Results 111 to 120 of about 126,155 (293)
Submicroscopic aberrations of chromosome 16 in prenatal diagnosis
Molecular Cytogenetics, 2019 Background Nearly 9.89% of chromosome 16 consists of segmental duplications, which makes it prone to non-homologous recombination. The present study aimed to investigate the incidence and perinatal characteristics of submicroscopic chromosome 16 ...
Xiaoqing Wu +9 more
doaj +1 more source
Background Level of Unstable Chromosome Aberrations in the Kazakhstan Population: A Human Biomonitoring Study. [PDF]
Int J Environ Res Public Health, 2022 Kenzhina LB +10 more
europepmc +1 more source
Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis [PDF]
, 2016 Lenka Pavlištová +6 more
openalex +1 more source
Advanced Healthcare Materials, EarlyView.Metallofullerenol Sc3N@C80(OH)18 demonstrates strong radioprotective properties as a scavenger of both short‐ and long‐lived radicals. The study reveals protection of human erythrocytes from γ‐radiation–induced biochemical damage via post‐irradiation removal of primary and secondary reactive oxidants, supported by pulse radiolysis kinetics.
Jacek Grebowski +6 more
wiley +1 more source
The Relationship between Screening Markers in the First Trimester of Pregnancy and Chromosome Aberrations. [PDF]
Int J Prev Med, 2022 Mirsafaie M +2 more
europepmc +1 more source
Chromosomal integrity after UV irradiation requires FANCD2-mediated repair of double strand breaks [PDF]
, 2016 Fanconi Anemia (FA) is a rare autosomal recessive disorder characterized by hypersensitivity to inter-strand crosslinks (ICLs). FANCD2, a central factor of the FA pathway, is essential for the repair of double strand breaks (DSBs) generated during fork ...
Bocco, Jose Luis +7 more
core +3 more sources
Advanced Healthcare Materials, EarlyView.Novel photo‐clickable triazine‐trione thermosets can be shaped and cured under mild conditions, including room and physiological temperatures. These materials are biocompatible and support osteogenic differentiation of bone marrow–derived mesenchymal stem cells on their surface.
Åshild Johansen +7 more
wiley +1 more source
Haematologica, 2013 Waldenström's macroglobulinemia is a disease of mature B cells, the genetic basis of which is poorly understood. Few recurrent chromosomal abnormalities have been reported, and their prognostic value is not known.
Florence Nguyen-Khac +28 more
doaj +1 more source
A cloud-based resource for genome coordinate-based exploration and large-scale analysis of chromosome aberrations and gene fusions in cancer. [PDF]
Genes Chromosomes Cancer, 2023 Wang J +12 more
europepmc +1 more source