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Animal : an International Journal of Animal Bioscience
|
November 3, 2016
Estimates of heritability and genetic correlations for milk coagulation properties and individual laboratory cheese yield in Sarda ewes
A Puledda, G Gaspa, M G Manca, et al.
Neuromuscular Disorders : NMD
|
January 1, 1993
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA
C T Moraes, F Ciacci, G Silvestri, et al.
Muscle & Nerve
|
January 1, 1979
Lipid storage myopathy, ichthyosis, and steatorrhea
A Miranda, S DiMauro, A Eastwood, et al.
Biochemical and Biophysical Research Communications
|
November 22, 1995
A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy
F M Santorelli, S C Mak, M Vàzquez-Acevedo, et al.
Annals of Neurology
|
August 1, 1997
Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?
G Manfredi, T Vu, E Bonilla, et al.
Journal of the Neurological Sciences
|
February 18, 2011
Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutation
Valentina Emmanuele, Evangelia Sotiriou, Maryam Shirazi, et al.
Plos One
|
August 7, 2010
Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effects
Luis C López, Catarina M Quinzii, Estela Area, et al.
Optics Letters
|
September 29, 2017
High-order harmonic generations in intense MIR fields by cascade three-wave mixing in a fractal-poled LiNbO<sub>3</sub> photonic crystal
Hyunwook Park, Antoine Camper, Kyle Kafka, et al.
American Journal of Human Genetics
|
December 23, 2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations
Luis Carlos López, Markus Schuelke, Catarina M Quinzii, et al.
American Journal of Medical Genetics. Part A
|
September 17, 2004
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosis
Sara Shanske, Jacklyn Pancrudo, Petra Kaufmann, et al.
Page
of 95
Search research articles
Search
Showing results (581-590 of 942) with videos related to
Sort By:
Page
of 95
Animal : an International Journal of Animal Bioscience
|
November 3, 2016
Estimates of heritability and genetic correlations for milk coagulation properties and individual laboratory cheese yield in Sarda ewes
A Puledda, G Gaspa, M G Manca, et al.
Neuromuscular Disorders : NMD
|
January 1, 1993
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA
C T Moraes, F Ciacci, G Silvestri, et al.
Muscle & Nerve
|
January 1, 1979
Lipid storage myopathy, ichthyosis, and steatorrhea
A Miranda, S DiMauro, A Eastwood, et al.
Biochemical and Biophysical Research Communications
|
November 22, 1995
A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy
F M Santorelli, S C Mak, M Vàzquez-Acevedo, et al.
Annals of Neurology
|
August 1, 1997
Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?
G Manfredi, T Vu, E Bonilla, et al.
Journal of the Neurological Sciences
|
February 18, 2011
Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutation
Valentina Emmanuele, Evangelia Sotiriou, Maryam Shirazi, et al.
Plos One
|
August 7, 2010
Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effects
Luis C López, Catarina M Quinzii, Estela Area, et al.
Optics Letters
|
September 29, 2017
High-order harmonic generations in intense MIR fields by cascade three-wave mixing in a fractal-poled LiNbO<sub>3</sub> photonic crystal
Hyunwook Park, Antoine Camper, Kyle Kafka, et al.
American Journal of Human Genetics
|
December 23, 2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations
Luis Carlos López, Markus Schuelke, Catarina M Quinzii, et al.
American Journal of Medical Genetics. Part A
|
September 17, 2004
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosis
Sara Shanske, Jacklyn Pancrudo, Petra Kaufmann, et al.
Page
of 95