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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
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