Search Results - "chromosome"
- Chromosomes 3
- Bibliography 1
- Catalogs 1
- Cause and determination 1
- Cell nuclei 1
- Chromosome Mapping 1
- Chromosome aberrations 1
- Chromosome abnormalities 1
- Cytogenetics 1
- Cytology 1
- Ethics, Medical 1
- Genetic Screening 1
- Genetics 1
- Genetics, Medical 1
- Human chromosome abnormalities 1
- Human chromosomes 1
- Human gene mapping 1
- Karyotypes 1
- Law and legislation 1
- Moral and ethical aspects 1
- Public Policy 1
- Sex 1
- Sex chromosome abnormalities 1
- Sex chromosomes 1
- Technique 1
- legislation 1
- methods 1
-
1
CHROMOSOME SET AND SOME PROBLEMS OF CANIS AUREUS IN CAUCASICA
Published 2014-11-01Subjects: “…chromosome set…”For the first time in the present resort chromosome set and some problems of Canis aureus ecology is described taking into account the structure of hail high altitude zone of mountain ecosystem.
Get full text
Article -
2
Chromosomal variation in man : a catalog of chromosomal variants and anomalies /
Published 1984 Subjects:Book -
3
What defines a bimodal karyotype? Bimodality revisited
Published 2025-07-01Subjects: Get full textBimodal karyotypes, initially defined by Avdulov, are characterized by one large and one small set of chromosomes, reflecting a particular type of karyotype asymmetry. Despite later discussions by Stebbins, the absence of a quantitative criterion has led to subjective classifications. This study rev...
Article -
4
Advances in insect chromosome evolution
Published 2025-04-01Subjects: Get full textInsects play an indispensable role in ecosystems, and studies on their chromosome evolution are crucial for understanding mechanisms of speciation, trait evolution and environmental adaptation. This paper systematically summarized the research progress in the field of insect chromosome evolution, fo...
Article -
5
Evaluation of oral findings and treatment approach of a child patient with Williams Syndrome: Case report
Published 2025-01-01Subjects: “…chromosome…”Williams syndrome (WS), also known as Williams-Beuren syndrome, is an autosomal dominant disorder. Although the exact incidence is unknown, it is estimated to occur in approximately 1 in 20,000 live births. The syndrome has been identified in all ethnic groups worldwide and affects both sexes equall...
Get full text
Article -
6
Rare human diseases: 9p deletion syndrome.
Published 2014-09-01Subjects: “…monosomy of chromosome 9…”Objective of the study was to review the anamnesis, pheno - and genotype in patients with rare chromosome disorders such as 9p deletion syndrome. Genetic methods of investigation (clinical and genealogical, cytogenetic, FISH- method), paraclinical and instrumental methods of examination were used. K...
Get full text
Article -
7
Generation of microdissected DNA probes from metaphase chromosomes when chromosome identification by routine staining is impossible
Published 2020-08-01Subjects: Get full textApplication of microdissected DNA libraries and DNA probes in numerous and various modern molecular cytogenetic studies showed them as an efficient and reliable tool in the analysis of chromosome reorganization during karyotypic evolution and in the diagnosis of human chromosome pathology. An import...
Article -
8
Sexual dimorphism in cancer
Published 2023-10-01Subjects: Get full textThe incidence and mortality of malignant neoplasms of non-reproductive organs both carcinomas and sarcomas in men is one and a half times higher than in women. This is based on genetic differences, which are superimposed by patterns of epigenetic regulation of the expression of sex chromosome genes...
Article -
9
THE DIVERSITY OF LIFE CYCLES AND THEIR ROLE IN THE EVOLUTION OF BASIC CHROMOSOME NUMBERS IN VARIOUS ORGANISMS
Published 2014-12-01Subjects: “…basic chromosome number…”Basic chromosome numbers are compared among species of four gymnosperm divisions, three Anthophyta families, and three Mammalia subclasses, with different life cycle types. Gymnosperm and angiosperm species characterized by alternation of haploid and diploid phases, sporic meiotic reduction, hermaph...
Get full text
Article -
10
Assessing cell lines with inducible depletion of cohesin and condensins components through analysis of metaphase chromosome morphology
Published 2024-04-01Subjects: Get full textOne of the most productive strategies for finding the functions of proteins is to study the consequences of loss of protein function. For this purpose, cells or organisms with a knockout of the gene encoding the protein of interest are obtained. However, many proteins perform important functions and...
Article -
11
Kinship analyses in forensic genetics: when complex hypotheses meet (very) complex genotypes
Published 2025-06-01Subjects: “…X chromosome aneuploidies, Kinship analyses…”Kinship analyses unlock the power of genetic data to unravel biological relationships and identify individuals. While most cases involve paternity/maternity problems using autosomal markers, more challenges arise when more complex kinship cases are investigated or when the information given by auto...
Get full text
Article -
12
Association Between Chromosome 4Q25 Polymorphism RS2200733 and the Incidence of Atrial Fibrillation in Bulgarian Patients
Published 2014-01-01Subjects: Get full textAtrial fibrillation (AF) is the commonest type of arrhythmia seen in everyday clinical practice, which leads to a significant increase in both morbidity and mortality. Its incidence increases with age and tends to turn into an epidemic. The cause of AF in 10-20% of cases remains unknown. Several mut...
Article -
13
A case of inversion of chromosome 4 and an unbalanced transloca- tion between the short arm of chromosome 4 and long arm of chromosome 18 in a girl: evolution of clinical and elect...
Published 2021-02-01Subjects: Get full textWe report a case of a girl with a chromosomal disorder that has never been described in the literature: inversion of chromosome 4 with an unbalanced translocation between the short arm of chromosome 4 and long arm of chromosome 18. Clinical manifestations of this syndrome included severe growth reta...
Article -
14
Corrigenda: Bhowmick BK, Jha S (2022) A critical review on cytogenetics of Cucurbitaceae with updates on Indian taxa. Comparative Cytogenetics 16(2): 93–126. https://doi.org/10.389...
Published 2025-07-01Subjects: “…chromosome…”The cytogenetic relationships in the species of Cucurbitaceae are becoming immensely important to answer questions pertaining to genome evolution. Here, a simplified and updated data resource on cytogenetics of Cucurbitaceae is presented on the basis of foundational parameters (basic, zygotic and ga...
Get full text
Article -
15
Acute non-lymphoblastic leukemia: characteristics of cytogenetic anomalies and their influence on clinical course of the disease
Published 2022-11-01Subjects: Get full textCytogenetic changes in bone marrow cells and their influence on clinical course of the disease were analyzed in 106 patients with acute non-lymphoblastic leukemia (ANLL). According to rearrangements of chromosomes the patients were divided into three groups. The first group consisted of patients wit...
Article -
16
Forensic Genetics: A Machine Learning Algorithm for Mutation Modelling
Published 2025-06-01Subjects: “…Y chromosome, mutation, microsatellites, Y-STRs…”Microsatellites or short tandem repeats (STRs) are the most used markers in population and forensic genetics due to their high polymorphism that is consequence of high germinal mutation rates. Mutation modeling has been a topic of intense research as its proper estimation is crucial for a wide rang...
Get full text
Article -
17
Karyotype variability of the genus Colocasia (Araceae) of Assam, North East India
Published 2025-07-01Subjects: Get full textCytological study in four species of Colocasia (Araceae) of Assam showed a variation of chromosome numbers. Basic chromosome number of the species was reported as n= 14. Dominance of metacentric chromosomes in all the four species and symmetric karyotypes indicate the primitive evolutionary status...
Article -
18
ADF1 and BEAF-32 chromatin proteins affect nucleosome positioning and DNA decompaction in 61C7/C8 interband region of Drosophila melanogaster polytene chromosomes
Published 2019-03-01Subjects: Get full textThe formation of interphase chromosomes is a multi-level process in which DNA is compacted several thousandfold by association with histones and non-histone proteins. The first step of compaction includes the formation of nucleosomes – the basic repeating units of chromatin. Further packaging occurs...
Article -
19
Direct cytogenetic study of chorionic samples of the arrested pregnancy tissues according to the Regional Reproductive Center materials
Published 2015-12-01Subjects: Get full textAim. Detection of chromosomal aberrations in patients during spontaneous abortion. Methods and results. Cytogenetic study of chorionic samples of the abortions on first trimester of pregnancy. According to the study, the karyotype anomalies were the cause of cardiac embryonic development in 59% o...
Article -
20
Drug-resistant epilepsy cases in chromosomal pathology
Published 2024-10-01Subjects: Get full textTwo cases of epilepsy in patients with a rare hereditary pathology associated with a chromosomal mutation caused deletion of chromosome 14 are presented. In the first case, this pathology was manifested in the child by generalized tonic-clonic seizures, delayed psycho-verbal development, and facial...
Article


