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Gert Vriend

Showing results (81-90 of 108) with videos related to

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Journal of Biomolecular NMR|October 8, 2009
The NMR restraints grid at BMRB for 5,266 protein and nucleic acid PDB entriesJurgen F Doreleijers, Wim F Vranken, Christopher Schulte, et al.
Structure (London, England : 1993)|May 9, 2008
The molecular mechanism of toxin-induced conformational changes in a potassium channel: relation to C-type inactivationUlrich Zachariae, Robert Schneider, Phanindra Velisetty, et al.
Journal of Biomolecular NMR|September 19, 2012
CING: an integrated residue-based structure validation program suiteJurgen F Doreleijers, Alan W Sousa da Silva, Elmar Krieger, et al.
Proteins|March 11, 2009
Correlated mutation analyses on super-family alignments reveal functionally important residuesRemko K P Kuipers, Henk-Jan Joosten, Eugene Verwiel, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 22, 2012
A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domainHyun-Ju Cho, Hong-Joon Park, Maria Trexler, et al.
Iscience|December 13, 2023
Quantifying the deformability of malaria-infected red blood cells using deep learning trained on synthetic cellsDaniel T Rademaker, Joshua J Koopmans, Gwendolyn M S M Thyen, et al.
Protein Engineering, Design & Selection : PEDS|May 6, 2017
NewProt - a protein engineering portalAndreas Schwarte, Maika Genz, Lilly Skalden, et al.
Open Biology|August 1, 2014
The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing lossTae-Jun Kwon, Se-Kyung Oh, Hong-Joon Park, et al.
Journal of Chemical Information and Modeling|January 28, 2015
Discovery of small molecule CD40-TRAF6 inhibitorsBarbara Zarzycka, Tom Seijkens, Sander B Nabuurs, et al.
Human Mutation|January 30, 2008
Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA bindingRob W J Collin, Ramesh Chellappa, Robert-Jan Pauw, et al.
Pageof 11

Showing results (81-90 of 108) with videos related to

Sort By:
Pageof 11
Journal of Biomolecular NMR|October 8, 2009
The NMR restraints grid at BMRB for 5,266 protein and nucleic acid PDB entriesJurgen F Doreleijers, Wim F Vranken, Christopher Schulte, et al.
Structure (London, England : 1993)|May 9, 2008
The molecular mechanism of toxin-induced conformational changes in a potassium channel: relation to C-type inactivationUlrich Zachariae, Robert Schneider, Phanindra Velisetty, et al.
Journal of Biomolecular NMR|September 19, 2012
CING: an integrated residue-based structure validation program suiteJurgen F Doreleijers, Alan W Sousa da Silva, Elmar Krieger, et al.
Proteins|March 11, 2009
Correlated mutation analyses on super-family alignments reveal functionally important residuesRemko K P Kuipers, Henk-Jan Joosten, Eugene Verwiel, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 22, 2012
A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domainHyun-Ju Cho, Hong-Joon Park, Maria Trexler, et al.
Iscience|December 13, 2023
Quantifying the deformability of malaria-infected red blood cells using deep learning trained on synthetic cellsDaniel T Rademaker, Joshua J Koopmans, Gwendolyn M S M Thyen, et al.
Protein Engineering, Design & Selection : PEDS|May 6, 2017
NewProt - a protein engineering portalAndreas Schwarte, Maika Genz, Lilly Skalden, et al.
Open Biology|August 1, 2014
The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing lossTae-Jun Kwon, Se-Kyung Oh, Hong-Joon Park, et al.
Journal of Chemical Information and Modeling|January 28, 2015
Discovery of small molecule CD40-TRAF6 inhibitorsBarbara Zarzycka, Tom Seijkens, Sander B Nabuurs, et al.
Human Mutation|January 30, 2008
Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA bindingRob W J Collin, Ramesh Chellappa, Robert-Jan Pauw, et al.
Pageof 11