Pdgfrb‐Cre targets lymphatic endothelial cells of both venous and non‐venous origins

Por Ulvmar, Maria H., Martinez‐Corral, Ines, Stanczuk, Lukas, Mäkinen, Taija
Publicado no Genesis (2016)

In vivo imaging of lymphatic vessels in development, wound healing, inflammation, and tumor metastasis

Por Martínez-Corral, Inés, Olmeda, David, Diéguez-Hurtado, Rodrigo, Tammela, Tuomas, Alitalo, Kari, Ortega, Sagrario
Publicado em 2012

Lymph Node Transplantation Decreases Swelling and Restores Immune Responses in a Transgenic Model of Lymphedema

Por Huang, Jung-Ju, Gardenier, Jason C., Hespe, Geoffrey E., García Nores, Gabriela D., Kataru, Raghu P., Ly, Catherine L., Martínez-Corral, Inés, Ortega, Sagrario, Mehrara, Babak J.
Publicado no PLoS One (2016)

Diphtheria toxin–mediated ablation of lymphatic endothelial cells results in progressive lymphedema

Por Gardenier, Jason C., Hespe, Geoffrey E., Kataru, Raghu P., Savetsky, Ira L., Torrisi, Jeremy S., Nores, Gabriela D. García, Dayan, Joseph J., Chang, David, Zampell, Jamie, Martínez-Corral, Inés, Ortega, Sagrario, Mehrara, Babak J.
Publicado no JCI Insight (2016)

FOXC2 and fluid shear stress stabilize postnatal lymphatic vasculature

Por Sabine, Amélie, Bovay, Esther, Demir, Cansaran Saygili, Kimura, Wataru, Jaquet, Muriel, Agalarov, Yan, Zangger, Nadine, Scallan, Joshua P., Graber, Werner, Gulpinar, Elgin, Kwak, Brenda R., Mäkinen, Taija, Martinez-Corral, Inés, Ortega, Sagrario, Delorenzi, Mauro, Kiefer, Friedemann, Davis, Michael J., Djonov, Valentin, Miura, Naoyuki, Petrova, Tatiana V.
Publicado no J Clin Invest (2015)

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

Por Martin-Almedina, Silvia, Martinez-Corral, Ines, Holdhus, Rita, Vicente, Andres, Fotiou, Elisavet, Lin, Shin, Petersen, Kjell, Simpson, Michael A., Hoischen, Alexander, Gilissen, Christian, Jeffery, Heather, Atton, Giles, Karapouliou, Christina, Brice, Glen, Gordon, Kristiana, Wiseman, John W., Wedin, Marianne, Rockson, Stanley G., Jeffery, Steve, Mortimer, Peter S., Snyder, Michael P., Berland, Siren, Mansour, Sahar, Makinen, Taija, Ostergaard, Pia
Publicado no J Clin Invest (2016)

Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy

Por Ostergaard, Pia, Simpson, Michael A., Mendola, Antonella, Vasudevan, Pradeep, Connell, Fiona C., van Impel, Andreas, Moore, Anthony T., Loeys, Bart L., Ghalamkarpour, Arash, Onoufriadis, Alexandros, Martinez-Corral, Ines, Devery, Sophie, Leroy, Jules G., van Laer, Lut, Singer, Amihood, Bialer, Martin G., McEntagart, Meriel, Quarrell, Oliver, Brice, Glen, Trembath, Richard C., Schulte-Merker, Stefan, Makinen, Taija, Vikkula, Miikka, Mortimer, Peter S., Mansour, Sahar, Jeffery, Steve
Publicado em 2012