Results 11 to 20 of about 88,181 (213)

Cytogenetic analysis for research and services [PDF]

open access: yesJournal of thee Medical Sciences (Berkala Ilmu Kedokteran), 2016
AbstractThat the correct chromosome number in man is 46 was first recognized by Tjio and Levan in 1956. Perhaps few Indonesians know that Tjio was an Indonesian scientist studying in Sweden and then living in the US. Cytogenetic analyses are commonly performed to determine both structural and numerical chromosome aberration, whilst changes in ...
Sultana MH Faradz, Faradz, Sultana MH
openaire   +3 more sources

A genome assembly-integrated dog 1 Mb BAC microarray : a cytogenetic resource for canine cancer studies and comparative genomic analysis [PDF]

open access: yes, 2008
Molecular cytogenetic studies have been instrumental in defining the nature of numerical and structural chromosome changes in human cancers, but their significance remains to be fully understood.
Evans, A   +7 more
core   +2 more sources

Molecular and classical cytogenetic analyses demonstrate an apomorphic reciprocal chromosomal translocation in Gorilla gorilla [PDF]

open access: yes, 1992
The existence of an apomorphic reciprocal chromosomal translocation in the gorilla lineage has been asserted or denied by various cytogeneticists. We employed a new molecular cytogenetic strategy (chromosomal in situ suppression hybridization) combined ...
Stanyon, Roscoe   +11 more
core   +1 more source

Molecular markers and cytogenetics of Eleven O’Clock Portulaca umbraticola: a non-conventional edible ornamental crop [PDF]

open access: yesBrazilian Journal of Biology
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

open access: yesRomanian Journal of Laboratory Medicine, 2020
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

open access: yesTurkish Journal of Hematology, 2022
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

A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X)

open access: yesThe Journal of Pediatric Academy, 2023
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

Comparative genomics in chicken and Pekin duck using FISH mapping and microarray analysis [PDF]

open access: yes, 2009
BACKGROUND: The availability of the complete chicken (Gallus gallus) genome sequence as well as a large number of chicken probes for fluorescent in-situ hybridization (FISH) and microarray resources facilitate comparative genomic studies between ...
Ioannou, D.   +30 more
core   +1 more source

Mixoploidia em híbridos de capim-elefante x milheto tratados com agentes antimitóticos Mixoploidy in napiergrass x pearl millet hybrids treated with antimitotic agents

open access: yesPesquisa Agropecuária Brasileira, 2006
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

Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma

open access: yesLeukemia Research Reports, 2020
Cytogenetic and iFISH plays a major part in the diagnosis of the MM and have an important prognostic significance.10–15% of patients with amyloidosis will also have multiple myeloma (MM).
Hasna Hamdaoui   +6 more
doaj   +1 more source

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