Literature DB >> 25830521

Endothelial chromosome 13 deletion in congenital heart disease-associated pulmonary arterial hypertension dysregulates SMAD9 signaling.

Kylie M Drake1, Suzy A Comhair, Serpil C Erzurum, Rubin M Tuder, Micheala A Aldred.   

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Year:  2015        PMID: 25830521      PMCID: PMC4407488          DOI: 10.1164/rccm.201411-1985LE

Source DB:  PubMed          Journal:  Am J Respir Crit Care Med        ISSN: 1073-449X            Impact factor:   21.405


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  22 in total

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4.  Somatic chromosome abnormalities in the lungs of patients with pulmonary arterial hypertension.

Authors:  Micheala A Aldred; Suzy A Comhair; Marileila Varella-Garcia; Kewal Asosingh; Weiling Xu; George P Noon; Patricia A Thistlethwaite; Rubin M Tuder; Serpil C Erzurum; Mark W Geraci; Christopher D Coldren
Journal:  Am J Respir Crit Care Med       Date:  2010-06-25       Impact factor: 21.405

5.  Mosaic ACVRL1 and ENG mutations in hereditary haemorrhagic telangiectasia patients.

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7.  Pulmonary arterial hypertension: baseline characteristics from the REVEAL Registry.

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8.  A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension.

Authors:  M Shintani; H Yagi; T Nakayama; T Saji; R Matsuoka
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9.  Multiple sequence variants in hereditary hemorrhagic telangiectasia cases: illustration of complexity in molecular diagnostic interpretation.

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10.  Defective pulmonary vascular remodeling in Smad8 mutant mice.

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1.  Translational Advances in the Field of Pulmonary Hypertension Molecular Medicine of Pulmonary Arterial Hypertension. From Population Genetics to Precision Medicine and Gene Editing.

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Review 4.  'There and Back Again'-Forward Genetics and Reverse Phenotyping in Pulmonary Arterial Hypertension.

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5.  Increased Mutagen Sensitivity and DNA Damage in Pulmonary Arterial Hypertension.

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8.  Genomic stability of pulmonary artery endothelial colony-forming cells in culture.

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Review 9.  Genetics and genomics of pulmonary arterial hypertension.

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