Cas Simons

Affiliations

Murdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Victoria 3052, Australia.
Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland 4072, Australia.

Réseau de co-auteurs

Ryan J Taft 3 collaborations

Adeline Vanderver 2 collaborations

Guy Helman 2 collaborations

Neil I Bower 2 collaborations

Katarzyna Koltowska 2 collaborations

Benjamin M Hogan 2 collaborations

Debdeep Dutta 1 collaboration

Lauren C Briere 1 collaboration

Oguz Kanca 1 collaboration

Paul C Marcogliese 1 collaboration

Melissa A Walker 1 collaboration

Frances A High 1 collaboration

Joel Krier 1 collaboration

Nikkola Carmichael 1 collaboration

Christine Callahan 1 collaboration

Undiagnosed Diseases Network 1 collaboration

Michael F Wangler 1 collaboration

Shinya Yamamoto 1 collaboration

David A Sweetser 1 collaboration

Hugo J Bellen 1 collaboration

Maja Bilip 1 collaboration

Shreya Shah 1 collaboration

Mayuran Mathiyalakan 1 collaboration

Aristides D Tagalakis 1 collaboration

Stephen L Hart 1 collaboration

Ruhina Maeshima 1 collaboration

Simon Eaton 1 collaboration

Michael Orford 1 collaboration

Elsa Irving 1 collaboration

Alessia Di Florio 1 collaboration

Claire Simons 1 collaboration

Andrew W Stoker 1 collaboration

Maria Rondon-Galeano 1 collaboration

Renae Skoczylas 1 collaboration

Emma Gordon 1 collaboration

Mathias Francois 1 collaboration

Smrita Chaudhury 1 collaboration

Kazuhide S Okuda 1 collaboration

Anne K Lagendijk 1 collaboration

Scott Paterson 1 collaboration

Gregory J Baillie 1 collaboration

Kelly A Smith 1 collaboration

Huifang Yan 1 collaboration

Swetha E Murthy 1 collaboration

Haoran Ji 1 collaboration

Joanna Crawford 1 collaboration

Thomas Kubisiak 1 collaboration

Stephen J Bent 1 collaboration

Jiangxi Xiao 1 collaboration

Adam Coombs 1 collaboration

Ye Wu 1 collaboration

Ana Pop 1 collaboration

Dongxiao Li 1 collaboration

Linda S de Vries 1 collaboration

Yuwu Jiang 1 collaboration

Gajja S Salomons 1 collaboration

Marjo S van der Knaap 1 collaboration

Ardem Patapoutian 1 collaboration

Margit Burmeister 1 collaboration

Jingmin Wang 1 collaboration

Nicole I Wolf 1 collaboration

Long Guo 1 collaboration

Débora Romeo Bertola 1 collaboration

Asako Takanohashi 1 collaboration

Asuka Saito 1 collaboration

Yuko Segawa 1 collaboration

Takanori Yokota 1 collaboration

Satoru Ishibashi 1 collaboration

Yoichiro Nishida 1 collaboration

Guilherme Lopes Yamamoto 1 collaboration

José Francisco da Silva Franco 1 collaboration

Rachel Sayuri Honjo 1 collaboration

Chong Ae Kim 1 collaboration

Camila Manso Musso 1 collaboration

Margaret Timmons 1 collaboration

Amy Pizzino 1 collaboration

Bryan Lajoie 1 collaboration

Melanie A Knight 1 collaboration

Kenneth H Fischbeck 1 collaboration

Andrew B Singleton 1 collaboration

Carlos R Ferreira 1 collaboration

Zheng Wang 1 collaboration

Li Yan 1 collaboration

James Y Garbern 1 collaboration

Pelin O Simsek-Kiper 1 collaboration

Hirofumi Ohashi 1 collaboration

Pamela G Robey 1 collaboration

Alan Boyde 1 collaboration

Naomichi Matsumoto 1 collaboration

Noriko Miyake 1 collaboration

Jürgen Spranger 1 collaboration

Raphael Schiffmann 1 collaboration

Gen Nishimura 1 collaboration

Maria Rita Dos Santos Passos-Bueno 1 collaboration

Kinya Ishikawa 1 collaboration

Shiro Ikegawa 1 collaboration

Cas Simons

Affiliations

Publications (6)

De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment.

Liposomal delivery of hydrophobic RAMBAs provides good bioavailability and significant enhancement of retinoic acid signalling in neuroblastoma tumour cells.

MAFB modulates the maturation of lymphatic vascular networks in mice.

Localised Collagen2a1 secretion supports lymphatic endothelial cell migration in the zebrafish embryo.

Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during Infancy.

Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation.

Réseau de co-auteurs