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Lisbeth Birk Møller

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Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)|August 31, 2014
Small amounts of functional ATP7A protein permit mild phenotypeLisbeth Birk Møller
Clinical Medicine. Pathology|August 31, 2011
Mutation Detection in the Menkes Gene ATP7A Using the Protein Truncation TestLisbeth Birk Møller, Nina Horn
Scandinavian Journal of Pain|June 20, 2018
GCH1 variants, tetrahydrobiopterin and their effects on pain sensitivityArafat Nasser, Lisbeth Birk Møller
Cells|October 21, 2020
Crosstalk of Hedgehog and mTORC1 PathwaysLasse Jonsgaard Larsen, Lisbeth Birk Møller
Stem Cell Research|July 31, 2023
Generation of induced pluripotent stem cells, KCi004-A derived from a male with Parkinson's disease and homozygous for the PINK1 variant c.1366C > T, p.Gln456Lasse Jonsgaard Larsen, Lisbeth Birk Møller
Frontiers in Pharmacology|October 12, 2012
Impairment of interrelated iron- and copper homeostatic mechanisms in brain contributes to the pathogenesis of neurodegenerative disordersTina Skjørringe, Lisbeth Birk Møller, Torben Moos
Biochimie|June 9, 2009
Molecular diagnosis of Menkes disease: genotype-phenotype correlationLisbeth Birk Møller, Mie Mogensen, Nina Horn
Plos One|April 16, 2011
Splice site mutations in the ATP7A geneTina Skjørringe, Zeynep Tümer, Lisbeth Birk Møller
Human Mutation|November 25, 2003
Screening of 383 unrelated patients affected with Menkes disease and finding of 57 gross deletions in ATP7AZeynep Tümer, Lisbeth Birk Møller, Nina Horn
The Journal of Biological Chemistry|June 22, 2002
The cryptic adenine deaminase gene of Escherichia coli. Silencing by the nucleoid-associated DNA-binding protein, H-NS, and activation by insertion elementsCarsten Petersen, Lisbeth Birk Møller, Poul Valentin-Hansen
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)|August 31, 2014
Small amounts of functional ATP7A protein permit mild phenotypeLisbeth Birk Møller
Clinical Medicine. Pathology|August 31, 2011
Mutation Detection in the Menkes Gene ATP7A Using the Protein Truncation TestLisbeth Birk Møller, Nina Horn
Scandinavian Journal of Pain|June 20, 2018
GCH1 variants, tetrahydrobiopterin and their effects on pain sensitivityArafat Nasser, Lisbeth Birk Møller
Cells|October 21, 2020
Crosstalk of Hedgehog and mTORC1 PathwaysLasse Jonsgaard Larsen, Lisbeth Birk Møller
Stem Cell Research|July 31, 2023
Generation of induced pluripotent stem cells, KCi004-A derived from a male with Parkinson's disease and homozygous for the PINK1 variant c.1366C > T, p.Gln456Lasse Jonsgaard Larsen, Lisbeth Birk Møller
Frontiers in Pharmacology|October 12, 2012
Impairment of interrelated iron- and copper homeostatic mechanisms in brain contributes to the pathogenesis of neurodegenerative disordersTina Skjørringe, Lisbeth Birk Møller, Torben Moos
Biochimie|June 9, 2009
Molecular diagnosis of Menkes disease: genotype-phenotype correlationLisbeth Birk Møller, Mie Mogensen, Nina Horn
Plos One|April 16, 2011
Splice site mutations in the ATP7A geneTina Skjørringe, Zeynep Tümer, Lisbeth Birk Møller
Human Mutation|November 25, 2003
Screening of 383 unrelated patients affected with Menkes disease and finding of 57 gross deletions in ATP7AZeynep Tümer, Lisbeth Birk Møller, Nina Horn
The Journal of Biological Chemistry|June 22, 2002
The cryptic adenine deaminase gene of Escherichia coli. Silencing by the nucleoid-associated DNA-binding protein, H-NS, and activation by insertion elementsCarsten Petersen, Lisbeth Birk Møller, Poul Valentin-Hansen
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