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C R Merril

Showing results (131-140 of 145) with videos related to

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Lancet (London, England)|September 2, 1989
Reduced plasma dehydroepiandrosterone concentrations in Alzheimer's diseaseT Sunderland, C R Merril, M G Harrington, et al.
Lancet (London, England)|January 29, 1983
Maternal transmission in Huntington's diseaseR H Myers, D Goldman, E D Bird, et al.
Electrophoresis|July 1, 1995
The protein disease databaseP F Lemkin, G A Orr, M P Goldstein, et al.
Brain Research|August 19, 1985
Genetic brain polypeptide variants in inbred mice and in mouse strains with high and low sensitivity to alcoholD Goldman, R Nelson, R A Deitrich, et al.
Journal of Forensic Sciences|May 1, 1993
Mitochondrial DNA sequence analysis of human skeletal remains: identification of remains from the Vietnam WarM M Holland, D L Fisher, L G Mitchell, et al.
Rejuvenation Research|March 31, 2005
Stable transformation of CHO Cells and human NARP cybrids confers oligomycin resistance (oli(r)) following transfer of a mitochondrial DNA-encoded oli(r) ATPase6 gene to the nuclear genome: a model system for mtDNA gene therapyS J Zullo, W T Parks, M Chloupkova, et al.
Neurobiology of Aging|November 1, 1994
Protein alterations in olfactory neuroblasts from Alzheimer donorsG S Johnson, J Basaric-Keys, H A Ghanbari, et al.
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society|January 1, 1992
Haloperidol induced CSF protein variations in schizophrenic patients: as studied by two-dimensional electrophoresisG Johnson, D Brane, D P van Kammen, et al.
Archives of Biochemistry and Biophysics|February 1, 1996
Possible relationship between conditions associated with chronic hypoxia and brain mitochondrial DNA deletionsC R Merril, S Zullo, H Ghanbari, et al.
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society|January 1, 1991
Abnormal protein in the cerebrospinal fluid of patients with a submicroscopic X-chromosomal deletion associated with Norrie disease: preliminary reportJ E Joy, R Poglod, D L Murphy, et al.
Pageof 15

Showing results (131-140 of 145) with videos related to

Sort By:
Pageof 15
Lancet (London, England)|September 2, 1989
Reduced plasma dehydroepiandrosterone concentrations in Alzheimer's diseaseT Sunderland, C R Merril, M G Harrington, et al.
Lancet (London, England)|January 29, 1983
Maternal transmission in Huntington's diseaseR H Myers, D Goldman, E D Bird, et al.
Electrophoresis|July 1, 1995
The protein disease databaseP F Lemkin, G A Orr, M P Goldstein, et al.
Brain Research|August 19, 1985
Genetic brain polypeptide variants in inbred mice and in mouse strains with high and low sensitivity to alcoholD Goldman, R Nelson, R A Deitrich, et al.
Journal of Forensic Sciences|May 1, 1993
Mitochondrial DNA sequence analysis of human skeletal remains: identification of remains from the Vietnam WarM M Holland, D L Fisher, L G Mitchell, et al.
Rejuvenation Research|March 31, 2005
Stable transformation of CHO Cells and human NARP cybrids confers oligomycin resistance (oli(r)) following transfer of a mitochondrial DNA-encoded oli(r) ATPase6 gene to the nuclear genome: a model system for mtDNA gene therapyS J Zullo, W T Parks, M Chloupkova, et al.
Neurobiology of Aging|November 1, 1994
Protein alterations in olfactory neuroblasts from Alzheimer donorsG S Johnson, J Basaric-Keys, H A Ghanbari, et al.
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society|January 1, 1992
Haloperidol induced CSF protein variations in schizophrenic patients: as studied by two-dimensional electrophoresisG Johnson, D Brane, D P van Kammen, et al.
Archives of Biochemistry and Biophysics|February 1, 1996
Possible relationship between conditions associated with chronic hypoxia and brain mitochondrial DNA deletionsC R Merril, S Zullo, H Ghanbari, et al.
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society|January 1, 1991
Abnormal protein in the cerebrospinal fluid of patients with a submicroscopic X-chromosomal deletion associated with Norrie disease: preliminary reportJ E Joy, R Poglod, D L Murphy, et al.
Pageof 15