| Year |
Citation |
Score |
| 2014 |
Strader MB, Hicks WA, Kassa T, Singleton E, Soman J, Olson JS, Weiss MJ, Mollan TL, Wilson MT, Alayash AI. Post-translational transformation of methionine to aspartate is catalyzed by heme iron and driven by peroxide: a novel subunit-specific mechanism in hemoglobin. The Journal of Biological Chemistry. 289: 22342-57. PMID 24939847 DOI: 10.1074/Jbc.M114.568980 |
0.559 |
|
| 2014 |
Mollan TL, Jia Y, Banerjee S, Wu G, Kreulen RT, Tsai AL, Olson JS, Crumbliss AL, Alayash AI. Redox properties of human hemoglobin in complex with fractionated dimeric and polymeric human haptoglobin. Free Radical Biology & Medicine. 69: 265-77. PMID 24486321 DOI: 10.1016/J.Freeradbiomed.2014.01.030 |
0.563 |
|
| 2014 |
Soman J, Strader M, Hicks W, Kassa T, Singleton E, Olson J, Weiss M, Mollan T, Wilson M, Alayash A. Crystallographic evidence for oxidative Met→Asp conversion in human hemoglobin Acta Crystallographica Section a Foundations and Advances. 70: C310-C310. DOI: 10.1107/S2053273314096892 |
0.589 |
|
| 2013 |
Dickson CF, Rich AM, D'Avigdor WM, Collins DA, Lowry JA, Mollan TL, Khandros E, Olson JS, Weiss MJ, Mackay JP, Lay PA, Gell DA. α-Hemoglobin-stabilizing protein (AHSP) perturbs the proximal heme pocket of oxy-α-hemoglobin and weakens the iron-oxygen bond. The Journal of Biological Chemistry. 288: 19986-20001. PMID 23696640 DOI: 10.1074/Jbc.M112.437509 |
0.585 |
|
| 2013 |
Mollan TL, Alayash AI. Redox reactions of hemoglobin: mechanisms of toxicity and control. Antioxidants & Redox Signaling. 18: 2251-3. PMID 23330885 DOI: 10.1089/ars.2013.5195 |
0.325 |
|
| 2013 |
Mollan TL, Banerjee S, Wu G, Parker Siburt CJ, Tsai AL, Olson JS, Weiss MJ, Crumbliss AL, Alayash AI. α-Hemoglobin stabilizing protein (AHSP) markedly decreases the redox potential and reactivity of α-subunits of human HbA with hydrogen peroxide. The Journal of Biological Chemistry. 288: 4288-98. PMID 23264625 DOI: 10.1074/Jbc.M112.412064 |
0.602 |
|
| 2013 |
Varnado CL, Mollan TL, Birukou I, Smith BJ, Henderson DP, Olson JS. Development of recombinant hemoglobin-based oxygen carriers. Antioxidants & Redox Signaling. 18: 2314-28. PMID 23025383 DOI: 10.1089/Ars.2012.4917 |
0.571 |
|
| 2012 |
Mollan TL, Abraham B, Strader MB, Jia Y, Lozier JN, Olson JS, Alayash AI. Familial secondary erythrocytosis due to increased oxygen affinity is caused by destabilization of the T state of hemoglobin Brigham (α₂β₂(Pro100Leu)). Protein Science : a Publication of the Protein Society. 21: 1444-55. PMID 22821886 DOI: 10.1002/Pro.2130 |
0.548 |
|
| 2012 |
Mollan TL, Khandros E, Weiss MJ, Olson JS. Kinetics of α-globin binding to α-hemoglobin stabilizing protein (AHSP) indicate preferential stabilization of hemichrome folding intermediate. The Journal of Biological Chemistry. 287: 11338-50. PMID 22298770 DOI: 10.1074/Jbc.M111.313247 |
0.556 |
|
| 2012 |
Khandros E, Mollan TL, Yu X, Wang X, Yao Y, D'Souza J, Gell DA, Olson JS, Weiss MJ. Insights into hemoglobin assembly through in vivo mutagenesis of α-hemoglobin stabilizing protein. The Journal of Biological Chemistry. 287: 11325-37. PMID 22287545 DOI: 10.1074/Jbc.M111.313205 |
0.606 |
|
| 2011 |
Crowley MA, Mollan TL, Abdulmalik OY, Butler AD, Goodwin EF, Sarkar A, Stolle CA, Gow AJ, Olson JS, Weiss MJ. A hemoglobin variant associated with neonatal cyanosis and anemia. The New England Journal of Medicine. 364: 1837-43. PMID 21561349 DOI: 10.1056/Nejmoa1013579 |
0.566 |
|
| 2010 |
Mollan TL, Yu X, Weiss MJ, Olson JS. The role of alpha-hemoglobin stabilizing protein in redox chemistry, denaturation, and hemoglobin assembly. Antioxidants & Redox Signaling. 12: 219-31. PMID 19659437 DOI: 10.1089/Ars.2009.2780 |
0.482 |
|
| 2009 |
Yu X, Mollan TL, Butler A, Gow AJ, Olson JS, Weiss MJ. Analysis of human alpha globin gene mutations that impair binding to the alpha hemoglobin stabilizing protein. Blood. 113: 5961-9. PMID 19349619 DOI: 10.1182/Blood-2008-12-196030 |
0.533 |
|
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