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

N A Parfrey

Showing results (21-30 of 33) with videos related to

Pageof 4
Sort By:
The Journal of Experimental Medicine|October 1, 1986
Dendritic cell-lymphoid cell aggregation and major histocompatibility antigen expression during rat cardiac allograft rejectionR D Forbes, N A Parfrey, M Gomersall, et al.
Neurology|January 3, 2001
Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutationsP McMonagle, P C Byrne, B Fitzgerald, et al.
Transplantation|February 1, 1986
The decreased incidence of aseptic necrosis in renal transplant recipients--a case control studyP S Parfrey, D Farge, N A Parfrey, et al.
The Journal of Pathology|December 1, 1996
Prognostic significance of p53 abnormalities in colorectal carcinoma detected by PCR-SSCP and immunohistochemical analysisD T Leahy, R Salman, H Mulcahy, et al.
Neurology|April 6, 2000
Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2pP C Byrne, P Mc Monagle, S Webb, et al.
Journal of Hepatology|February 15, 2000
Expansion of peripheral blood CD5+ B cells is associated with mild disease in chronic hepatitis C virus infectionM P Curry, L Golden-Mason, N Nolan, et al.
Neurology|May 9, 2001
SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14qC A Hughes, P C Byrne, S Webb, et al.
The British Journal of Ophthalmology|April 21, 1999
Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinctM Callaghan, C K Hand, S M Kennedy, et al.
The Journal of Pathology|August 19, 1999
Interferon-gamma gene expression during acute graft-versus-host disease: relationship to MHC induction and tissue injuryN A Parfrey, A El-Sheikh, E A Monckton, et al.
Genomics|October 8, 1999
Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mappingC K Hand, D L Harmon, S M Kennedy, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
The Journal of Experimental Medicine|October 1, 1986
Dendritic cell-lymphoid cell aggregation and major histocompatibility antigen expression during rat cardiac allograft rejectionR D Forbes, N A Parfrey, M Gomersall, et al.
Neurology|January 3, 2001
Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutationsP McMonagle, P C Byrne, B Fitzgerald, et al.
Transplantation|February 1, 1986
The decreased incidence of aseptic necrosis in renal transplant recipients--a case control studyP S Parfrey, D Farge, N A Parfrey, et al.
The Journal of Pathology|December 1, 1996
Prognostic significance of p53 abnormalities in colorectal carcinoma detected by PCR-SSCP and immunohistochemical analysisD T Leahy, R Salman, H Mulcahy, et al.
Neurology|April 6, 2000
Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2pP C Byrne, P Mc Monagle, S Webb, et al.
Journal of Hepatology|February 15, 2000
Expansion of peripheral blood CD5+ B cells is associated with mild disease in chronic hepatitis C virus infectionM P Curry, L Golden-Mason, N Nolan, et al.
Neurology|May 9, 2001
SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14qC A Hughes, P C Byrne, S Webb, et al.
The British Journal of Ophthalmology|April 21, 1999
Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinctM Callaghan, C K Hand, S M Kennedy, et al.
The Journal of Pathology|August 19, 1999
Interferon-gamma gene expression during acute graft-versus-host disease: relationship to MHC induction and tissue injuryN A Parfrey, A El-Sheikh, E A Monckton, et al.
Genomics|October 8, 1999
Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mappingC K Hand, D L Harmon, S M Kennedy, et al.
Pageof 4