Results 21 to 30 of about 22,374,088 (435)

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

An explainable model to support the decision about the therapy protocol for AML [PDF]

open access: yes, 2023
Acute Myeloid Leukemia (AML) is one of the most aggressive types of hematological neoplasm. To support the specialists' decision about the appropriate therapy, patients with AML receive a prognostic of outcomes according to their cytogenetic and molecular characteristics, often divided into three risk categories: favorable, intermediate, and adverse ...
arxiv   +1 more source

In silico karyotyping of chromosomally polymorphic malaria mosquitoes in the Anopheles gambiae complex [PDF]

open access: yes, 2019
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

Cytogenetic Analysis and Chromosomal Mapping of Repetitive DNA in Melipona Species (Hymenoptera, Meliponini)

open access: yesCytogenetic and Genome Research, 2019
Stingless bees of the genus Melipona are subdivided into 4 subgenera called Eomelipona, Melikerria, Melipona sensu stricto, and Michmelia according to species morphology. Cytogenetically, the species of the genus Melipona show variation in the amount and
N. Travenzoli   +5 more
semanticscholar   +1 more source

Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2014
Objective: Prenatal detection of trisomy 8 mosaicism can be misleading and remains challenging in genetic counseling. Identifying cases of partial or complete trisomy 8 mosaicism will highlight the pitfalls of conventional karyotyping in prenatal ...
Meng-Che Tsai   +4 more
doaj   +1 more source

The micronucleus assay as a biological dosimeter of in vivo ionising radiation exposure [PDF]

open access: yes, 2010
Biological dosimetry, based on the analysis of micronuclei (MN) in the cytokinesis-block micronucleus (CBMN) assay can be used as an alternative method for scoring dicentric chromosomes in the field of radiation protection.
Fenech, Michel   +2 more
core   +2 more sources

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

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

Comparative Cytogenetic Analysis of Spontaneous Abortions in Recurrent and Sporadic Pregnancy Losses

open access: yesBiomedicine hub, 2016
Background: The majority of miscarriages are sporadic; however, 1-5% of couples experience recurrent pregnancy loss (RPL). Approximately 50-60% of miscarriages result from chromosomal abnormalities.
T. Nikitina   +9 more
semanticscholar   +1 more source

Нypeгtriploidy as a cause of early embryonic arrest

open access: yesФундаментальная и клиническая медицина, 2020
Chromosomal abnormalities are a leading cause of early embryonic arrest Identification of genetic abnormalities incompatible with embryonic development significantly contributes to the understanding of early embryonic arrest causes and to the development
A. N. Volkov, L. V. Nacheva
doaj   +1 more source

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