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Publications by Roland Werner
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , Which Encode Subcomponents C1r and C1s of Complement
American Journal of Human Genetics
Genetics
Related publications
Assembly of Subcomponents C1r and C1s of First Component of Complement: Electron Microscopic and Ultracentrifugal Studies.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
The Structure and Enzymic Activities of the C1r and C1s Subcomponents of C1, the First Component of Human Serum Complement
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Prohaptoglobin Is Proteolytically Cleaved in the Endoplasmic Reticulum by the Complement C1r-Like Protein
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Hypermobile Ehlers-Danlos Syndrome (a.k.a. Ehlers-Danlos Syndrome Type III and Ehlers-Danlos Syndrome Hypermobility Type): Clinical Description and Natural History
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
Genetics
Classical Ehlers-Danlos Syndrome Caused by a Mutation in Type I Collagen
American Journal of Human Genetics
Genetics
Hypermobile Ehlers Danlos Syndrome
Balkan Medical Journal
Medicine
Proprioceptive Precision Is Impaired in Ehlers–Danlos Syndrome
SpringerPlus
Multidisciplinary
Assembly and Enzymatic Properties of the Catalytic Domain of Human Complement Protease C1r
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
The Purification and Characterization of Subcomponent C1s of the First Component of Bovine Complement
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
