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Circulation
|
November 1, 1996
ECG repolarization patterns in chromosome 7-linked QT syndrome (LQTS 2)
E Schulze-Bahr, W Haverkamp, G Breithardt, et al.
Biochemical Society Transactions
|
May 1, 1993
Phenotypic variation of mutations in the human lipoprotein-lipase gene
M R Hayden, J J Kastelein, H Funke, et al.
Angewandte Chemie (International Ed. in English)
|
July 3, 2015
Enhanced Hydrogen Production from DNA-Assembled Z-Scheme TiO2-CdS Photocatalyst Systems
Ke Ma, Omer Yehezkeli, Dylan W Domaille, et al.
Journal of Lipid Research
|
October 3, 2000
Apolipoprotein A4-1/2 polymorphism and response of serum lipids to dietary cholesterol in humans
R M Weggemans, P L Zock, S Meyboom, et al.
The Journal of Clinical Investigation
|
December 1, 1989
Apolipoprotein A-I variants. Naturally occurring substitutions of proline residues affect plasma concentration of apolipoprotein A-I
A von Eckardstein, H Funke, A Henke, et al.
Nanoscale
|
September 27, 2014
Copper plasmonics and catalysis: role of electron-phonon interactions in dephasing localized surface plasmons
Qi-C Sun, Yuchen Ding, Samuel M Goodman, et al.
The Journal of Biological Chemistry
|
May 25, 1990
Structural analysis of human apolipoprotein A-I variants. Amino acid substitutions are nonrandomly distributed throughout the apolipoprotein A-I primary structure
A von Eckardstein, H Funke, M Walter, et al.
Muscle & Nerve
|
August 14, 1998
Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene
F Stögbauer, P Young, M Kerschensteiner, et al.
Deutsche Medizinische Wochenschrift (1946)
|
March 11, 1977
[Successful treatment of a supraventricular re-entry tachycardia in a patient with WPW and sick-sinus syndrome with permanent rapid atrial and QRS-inhibited ventricular pacemaker stimulation (author's transl)]
G Neumann, H Funke, J Wagner, et al.
Human Mutation
|
April 27, 2018
NGS testing for cardiomyopathy: Utility of adding RASopathy-associated genes
Ozge Ceyhan-Birsoy, Maya M Miatkowski, Elizabeth Hynes, et al.
Page
of 21
Search research articles
Search
Showing results (71-80 of 203) with videos related to
Sort By:
Page
of 21
Circulation
|
November 1, 1996
ECG repolarization patterns in chromosome 7-linked QT syndrome (LQTS 2)
E Schulze-Bahr, W Haverkamp, G Breithardt, et al.
Biochemical Society Transactions
|
May 1, 1993
Phenotypic variation of mutations in the human lipoprotein-lipase gene
M R Hayden, J J Kastelein, H Funke, et al.
Angewandte Chemie (International Ed. in English)
|
July 3, 2015
Enhanced Hydrogen Production from DNA-Assembled Z-Scheme TiO2-CdS Photocatalyst Systems
Ke Ma, Omer Yehezkeli, Dylan W Domaille, et al.
Journal of Lipid Research
|
October 3, 2000
Apolipoprotein A4-1/2 polymorphism and response of serum lipids to dietary cholesterol in humans
R M Weggemans, P L Zock, S Meyboom, et al.
The Journal of Clinical Investigation
|
December 1, 1989
Apolipoprotein A-I variants. Naturally occurring substitutions of proline residues affect plasma concentration of apolipoprotein A-I
A von Eckardstein, H Funke, A Henke, et al.
Nanoscale
|
September 27, 2014
Copper plasmonics and catalysis: role of electron-phonon interactions in dephasing localized surface plasmons
Qi-C Sun, Yuchen Ding, Samuel M Goodman, et al.
The Journal of Biological Chemistry
|
May 25, 1990
Structural analysis of human apolipoprotein A-I variants. Amino acid substitutions are nonrandomly distributed throughout the apolipoprotein A-I primary structure
A von Eckardstein, H Funke, M Walter, et al.
Muscle & Nerve
|
August 14, 1998
Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene
F Stögbauer, P Young, M Kerschensteiner, et al.
Deutsche Medizinische Wochenschrift (1946)
|
March 11, 1977
[Successful treatment of a supraventricular re-entry tachycardia in a patient with WPW and sick-sinus syndrome with permanent rapid atrial and QRS-inhibited ventricular pacemaker stimulation (author's transl)]
G Neumann, H Funke, J Wagner, et al.
Human Mutation
|
April 27, 2018
NGS testing for cardiomyopathy: Utility of adding RASopathy-associated genes
Ozge Ceyhan-Birsoy, Maya M Miatkowski, Elizabeth Hynes, et al.
Page
of 21