Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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Biology of Vascular Endothelial Growth Factor C in the Morphogenesis of Lymphatic Vessels.

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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type

Item

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

@nl

P1476

Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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P2093

Alain Colige

http://www.w3.org/2001/XMLSchema#string

George E Tiller

http://www.w3.org/2001/XMLSchema#string

Joseph Peeden

http://www.w3.org/2001/XMLSchema#string

Laura Dupont

http://www.w3.org/2001/XMLSchema#string

Pascal Brouillard

http://www.w3.org/2001/XMLSchema#string

Raphael Helaers

http://www.w3.org/2001/XMLSchema#string

Richard Coulie

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P2860

Protein tyrosine phosphatase PTPN14 is a regulator of lymphatic function and choanal development in humans

CCBE1 is essential for mammalian lymphatic vascular development and enhances the lymphangiogenic effect of vascular endothelial growth factor-C in vivo

Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans

CCBE1 enhances lymphangiogenesis via A disintegrin and metalloprotease with thrombospondin motifs-3-mediated vascular endothelial growth factor-C activation

EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

Domains and maturation processes that regulate the activity of ADAMTS-2, a metalloproteinase cleaving the aminopropeptide of fibrillar procollagens types I-III and V

Genetics of lymphatic anomalies

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

Efficient activation of the lymphangiogenic growth factor VEGF-C requires the C-terminal domain of VEGF-C and the N-terminal domain of CCBE1

P304

4095-4104

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scholarly article

P356

10.1093/HMG/DDX297

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http://www.w3.org/2001/XMLSchema#string

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Miikka Vikkula

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2017-08-02T00:00:00Z

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28985353

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.

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P2093

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P698

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P577

P698