S. Natarajan

发表

Tyrosine Phosphorylation Profiling in FGF-2 Stimulated Human Embryonic Stem Cells

B. Snel, S. Lemeer, A. Heck, 2011, PloS one.

The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5

Colin A. Johnson, C. Inglehearn, C. Toomes, 2019, Scientific Reports.

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Colin A. Johnson, Teunis J. P. van Dam, J. Shendure, 2015, Nature Cell Biology.

Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects.

Colin A. Johnson, C. Inglehearn, C. Toomes, 2013, Human molecular genetics.

Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

Colin A. Johnson, M. Hurles, D. Bonthron, 2013, Nature Genetics.

FGF‐2 modulates Wnt signaling in undifferentiated hESC and iPS cells through activated PI3‐K/GSK3β signaling

M. Yap, S. Cool, A. Choo, 2010, Journal of cellular physiology.

HEXIM1 Induces Differentiation of Human Pluripotent Stem Cells

Qiao Jing Lew, M. Gurumurthy, S. Chao, 2013, PloS one.

Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel-Gruber syndrome.

Colin A. Johnson, C. Inglehearn, C. Toomes, 2013, Developmental biology.

Proceedings of the Second International Cilia in Development and Disease Scientific Conference

R. Roepman, N. Sorusch, U. Wolfrum, 2015 .

Drug and siRNA screens identify ROCK2 as a therapeutic target for ciliopathies

Colin A. Johnson, S. Grellscheid, J. Bond, 2020 .

The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway

Colin A. Johnson, D. Jagger, C. Inglehearn, 2015, Disease Models & Mechanisms.

A high-throughput genome-wide siRNA screen for ciliogenesis identifies new ciliary functional components and ciliopathy genes

R. Roepman, N. Sorusch, U. Wolfrum, 2015, Cilia.