期刊： CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (4)
This study aimed to detect differences in BCR-ABL1 kinase domain (KD) variants in patients with chronic myeloid leukemia (CML) who have been warned an......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (3)
RAD21 plays multiple roles in numerous cancers. In breast cancer (BC), a high level of RAD21 correlates with poor disease outcomes and resistance to c......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (4)
Noncoding RNAs (ncRNA) are a kind of endogenous RNA that regulate many vital bioprocesses with limited ability to encode polypeptides. Most of them ar......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2021; 160 (11-12)
High-throughput sequencing based on copy number variation (CNV-seq) is commonly used to detect chromosomal abnormalities. This study identifies chromo......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2021; 161 (3-4)
In the present study, we retrospectively recruited 340 patients who underwent spontaneous abortions to investigate chromosomal abnormalities of the co......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2021; 161 (3-4)
The genera of the tribe Triticeae (family Poaceae), constituting many economically important plants with abundant genetic resources, carry genomes suc......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2021; 161 (3-4)
The barrier-to-autointegration factor (BAF) is widely expressed in most human tissues and plays a critical role in chromatin organization, nuclear env......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2021; 161 (3-4)
Coronary heart disease (CHD) is a serious condition comprising atherosclerosis-mediated ischaemic and hypoxic myocardial injury. This study aimed to i......
期刊： CYTOGENETIC AND GENOME RESEARCH, ; ()
The purpose of this study was to evaluate the effectiveness of next-generation sequencing (NGS)-based preimplantation genetic testing (PGT) for balanc......
期刊： CYTOGENETIC AND GENOME RESEARCH, ; ()
Ajuba has been found to be mutated or aberrantly regulated in several human cancers and plays important roles in cancer progression via different sign......
期刊： CYTOGENETIC AND GENOME RESEARCH, ; ()
Congenital cardiovascular malformations (CVMs) due to genomic mutations bring a greater risk of morbidity and comorbidity and increase the risks relat......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2020; 160 (5)
Saccharum spontaneumis a wild germplasm resource of the genusSaccharumthat has many valuable traits. Ty1-copia retrotransposons constitute a large pro......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2020; 160 (5)
X-linked Alport syndrome (XLAS) is a common hereditary nephropathy caused byCOL4A5gene mutations. To date, many splice site mutations have been descri......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2020; 160 (2)
Chloroplasts and mitochondria are semi-autonomous organelles and have their own genomes (cytoplasmic genomes). Physical radiations (e.g., gamma-rays) ......
期刊： CYTOGENETIC AND GENOME RESEARCH, 2020; 160 (2)
DCC netrin 1 receptor (DCC) affects the structure and function of the dopamine circuitry, which in turn affects the susceptibility to developing addic......
