Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome
10.1038/srep30293
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sg-nus-scholar.10635-1740002024-04-04T01:08:59Z Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome Pucheta-Martinez, E D'Amelio, N Lelli, M Martinez-Torrecuadrada, J.L Sudol, M Saladino, G Gervasio, F.L PHYSIOLOGY carrier protein DNA binding protein messenger RNA nuclear protein PQBP1 protein, human protein binding WBP11 protein, human beta sheet cerebral palsy chemistry genetics human intellectual impairment molecular dynamics nuclear magnetic resonance pathology point mutation protein folding WW domain X linked mental retardation Carrier Proteins Cerebral Palsy DNA-Binding Proteins Humans Intellectual Disability Mental Retardation, X-Linked Molecular Dynamics Simulation Nuclear Magnetic Resonance, Biomolecular Nuclear Proteins Point Mutation Protein Binding Protein Conformation, beta-Strand Protein Folding RNA, Messenger WW Domains 10.1038/srep30293 Scientific Reports 6 30293 2020-09-02T06:52:11Z 2020-09-02T06:52:11Z 2016 Article Pucheta-Martinez, E, D'Amelio, N, Lelli, M, Martinez-Torrecuadrada, J.L, Sudol, M, Saladino, G, Gervasio, F.L (2016). Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome. Scientific Reports 6 : 30293. ScholarBank@NUS Repository. https://doi.org/10.1038/srep30293 20452322 https://scholarbank.nus.edu.sg/handle/10635/174000 Unpaywall 20200831 |
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carrier protein DNA binding protein messenger RNA nuclear protein PQBP1 protein, human protein binding WBP11 protein, human beta sheet cerebral palsy chemistry genetics human intellectual impairment molecular dynamics nuclear magnetic resonance pathology point mutation protein folding WW domain X linked mental retardation Carrier Proteins Cerebral Palsy DNA-Binding Proteins Humans Intellectual Disability Mental Retardation, X-Linked Molecular Dynamics Simulation Nuclear Magnetic Resonance, Biomolecular Nuclear Proteins Point Mutation Protein Binding Protein Conformation, beta-Strand Protein Folding RNA, Messenger WW Domains |
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carrier protein DNA binding protein messenger RNA nuclear protein PQBP1 protein, human protein binding WBP11 protein, human beta sheet cerebral palsy chemistry genetics human intellectual impairment molecular dynamics nuclear magnetic resonance pathology point mutation protein folding WW domain X linked mental retardation Carrier Proteins Cerebral Palsy DNA-Binding Proteins Humans Intellectual Disability Mental Retardation, X-Linked Molecular Dynamics Simulation Nuclear Magnetic Resonance, Biomolecular Nuclear Proteins Point Mutation Protein Binding Protein Conformation, beta-Strand Protein Folding RNA, Messenger WW Domains Pucheta-Martinez, E D'Amelio, N Lelli, M Martinez-Torrecuadrada, J.L Sudol, M Saladino, G Gervasio, F.L Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome |
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10.1038/srep30293 |
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PHYSIOLOGY |
author_facet |
PHYSIOLOGY Pucheta-Martinez, E D'Amelio, N Lelli, M Martinez-Torrecuadrada, J.L Sudol, M Saladino, G Gervasio, F.L |
format |
Article |
author |
Pucheta-Martinez, E D'Amelio, N Lelli, M Martinez-Torrecuadrada, J.L Sudol, M Saladino, G Gervasio, F.L |
author_sort |
Pucheta-Martinez, E |
title |
Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome |
title_short |
Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome |
title_full |
Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome |
title_fullStr |
Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome |
title_full_unstemmed |
Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome |
title_sort |
changes in the folding landscape of the ww domain provide a molecular mechanism for an inherited genetic syndrome |
publishDate |
2020 |
url |
https://scholarbank.nus.edu.sg/handle/10635/174000 |
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1795374316288737280 |