6 results for author:"Kostareva A." in Literature citations
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| Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins. Kostareva A., Sjoberg G., Gudkova A., Smolina N., Semernin E., Shlyakhto E., Sejersen T. |
| Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population. Zhebrun D., Kudryashova Y., Babenko A., Maslyansky A., Kunitskaya N., Popcova D., Klushina A., Grineva E., Kostareva A., Shlyakhto E. Aging (Albany NY) 3:368-373(2011) · Mapped (5) |
| Type 2 deiodinase Thr92Ala polymorphism impact on clinical course and myocardial remodeling in patients with Graves' disease. Grineva E., Babenko A., Vahrameeva N., Bogdanova M., Kostareva A., Popcova D., Larionova V. Cell Cycle 8:2565-2569(2009) · Mapped (6) |
| Deletion in TNNI3 gene is associated with restrictive cardiomyopathy. Kostareva A., Gudkova A., Sjoberg G., Morner S., Semernin E., Krutikov A., Shlyakhto E., Sejersen T. Int. J. Cardiol. 131:410-412(2009) · UniProtKB (1) |
| Desmin mutations in a St. Petersburg cohort of cardiomyopathies. Kostareva A., Gudkova A., Sjoberg G., Kiselev I., Moiseeva O., Karelkina E., Goldfarb L., Schlyakhto E., Sejersen T. Acta Myol 25:109-115(2006) · Mapped (13) |
| Variable pathogenic potentials of mutations located in the desmin alpha-helical domain. Goudeau B., Rodrigues-Lima F., Fischer D., Casteras-Simon M., Sambuughin N., de Visser M., Laforet P., Ferrer X., Chapon F., Sjoberg G. et al. Hum. Mutat. 27:906-913(2006) · UniProtKB (1) |