Zobrazeno 1 - 10 of 24 pro vyhledávání: '"Adriana, Sireteanu"'
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Akademický článek
B7-Positive and B7-Negative Acute Myeloid Leukemias Display Distinct T Cell Maturation Profiles, Immune Checkpoint Receptor Expression, and European Leukemia Net Risk Profiles
Autor: Ion Antohe, Angela Dǎscǎlescu, Cǎtǎlin Dǎnǎilǎ, Amalia Titieanu, Mihaela Zlei, Iuliu Ivanov, Adriana Sireteanu, Mariana Pavel, Petru Cianga
Publikováno v: Frontiers in Oncology, Vol 10 (2020)
Acute myeloid leukemia (AML) is generally considered a poorly immunogenic malignancy, displaying a “non-inflamed” leukemia microenvironment (LME), leading to T cell tolerance. However, the immune landscape of AML is much more heterogeneous. Since
Externí odkaz: https://doaj.org/article/5c69fd3ddaa0482abbda5869c9efe179
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2
Prognostic Value of Association of Copy Number Alterations and Cell-Surface Expression Markers in Newly Diagnosed Multiple Myeloma Patients
Autor: Mihaiela L. Dragoș, Iuliu C. Ivanov, Mihaela Mențel, Irina C. Văcărean-Trandafir, Adriana Sireteanu, Amalia A. Titianu, Angela S. Dăscălescu, Alexandru B. Stache, Daniela Jitaru, Dragoș L. Gorgan
Publikováno v: International Journal of Molecular Sciences; Volume 23; Issue 14; Pages: 7530
Multiple myeloma results from the clonal proliferation of abnormal plasma cells (PCs) in the bone marrow (BM). In this study, the cell surface expression markers (CD) on atypical PCs (detected by multiparametric flow cytometry (MFC)) were correlated
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::138cfe062b8350504fb401bebcab36a8
https://doi.org/10.3390/ijms23147530
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3
Pallister–Killian Syndrome versus Trisomy 12p—A Clinical Study of 5 New Cases and a Literature Review
Autor: Adriana Sireteanu, Sorina Mihaela Papuc, Andreea Tutulan-Cunita, Roxana Popescu, Monica Panzaru, Aurora Arghir, Lăcrămioara Butnariu, Cristina Rusu, Mihaela Gramescu, Eusebiu Vlad Gorduza, Magdalena Budisteanu, Irina Resmerita
Publikováno v: Genes
Volume 12
Issue 6
Genes, Vol 12, Iss 811, p 811 (2021)
Pallister–Killian syndrome (PKS) is a rare, sporadic disorder defined by a characteristic dysmorphic face, pigmentary skin anomalies, intellectual disability, hypotonia, and seizures caused by 12p tetrasomy due to an extra isochromosome 12p. We pre
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec1d8bd412f6268f3470fb838ea68ce8
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4
The MHC-II antigen presentation machinery and B7 checkpoint ligands display distinctive patterns correlated with acute myeloid leukaemias blast cells HLA-DR expression
Autor: Adriana Sireteanu, Amalia Titieanu, Iuliu Ivanov, Angela Dascalescu, Petru Cianga, Catalin Danaila, Mihaela Zlei, Ion Antohe, Mariana Pavel Tanasa
Publikováno v: Immunobiology. 226(1)
Acute Myeloid Leukaemia (AML) is a neoplasia characterised by rapid proliferation and an increased rate of relapses. The AML blasts display features of antigen-presenting cells (APC), and thus can directly modulate the anti-tumour T cell responses. T
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9ccdd80d7cc3e50989253d5eec858dd
https://pubmed.ncbi.nlm.nih.gov/33352400
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5
FLT-3 ITD Positive Acute Basophilic Leukemia with Rare Complex Karyotype Presenting with Acute Respiratory Failure: Case Report
Autor: Mihaela Zlei, Adriana Sireteanu, Iuliu Ivanov, Raluca Oană, Oana Boca, Petru Cianga, Ion Antohe, Angela Dascalescu, Catalin Danaila
Publikováno v: Romanian Journal of Laboratory Medicine, Vol 26, Iss 1, Pp 87-94 (2018)
Background: Acute basophilic leukemia is a rare subtype of acute myeloid leukemia, as categorized by the 2008 World Health Organization classification of myeloid neoplasms. Acute basophilic leukemia diagnosis requires thorough morphological, cytochem
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4212ab1bc6e9310d9f50136ce57f8b14
https://doaj.org/article/2c3530f121574bfbb0d03a0debdcb06c
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7
Detection of chromosomal imbalances using combined MLPA kits in patients with syndromic intellectual disability
Autor: Eusebiu Vlad Gorduza, Lavinia Caba, Iuliu Ivanov, C Bujoran, Elena Graur, Elena Braha, Monica Pânzaru, Cristina Rusu, Mihaela Gramescu, Roxana Popescu, Lăcrămioara Butnariu, Adriana Sireteanu
Publikováno v: Romanian Journal of Laboratory Medicine, Vol 22, Iss 2, Pp 157-164 (2014)
Dizabilitatea intelectuală (DI) este o afecțiune frecventă, cu consecințe majore pentru individ, familie și societate. Datorită heterogenității sale clinice și genetice, în aproximativ 50% din cazuri etiologia bolii nu poate fi stabilită.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::753c0f21216d3229c8d6bd607f7bc9bd
https://doaj.org/article/2920e16aae1c457385ebdd117f4a7b14
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8
DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
Autor: Adriana Sireteanu, Cristina Rusu, Eusebiu Vlad Gorduza, M Voloşciuc, Carmen Vulpoi, Mihaela Gramescu, I Frunză
Publikováno v: Balkan Journal of Medical Genetics, Vol 16, Iss 2, Pp 67-72 (2013)
Balkan Journal of Medical Genetics : BJMG
We report a 20-year-old female with features evocative of Turner syndrome (short stature, broad trunk, mild webbed neck), dysmorphic face, minor features of holo-prosencephaly (HPE), small hands and feet, excessive hair growth on anterior trunk and i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ad35e5ca37b5d3d5db9247f4960b105
https://doi.org/10.2478/bjmg-2013-0034
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9
Ring Autosomes: Some Unexpected Findings
Autor: Lăcrămioara Butnariu, Mihaela Gramescu, Cristina Rusu, G. Gug, Adriana Sireteanu, Roxana Popescu, D. Ochiană, M Covic, Elena Braha, Lavinia Caba, Eusebiu Vlad Gorduza, Monica Pânzaru, V. Plăiaşu, C Bujoran, M Voloşciuc
Publikováno v: Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics, Vol 15, Iss 2, Pp 35-46 (2012)
Ring chromosomes are rare entities, usually associated with phenotypic abnormalities in correlation with the loss of genetic material. There are various breakpoints and sometimes there is a dynamic mosaicism that is reflected in clinical features. Mo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::236a6bcade1817c685f05c5de41507b7
https://doi.org/10.2478/bjmg-2013-0005
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10
Co-expression of the CBFβ-MYH11 and BCR-ABL fusion genes in chronic myeloid leukaemia / Coexistenţa genelor de fuziune CBFβ-MYH11 şi BCR-ABL în leucemia mieloidă cronică
Autor: Anca Ivanov, Angela Dascalescu, Eusebiu Vlad Gorduza, Catalin Danaila, Roxana Popescu, Mihaela Zlei, Doina Azoicai, Doramina Ghiorghiu, Adriana Sireteanu
Publikováno v: Romanian Journal of Laboratory Medicine, Vol 23, Iss 2, Pp 221-230 (2015)
The coexistence of t(9;22) and inv(16) has been described in a very limited number of cases of CML, de novo or therapy-related AML. We report a patient with CML who presented both inversion of chromosome 16 and Philadelphia chromosome and evolved tow
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04ba0c781bd1d08853eaa12e4fec526f
https://doi.org/10.1515/rrlm-2015-0013
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