Results 11 to 20 of about 154,528 (340)

Toxicological Investigations of Aristolochia longa Root Extracts

open access: yesJournal of Toxicology, 2020
Aristolochia longa L. (Aristolochiaceae) is an herbaceous plant recognized in alternative medicine for its many therapeutic virtues. The aim of this study was to determine the pharmacotoxicological effects of this plant in order to ensure safe clinical ...
Nasreddine El Omari   +9 more
doaj   +1 more source

Cytogenetic analysis of meningiomas [PDF]

open access: yesJournal of Korean Medical Science, 1992
Cytogenetic analysis of 4 cases of meningiomas from 3 male and 1 female patients is reported. One of male patients suffered from neurofibromatosis type 2. Histologically, the meningiomas were meningotheliomatous (1), transitional (2), and psammomatous (1). Chromosomal abnormalities were found in all cases with a karyotype 45,XY,-22, 45,XY,-16, 45,XX,-2,
J H, Cho   +5 more
openaire   +2 more sources

Individual Risk Assessment for Population Living on the Territories Long-Term Polluted by Organochlorine Pesticides

open access: yesToxics, 2023
The long-term storage of unutilized pesticides raised new problems of long-term environmental contamination. The study presents the results of surveying 151 individuals in 7 villages living close to pesticide-contaminated localities. All individuals have
Aleksandr Garshin   +11 more
doaj   +1 more source

Cytogenetic Analysis of Telomere Dysfunction [PDF]

open access: yes, 2017
Dysfunctional telomeres arising either through natural attrition due to telomerase deficiency or by the removal of telomere-binding proteins are recognized as double-stranded breaks (DSBs). Repair of DSBs is crucial for the maintenance of genome stability.
Rekha, Rai   +2 more
openaire   +4 more sources

Clinical genetic description and analysis of the case of chromosomal mosaicism mos47,XY,+8/46,XY

open access: yesБюллетень сибирской медицины, 2021
The article describes a clinical case of chromosomal mosaicism in a boy, 4 months and 3 weeks old. Cytogenetic analysis of peripheral blood lymphocytes of the child made it possible to establish the karyotype mos47,XY,+8/46,XY with an approximately equal
s L. Nersesyan   +2 more
doaj   +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

Detection of monosomy 7 in interphase cells of patients with myeloid disorders [PDF]

open access: yes, 1990
Six patients, five with acute myeloid leukemia (AML) and one with a myelodysplastic syndrome (MDS), were found to have monosomy 7 by conventional cytogenetics at diagnosis.
Cremer, Thomas   +5 more
core   +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

Clonal karyotype evolution involving ring chromosome 1 with myelodysplastic syndrome subtype RAEB-t progressing into acute leukemia [PDF]

open access: yes, 2006
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

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