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C Gaskell

Showing results (11-20 of 66) with videos related to

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Veterinary Immunology and Immunopathology|June 1, 1996
Systemic and pulmonary immune response to intrabronchial administration of ovalbumin in calvesH HogenEsch, S E Torregrosa, D Borie, et al.
Acta Neuropathologica|August 30, 2000
Lewy body and Alzheimer pathology in a family with the amyloid-beta precursor protein APP717 gene mutationC K Rosenberg, M A Pericak-Vance, A M Saunders, et al.
Neurogenetics|December 17, 2002
Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432Marcy C Speer, Felicia Lennon Graham, Erin Bonner, et al.
Nucleic Acids Research|July 25, 1991
RsaI RFLP for electron transport flavoprotein-beta(ETFB)V Royal, M J Alberts, M A Pericak-Vance, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, et al.
Neurobiology of Aging|July 1, 1995
Delayed onset of Alzheimer's disease with nonsteroidal anti-inflammatory and histamine H2 blocking drugsJ C Breitner, K A Welsh, M J Helms, et al.
Neurogenetics|March 28, 2006
A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12Stephan Züchner, Melanie E Kail, Martha A Nance, et al.
Australian Paediatric Journal|January 1, 1988
Systematic gene mapping in man: data management considerationsM A Pericak-Vance, W Y Hung, L Yamaoka, et al.
Neurology|March 1, 1992
Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entitiesL J Loprest, M A Pericak-Vance, J Stajich, et al.
Prenatal Diagnosis|July 1, 1988
Prenatal diagnosis using deletion studies in Duchenne muscular dystrophyM C Speer, M A Pericak-Vance, L H Yamaoka, et al.
Pageof 7

Showing results (11-20 of 66) with videos related to

Sort By:
Pageof 7
Veterinary Immunology and Immunopathology|June 1, 1996
Systemic and pulmonary immune response to intrabronchial administration of ovalbumin in calvesH HogenEsch, S E Torregrosa, D Borie, et al.
Acta Neuropathologica|August 30, 2000
Lewy body and Alzheimer pathology in a family with the amyloid-beta precursor protein APP717 gene mutationC K Rosenberg, M A Pericak-Vance, A M Saunders, et al.
Neurogenetics|December 17, 2002
Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432Marcy C Speer, Felicia Lennon Graham, Erin Bonner, et al.
Nucleic Acids Research|July 25, 1991
RsaI RFLP for electron transport flavoprotein-beta(ETFB)V Royal, M J Alberts, M A Pericak-Vance, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, et al.
Neurobiology of Aging|July 1, 1995
Delayed onset of Alzheimer's disease with nonsteroidal anti-inflammatory and histamine H2 blocking drugsJ C Breitner, K A Welsh, M J Helms, et al.
Neurogenetics|March 28, 2006
A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12Stephan Züchner, Melanie E Kail, Martha A Nance, et al.
Australian Paediatric Journal|January 1, 1988
Systematic gene mapping in man: data management considerationsM A Pericak-Vance, W Y Hung, L Yamaoka, et al.
Neurology|March 1, 1992
Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entitiesL J Loprest, M A Pericak-Vance, J Stajich, et al.
Prenatal Diagnosis|July 1, 1988
Prenatal diagnosis using deletion studies in Duchenne muscular dystrophyM C Speer, M A Pericak-Vance, L H Yamaoka, et al.
Pageof 7