Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anna Ploszynska"'
Autor:
Anna Płoszyńska, Katarzyna Ruckemann-Dziurdzińska, Agnieszka Jóźwik, Anna Mikosik, Katarzyna Lisowska, Anna Balcerska, Jacek M. Witkowski
Publikováno v:
Folia Histochemica et Cytobiologica, Vol 50, Iss 2, Pp 304-311 (2012)
Transferrin receptor 1 (CD71) is a transmembrane glycoprotein responsible for cellular iron uptake. Higher expression of CD71 has been identified as a negative prognostic marker for numerous solid tumor types and for some lymphomas. The aim of this s
Externí odkaz:
https://doaj.org/article/6fd661b7301e402b90ddef095dd7a0cc
Autor:
Anna Mikosik, Izabella Henc, Katarzyna Ruckemann-Dziurdzińska, Joanna E Frąckowiak, Anna Płoszyńska, Anna Balcerska, Ewa Bryl, Jacek M Witkowski
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0136615 (2015)
Childhood acute lymphoblastic leukemia (ALL) blasts are characterized by inhibited apoptosis promoting fast disease progress. It is known that in chronic lymphocytic and acute myeloid leukemias the reduced apoptosis is strongly related with the activ
Externí odkaz:
https://doaj.org/article/12f0f3bb59b84f5c9ddd04e939d10636
Autor:
David Viskochil, Alan H. Beggs, Edyta Niewiadomska, Evangelia Atsidaftos, Lilia Long, Roma Rokicka-Milewska, Colin A. Sieff, Adrianna Vlachos, Rong Zhong, Dagmar Pospisilova, Jan Maciej Zaucha, David G. Nathan, Anna Ploszynska, Charlotte M. Niemeyer, Joerg J Meerpohl, W. Wiktor-Jedrzejczak, Hanna T. Gazda, Jeffrey M. Lipton
Publikováno v:
British Journal of Haematology. 127:105-113
Summary The genetic basis of Diamond–Blackfan anaemia (DBA), a congenital erythroid hypoplasia that shows marked clinical heterogeneity, remains obscure. However, the fact that nearly one-quarter of patients harbour a variety of mutations in RPS19,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c48181f04aace961acd1e2c572464da7
https://doi.org/10.1111/j.1365-2141.2004.05152.x
https://doi.org/10.1111/j.1365-2141.2004.05152.x
Autor:
Bertil Glader, Mark J. Daly, Thiebaut Noel Willig, Adrianna Vlachos, Gil Tchernia, Narla Mohandas, Allison Webber, Colin A. Sieff, Charlotte M. Niemeyer, Akira Ohara, David G. Nathan, Karen A. Orfali, Roma Rokicka-Milewska, Alan H. Beggs, Jeffrey M. Lipton, Anna Ploszynska, Sarah E. Ball, Dagmar Pospisilova, Hanna T. Gazda, David L. Baker, David Viskochil
Publikováno v:
Blood. 97:2145-2150
Diamond-Blackfan anemia (DBA) is a rare congenital hypoplastic anemia that usually presents early in infancy and is inherited in 10% to 20% of cases. Linkage analysis has shown that DBA in many of both dominant and recessive DBA families mapped to ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adc87df092cb238f5d7aac0d2b925a49
https://doi.org/10.1182/blood.v97.7.2145
https://doi.org/10.1182/blood.v97.7.2145
Autor:
Hanna T, Gazda, Rong, Zhong, Lilia, Long, Edyta, Niewiadomska, Jeffrey M, Lipton, Anna, Ploszynska, Jan M, Zaucha, Adrianna, Vlachos, Evangelia, Atsidaftos, David H, Viskochil, Charlotte M, Niemeyer, Joerg J, Meerpohl, Roma, Rokicka-Milewska, Dagmar, Pospisilova, W, Wiktor-Jedrzejczak, David G, Nathan, Alan H, Beggs, Colin A, Sieff
Publikováno v:
British journal of haematology. 127(1)
The genetic basis of Diamond-Blackfan anaemia (DBA), a congenital erythroid hypoplasia that shows marked clinical heterogeneity, remains obscure. However, the fact that nearly one-quarter of patients harbour a variety of mutations in RPS19, a ribosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b21b92f3d36fc598f4d3ec477de7996c
https://pubmed.ncbi.nlm.nih.gov/15384984
https://pubmed.ncbi.nlm.nih.gov/15384984
Autor:
Colin A. Sieff, N. Mohandas, Jeffrey M. Lipton, Adrianna Vlachos, T.N. Willig, Sarah W. Ball, G. Tchernia, A. Ohara, Mark J. Daly, Alan H. Beggs, Anna Ploszynska, David Viskochil, D. Pospisilova, D. Baker, Roma Rokicka-Milewska, Hanna T. Gazda, Bertil Glader, David G. Nathan, Niemeyer Cm, Karen A. Orfali, A. Webber
Publikováno v:
Experimental Hematology. 28:1493
Diamond-Blackfan Anemia (DBA) is a rare congenital hypoplastic anemia that usually presents early in infancy and is inherited in 10–20% of cases. Recently, identification of a patient with a translocation t(X;19)(p21;q13) led to the cloning of a ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99ca70ef085880e62bec24027c9faf51
https://doi.org/10.1016/s0301-472x(00)00565-8
https://doi.org/10.1016/s0301-472x(00)00565-8