scholarly article | Q13442814 |
P50 | author | Carla Esposito | Q57631620 |
P2093 | author name string | Margherita Ruoppolo | |
Gennaro Marino | |||
Simona Francese | |||
Luigi Vitagliano | |||
Stefania Orru | |||
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Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase | Q28293728 | ||
Human-immunodeficiency-virus transmembrane glycoprotein gp41 is an amino acceptor and donor substrate for transglutaminase in vitro | Q28298228 | ||
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The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1 | Q28589800 | ||
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Transglutaminase-catalyzed inactivation of glyceraldehyde 3-phosphate dehydrogenase and alpha-ketoglutarate dehydrogenase complex by polyglutamine domains of pathological length | Q36826440 | ||
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Tissue transglutaminase-catalyzed formation of high-molecular-weight aggregates in vitro is favored with long polyglutamine domains: a possible mechanism contributing to CAG-triplet diseases. | Q41042815 | ||
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Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH. | Q45291767 | ||
Huntington's disease gene product, huntingtin, associates with microtubules in vitro | Q45295496 | ||
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Neurokinin receptors could be differentiated by their capacity to respond to the transglutaminase-synthesized gamma-(glutamyl5)spermine derivative of substance P. | Q46222360 | ||
Mass spectrometric identification of the amino donor and acceptor sites in a transglutaminase protein substrate secreted from rat seminal vesicles. | Q46251766 | ||
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P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 137-46 | |
P577 | publication date | 2002-01-01 | |
P1433 | published in | Protein Science | Q7251445 |
P1476 | title | Identification of tissue transglutaminase-reactive lysine residues in glyceraldehyde-3-phosphate dehydrogenase | |
P478 | volume | 11 |
Q55499802 | Biological functionalities of transglutaminase 2 and the possibility of its compensation by other members of the transglutaminase family. |
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Q38755364 | Possible Function of Molecular Chaperones in Diseases Caused by Propagating Amyloid Aggregates |
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