Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Beverly Vaughan"'
Autor:
Hock, Beverly Vaughan
Publikováno v:
The Oxford Encyclopedia of Children's Literature, 1 ed., 2006.
Externí odkaz:
http://www.oxfordreference.com/view/10.1093/acref/9780195146561.001.0001/acref-9780195146561-e-1573
Autor:
Garikai Kushinga, Hara Keisuke, Magdalena Sztyler, Daizo Kurishita, Yasuhiro Oshima, Tomoaki Kurakazu, Sakina Gooljar, Assa Oumie, Tomohisa Nagata, R.P. Baptista, Marc-Olivier Baradez, Celia Murray-Dunning, Hannah Smith, Rhys Macown, Beverly Vaughan
Publikováno v:
Cytotherapy. 19:e19-e20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7f183b30400d1f39452e4e3170a4558
https://doi.org/10.1016/j.jcyt.2017.03.047
https://doi.org/10.1016/j.jcyt.2017.03.047
Publikováno v:
Cancer Genetics and Cytogenetics. 175:98-106
Conventional cytogenetic methods rely on culturing bone marrow aspirates to obtain suitable and sufficient mitotic figures for G-banded analysis. Samples from patients with chronic myeloproliferative disorders (CMPD) often have increased failure rate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbc4eb3ffe32a60bf92b29cc5117f0b4
https://doi.org/10.1016/j.cancergencyto.2007.02.001
https://doi.org/10.1016/j.cancergencyto.2007.02.001
Publikováno v:
Blood. 108:4459-4459
Acute Myeloid Leukaemia is a heterogeneous clonal disorder of the bone marrow, which has characteristic acquired chromosomal abnormalities. Cytogenetic rearrangements of chromosome 16 have a well-established association with AML subtype M4Eo although
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf10349d7aa7d3abd2228aaf8a9b3520
https://doi.org/10.1182/blood.v108.11.4459.4459
https://doi.org/10.1182/blood.v108.11.4459.4459
Publikováno v:
Blood. 108:4810-4810
Chronic Myeloproiferative Disorders (CMPDs) are a spectrum of haematological malignancies of which the molecular pathogenesis remains unknown. Chronic Myeloid Leukaemia (CML) being the only disorder with a recognisable pathogenomic abnormality, the P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c0b3f84f6e103dbb13c11a2a83028b
https://doi.org/10.1182/blood.v108.11.4810.4810
https://doi.org/10.1182/blood.v108.11.4810.4810