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Clinical Genetics
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June 29, 2017
A 37-year-old Menkes disease patient-Residual ATP7A activity and early copper administration as key factors in beneficial treatment
Z 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 syndrome
J 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 syndrome
L 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 oocytes
Lars 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 membranes
Gerd P Bienert, Anders L B Møller, Kim A Kristiansen, et al.
FEBS Letters
|
September 11, 2004
Aquaporin homologues in plants and mammals transport ammonia
Thomas 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 banana
A 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 Construction
Florian 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 interaction
A 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 deficiency
J L K Van Hove, J Steyaert, G Matthijs, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 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 treatment
Z 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 syndrome
J 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 syndrome
L 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 oocytes
Lars 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 membranes
Gerd P Bienert, Anders L B Møller, Kim A Kristiansen, et al.
FEBS Letters
|
September 11, 2004
Aquaporin homologues in plants and mammals transport ammonia
Thomas 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 banana
A 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 Construction
Florian 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 interaction
A 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 deficiency
J L K Van Hove, J Steyaert, G Matthijs, et al.
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of 4