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Entry ID Original Release date Data summary Entry Title Citation Title Authors
51744 2023-05-24 Chemical Shifts: 1 set
AbpSH3 0 mM NaCl How a highly acidic SH3 domain folds in the absence of its charged peptide target Download bibtex for citation iamge Aaron J Adkins, Anna H Carhart, Benjamin J Lantz, Elahe Masoumzadeh, Elliott J Stollar, Gemma M Bell, K Aurelia A Ball, M Adriana A Cuibus, Matthew J Dominguez, Megan E Souness, Michael P Latham, Valeria Jaramillo-Martinez
51745 2023-05-24 Chemical Shifts: 1 set
AbpSH3 100 mM NaCl How a highly acidic SH3 domain folds in the absence of its charged peptide target Download bibtex for citation iamge Aaron J Adkins, Anna H Carhart, Benjamin J Lantz, Elahe Masoumzadeh, Elliott J Stollar, Gemma M Bell, K Aurelia A Ball, M Adriana A Cuibus, Matthew J Dominguez, Megan E Souness, Michael P Latham, Valeria Jaramillo-Martinez
51746 2023-05-24 Chemical Shifts: 1 set
AbpSH3 800 mM NaCl How a highly acidic SH3 domain folds in the absence of its charged peptide target Download bibtex for citation iamge Aaron J Adkins, Anna H Carhart, Benjamin J Lantz, Elahe Masoumzadeh, Elliott J Stollar, Gemma M Bell, K Aurelia A Ball, M Adriana A Cuibus, Matthew J Dominguez, Megan E Souness, Michael P Latham, Valeria Jaramillo-Martinez
51384 2022-04-13 Chemical Shifts: 1 set
SH3-DNAse1L3-CTD Structural features of Dnase1L3 responsible for serum antigen clearance Download bibtex for citation iamge Britney Mapp, Elahe Masoumzadeh, Johanna Villarreal, Jon J McCord, Michael P Latham, Minal Engavale, Peter A Keyel, R Bryan B Sutton
30653 2020-08-14 Chemical Shifts: 1 set
Human CstF-64 RRM mutant - D50A A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans Download bibtex for citation iamge Clinton C MacDonald, Elahe Masoumzadeh, Marie-Ange A Delrue, Michael P Latham, Petar N Grozdanov, Pierre Billuart, Thierry Bienvenu, Vera M Kalscheuer
30652 2020-08-03 Chemical Shifts: 1 set
Human CstF-64 RRM A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans Download bibtex for citation iamge Clinton C MacDonald, Elahe Masoumzadeh, Marie-Ange A Delrue, Michael P Latham, Petar N Grozdanov, Pierre Billuart, Thierry Bienvenu, Vera M Kalscheuer