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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 immunofluorescence
A 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 IV
A 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 collagen
P 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 child
D 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 phenotype
P 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 procollagen
S 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 skin
I 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 imperfecta
F 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 folding
J E Oliver, E M Thompson, F M Pope, et al.
Page
of 17
Search research articles
Search
Showing results (61-70 of 168) with videos related to
Sort By:
Page
of 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 immunofluorescence
A 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 IV
A 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 collagen
P 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 child
D 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 phenotype
P 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 procollagen
S 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 skin
I 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 imperfecta
F 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 folding
J E Oliver, E M Thompson, F M Pope, et al.
Page
of 17