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Paper Details

TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone.
J Cell Biol
78
2015
Arl13b, B9d1, Caenorhabditis, Caenorhabditis elegans, Inpp5e, MKS, MKS complex, Meckel syndrome, Mks1, OFD3, TMEM231, Tmem231, kidney cysts, mouse, mouse Tmem231, patients, polydactyly
Author NameAffiliation
Heidi CopeCenter for Human Disease Modeling, and Duke Molecular Physiology Institute, Duke University Medical Center
Allison E Ashley-KochCenter for Human Disease Modeling, and Duke Molecular Physiology Institute, Duke University Medical Center, NC 22710 Center for Human Disease Modeling
John A SayerInstitute of Genetic Medicine, Newcastle University, UK Newcastle Hospitals National Health Service Foundation Trust
Nicholas KatsanisCenter for Human Disease Modeling, and Duke Molecular Physiology Institute, Duke University Medical Center
Nicholas KatsanisCenter for Human Disease Modeling, and Duke Molecular Physiology Institute, Duke University Medical Center
Friedhelm HildebrandtBoston Children's Hospital and Harvard Medical School, MA 02115 Howard Hughes Medical Institute
Jeremy F ReiterDepartment of Biochemistry and Biophysics and Cardiovascular Research Institute, University of California san francisco
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