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Investigation of genetic instability in patients with Diabetes Mellitus type I, II and LADA using buccal micronucleus cytome assay.
Mutat Res Genet Toxicol Environ Mutagen
December 2024
Medline Clinic MC, Yerevan, Armenia.
Article Synopsis
- The pilot study focused on the presence of micronuclei (MN) and other nuclear abnormalities in oral mucosa cells from patients with type I, II, and LADA diabetes, comparing results to healthy individuals.
- Cytogenetic analysis indicated that diabetes patients had significantly higher levels of MN, particularly in type I and LADA groups, suggesting potential cytotoxic and genotoxic effects of the disease.
- There was a strong correlation found between MN levels, blood glucose concentration, and glycosylated hemoglobin, highlighting the impact of diabetes on cellular health.
Sex assignment and psychosexual peculiarities of individuals with different forms of androgen insensitivity syndrome: A qualitative study.
Int J Reprod Biomed
December 2023
Center for Reproductive Medicine Universe, Tbilisi, Georgia.
Background: A mismatch between chromosomal, gonadal, and phenotypic sexes in individuals with androgen insensitivity syndrome (AIS) creates problems in sex assignment and psychosexual identification.
Objective: To identify psychosexual and sex assignment peculiarities of individuals with different forms of AIS.
Materials And Methods: In this qualitative study, 41 individuals with AIS aged between 15 and 31 yr who referred to the Universe Center for Reproductive Medicine Tbilisi, Georgia between 2016 and 2021 were studied.
Genetic diversity and forensic characterization of 15 autosomal microsatellite markers in the North-east Indian Tripuri population.
Int J Legal Med
September 2021
DNA Fingerprinting Unit, State Forensic Science Laboratory, Department of Home (Police), Govt. of MP, Sagar, 470001, India.
This study was conducted to explore the genomic diversity and forensic characterization of 15 autosomal microsatellite markers in the East Indian Tripuri population. In the studied population, we observed 158 different alleles with the average 10.53 alleles per locus.
View Article and Find Full Text PDFA study of genomic diversity in populations of Maharashtra, India, inferred from 20 autosomal STR markers.
BMC Res Notes
February 2021
DNA Fingerprinting Unit, State Forensic Science Laboratory, Sagar, M.P., 470001, India.
Objective: This study was planned to evaluate the genetic diversity in the admixed and Teli (a Hindu caste) populations of Maharashtra, India using 20 autosomal Short Tandem Repeat (STR) genetic markers. We further investigated the genetic relatedness of the studied populations with other Indian populations.
Results: The studied populations showed a wide range of observed heterozygosity viz.
Congenital short tail in Macaca mulatta.
J Med Primatol
April 2021
Department of Primatology, Institute of Science and Technology in Biomodels, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
In a captive Macaca mulatta breeding colony, a single family group with 39 animals showed 19 individuals being born with dramatic tail shortening. Through clinical, genealogical, radiographic, and cytogenetic evaluation, it was related to a probable dominant autosomal inheritance of the reduction in the number of distal caudal vertebrae.
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