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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 1 |
2010 | 2 |
2011 | 2 |
2012 | 2 |
2015 | 1 |
2024 | 0 |
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7 results
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Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis.
Clin Genet. 2011 Apr;79(4):335-44. doi: 10.1111/j.1399-0004.2010.01596.x. Epub 2010 Dec 16.
Clin Genet. 2011.
PMID: 21158752
Bioinformatic analysis of pathogenic missense mutations of activin receptor like kinase 1 ectodomain.
Scotti C, Olivieri C, Boeri L, Canzonieri C, Ornati F, Buscarini E, Pagella F, Danesino C.
Scotti C, et al.
PLoS One. 2011;6(10):e26431. doi: 10.1371/journal.pone.0026431. Epub 2011 Oct 18.
PLoS One. 2011.
PMID: 22028876
Free PMC article.
Item in Clipboard
Specificity and structure of a high affinity activin receptor-like kinase 1 (ALK1) signaling complex.
Townson SA, Martinez-Hackert E, Greppi C, Lowden P, Sako D, Liu J, Ucran JA, Liharska K, Underwood KW, Seehra J, Kumar R, Grinberg AV.
Townson SA, et al.
J Biol Chem. 2012 Aug 10;287(33):27313-25. doi: 10.1074/jbc.M112.377960. Epub 2012 Jun 20.
J Biol Chem. 2012.
PMID: 22718755
Free PMC article.
Item in Clipboard
Structure of the Alk1 extracellular domain and characterization of its bone morphogenetic protein (BMP) binding properties.
Mahlawat P, Ilangovan U, Biswas T, Sun LZ, Hinck AP.
Mahlawat P, et al.
Biochemistry. 2012 Aug 14;51(32):6328-41. doi: 10.1021/bi300942x. Epub 2012 Aug 2.
Biochemistry. 2012.
PMID: 22799562
Free PMC article.
Item in Clipboard
Functional analysis of the BMP9 response of ALK1 mutants from HHT2 patients: a diagnostic tool for novel ACVRL1 mutations.
Ricard N, Bidart M, Mallet C, Lesca G, Giraud S, Prudent R, Feige JJ, Bailly S.
Ricard N, et al.
Blood. 2010 Sep 2;116(9):1604-12. doi: 10.1182/blood-2010-03-276881. Epub 2010 May 25.
Blood. 2010.
PMID: 20501893
Free article.
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Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia.
Alaa El Din F, Patri S, Thoreau V, Rodriguez-Ballesteros M, Hamade E, Bailly S, Gilbert-Dussardier B, Abou Merhi R, Kitzis A.
Alaa El Din F, et al.
PLoS One. 2015 Jul 15;10(7):e0132111. doi: 10.1371/journal.pone.0132111. eCollection 2015.
PLoS One. 2015.
PMID: 26176610
Free PMC article.
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Novel mutations in the ENG and ACVRL1 genes causing hereditary hemorrhagic teleangiectasia.
Argyriou L, Twelkemeyer S, Panchulidze I, Wehner LE, Teske U, Engel W, Nayernia K.
Argyriou L, et al.
Int J Mol Med. 2006 Apr;17(4):655-9.
Int J Mol Med. 2006.
PMID: 16525724
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