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Neurobiology of Aging
|
January 19, 2000
Mitochondrial DNA rearrangements in aging human brain and in situ PCR of mtDNA
S Melov, J A Schneider, P E Coskun, et al.
The Annals of Otology, Rhinology, and Laryngology
|
February 4, 1999
Carotid artery occlusion due to bacterial paranasal sinusitis
M Z Ozüer, F N Ardiç, E Coskun, et al.
Journal of Pediatric Hematology/Oncology
|
April 24, 2018
Respiratory Distress and Severe Anemia in a Child With Idiopathic Pulmonary Hemosiderosis
Münevver T Temel, Levent Temel, Mehmet E Coskun, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
January 1, 2019
Dynamic thiol/disulfide homeostasis in children with community-acquired pneumonia
Münevver Tugba Temel, Seniz Demiryürek, Levent Temel, et al.
Biochimica Et Biophysica Acta
|
April 29, 2008
MITOCHIP assessment of differential gene expression in the skeletal muscle of Ant1 knockout mice: coordinate regulation of OXPHOS, antioxidant, and apoptotic genes
Vaidya Subramaniam, Pawel Golik, Deborah G Murdock, et al.
Cardiology in the Young
|
April 2, 2019
Determination of dynamic thiol/disulphide homeostasis in children with tetralogy of Fallot and ventricular septal defect
Münevver T Temel, Seniz Demiryürek, Ahmet Saracaloglu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 19, 2001
Lifespan extension and rescue of spongiform encephalopathy in superoxide dismutase 2 nullizygous mice treated with superoxide dismutase-catalase mimetics
S Melov, S R Doctrow, J A Schneider, et al.
Journal of Alzheimer'S Disease : JAD
|
May 14, 2010
Systemic mitochondrial dysfunction and the etiology of Alzheimer's disease and down syndrome dementia
Pinar E Coskun, Joanne Wyrembak, Olga Derbereva, et al.
Science (New York, N.Y.)
|
February 16, 2008
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations
Weiwei Fan, Katrina G Waymire, Navneet Narula, et al.
Clinical and Translational Science
|
October 17, 2013
Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndrome
Puya G Yazdi, Hailing Su, Svetlana Ghimbovschi, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Neurobiology of Aging
|
January 19, 2000
Mitochondrial DNA rearrangements in aging human brain and in situ PCR of mtDNA
S Melov, J A Schneider, P E Coskun, et al.
The Annals of Otology, Rhinology, and Laryngology
|
February 4, 1999
Carotid artery occlusion due to bacterial paranasal sinusitis
M Z Ozüer, F N Ardiç, E Coskun, et al.
Journal of Pediatric Hematology/Oncology
|
April 24, 2018
Respiratory Distress and Severe Anemia in a Child With Idiopathic Pulmonary Hemosiderosis
Münevver T Temel, Levent Temel, Mehmet E Coskun, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
January 1, 2019
Dynamic thiol/disulfide homeostasis in children with community-acquired pneumonia
Münevver Tugba Temel, Seniz Demiryürek, Levent Temel, et al.
Biochimica Et Biophysica Acta
|
April 29, 2008
MITOCHIP assessment of differential gene expression in the skeletal muscle of Ant1 knockout mice: coordinate regulation of OXPHOS, antioxidant, and apoptotic genes
Vaidya Subramaniam, Pawel Golik, Deborah G Murdock, et al.
Cardiology in the Young
|
April 2, 2019
Determination of dynamic thiol/disulphide homeostasis in children with tetralogy of Fallot and ventricular septal defect
Münevver T Temel, Seniz Demiryürek, Ahmet Saracaloglu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 19, 2001
Lifespan extension and rescue of spongiform encephalopathy in superoxide dismutase 2 nullizygous mice treated with superoxide dismutase-catalase mimetics
S Melov, S R Doctrow, J A Schneider, et al.
Journal of Alzheimer'S Disease : JAD
|
May 14, 2010
Systemic mitochondrial dysfunction and the etiology of Alzheimer's disease and down syndrome dementia
Pinar E Coskun, Joanne Wyrembak, Olga Derbereva, et al.
Science (New York, N.Y.)
|
February 16, 2008
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations
Weiwei Fan, Katrina G Waymire, Navneet Narula, et al.
Clinical and Translational Science
|
October 17, 2013
Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndrome
Puya G Yazdi, Hailing Su, Svetlana Ghimbovschi, et al.
Page
of 4