Prediction of protein domain boundaries from inverse covariances

ανά Sadowski, Michael I
Έκδοση 2013

An automatic method for assessing structural importance of amino acid positions

ανά Sadowski, Michael I, Jones, David T
Έκδοση 2009

Structural Constraints on the Covariance Matrix Derived from Multiple Aligned Protein Sequences

ανά Taylor, William R., Sadowski, Michael I.
Έκδοση 2011

Direct correlation analysis improves fold recognition

ανά Sadowski, Michael I., Maksimiak, Katarzyna, Taylor, William R.
Έκδοση 2011

Protein topology from predicted residue contacts

ανά Taylor, William R, Jones, David T, Sadowski, Michael I
Έκδοση 2012

De novo backbone scaffolds for protein design

ανά MacDonald, James T, Maksimiak, Katarzyna, Sadowski, Michael I, Taylor, William R
Έκδοση 2010

Exploring the limits of fold discrimination by structural alignment: A large scale benchmark using decoys of known fold

ανά Hollup, Siv Midtun, Sadowski, Michael I., Jonassen, Inge, Taylor, William R.
Έκδοση 2011

Analytic Markovian Rates for Generalized Protein Structure Evolution

ανά Coluzza, Ivan, MacDonald, James T., Sadowski, Michael I., Taylor, William R., Goldstein, Richard A.
Έκδοση 2012

Genome-wide analysis of repressor element 1 silencing transcription factor/neuron-restrictive silencing factor (REST/NRSF) target genes

ανά Bruce, Alexander W., Donaldson, Ian J., Wood, Ian C., Yerbury, Sally A., Sadowski, Michael I., Chapman, Michael, Göttgens, Berthold, Buckley, Noel J.
Έκδοση 2004

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy

ανά Fassone, Elisa, Duncan, Andrew J., Taanman, Jan-Willem, Pagnamenta, Alistair T., Sadowski, Michael I., Holand, Tatjana, Qasim, Waseem, Rutland, Paul, Calvo, Sarah E., Mootha, Vamsi K., Bitner-Glindzicz, Maria, Rahman, Shamima
Τόπος έκδοσης Hum Mol Genet (2015)

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy

ανά Fassone, Elisa, Duncan, Andrew J., Taanman, Jan-Willem, Pagnamenta, Alistair T., Sadowski, Michael I., Holand, Tatjana, Qasim, Waseem, Rutland, Paul, Calvo, Sarah E., Mootha, Vamsi K., Bitner-Glindzicz, Maria, Rahman, Shamima
Τόπος έκδοσης Hum Mol Genet (2010)

A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q(10) Deficiency: A Potentially Treatable Form of Mitochondrial Disease

ανά Duncan, Andrew J., Bitner-Glindzicz, Maria, Meunier, Brigitte, Costello, Harry, Hargreaves, Iain P., López, Luis C., Hirano, Michio, Quinzii, Catarina M., Sadowski, Michael I., Hardy, John, Singleton, Andrew, Clayton, Peter T., Rahman, Shamima
Έκδοση 2009

The implications of alternative splicing in the ENCODE protein complement

ανά Tress, Michael L., Martelli, Pier Luigi, Frankish, Adam, Reeves, Gabrielle A., Wesselink, Jan Jaap, Yeats, Corin, Ólason, Páll ĺsólfur, Albrecht, Mario, Hegyi, Hedi, Giorgetti, Alejandro, Raimondo, Domenico, Lagarde, Julien, Laskowski, Roman A., López, Gonzalo, Sadowski, Michael I., Watson, James D., Fariselli, Piero, Rossi, Ivan, Nagy, Alinda, Kai, Wang, Størling, Zenia, Orsini, Massimiliano, Assenov, Yassen, Blankenburg, Hagen, Huthmacher, Carola, Ramírez, Fidel, Schlicker, Andreas, Denoeud, France, Jones, Phil, Kerrien, Samuel, Orchard, Sandra, Antonarakis, Stylianos E., Reymond, Alexandre, Birney, Ewan, Brunak, Søren, Casadio, Rita, Guigo, Roderic, Harrow, Jennifer, Hermjakob, Henning, Jones, David T., Lengauer, Thomas, A. Orengo, Christine, Patthy, László, Thornton, Janet M., Tramontano, Anna, Valencia, Alfonso
Έκδοση 2007