Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F M Pope

Showing results (111-120 of 168) with videos related to

Pageof 17
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1993
The gene responsible for Werner syndrome may be a cell division "counting" geneR G Faragher, I R Kill, J A Hunter, et al.
Cardiovascular Surgery (London, England)|February 8, 2000
Emergency repair of type A aortic dissection in type IV Ehlers-Danlos syndromeR Ascione, W J Gomes, M Bates, et al.
Journal of Medical Genetics|June 1, 1992
Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locusL al-Imara, A J Richards, R A Eady, et al.
Journal of Medical Genetics|November 10, 2000
Clinical phenotypes and molecular characterisation of three patients with Ehlers-Danlos syndrome type VIIA C Nicholls, J L Sher, M J Wright, et al.
American Journal of Medical Genetics|May 15, 1993
Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IVP Narcisi, Y Wu, G Tromp, et al.
Clinical and Experimental Dermatology|June 30, 2009
An atypical cutaneous presentation of vasculitis with features of Churg-Strauss syndrome, associated with anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane antibodiesC M Gleeson, J B Levy, H T Cook, et al.
Human Genetics|June 1, 1992
A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid in a family with Ehlers-Danlos syndrome type IV. An unaffected family member is mosaic for the mutationA J Richards, P N Ward, P Narcisi, et al.
Journal of Medical Genetics|July 1, 1991
Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P N Ward, et al.
Clinical and Experimental Dermatology|October 27, 2001
Elastosis perforans serpiginosa and associated disordersR K Mehta, N P Burrows, C M Payne, et al.
Journal of Medical Genetics|October 23, 1998
A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type IIA J Richards, S Martin, A C Nicholls, et al.
Pageof 17

Showing results (111-120 of 168) with videos related to

Sort By:
Pageof 17
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1993
The gene responsible for Werner syndrome may be a cell division "counting" geneR G Faragher, I R Kill, J A Hunter, et al.
Cardiovascular Surgery (London, England)|February 8, 2000
Emergency repair of type A aortic dissection in type IV Ehlers-Danlos syndromeR Ascione, W J Gomes, M Bates, et al.
Journal of Medical Genetics|June 1, 1992
Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locusL al-Imara, A J Richards, R A Eady, et al.
Journal of Medical Genetics|November 10, 2000
Clinical phenotypes and molecular characterisation of three patients with Ehlers-Danlos syndrome type VIIA C Nicholls, J L Sher, M J Wright, et al.
American Journal of Medical Genetics|May 15, 1993
Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IVP Narcisi, Y Wu, G Tromp, et al.
Clinical and Experimental Dermatology|June 30, 2009
An atypical cutaneous presentation of vasculitis with features of Churg-Strauss syndrome, associated with anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane antibodiesC M Gleeson, J B Levy, H T Cook, et al.
Human Genetics|June 1, 1992
A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid in a family with Ehlers-Danlos syndrome type IV. An unaffected family member is mosaic for the mutationA J Richards, P N Ward, P Narcisi, et al.
Journal of Medical Genetics|July 1, 1991
Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P N Ward, et al.
Clinical and Experimental Dermatology|October 27, 2001
Elastosis perforans serpiginosa and associated disordersR K Mehta, N P Burrows, C M Payne, et al.
Journal of Medical Genetics|October 23, 1998
A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type IIA J Richards, S Martin, A C Nicholls, et al.
Pageof 17