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M W Head

Showing results (21-30 of 45) with videos related to

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The International Journal of Developmental Biology|September 1, 1992
Localization of delta-crystallin RNA during lens morphogenesis and differentiation in the normal and talpid3 chick embryoM W Head, E L Triplett, D A Ede, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 1, 1997
Macular holes: migratory gaps and vitreous as obstacles to glial closureH D Schubert, K Kuang, F Kang, et al.
Neuropathology and Applied Neurobiology|May 29, 2009
Panencephalopathic Creutzfeldt-Jakob disease in the Netherlands and the UK: clinical and pathological characteristics of nine patientsC Jansen, M W Head, A J M Rozemuller, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|June 18, 2002
Pathological diagnosis of variant Creutzfeldt-Jakob diseaseJ W Ironside, L McCardle, A Horsburgh, et al.
Clinics in Laboratory Medicine|May 8, 2003
Variant Creutzfeldt-Jakob diseaseH J T Ward, M W Head, R G Will, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|May 29, 1998
Suppression of fibroblast growth factor 2 expression by antisense oligonucleotides inhibits embryonic chick neural retina cell differentiation and survival in vivoL Désiré, M W Head, N A Fayein, et al.
Journal of Neuroscience Research|March 1, 1996
Expression of the chicken cysteine-rich fibroblast growth factor receptor (CFR) during embryogenesis and retina developmentN A Fayein, M W Head, J C Jeanny, et al.
Neuropathology and Applied Neurobiology|August 13, 2009
A case of protease sensitive prionopathy in a patient in the UKM W Head, R Knight, M Zeidler, et al.
Neuropathology and Applied Neurobiology|February 4, 2009
Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene (PRNP)D A Hilton, M W Head, V K Singh, et al.
Histopathology|August 10, 2000
Laboratory diagnosis of variant Creutzfeldt-Jakob diseaseJ W Ironside, M W Head, J E Bell, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
The International Journal of Developmental Biology|September 1, 1992
Localization of delta-crystallin RNA during lens morphogenesis and differentiation in the normal and talpid3 chick embryoM W Head, E L Triplett, D A Ede, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 1, 1997
Macular holes: migratory gaps and vitreous as obstacles to glial closureH D Schubert, K Kuang, F Kang, et al.
Neuropathology and Applied Neurobiology|May 29, 2009
Panencephalopathic Creutzfeldt-Jakob disease in the Netherlands and the UK: clinical and pathological characteristics of nine patientsC Jansen, M W Head, A J M Rozemuller, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|June 18, 2002
Pathological diagnosis of variant Creutzfeldt-Jakob diseaseJ W Ironside, L McCardle, A Horsburgh, et al.
Clinics in Laboratory Medicine|May 8, 2003
Variant Creutzfeldt-Jakob diseaseH J T Ward, M W Head, R G Will, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|May 29, 1998
Suppression of fibroblast growth factor 2 expression by antisense oligonucleotides inhibits embryonic chick neural retina cell differentiation and survival in vivoL Désiré, M W Head, N A Fayein, et al.
Journal of Neuroscience Research|March 1, 1996
Expression of the chicken cysteine-rich fibroblast growth factor receptor (CFR) during embryogenesis and retina developmentN A Fayein, M W Head, J C Jeanny, et al.
Neuropathology and Applied Neurobiology|August 13, 2009
A case of protease sensitive prionopathy in a patient in the UKM W Head, R Knight, M Zeidler, et al.
Neuropathology and Applied Neurobiology|February 4, 2009
Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene (PRNP)D A Hilton, M W Head, V K Singh, et al.
Histopathology|August 10, 2000
Laboratory diagnosis of variant Creutzfeldt-Jakob diseaseJ W Ironside, M W Head, J E Bell, et al.
Pageof 5