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C Speer

Showing results (71-80 of 158) with videos related to

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Journal of Nutrition for the Elderly|December 25, 2010
Natural food folate and late-life depressionMartha E Payne, Brenda D Jamerson, Christopher F Potocky, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 1, 2000
A Bethlem myopathy Gly to Glu mutation in the von Willebrand factor A domain N2 of the collagen alpha3(VI) chain interferes with protein foldingT Sasaki, E Hohenester, R Z Zhang, et al.
Neurology|April 1, 1990
Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studiesM C Speer, M A Pericak-Vance, L Yamaoka, et al.
Journal of Animal Science|April 28, 2000
Injection of beef strip loins with solutions containing sodium tripolyphosphate, sodium lactate, and sodium chloride to enhance palatabilityD J Vote, W J Platter, J D Tatum, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermiaDemetra S Stamm, Arthur S Aylsworth, Jeffrey M Stajich, et al.
Nature Genetics|September 1, 1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contracturesG J Jöbsis, H Keizers, J P Vreijling, et al.
Human Molecular Genetics|August 12, 2008
Human neural crest cells display molecular and phenotypic hallmarks of stem cellsSophie Thomas, Marie Thomas, Patrick Wincker, et al.
Genetic Epidemiology|January 17, 2002
Life after the screen: making sense of many P-valuesS Schmidt, Y Shao, E R Hauser, et al.
Teratology|February 8, 2000
Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomaliesJ S Nye, E A Hayes, M Amendola, et al.
Genomics|April 7, 1999
A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequencesS K Horrigan, L Bartoloni, M C Speer, et al.
Pageof 16

Showing results (71-80 of 158) with videos related to

Sort By:
Pageof 16
Journal of Nutrition for the Elderly|December 25, 2010
Natural food folate and late-life depressionMartha E Payne, Brenda D Jamerson, Christopher F Potocky, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 1, 2000
A Bethlem myopathy Gly to Glu mutation in the von Willebrand factor A domain N2 of the collagen alpha3(VI) chain interferes with protein foldingT Sasaki, E Hohenester, R Z Zhang, et al.
Neurology|April 1, 1990
Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studiesM C Speer, M A Pericak-Vance, L Yamaoka, et al.
Journal of Animal Science|April 28, 2000
Injection of beef strip loins with solutions containing sodium tripolyphosphate, sodium lactate, and sodium chloride to enhance palatabilityD J Vote, W J Platter, J D Tatum, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermiaDemetra S Stamm, Arthur S Aylsworth, Jeffrey M Stajich, et al.
Nature Genetics|September 1, 1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contracturesG J Jöbsis, H Keizers, J P Vreijling, et al.
Human Molecular Genetics|August 12, 2008
Human neural crest cells display molecular and phenotypic hallmarks of stem cellsSophie Thomas, Marie Thomas, Patrick Wincker, et al.
Genetic Epidemiology|January 17, 2002
Life after the screen: making sense of many P-valuesS Schmidt, Y Shao, E R Hauser, et al.
Teratology|February 8, 2000
Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomaliesJ S Nye, E A Hayes, M Amendola, et al.
Genomics|April 7, 1999
A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequencesS K Horrigan, L Bartoloni, M C Speer, et al.
Pageof 16