Search Within
Applied Filters:
Showing 1-30 of 173 results for "


" within Papers
[Transcription factor Kaiso does not interact with hydroxymethylated DNA within CTGCNA sequence context].
S V Zhenilo et al.
Molekuliarnaia biologiia, 47(3), 522-525 (2013-07-31)
Francesca Trojsi et al.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 32(1), 23-26 (2013-07-16)
We report the first Italian kindred with Familial Amyotrophic Lateral Sclerosis (FALS) due to c.149T>C mutation in the exon 5 of superoxide dismutase-1 (SOD1) gene. The proband was a 49-year-old woman who came to our observation because of an history
Tritiated thymidine: xeroderma pigmentosum and DNA repair.
James E Cleaver
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 28(7), 2742-2745 (2014-07-06)
Xin Cai et al.
Molecular cell, 54(2), 289-296 (2014-04-29)
The innate immune system deploys a variety of sensors to detect signs of infection. Nucleic acids represent a major class of pathogen signatures that can trigger robust immune responses. The presence of DNA in the cytoplasm of mammalian cells is
Yuzhong Cheng et al.
Developmental biology, 395(1), 131-143 (2014-08-31)
invected (inv) and engrailed (en) form a gene complex that extends about 115 kb. These two genes encode highly related homeodomain proteins that are co-regulated in a complex manner throughout development. Our dissection of inv/en regulatory DNA shows that most
Liying Liu et al.
Biochemical and biophysical research communications, 450(1), 851-856 (2014-06-28)
High mobility group box 1 (HMGB1) is a prototype damage-associated molecular pattern (DAMP) that can induce inflammatory and immune responses alone as well as in combination with other molecules such as DNA. However, the intricate molecular mechanisms underlying HMGB1-DNA complex-mediated
Pantelis S Karatzas et al.
Medicine, 93(28), e309-e309 (2014-12-20)
The contribution of epigenetic alterations to disease pathogenesis is emerging as a research priority. In this study, we aimed to seek DNA methylation changes in peripheral blood and tissue biopsies from patients with inflammatory bowel disease. The promoter methylation status
Zhi-Hua Li et al.
Ecotoxicology and environmental safety, 109, 10-14 (2014-08-19)
The effect of long-term exposure to tributyltin (TBT) on the intestine-related biochemical biomarkers in common carp was investigated in this study. Fish were exposed at sub-lethal concentrations of TBT (75 ng/L, 0.75 and 7.5 μg/L) for 60 days. Multiple biomarkers
Rosaiah Kotikalapudi et al.
Pakistan journal of biological sciences : PJBS, 16(23), 1823-1825 (2014-02-11)
The aim of the study is to standardize the simple method for extracting DNA from cells fixed in fixative (3:1 ratio of methanol and acetic acid glacial) mostly used for chromosomal studies in cattle and buffaloes. These fixed cells were
Arnaud Obri et al.
Nature, 505(7485), 648-653 (2014-01-28)
H2A.Z is an essential histone variant implicated in the regulation of key nuclear events. However, the metazoan chaperones responsible for H2A.Z deposition and its removal from chromatin remain unknown. Here we report the identification and characterization of the human protein
Look Ma, no PCNA: how DNA polymerase ε synthesizes long stretches of DNA without a processivity factor.
Karl E Zahn et al.
Nature structural & molecular biology, 21(1), 12-14 (2014-01-07)
Dennis Lo elected to the US National Academy of Sciences.
Clinical chemistry, 59(7), 1133-1133 (2013-08-24)
Piero Stratta et al.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 29(10), 1902-1909 (2014-08-12)
Inactivating mutations of the calcium-sensing receptor (CaSR), of the G-protein subunit α11 (GNA11) and of the adaptor-related protein complex 2, sigma 1 subunit (AP2S1) genes are responsible for familial hypocalciuric hypercalcaemia (FHH). The aim of this study was to analyse
Louise R A Olde Nordkamp et al.
The American journal of cardiology, 114(8), 1223-1228 (2014-09-01)
Unaffected long-QT syndrome family members (FMs) frequently experience syncope. The aims of this study were to test the hypothesis that syncope events in FMs are benign events and to compare clinical characteristics, triggers eliciting the syncope events, and long-term outcomes
Henrique Lemos et al.
European journal of immunology, 44(10), 2847-2853 (2014-08-22)
DNA is immunogenic and many cells express cytosolic DNA sensors that activate the stimulator of interferon genes (STING) adaptor to trigger interferon type I (IFN-β) release, a potent immune activator. DNA sensing to induce IFN-β triggers host immunity to pathogens
Artur V Cideciyan et al.
Investigative ophthalmology & visual science, 56(1), 526-537 (2014-12-30)
The purpose of this study was to evaluate fixation location and oculomotor characteristics of 15 patients with Leber congenital amaurosis (LCA) caused by RPE65 mutations (RPE65-LCA) who underwent retinal gene therapy. Eye movements were quantified under infrared imaging of the
Ancient DNA. Indo-European languages tied to herders.
Michael Balter et al.
Science (New York, N.Y.), 347(6224), 814-815 (2015-02-24)
B Shapiro et al.
Science (New York, N.Y.), 343(6169), 1236573-1236573 (2014-01-25)
The publication of partial and complete paleogenomes within the last few years has reinvigorated research in ancient DNA. No longer limited to short fragments of mitochondrial DNA, inference of evolutionary processes through time can now be investigated from genome-wide data
Alexandre Rodrigues-Correia et al.
Organic letters, 16(19), 5128-5131 (2014-09-19)
The synthesis and use of the new nucleobase-caged nucleotides dT(pHP) and dT(NDEACM) is reported. Through a combination of time and wavelength selectivity four levels of selective uncaging with only two cages, and only two wavelengths, were obtained. The new residue
Nicola Carboni et al.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 32(1), 7-17 (2013-07-16)
Mutations on the LMNA gene are responsible for an heterogeneous group of diseases. Overlapping syndromes related to LMNA gene alterations have been extensively reported. Study scope is to perform a systematic analysis of the overlapping syndromes so far described and
Ming Zeng et al.
Science (New York, N.Y.), 346(6216), 1486-1492 (2014-12-20)
Multivalent molecules with repetitive structures including bacterial capsular polysaccharides and viral capsids elicit antibody responses through B cell receptor (BCR) crosslinking in the absence of T cell help. We report that immunization with these T cell-independent type 2 (TI-2) antigens
Ching-Yu Cheng et al.
Investigative ophthalmology & visual science, 56(1), 478-483 (2014-12-30)
Recently the common SIX6 missense variant rs33912345 was found to be highly associated with glaucoma. The aim of this study was to investigate the association between this SIX6 variant and peripapillary retinal nerve fiber layer (RNFL) thickness measured by spectral-domain
Nanoparticle self-assembly: Bonding them all.
Ulrich Simon
Nature materials, 12(8), 694-696 (2013-07-24)
Kieren J Mitchell et al.
Science (New York, N.Y.), 344(6186), 898-900 (2014-05-24)
The evolution of the ratite birds has been widely attributed to vicariant speciation, driven by the Cretaceous breakup of the supercontinent Gondwana. The early isolation of Africa and Madagascar implies that the ostrich and extinct Madagascan elephant birds (Aepyornithidae) should
Florence F Roussotte et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 34(19), 6537-6545 (2014-05-09)
The C allele at the rs11136000 locus in the clusterin (CLU) gene is the third strongest known genetic risk factor for late-onset Alzheimer's disease (LOAD). A recent genome-wide association study of LOAD found the strongest evidence of association with CLU
Yong S Joe et al.
Journal of nanoscience and nanotechnology, 13(6), 3889-3896 (2013-07-19)
We utilize a two-dimensional four-channel DNA model, with a tight-binding (TB) Hamiltonian, and investigate the temperature and the magnetic field dependence of the transport behavior of a short DNA molecule. Random variation of the hopping integrals due to the thermal
Limb K Hapairai et al.
Journal of medical entomology, 50(4), 731-739 (2013-08-10)
The efficacy of the BG-Sentinel (BGS) and the BG-Mosquitito (BGM) mosquito traps for sampling populations of the important filariasis and dengue vector Aedes (Stegomyia) polynesiensis (Marks) was evaluated in French Polynesia against human bait collections (HBC) using a modified Centers
Ashish Gupta et al.
Biochemistry, 53(27), 4368-4380 (2014-06-24)
Members of the multiple antibiotic resistance regulator (MarR) family often regulate gene activity by responding to a specific ligand. In the absence of ligand, most MarR proteins function as repressors, while ligand binding causes attenuated DNA binding and therefore increased
Giang Huong Nguyen et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(27), 9905-9910 (2014-06-25)
Bloom syndrome is a rare autosomal recessive disorder characterized by genetic instability and cancer predisposition, and caused by mutations in the gene encoding the Bloom syndrome, RecQ helicase-like (BLM) protein. To determine whether altered gene expression might be responsible for
M V Ploskonos
Klinicheskaia laboratornaia diagnostika, (4)(4), 3-8 (2013-08-30)
The article presents the classification and evaluation of techniques applied in documentation of apoptosis of spermatozoids. The main point of techniques detecting the changes in DNA of apoptosis spermatozoids (SCSA technique, TUNEL test and Comet assay) is revealed The annexin
Page 1 of 6
Page 1 of 6