Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in FBRSL1 to AUTS2 Syndrome

por Pauli, Silke, Berger, Hanna, Ufartes, Roser, Borchers, Annette
Publicado 2021

Periodic expression of Kv10.1 driven by pRb/E2F1 contributes to G2/M progression of cancer and non-transformed cells

por Urrego, Diana, Movsisyan, Naira, Ufartes, Roser, Pardo, Luis A.
Publicado 2016

3D virtual histology of murine kidneys –high resolution visualization of pathological alterations by micro computed tomography

por Missbach-Guentner, Jeannine, Pinkert-Leetsch, Diana, Dullin, Christian, Ufartes, Roser, Hornung, Daniel, Tampe, Bjoern, Zeisberg, Michael, Alves, Frauke
Publicado 2018

μCT of ex-vivo stained mouse hearts and embryos enables a precise match between 3D virtual histology, classical histology and immunochemistry

por Dullin, Christian, Ufartes, Roser, Larsson, Emanuel, Martin, Sabine, Lazzarini, Marcio, Tromba, Giuliana, Missbach-Guentner, Jeannine, Pinkert-Leetsch, Diana, Katschinski, Dörthe M., Alves, Frauke
Publicado 2017

De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome

por Ufartes, Roser, Berger, Hanna, Till, Katharina, Salinas, Gabriela, Sturm, Marc, Altmüller, Janine, Nürnberg, Peter, Thiele, Holger, Funke, Rudolf, Apeshiotis, Neophytos, Langen, Hendrik, Wollnik, Bernd, Borchers, Annette, Pauli, Silke
Publicado 2020

Behavioural and functional characterization of K(v)10.1 (Eag1) knockout mice

por Ufartes, Roser, Schneider, Tomasz, Mortensen, Lena Sünke, de Juan Romero, Camino, Hentrich, Klaus, Knoetgen, Hendrik, Beilinson, Vadim, Moebius, Wiebke, Tarabykin, Victor, Alves, Frauke, Pardo, Luis A., Rawlins, J. Nicholas P., Stuehmer, Walter
Publicado 2013