Recently, non-clonal chromosomal alterations previously unappreciated are being proposed to be included in cytogenetic practice. The aim of this inclusion is to obtain a greater …
HHQ Heng, SM Regan, G Liu, CJ Ye - Molecular cytogenetics, 2016 - Springer
Current cytogenetics has largely focused its efforts on the identification of recurrent karyotypic alterations, also known as clonal chromosomal aberrations (CCAs). The rationale …
Background The genetic basis of metastasis is still unclear because metastases carry individual karyotypes and phenotypes, rather than consistent mutations, and are rare …
Cancer is a disease of cellular evolution. For this cellular evolution to take place, a population of cells must contain functional heterogeneity and an assessment of this …
A Stepanenko, S Andreieva, K Korets… - Mutation Research …, 2015 - Elsevier
The pattern of genome evolution can be divided into two phases: the step-wise continuous phase (step-wise clonal evolution, stable dominant clonal chromosome aberrations (CCAs) …
Uniparental disomy (UPD) is a topic, which normally is considered to be something molecular genetics has to take care of exclusively. As UPD is characterized by microsatellite …
M Weber, A Weise, F Vasheghani, C Göhner… - Placenta, 2021 - Elsevier
Trophoblastic cell lines are established models used to examine human placenta physiology and disease. We performed concurrent cytogenetic analyses of six established …
It has been known for over 100 years that cancers have individual karyotypes and arise only years to decades after initiating carcinogens. However, there is still no coherent theory to …
Background Despite over 50 years of research, it remains unclear how the DNA tumor viruses SV40 and Polyoma cause cancers. Prevailing theories hold that virus-coded Tumor …