نتایج جستجو برای: somatic chromosome

تعداد نتایج: 159086  

2018
Wulfran Cacheux Virginie Dangles-Marie Etienne Rouleau Julien Lazartigues Elodie Girard Adrien Briaux Pascale Mariani Sophie Richon Sophie Vacher Bruno Buecher Marion Richard-Molard Emmanuelle Jeannot Nicolas Servant Fereshteh Farkhondeh Odette Mariani Thomas Rio-Frio Sergio Roman-Roman Emmanuel Mitry Ivan Bieche Astrid Lièvre

Anal squamous cell carcinomas (ASCC) are rare tumours in humans. The etiological role of HPV infection is now well established but little is known about the molecular landscape and signalling pathways involved in the pathogenesis of this cancer. Here we report the results from a whole exome sequencing of a homogeneous group of 20 treatment-naive ASCC. A total of 2422 somatic single nucleotide v...

2010
Thomas Liehr Tatyana Karamysheva Martina Merkas Lukrecija Brecevic Ahmed B. Hamid Elisabeth Ewers Kristin Mrasek Nadezda Kosyakova Anja Weise

Somatic mosaicism is something that is observed in everyday lives of cytogeneticists. Chromosome instability is one of the leading causes of large-scale genome variation analyzable since the correct human chromosome number was established in 1956. Somatic mosaicism is also a well-known fact to be present in cases with small supernumerary marker chromosomes (sSMC), i.e. karyotypes of 47,+mar/46....

Journal: :Blood advances 2017
Koichi Takahashi Feng Wang Hagop Kantarjian Xingzhi Song Keyur Patel Sattva Neelapu Curtis Gumbs Latasha Little Samantha Tippen Rebecca Thornton Courtney D DiNardo Farhad Ravandi Carlos Bueso-Ramos Jianhua Zhang Xifeng Wu Guillermo Garcia-Manero P Andrew Futreal

Recent studies have revealed that clonal hematopoiesis of indeterminate potential (CHIP) is an important risk factor for therapy-related myeloid neoplasms (t-MNs). CHIP is currently defined as a clonal hematopoietic population carrying somatic point mutations in 1 of the leukemia-associated genes. Patients with t-MNs often present with chromosomal abnormalities in addition to somatic point muta...

2010
Yuri B. Yurov Ivan Y. Iourov

Somatic Genome Variations: First Steps Towards a Deeper Understanding of an Underappreciated Source of Biodiversity and Disease Somatic Genome Variations (SGV) are referred to as intercellular variability of genomes in somatic tissues of the same organism. These can manifest as single-nucleotide changes, short DNA sequence changes (<1kb), short tandem repeat variations, retrotransposition of mo...

Journal: :Genetics 1993
C E Williams S M Wielgus G T Haberlach C Guenther H Kim-Lee J P Helgeson

Segregation of restriction fragment length polymorphism (RFLP) loci was monitored to determine the degree of homeologous pairing and recombination in a hexaploid somatic hybrid, A206, the result of protoplast fusion between Solanum tuberosum (PI 203900, a tetraploid cultivated potato) and Solanum brevidens (PI 218228), a diploid, sexually incompatible, distant relative harboring several traits ...

2003
B. R. NEBEL

T WAS recently found (NEBEL and RUTTLE, in press) that Tradescantia I reflexa Raf. shows four threads1 per chromosome during all somatic as well as during all premeiotic stages. Multiplication of threads occurs a t metaphase during somatic division (fig. I). In meiosis of T . reflexa the four threads multiply a t early interkinesis and do not do so again until the metaphase of the first pollen ...

Journal: :Genetics 1975
B S Baker

The effects of a male-specific meiotic mutant, paternal los (pal), in D. melanogaster have been examined genetically. The results indicate the following: (1) When homozygous in males, pal can cause loss, but not nondisjunction, of any chromosome pair. The pal-induced chromosome loss produces exceptional progeny that apparently failed to receive one, or more, paternal chromosomes and, in additio...

2014
Mateus Mondin Janay A. Santos-Serejo Mônica R. Bertäo Prianda Laborda Daniel Pizzaia Margarida L. R. Aguiar-Perecin

Maize karyotype variability has been extensively investigated. The identification of maize somatic and pachytene chromosomes has improved with the development of fluorescence in situ hybridization (FISH) using tandemly repeated DNA sequences as probes. We identified the somatic chromosomes of sister inbred lines that were derived from a tropical flint maize population (Jac Duro [JD]), and hybri...

Journal: :Frontiers in bioscience : a journal and virtual library 2007
Tetsuya Tani Yoko Kato Yukio Tsunoda

Nuclear, microtubular dynamics and spindle assembly checkpoint (SAC) in bovine somatic cell nuclear transfer (SCNT) oocytes receiving G1/0 or M phase somatic cell nuclei were studied. SCNT oocytes assembled microtubules, however, the spindles were structurally abnormal, including bi-, tri-polar or elongated spindles with scattered premature chromosome condensation (PCC) in G1/0 phase nuclei, an...

Journal: :Investigative ophthalmology & visual science 1987
D J Barrett J B Bateman R S Sparkes T Mohandas I Klisak G Inana

Gyrate atrophy is a hereditary chorioretinal degeneration associated with a deficiency of ornithine aminotransferase (OAT). By means of a complementary DNA clone encoding human OAT, the OAT gene sequences were mapped by somatic cell hybrids and in situ hybridization to human chromosome regions 10q26 and Xp11.2. A review of 80 biochemically confirmed cases of gyrate atrophy confirmed the autosom...

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