Berg J, Porteous M, Reinhardt D, Gallione C, Holloway S, Umasunthar T, Lux A, McKinnon W, Marchuk D, Guttmacher A. Berg J, et al. J Med Genet. 2003 Aug;40(8):585-90. doi: 10.1136/jmg.40.8.585. J Med Genet. 2003. PMID: 12920067 Free PMC article.

6

Visceral manifestations in hereditary haemorrhagic telangiectasia type 2.

Abdalla SA, Geisthoff UW, Bonneau D, Plauchu H, McDonald J, Kennedy S, Faughnan ME, Letarte M. Abdalla SA, et al. J Med Genet. 2003 Jul;40(7):494-502. doi: 10.1136/jmg.40.7.494. J Med Genet. 2003. PMID: 12843319 Free PMC article.

7

Disease-associated mutations in conserved residues of ALK-1 kinase domain.

Abdalla SA, Cymerman U, Johnson RM, Deber CM, Letarte M. Abdalla SA, et al. Eur J Hum Genet. 2003 Apr;11(4):279-87. doi: 10.1038/sj.ejhg.5200919. Eur J Hum Genet. 2003. PMID: 12700602

8

Vascular morphogenesis: tales of two syndromes.

Marchuk DA, Srinivasan S, Squire TL, Zawistowski JS. Marchuk DA, et al. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R97-112. doi: 10.1093/hmg/ddg103. Hum Mol Genet. 2003. PMID: 12668602 Review.

9

A mouse model for hereditary hemorrhagic telangiectasia (HHT) type 2.

Srinivasan S, Hanes MA, Dickens T, Porteous ME, Oh SP, Hale LP, Marchuk DA. Srinivasan S, et al. Hum Mol Genet. 2003 Mar 1;12(5):473-82. doi: 10.1093/hmg/ddg050. Hum Mol Genet. 2003. PMID: 12588795

10

Genetic clues to the cause of primary pulmonary hypertension.

Loscalzo J. Loscalzo J. N Engl J Med. 2001 Aug 2;345(5):367-71. doi: 10.1056/NEJM200108023450511. N Engl J Med. 2001. PMID: 11484696 No abstract available.

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