نتایج جستجو برای: chromosomal sensitivity

تعداد نتایج: 380653  

2016
Takumi Ishizuka Hong Shan Liu Kenichiro Ito Yan Xu

Chromosome visualization is essential for chromosome analysis and genetic diagnostics. Here, we developed a click chemistry approach for multicolor imaging of chromosomal DNA instead of the traditional dye method. We first demonstrated that the commercially available reagents allow for the multicolor staining of chromosomes. We then prepared two pro-fluorophore moieties that served as light-up ...

Journal: :Cell 2011
Jing Pan Mariko Sasaki Ryan Kniewel Hajime Murakami Hannah G. Blitzblau Sam E. Tischfield Xuan Zhu Matthew J. Neale Maria Jasin Nicholas D. Socci Andreas Hochwagen Scott Keeney

The nonrandom distribution of meiotic recombination influences patterns of inheritance and genome evolution, but chromosomal features governing this distribution are poorly understood. Formation of the DNA double-strand breaks (DSBs) that initiate recombination results in the accumulation of Spo11 protein covalently bound to small DNA fragments. By sequencing these fragments, we uncover a genom...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1980
J McEwen P Silverman

We have identified two chromosomal genes of Escherichia coli K12 that are required for the expression of conjugative plasmid functions in the presence of normal plasmid DNA. Hfr cells with mutations in both of these genes are resistant to donor-specific bacteriophage and defective as conjugal donors. These characteristics can be attributed to the inability of mutant Hfr cells to elaborate F-pil...

2014
Josien C. Haan Mariette Labots Christian Rausch Miriam Koopman Jolien Tol Leonie J. M. Mekenkamp Mark A. van de Wiel Danielle Israeli Hendrik F. van Essen Nicole C. T. van Grieken Quirinus J. M. Voorham Linda J. W. Bosch Xueping Qu Omar Kabbarah Henk M. W. Verheul Iris D. Nagtegaal Cornelis J. A. Punt Bauke Ylstra Gerrit A. Meijer

Response to drug therapy in individual colorectal cancer (CRC) patients is associated with tumour biology. Here we describe the genomic landscape of tumour samples of a homogeneous well-annotated series of patients with metastatic CRC (mCRC) of two phase III clinical trials, CAIRO and CAIRO2. DNA copy number aberrations of 349 patients are determined. Within three treatment arms, 194 chromosoma...

Journal: :Trends in genetics : TIG 2009
Rossa W K Chiu Charles R Cantor Y M Dennis Lo

Non-invasive prenatal diagnosis of fetal chromosomal aneuploidies and monogenic diseases by analysing fetal DNA present in maternal plasma poses a challenging goal. In particular, the presence of background maternal DNA interferes with the analysis of fetal DNA. Using single molecule counting methods, including digital PCR and massively parallel sequencing, many of the former problems have been...

2012
S. B. TEOH A.

The effects of gamma-rays on three varieties of long bean (Vigna sesquipedalis, Fruw), namely Melaka, Local Black and Local Long were studied using five doses ranging from 10 to 50 kR. Both Chromosomal aberrations and characteristics related to physiological damage were used to study radiation sensitivity of the varieties. In general, gamma radiation did not affect % seed germination but caused...

2017
Supawat Thongthip Brooke A. Conti Francis P. Lach Agata Smogorzewska

Severe cellular sensitivity and aberrant chromosomal rearrangements in response to DNA interstrand crosslink (ICL) inducing agents are hallmarks of Fanconi anemia (FA) deficient cells. These phenotypes have previously been ascribed to inappropriate activity of non-homologous end joining (NHEJ) rather than a direct consequence of DNA ICL repair defects. Here we used chemical inhibitors, RNAi, an...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Sven Kracker Yvonne Bergmann Ilja Demuth Pierre-Olivier Frappart Gabriele Hildebrand Rainer Christine Zhao-Qi Wang Karl Sperling Martin Digweed Andreas Radbruch

Nijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by predisposition to hematopoietic malignancy, cell-cycle checkpoint defects, and ionizing radiation sensitivity. NBS is caused by a hypomorphic mutation of the NBS1 gene, encoding nibrin, which forms a protein complex with Mre11 and Rad50, both involved in DNA repair. Nibrin localizes to chromosomal sites of ...

Journal: :Human molecular genetics 1998
T Ried E Schröck Y Ning J Wienberg

Chromosome 'painting' refers to the hybridization of fluorescently labeled chromosome-specific, composite probe pools to cytological preparations. Chromosome painting allows the visualization of individual chromosomes in metaphase or interphase cells and the identification of both numerical and structural chromosomal aberrations in human pathology with high sensitivity and specificity. In addit...

2017
Peter J. Cook Rozario Thomas Ram Kannan Esther Sanchez de Leon Alexander Drilon Marc K. Rosenblum Maurizio Scaltriti Robert Benezra Andrea Ventura

The widespread application of high-throughput sequencing methods is resulting in the identification of a rapidly growing number of novel gene fusions caused by tumour-specific chromosomal rearrangements, whose oncogenic potential remains unknown. Here we describe a strategy that builds upon recent advances in genome editing and combines ex vivo and in vivo chromosomal engineering to rapidly and...

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