Bateman, John F.
Royal Children's Hospital · The University of Melbourne · Murdoch Children's Research Institute
3 papers on CoChatORCID 0000-0001-8542-0730
Most cited papers
- Verified
Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations
Bateman, J. F., Boot-Handford, R. P., & Lamandé, S. R. (2009) · Nature Reviews Genetics
Connective tissue disorders researchDermatological and Skeletal Disorders
Cited by 338
- Verified
Autophagic elimination of misfolded procollagen aggregates in the endoplasmic reticulum as a means of cell protection
Ishida, Y., Yamamoto, A., Kitamura, A., Lamandé, S. R., Yoshimori, T., Bateman, J. F., Kubota, H., & Nagata, K. (2009) · Molecular Biology of the Cell
Autophagy in Disease and TherapyEndoplasmic Reticulum Stress and Disease
Cited by 221
- Verified
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
McGillivray, G., Savarirayan, R., Cox, T. C., Stojkoski, C., McNeil, R., Bankier, A., Bateman, J. F., Roscioli, T., Gardner, R. J. M., & Lamandé, S. R. (2005) · Journal of Medical Genetics
Craniofacial Disorders and TreatmentsGenomics and Rare Diseases
Cited by 34
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