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F M Pope

Showing results (61-70 of 168) with videos related to

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The British Journal of Dermatology|January 1, 1988
Detection of type III collagen in skin fibroblasts from patients with Ehlers-Danlos syndrome type IV by immunofluorescenceA S Temple, P Hinton, P Narcisi, et al.
Journal of Medical Genetics|August 1, 1993
The substitution of glycine 661 by arginine in type III collagen produces mutant molecules with different thermal stabilities and causes Ehlers-Danlos syndrome type IVA Richards, P Narcisi, J Lloyd, et al.
Human Molecular Genetics|September 1, 1994
A family with Ehlers-Danlos syndrome type III/articular hypermobility syndrome has a glycine 637 to serine substitution in type III collagenP Narcisi, A J Richards, S D Ferguson, et al.
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.
The Journal of Pathology|October 31, 2000
A light and electron microscopic study of osteogenesis imperfecta bone samples, with reference to collagen chemistry and clinical phenotypeP Sarathchandra, F M Pope, M V Kayser, et al.
The Journal of Biological Chemistry|December 25, 1983
The molecular defect in a nonlethal variant of osteogenesis imperfecta. Synthesis of pro-alpha 2(I) chains which are not incorporated into trimers of type I procollagenS B Deak, A Nicholls, F M Pope, et al.
The Biochemical Journal|January 1, 1989
A type VI collagen-related glycopolypeptide is the major concanavalin A-binding component in pig skinI A King, A Tabiowo, P R Fryer, et al.
Clinical Dysmorphology|October 1, 1995
A mother and three daughters with congenital dislocation of the hip and a characteristic facial appearance: a new syndrome?A L Collins, N R Dennis, N Clarke, et al.
Journal of Medical Genetics|August 1, 1986
Clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaF M Pope, A C Nicolls, G Osse, 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.
Pageof 17

Showing results (61-70 of 168) with videos related to

Sort By:
Pageof 17
The British Journal of Dermatology|January 1, 1988
Detection of type III collagen in skin fibroblasts from patients with Ehlers-Danlos syndrome type IV by immunofluorescenceA S Temple, P Hinton, P Narcisi, et al.
Journal of Medical Genetics|August 1, 1993
The substitution of glycine 661 by arginine in type III collagen produces mutant molecules with different thermal stabilities and causes Ehlers-Danlos syndrome type IVA Richards, P Narcisi, J Lloyd, et al.
Human Molecular Genetics|September 1, 1994
A family with Ehlers-Danlos syndrome type III/articular hypermobility syndrome has a glycine 637 to serine substitution in type III collagenP Narcisi, A J Richards, S D Ferguson, et al.
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.
The Journal of Pathology|October 31, 2000
A light and electron microscopic study of osteogenesis imperfecta bone samples, with reference to collagen chemistry and clinical phenotypeP Sarathchandra, F M Pope, M V Kayser, et al.
The Journal of Biological Chemistry|December 25, 1983
The molecular defect in a nonlethal variant of osteogenesis imperfecta. Synthesis of pro-alpha 2(I) chains which are not incorporated into trimers of type I procollagenS B Deak, A Nicholls, F M Pope, et al.
The Biochemical Journal|January 1, 1989
A type VI collagen-related glycopolypeptide is the major concanavalin A-binding component in pig skinI A King, A Tabiowo, P R Fryer, et al.
Clinical Dysmorphology|October 1, 1995
A mother and three daughters with congenital dislocation of the hip and a characteristic facial appearance: a new syndrome?A L Collins, N R Dennis, N Clarke, et al.
Journal of Medical Genetics|August 1, 1986
Clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaF M Pope, A C Nicolls, G Osse, 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.
Pageof 17