Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers. [PDF]
Duncavage EJ +26 more
europepmc +2 more sources
Assessment of Molecular Cytogenetic Methods for the Detection of Chromosomal Abnormalities [PDF]
Some marker chromosomes and chromosome rearrangements are difficult to identify using G-bands by Giemsa staining after trypsin treatment (G-banding) alone.
Maruyama, Hidehiko +5 more
core +1 more source
Molecular markers and cytogenetics of Eleven O’Clock Portulaca umbraticola: a non-conventional edible ornamental crop [PDF]
Portulaca umbraticola, commonly known as “Eleven o'clock”, is a popular ornamental plant in Brazil, but its potential as a non-conventional food source remains underexplored.
J. S. Souza +6 more
doaj +1 more source
Multiplex ligation-dependent probe amplification – a short overview
Multiplex Ligation-dependent Probe Amplification is a technique proposed for the detection of deletions or duplications that may lead to copy number variations in genomic DNA, mainly due to its higher resolution, and shorter overall diagnosis time, when ...
Moldovan Valeriu, Moldovan Elena
doaj +1 more source
Assessment of Bone Marrow Biopsy and Cytogenetic Findings in Patients with Multiple Myeloma
Objective: Multiple myeloma (MM) is a malignant condition characterized by the accumulation of malignant plasma cells. Although MM remains incurable, the survival of MM patients has improved considerably due to the application of autologous stem cell ...
Ahmet Seyhanlı +8 more
doaj +1 more source
In silico karyotyping of chromosomally polymorphic malaria mosquitoes in the Anopheles gambiae complex [PDF]
Chromosomal inversion polymorphisms play an important role in adaptation to environmental heterogeneities. For mosquito species in the Anopheles gambiae complex that are significant vectors of human malaria, paracentric inversion polymorphisms are ...
Besansky, N. J. +7 more
core +1 more source
A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X)
Pentasomy X syndrome is a very rare sex chromosome numerical anomaly of unknown frequency. The karyotype consists of 49,XXXXX. Musculoskeletal, craniofacial, cardiac, and kidney anomalies accompany psychomotor developmental delays. This report describes,
Kübra Aydoğan +5 more
doaj +1 more source
Management of imatinib-resistant CML patients [PDF]
Imatinib has had marked impact on outcomes in chronic myelogenous leukemia (CML) patients for all stages of the disease and is endorsed by international treatment guidelines as the first line option.
Branford S +21 more
core +1 more source
O objetivo deste trabalho foi avaliar métodos de duplicação cromossômica, com uso de agentes antimitóticos e diversos materiais botânicos como explantes dos híbridos entre capim-elefante (Pennisetum purpureum Schum.) e milheto (Pennisetum glaucum (L.) R.
Juscélio Clemente de Abreu +3 more
doaj +1 more source
Clonal karyotype evolution involving ring chromosome 1 with myelodysplastic syndrome subtype RAEB-t progressing into acute leukemia [PDF]
s Karyotypic evolution is a well-known phenomenon in patients with malignant hernatological disorders during disease progression. We describe a 50-year-old male patient who had originally presented with pancytopenia in October 1992.
Bennett JM +46 more
core +1 more source

