Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Abazis, D."'
Transferrin receptor (TfR, CD71) is an integral membrane glycoprotein that mediates cellular uptake of iron. In most tissues, TfR expression is correlated positively with proliferation and regulated at the post-transcriptional level. The available da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f567f52688225168bd3a0c010bcaf27a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3080751
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3080751
Acute promyelocytic leukemia was diagnosed in a 48-year-old man; the karyotype was normal, whereas reverse transcriptase polymerase chain reaction (RT-PCR) analysis identified PML/RAR alpha chimeric transcripts of the bcr3 type. Rather unexpectedly,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f978fc971fa8786ee2aa9d8bbd11faa3
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3052926
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3052926
Cytogenetic analysis was performed in 60 patients with primary myelodysplastic syndromes-diagnosed, treated, and followed in our department. In 41 cases, the presence of the NRAS mutation was also evaluated. The aim of this study was to evaluate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::698f680a9374046526509f0730b4b0e6
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3051824
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3051824
Cytogenetic analysis of bone marrow cells from a patient with myelodysplastic syndrome associated with eosinophilia showed a complex translocation with a 46,XY,t(2;18;2)(p23;q11;q32) karyotype The patient has refractory anemia (RA) according to the F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::cd1fb3a46362f9eec62578f36294907c
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3049392
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3049392
Partial trisomy 17q22-qter is a rare but well-recognized clinical entity, We present a case of partial trisomy for the long arm of chromosome 17, which was detected in a female infant with severe psychomotor and somatic retardation, Stargardt disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::51ff9503401164b3be643781cdf0c43b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3049298
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3049298
We report two cases with chronic myeloproliferative disorder which were found to carry simple variant Philadelphia (Ph) t(14;22)(q32;q11) in unstimulated bone marrow mononuclear cells. Both cases were characterized molecularly by Southern blot, rever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::2b427d8ba7ffef6a12af40d8a498f8f3
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3048586
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3048586
We report a man with de novo acute myeloid leukemia (M4 of the FAB classification) bearing two abnormal clones in the bone marrow cells. The clones showed trisomy 11 with loss of the Y chromosome and trisomy 13, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::9dddd18b808e3d38b902ee72e911515c
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3047756
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3047756
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.