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Helvetica Paediatrica Acta|January 1, 1981
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian familyJ Gehler, A C Sewell, C Becker, et al.Prenatal Diagnosis|December 13, 2000
Greenberg dysplasia: first reported case with additional non-skeletal malformations and without consanguinityL C Horn, R Faber, A Meiner, et al.Calcified Tissue International|January 1, 1992
Osteogenesis imperfecta: a clinical study of the first ten years of lifeU Vetter, B Pontz, E Zauner, et al.American Journal of Medical Genetics. Part A|May 12, 2005
Autosomal dominant inheritance of spondyloenchondrodysplasiaR Bhargava, N J Leonard, A K J Chan, et al.Chemical Society Reviews|February 12, 2019
Design, synthesis, and biomedical applications of synthetic sulphated polysaccharidesHannah E Caputo, John E Straub, Mark W GrinstaffDer Urologe. Ausg. A|May 1, 1977
[Vesicorenal reflux (author's transl)]K F Klippel, R Hohenfellner, E Straub, et al.Journal of the American Chemical Society|March 12, 2009
Transmembrane structures of amyloid precursor protein dimer predicted by replica-exchange molecular dynamics simulationsNaoyuki Miyashita, John E Straub, D Thirumalai, et al.Protein Science : a Publication of the Protein Society|June 19, 2002
Charge states rather than propensity for beta-structure determine enhanced fibrillogenesis in wild-type Alzheimer's beta-amyloid peptide compared to E22Q Dutch mutantFrancesca Massi, D Klimov, D Thirumalai, et al.Biophysical Journal|April 9, 2026
Accurate determination of the preferred aggregation number of a micelle-encapsulated membrane protein dimerJonathan J Harris, George A Pantelopulos, John E StraubProceedings of the National Academy of Sciences of the United States of America|August 26, 2016
Impact of membrane lipid composition on the structure and stability of the transmembrane domain of amyloid precursor proteinLaura Dominguez, Leigh Foster, John E Straub, et al.Pageof 46