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L Marklund

Showing results (241-250 of 256) with videos related to

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Genetics|June 11, 1998
Multiple marker mapping of quantitative trait loci in a cross between outbred wild boar and large white pigsS A Knott, L Marklund, C S Haley, et al.
Cardiovascular Diabetology|April 10, 2015
Plasma extracellular superoxide dismutase concentration, allelic variations in the SOD3 gene and risk of myocardial infarction and all-cause mortality in people with type 1 and type 2 diabetesKamel Mohammedi, Naïma Bellili-Muñoz, Stefan L Marklund, et al.
Neurology|March 1, 1997
Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotrophic lateral sclerosisR W Orrell, J J Habgood, I Gardiner, et al.
Brain : a Journal of Neurology|November 17, 2021
Infantile SOD1 deficiency syndrome caused by a homozygous SOD1 variant with absence of enzyme activityShlomit Ezer, Muhannad Daana, Julien H Park, et al.
Brain : a Journal of Neurology|August 1, 1996
Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patientsP M Andersen, L Forsgren, M Binzer, et al.
Human Molecular Genetics|May 19, 2012
Mutant superoxide dismutase-1 indistinguishable from wild-type causes ALSMatthis Synofzik, Dario Ronchi, Isil Keskin, et al.
Neurobiology of Disease|September 25, 2002
CuZn-superoxide dismutase in D90A heterozygotes from recessive and dominant ALS pedigreesP Andreas Jonsson, Asa Bäckstrand, Peter M Andersen, et al.
Neurobiology of Aging|September 22, 2018
A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanismsAntonio Canosa, Giovanni De Marco, Annarosa Lomartire, et al.
Scientific Reports|September 23, 2018
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral SclerosisBastien Paré, Manuela Lehmann, Marie Beaudin, et al.
Cells|April 12, 2022
Alteration of Mitochondrial Integrity as Upstream Event in the Pathophysiology of SOD1-ALSRené Günther, Arun Pal, Chloe Williams, et al.
Pageof 26

Showing results (241-250 of 256) with videos related to

Sort By:
Pageof 26
Genetics|June 11, 1998
Multiple marker mapping of quantitative trait loci in a cross between outbred wild boar and large white pigsS A Knott, L Marklund, C S Haley, et al.
Cardiovascular Diabetology|April 10, 2015
Plasma extracellular superoxide dismutase concentration, allelic variations in the SOD3 gene and risk of myocardial infarction and all-cause mortality in people with type 1 and type 2 diabetesKamel Mohammedi, Naïma Bellili-Muñoz, Stefan L Marklund, et al.
Neurology|March 1, 1997
Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotrophic lateral sclerosisR W Orrell, J J Habgood, I Gardiner, et al.
Brain : a Journal of Neurology|November 17, 2021
Infantile SOD1 deficiency syndrome caused by a homozygous SOD1 variant with absence of enzyme activityShlomit Ezer, Muhannad Daana, Julien H Park, et al.
Brain : a Journal of Neurology|August 1, 1996
Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patientsP M Andersen, L Forsgren, M Binzer, et al.
Human Molecular Genetics|May 19, 2012
Mutant superoxide dismutase-1 indistinguishable from wild-type causes ALSMatthis Synofzik, Dario Ronchi, Isil Keskin, et al.
Neurobiology of Disease|September 25, 2002
CuZn-superoxide dismutase in D90A heterozygotes from recessive and dominant ALS pedigreesP Andreas Jonsson, Asa Bäckstrand, Peter M Andersen, et al.
Neurobiology of Aging|September 22, 2018
A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanismsAntonio Canosa, Giovanni De Marco, Annarosa Lomartire, et al.
Scientific Reports|September 23, 2018
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral SclerosisBastien Paré, Manuela Lehmann, Marie Beaudin, et al.
Cells|April 12, 2022
Alteration of Mitochondrial Integrity as Upstream Event in the Pathophysiology of SOD1-ALSRené Günther, Arun Pal, Chloe Williams, et al.
Pageof 26