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L B Møller

Showing results (21-30 of 31) with videos related to

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Clinical Genetics|June 29, 2017
A 37-year-old Menkes disease patient-Residual ATP7A activity and early copper administration as key factors in beneficial treatmentZ Tümer, M Petris, S Zhu, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 9, 2002
Disturbed copper transport in humans. Part 1: mutations of the ATP7A gene lead to Menkes disease and occipital horn syndromeJ Seidel, L B Møller, H J Mentzel, et al.
American Journal of Human Genetics|March 31, 2000
Similar splice-site mutations of the ATP7A gene lead to different phenotypes: classical Menkes disease or occipital horn syndromeL B Møller, Z Tümer, C Lund, et al.
Pflugers Archiv : European Journal of Physiology|July 1, 2005
NH3 and NH4+ permeability in aquaporin-expressing Xenopus oocytesLars M Holm, Thomas P Jahn, Anders L B Møller, et al.
The Journal of Biological Chemistry|November 16, 2006
Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranesGerd P Bienert, Anders L B Møller, Kim A Kristiansen, et al.
FEBS Letters|September 11, 2004
Aquaporin homologues in plants and mammals transport ammoniaThomas P Jahn, Anders L B Møller, Thomas Zeuthen, et al.
Journal of Proteomics|February 22, 2011
A workflow for peptide-based proteomics in a poorly sequenced plant: a case study on the plasma membrane proteome of bananaA Vertommen, A L B Møller, J H G Cordewener, et al.
Journal of the American Chemical Society|December 23, 2025
Modular Total Synthesis of Lasalocid Acid A through Direct C(sp<sup>3</sup>)-C(sp<sup>3</sup>) Attached Ring ConstructionFlorian E H Kromm, Søren L B Møller, Adam S Jensen, et al.
The Journal of Cell Biology|June 13, 1998
Mannose 6-phosphate/insulin-like growth factor-II receptor targets the urokinase receptor to lysosomes via a novel binding interactionA Nykjaer, E I Christensen, H Vorum, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 20, 2005
Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiencyJ L K Van Hove, J Steyaert, G Matthijs, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Clinical Genetics|June 29, 2017
A 37-year-old Menkes disease patient-Residual ATP7A activity and early copper administration as key factors in beneficial treatmentZ Tümer, M Petris, S Zhu, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 9, 2002
Disturbed copper transport in humans. Part 1: mutations of the ATP7A gene lead to Menkes disease and occipital horn syndromeJ Seidel, L B Møller, H J Mentzel, et al.
American Journal of Human Genetics|March 31, 2000
Similar splice-site mutations of the ATP7A gene lead to different phenotypes: classical Menkes disease or occipital horn syndromeL B Møller, Z Tümer, C Lund, et al.
Pflugers Archiv : European Journal of Physiology|July 1, 2005
NH3 and NH4+ permeability in aquaporin-expressing Xenopus oocytesLars M Holm, Thomas P Jahn, Anders L B Møller, et al.
The Journal of Biological Chemistry|November 16, 2006
Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranesGerd P Bienert, Anders L B Møller, Kim A Kristiansen, et al.
FEBS Letters|September 11, 2004
Aquaporin homologues in plants and mammals transport ammoniaThomas P Jahn, Anders L B Møller, Thomas Zeuthen, et al.
Journal of Proteomics|February 22, 2011
A workflow for peptide-based proteomics in a poorly sequenced plant: a case study on the plasma membrane proteome of bananaA Vertommen, A L B Møller, J H G Cordewener, et al.
Journal of the American Chemical Society|December 23, 2025
Modular Total Synthesis of Lasalocid Acid A through Direct C(sp<sup>3</sup>)-C(sp<sup>3</sup>) Attached Ring ConstructionFlorian E H Kromm, Søren L B Møller, Adam S Jensen, et al.
The Journal of Cell Biology|June 13, 1998
Mannose 6-phosphate/insulin-like growth factor-II receptor targets the urokinase receptor to lysosomes via a novel binding interactionA Nykjaer, E I Christensen, H Vorum, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 20, 2005
Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiencyJ L K Van Hove, J Steyaert, G Matthijs, et al.
Pageof 4