Showing results (1-10 of 11) with videos related to
Sort By:
Pageof 2
Cell Cycle (Georgetown, Tex.)|April 1, 2016
Periodic expression of Kv10.1 driven by pRb/E2F1 contributes to G2/M progression of cancer and non-transformed cellsDiana Urrego, Naira Movsisyan, Roser Ufartes, et al.Frontiers in Cell and Developmental Biology|November 22, 2021
Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in FBRSL1 to AUTS2 SyndromeSilke Pauli, Hanna Berger, Roser Ufartes, et al.Human Genetics|July 14, 2025
FBRSL1 regulates the expression of chromatin regulators BRPF1 and KAT6AGina Kastens, Hanna Berger-Santangelo, Sarah Gerstner, et al.Scientific Reports|January 25, 2018
3D virtual histology of murine kidneys -high resolution visualization of pathological alterations by micro computed tomographyJeannine Missbach-Guentner, Diana Pinkert-Leetsch, Christian Dullin, et al.Human Molecular Genetics|July 7, 2021
CHARGE syndrome and related disorders: a mechanistic linkRoser Ufartes, Regina Grün, Gabriela Salinas, et al.Plos One|February 9, 2017
μCT of ex-vivo stained mouse hearts and embryos enables a precise match between 3D virtual histology, classical histology and immunochemistryChristian Dullin, Roser Ufartes, Emanuel Larsson, et al.The Journal of Physiology|January 6, 2015
KV 10.1 opposes activity-dependent increase in Ca²⁺ influx into the presynaptic terminal of the parallel fibre-Purkinje cell synapseLena Sünke Mortensen, Hartmut Schmidt, Zohreh Farsi, et al.Human Genetics|May 20, 2020
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndromeRoser Ufartes, Hanna Berger, Katharina Till, et al.Human Molecular Genetics|February 21, 2013
Behavioural and functional characterization of Kv10.1 (Eag1) knockout miceRoser Ufartes, Tomasz Schneider, Lena Sünke Mortensen, et al.Human Molecular Genetics|February 13, 2018
Sema3a plays a role in the pathogenesis of CHARGE syndromeRoser Ufartes, Janina Schwenty-Lara, Luisa Freese, et al.Pageof 2