Loss-of-function mutations of the TIE1 receptor tyrosine kinase cause late-onset primary lymphedema-Reference-Cited by-同舟云学术

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Loss-of-function mutations of the TIE1 receptor tyrosine kinase cause late-onset primary lymphedema

Published:2024-05-30 Issue:14 Volume:134 Page:
ISSN:1558-8238
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Brouillard Pascal^ORCID,Murtomäki Aino,Leppänen Veli-Matti^ORCID,Hyytiäinen Marko,Mestre Sandrine,Potier Lucas^ORCID,Boon Laurence M.^ORCID,Revencu Nicole,Greene Arin,Anisimov Andrey^ORCID,Salo Miia H.^ORCID,Hinttala Reetta,Eklund Lauri,Quéré Isabelle,Alitalo Kari^ORCID,Vikkula Miikka^ORCID

Funder

Fonds De La Recherche Scientifique - FNRS

Fund Generet managed by the King Baudouin Foundation

Région wallonne dans le cadre du financement de l’axe stratégique FRFS-WELBIO

Leducq Foundation Networks of Excellence Program

European Union’s Horizon 2020 research and innovation programme

Wihuri Foundation

European research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme

Jane and Aatos Erkko Foundation

The Research Council of Finland

Sigrid Jusélius Foundation

Novo Nordisk Foundation

Hospital District of Helsinki and Uusimaa Research Grant

Publisher

American Society for Clinical Investigation

Link

https://www.jci.org/articles/view/173586/files/pdf

Reference76 articles.

1. A model for gene therapy of human hereditary lymphedema

2. Primary lymphoedema

3. Vascular heterogeneity and specialization in development and disease

4. Organ-specific lymphatic vasculature: From development to pathophysiology

5. Biological functions of lymphatic vessels

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