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Myeloid-Specific Deletion of Epsins 1 and 2 Reduces Atherosclerosis by Preventing LRP-1 Downregulation

Publication: Journal Article

Brophy, Megan, Yunzhou Dong, Huan Tao, Patricia Yancey, Kai Song, Kun Zhang, Aiyun Wen, et al. 2019. “Myeloid-Specific Deletion of Epsins 1 and 2 Reduces Atherosclerosis by Preventing LRP-1 Downregulation”. Circ Res 124 (4): e6-e19.

Non-β-blocker enantiomers of propranolol and atenolol inhibit vasculogenesis in infantile hemangioma

Publication: Journal Article

Seebauer, Caroline, Matthew Graus, Lan Huang, Alex McCann, Jill Wylie-Sears, Frank Fontaine, Tara Karnezis, et al. 2021. “Non-β-Blocker Enantiomers of Propranolol and Atenolol Inhibit Vasculogenesis in Infantile Hemangioma”. J Clin Invest.

Isolation of Stem Cells, Endothelial Cells and Pericytes from Human Infantile Hemangioma

Publication: Journal Article

Huang, Lan, and Joyce Bischoff. 2020. “Isolation of Stem Cells, Endothelial Cells and Pericytes from Human Infantile Hemangioma”. Bio Protoc 10 (2): e3487.

Lan Huang, PhD, of Boston Children's Hospital Receives Lisa's Sturge-Weber Foundation Research Fellowship Award

News: May 11, 2016

The Sturge-Weber Foundation (SWF), a 501 (c)(3)nonprofit organization, has named Lan Huang, PhD, of Boston Children's Hospital the recipient of the inaugural Lisa's Sturge-Weber Research Fellowship Award. Research is defined as "patient-oriented research" conducted with human subjects, or...

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Vascular Malformations

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Vascular malformations are defects in the architecture and function of arteries, veins, capillaries and lymphatic vessels. The malformations can be familial or sporadic, and are often associated with tissue overgrowth, deformity and infections. We focus on capillary malformations (CM) - excessive...

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A “CRISPR” view of Sturge-Weber syndrome is coming into focus November 6, 2017 Three-dimensional modeling and CRISPR-Cas9 gene editing technology are giving scientists a new view into Sturge-Weber syndrome , a rare congenital disorder that causes small blood vessels, called capillaries, to be...

Patients’ brain tissue unlocks the cellular hideout of Sturge-Weber’s gene mutation

News: March 01, 2017

A person born with a port-wine birthmark on his or her face and eyelid(s) has an 8 to 15 percent chance of being diagnosed with Sturge-Weber syndrome. The rare disorder causes malformations in certain regions of the body’s capillaries (small blood vessels). Port-wine birthmarks appear on areas of...

A somatic GNA11 mutation is associated with extremity capillary malformation and overgrowth

Publication: Journal Article

Couto, Javier, Ugur Ayturk, Dennis Konczyk, Jeremy Goss, August Huang, Steve Hann, Jennifer Reeve, et al. 2017. “A Somatic GNA11 Mutation Is Associated With Extremity Capillary Malformation and Overgrowth”. Angiogenesis 20 (3): 303-6.

Endothelial Cells from Capillary Malformations Are Enriched for Somatic GNAQ Mutations

Publication: Journal Article

Couto, Javier, Lan Huang, Matthew Vivero, Nolan Kamitaki, Reid Maclellan, John Mulliken, Joyce Bischoff, Matthew Warman, and Arin Greene. 2016. “Endothelial Cells from Capillary Malformations Are Enriched for Somatic GNAQ Mutations”. Plast Reconstr Surg 137 (1): 77e-82e.