Endothelial Cells from Capillary Malformations Are Enriched for Somatic GNAQ Mutations-Reference-Cited by-同舟云学术

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Endothelial Cells from Capillary Malformations Are Enriched for Somatic GNAQ Mutations

Published:2016-01 Issue:1 Volume:137 Page:77e-82e
ISSN:0032-1052
Container-title:Plastic and Reconstructive Surgery
language:en
Short-container-title:Plastic and Reconstructive Surgery

Author:

Couto Javier A.,Huang Lan,Vivero Matthew P.,Kamitaki Nolan,Maclellan Reid A.,Mulliken John B.,Bischoff Joyce,Warman Matthew L.,Greene Arin K.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Surgery

Reference10 articles.

1. Histopathology of Vascular Anomalies

2. Sturge-Weber Syndrome

3. Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ

4. Mitogenic signaling pathways induced by G protein-coupled receptors

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1. Somatic Loss-of-Function PIK3R1 and Activating Non-hotspot PIK3CA Mutations Associated with Capillary Malformation with Dilated Veins (CMDV);Journal of Investigative Dermatology;2024-09

2. Pathophysiology in Brain Arteriovenous Malformations: Focus on Endothelial Dysfunctions and Endothelial-to-Mesenchymal Transition;Biomedicines;2024-08-07

3. Congenital Vascular and Lymphatic Diseases;Circulation Research;2024-06-21

4. Similarities and differences between brain and skinGNAQp.R183Q driven capillary malformations;2024-06-19

5. Capillary malformations;Journal of Clinical Investigation;2024-04-15

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