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Human Genetics|December 18, 1998
Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of XpB Fritz, W Küster, K H Orstavik, et al.
American Journal of Medical Genetics|May 3, 1996
Clinical and ultrastructural findings in three patients with geleophysic dysplasiaB F Pontz, H Stöss, F Henschke, et al.
Nature Genetics|April 1, 1993
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectA Winterpacht, M Hilbert, U Schwarze, et al.
The Journal of Pediatrics|July 1, 1991
Schimke immuno-osseous dysplasia: a newly recognized multisystem diseaseJ Spranger, G K Hinkel, H Stöss, et al.
Biophysical Journal|September 2, 2023
Characterizing the transmembrane domains of ADAM10 and BACE1 and the impact of membrane compositionConor B Abraham, Lin Xu, George A Pantelopulos, et al.
The Journal of Physical Chemistry Letters|June 22, 2011
Influence of Nanoparticle Size and Shape on Oligomer Formation of an Amyloidogenic PeptideEdward P O'Brien, John E Straub, Bernard R Brooks, et al.
The Journal of Chemical Physics|December 3, 2008
Probing the mechanisms of fibril formation using lattice modelsMai Suan Li, D K Klimov, J E Straub, et al.
American Journal of Medical Genetics|May 3, 1996
A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasiaB Zabel, K Hilbert, H Stöss, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 12, 2013
Expression in Escherichia coli of a cytochrome P450 enzyme with a cobalt protoporphyrin IX prosthetic groupWesley E Straub, Clinton R Nishida, Paul R Ortiz de Montellano
The Journal of Biological Chemistry|August 27, 2017
Cellular prion protein targets amyloid-β fibril ends via its C-terminal domain to prevent elongationErin Bove-Fenderson, Ryo Urano, John E Straub, et al.
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