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F M Pope

Showing results (131-140 of 168) with videos related to

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Lancet (London, England)|January 16, 1982
Basophils in allergen-induced patch test sites in atopic dermatitisE B Mitchell, J Crow, M D Chapman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988
Spontaneous carotid cavernous fistula in Ehlers Danlos syndromeR Fox, F M Pope, P Narcisi, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1975
Patients with Ehlers-Danlos syndrome type IV lack type III collagenF M Pope, G R Martin, J R Lichtenstein, et al.
The Journal of Biological Chemistry|November 10, 1984
Osteogenesis imperfecta: cloning of a pro-alpha 2(I) collagen gene with a frameshift mutationT Pihlajaniemi, L A Dickson, F M Pope, et al.
QJM : Monthly Journal of the Association of Physicians|August 20, 2003
A glycine to aspartic acid substitution of COL2A1 in a family with the Strudwick variant of spondyloepimetaphyseal dysplasiaC Tysoe, J Saunders, L White, et al.
Clinical Genetics|December 1, 1993
Restrictive dermopathy: a disorder of skin differentiation with abnormal integrin expressionJ C Dean, E S Gray, K N Stewart, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1992
Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptidesK Kainulainen, L Y Sakai, A Child, et al.
The Journal of Investigative Dermatology|August 1, 1996
Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosaM G Dunnill, J A McGrath, A J Richards, et al.
Human Molecular Genetics|September 1, 1996
A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagenA J Richards, J R Yates, R Williams, et al.
American Journal of Human Genetics|July 31, 1998
A point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British familiesN P Burrows, A C Nicholls, A J Richards, et al.
Pageof 17

Showing results (131-140 of 168) with videos related to

Sort By:
Pageof 17
Lancet (London, England)|January 16, 1982
Basophils in allergen-induced patch test sites in atopic dermatitisE B Mitchell, J Crow, M D Chapman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988
Spontaneous carotid cavernous fistula in Ehlers Danlos syndromeR Fox, F M Pope, P Narcisi, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1975
Patients with Ehlers-Danlos syndrome type IV lack type III collagenF M Pope, G R Martin, J R Lichtenstein, et al.
The Journal of Biological Chemistry|November 10, 1984
Osteogenesis imperfecta: cloning of a pro-alpha 2(I) collagen gene with a frameshift mutationT Pihlajaniemi, L A Dickson, F M Pope, et al.
QJM : Monthly Journal of the Association of Physicians|August 20, 2003
A glycine to aspartic acid substitution of COL2A1 in a family with the Strudwick variant of spondyloepimetaphyseal dysplasiaC Tysoe, J Saunders, L White, et al.
Clinical Genetics|December 1, 1993
Restrictive dermopathy: a disorder of skin differentiation with abnormal integrin expressionJ C Dean, E S Gray, K N Stewart, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1992
Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptidesK Kainulainen, L Y Sakai, A Child, et al.
The Journal of Investigative Dermatology|August 1, 1996
Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosaM G Dunnill, J A McGrath, A J Richards, et al.
Human Molecular Genetics|September 1, 1996
A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagenA J Richards, J R Yates, R Williams, et al.
American Journal of Human Genetics|July 31, 1998
A point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British familiesN P Burrows, A C Nicholls, A J Richards, et al.
Pageof 17