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Neurosurgery
|
December 7, 2005
Spontaneous spinal subarachnoid hemorrhage secondary to spinal aneurysms: diagnosis and treatment paradigm
L Fernando Gonzalez, Joseph M Zabramski, Peyman Tabrizi, et al.
Growth Regulation
|
March 1, 1993
Effects of interactions between IGFBPs and IGFs on the plasma clearance and in vivo biological activities of IGFs and IGF analogs
F J Ballard, P E Walton, S Bastian, et al.
Cell
|
June 15, 1990
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
J M Shoffner, M T Lott, A M Lezza, et al.
Applied and Environmental Microbiology
|
April 1, 1990
Cloning, sequence analysis, and expression of genes encoding xylan-degrading enzymes from the thermophile "Caldocellum saccharolyticum"
E Lüthi, D R Love, J McAnulty, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society
|
June 10, 1998
The maculatin peptides from the skin glands of the tree frog Litoria genimaculata: a comparison of the structures and antibacterial activities of maculatin 1.1 and caerin 1.1
T Rozek, R J Waugh, S T Steinborner, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1997
Mitochondrial DNA and Y chromosome-specific polymorphisms in the Seminole Tribe of Florida
K Huoponen, A Torroni, P R Wickman, et al.
Electrophoresis
|
December 1, 1996
Fast capillary electrophoresis-laser induced fluorescence analysis of ligase chain reaction products: human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy
J Muth, P M Williams, S J Williams, et al.
Human Mutation
|
April 23, 2008
Reduced half-life of holocarboxylase synthetase from patients with severe multiple carboxylase deficiency
Lisa M Bailey, Ruby A Ivanov, Sarawut Jitrapakdee, et al.
American Journal of Ophthalmology
|
August 15, 1994
Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team
N J Newman, A Torroni, M D Brown, et al.
Free Radical Biology & Medicine
|
April 8, 2000
Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene
L A Esposito, J E Kokoszka, K G Waymire, et al.
Page
of 146
Search research articles
Search
Showing results (841-850 of 1,458) with videos related to
Sort By:
Page
of 146
Neurosurgery
|
December 7, 2005
Spontaneous spinal subarachnoid hemorrhage secondary to spinal aneurysms: diagnosis and treatment paradigm
L Fernando Gonzalez, Joseph M Zabramski, Peyman Tabrizi, et al.
Growth Regulation
|
March 1, 1993
Effects of interactions between IGFBPs and IGFs on the plasma clearance and in vivo biological activities of IGFs and IGF analogs
F J Ballard, P E Walton, S Bastian, et al.
Cell
|
June 15, 1990
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
J M Shoffner, M T Lott, A M Lezza, et al.
Applied and Environmental Microbiology
|
April 1, 1990
Cloning, sequence analysis, and expression of genes encoding xylan-degrading enzymes from the thermophile "Caldocellum saccharolyticum"
E Lüthi, D R Love, J McAnulty, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society
|
June 10, 1998
The maculatin peptides from the skin glands of the tree frog Litoria genimaculata: a comparison of the structures and antibacterial activities of maculatin 1.1 and caerin 1.1
T Rozek, R J Waugh, S T Steinborner, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1997
Mitochondrial DNA and Y chromosome-specific polymorphisms in the Seminole Tribe of Florida
K Huoponen, A Torroni, P R Wickman, et al.
Electrophoresis
|
December 1, 1996
Fast capillary electrophoresis-laser induced fluorescence analysis of ligase chain reaction products: human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy
J Muth, P M Williams, S J Williams, et al.
Human Mutation
|
April 23, 2008
Reduced half-life of holocarboxylase synthetase from patients with severe multiple carboxylase deficiency
Lisa M Bailey, Ruby A Ivanov, Sarawut Jitrapakdee, et al.
American Journal of Ophthalmology
|
August 15, 1994
Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team
N J Newman, A Torroni, M D Brown, et al.
Free Radical Biology & Medicine
|
April 8, 2000
Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene
L A Esposito, J E Kokoszka, K G Waymire, et al.
Page
of 146