Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia
about
Activin receptor-like kinases: a diverse family playing an important role in cancerA mouse model of hereditary hemorrhagic telangiectasia generated by transmammary-delivered immunoblocking of BMP9 and BMP10.Tacrolimus rescues the signaling and gene expression signature of endothelial ALK1 loss-of-function and improves HHT vascular pathology.Myopenia and precision (P4) medicine.
P2860
Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia
description
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique PLoS ONE
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artikull shkencor
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artículu científicu espublizáu en 2015
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im Januar 2015 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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wetenschappelijk artikel
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наукова стаття, опублікована в січні 2015
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مقالة علمية (نشرت عام 2015)
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name
Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
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Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
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Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
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type
label
Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
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Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
@en
Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
@nl
prefLabel
Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
@ast
Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
@en
Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
@nl
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Functional and splicing defect ...... ary Hemorrhagic Telangiectasia
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P2093
Alain Kitzis
Ferdos Alaa El Din
Montserrat Rodriguez-Ballesteros
Raghida Abou Merhi
Sylvie Patri
Vincent Thoreau
P2860
P304
P356
10.1371/JOURNAL.PONE.0132111
P407
P577
2015-07-15T00:00:00Z