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A C Nicholls

Showing results (21-30 of 58) with videos related to

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The British Journal of Dermatology|September 1, 1984
Ehlers-Danlos syndrome type IV mimicking non-accidental injury in a childD L Roberts, F M Pope, A C Nicholls, et al.
Human Mutation|January 1, 1996
Mutation in the carboxy-terminal propeptide of the Pro alpha 1(I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): possible implications for protein foldingJ E Oliver, E M Thompson, F M Pope, et al.
Journal of Medical Genetics|December 1, 1985
Collagen genes and proteins in osteogenesis imperfectaF M Pope, A C Nicholls, J McPheat, et al.
Clinical Science and Molecular Medicine|July 1, 1978
Changes in the collagen of synovial membrane in rheumatoid arthritis and effect of D-penicillamineC R Lovell, A C Nicholls, M I Jayson, et al.
The British Journal of Dermatology|April 1, 1979
Characterization of dermal collagen in systemic sclerosisC R Lovell, A C Nicholls, V C Duance, et al.
Journal of Medical Genetics|November 1, 1991
Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfectaA C Nicholls, J Oliver, D V Renouf, et al.
Human Mutation|January 1, 1996
Splice site mutation causing deletion of exon 21 sequences from the pro alpha 2(I) chain of type I collagen in a patient with severe dentinogenesis imperfecta but very mild osteogenesis imperfectaA C Nicholls, J Oliver, S McCarron, et al.
Archives of Disease in Childhood|September 1, 1988
Clinical presentations of Ehlers Danlos syndrome type IVF M Pope, P Narcisi, A C Nicholls, et al.
Journal of Neurosurgery|July 1, 1983
Collagen deficiency and ruptured cerebral aneurysms. A clinical and biochemical studyG Neil-Dwyer, J R Bartlett, A C Nicholls, et al.
Journal of the Royal Society of Medicine|March 1, 1980
EDS IV (acrogeria): new autosomal dominant and recessive typesF M Pope, A C Nicholls, P M Jones, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
The British Journal of Dermatology|September 1, 1984
Ehlers-Danlos syndrome type IV mimicking non-accidental injury in a childD L Roberts, F M Pope, A C Nicholls, et al.
Human Mutation|January 1, 1996
Mutation in the carboxy-terminal propeptide of the Pro alpha 1(I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): possible implications for protein foldingJ E Oliver, E M Thompson, F M Pope, et al.
Journal of Medical Genetics|December 1, 1985
Collagen genes and proteins in osteogenesis imperfectaF M Pope, A C Nicholls, J McPheat, et al.
Clinical Science and Molecular Medicine|July 1, 1978
Changes in the collagen of synovial membrane in rheumatoid arthritis and effect of D-penicillamineC R Lovell, A C Nicholls, M I Jayson, et al.
The British Journal of Dermatology|April 1, 1979
Characterization of dermal collagen in systemic sclerosisC R Lovell, A C Nicholls, V C Duance, et al.
Journal of Medical Genetics|November 1, 1991
Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfectaA C Nicholls, J Oliver, D V Renouf, et al.
Human Mutation|January 1, 1996
Splice site mutation causing deletion of exon 21 sequences from the pro alpha 2(I) chain of type I collagen in a patient with severe dentinogenesis imperfecta but very mild osteogenesis imperfectaA C Nicholls, J Oliver, S McCarron, et al.
Archives of Disease in Childhood|September 1, 1988
Clinical presentations of Ehlers Danlos syndrome type IVF M Pope, P Narcisi, A C Nicholls, et al.
Journal of Neurosurgery|July 1, 1983
Collagen deficiency and ruptured cerebral aneurysms. A clinical and biochemical studyG Neil-Dwyer, J R Bartlett, A C Nicholls, et al.
Journal of the Royal Society of Medicine|March 1, 1980
EDS IV (acrogeria): new autosomal dominant and recessive typesF M Pope, A C Nicholls, P M Jones, et al.
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