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Experimental Neurology
|
May 19, 2001
Early degenerative changes in transgenic mice expressing mutant huntingtin involve dendritic abnormalities but no impairment of mitochondrial energy production
P Guidetti, V Charles, E Y Chen, et al.
Genome Research
|
January 5, 1999
Strategies for mutational analysis of the large multiexon ATM gene using high-density oligonucleotide arrays
J G Hacia, B Sun, N Hunt, et al.
Genomics
|
January 1, 1997
The complete sequences of the galago and rabbit beta-globin locus control regions: extended sequence and functional conservation outside the cores of DNase hypersensitive sites
J L Slightom, J H Bock, D A Tagle, et al.
Nature Genetics
|
November 1, 1993
Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues
T V Strong, D A Tagle, J M Valdes, et al.
Molecular and Cellular Biology
|
November 1, 1992
Phylogenetic footprinting reveals a nuclear protein which binds to silencer sequences in the human gamma and epsilon globin genes
D L Gumucio, H Heilstedt-Williamson, T A Gray, et al.
American Journal of Human Genetics
|
August 1, 1992
A recombination event that redefines the Huntington disease region
R G Snell, L M Thompson, D A Tagle, et al.
Human Molecular Genetics
|
December 1, 1996
Ataxia-telangiectasia: founder effect among north African Jews
S Gilad, A Bar-Shira, R Harnik, et al.
Science (New York, N.Y.)
|
July 11, 1997
Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene
S K Loftus, J A Morris, E D Carstea, et al.
Genomics
|
April 15, 1996
A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23
K Savitsky, Y Ziv, A Bar-Shira, et al.
Genomics
|
July 1, 1996
Identification and chromosomal localization of Atm, the mouse homolog of the ataxia-telangiectasia gene
I Pecker, K B Avraham, D J Gilbert, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Experimental Neurology
|
May 19, 2001
Early degenerative changes in transgenic mice expressing mutant huntingtin involve dendritic abnormalities but no impairment of mitochondrial energy production
P Guidetti, V Charles, E Y Chen, et al.
Genome Research
|
January 5, 1999
Strategies for mutational analysis of the large multiexon ATM gene using high-density oligonucleotide arrays
J G Hacia, B Sun, N Hunt, et al.
Genomics
|
January 1, 1997
The complete sequences of the galago and rabbit beta-globin locus control regions: extended sequence and functional conservation outside the cores of DNase hypersensitive sites
J L Slightom, J H Bock, D A Tagle, et al.
Nature Genetics
|
November 1, 1993
Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues
T V Strong, D A Tagle, J M Valdes, et al.
Molecular and Cellular Biology
|
November 1, 1992
Phylogenetic footprinting reveals a nuclear protein which binds to silencer sequences in the human gamma and epsilon globin genes
D L Gumucio, H Heilstedt-Williamson, T A Gray, et al.
American Journal of Human Genetics
|
August 1, 1992
A recombination event that redefines the Huntington disease region
R G Snell, L M Thompson, D A Tagle, et al.
Human Molecular Genetics
|
December 1, 1996
Ataxia-telangiectasia: founder effect among north African Jews
S Gilad, A Bar-Shira, R Harnik, et al.
Science (New York, N.Y.)
|
July 11, 1997
Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene
S K Loftus, J A Morris, E D Carstea, et al.
Genomics
|
April 15, 1996
A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23
K Savitsky, Y Ziv, A Bar-Shira, et al.
Genomics
|
July 1, 1996
Identification and chromosomal localization of Atm, the mouse homolog of the ataxia-telangiectasia gene
I Pecker, K B Avraham, D J Gilbert, et al.
Page
of 6