| scholarly article | Q13442814 |
| P50 | author | Vaclav Brazda | Q58870323 |
| Sergei Ryazansky | Q59674281 | ||
| Ekaterina Nikitina | Q60184243 | ||
| P2093 | author name string | Elena V Savvateeva-Popova | |
| Elena V Tokmatcheva | |||
| Olga G Zatsepina | |||
| Aleksandr V Zhuravlev | |||
| Michail B Evgen'ev | |||
| Dina A Kulikova | |||
| Alena N Kaminskaya | |||
| Gennady A Zakharov | |||
| Sergei Y Funikov | |||
| Anna V Medvedeva | |||
| Julia F Dolgaya | |||
| P2860 | cites work | MAPPER: a search engine for the computational identification of putative transcription factor binding sites in multiple genomes | Q21284278 |
| The rise of regulatory RNA | Q22121998 | ||
| Mechanisms of change in gene copy number | Q22122003 | ||
| Leucine-Rich Repeat Kinase 2 interacts with Parkin, DJ-1 and PINK-1 in a Drosophila melanogaster model of Parkinson's disease | Q24336655 | ||
| Birth of a chimeric primate gene by capture of the transposase gene from a mobile element | Q24545998 | ||
| MicroRNA-mediated up-regulation of an alternatively polyadenylated variant of the mouse cytoplasmic {beta}-actin gene | Q24645163 | ||
| SWISS-MODEL: An automated protein homology-modeling server | Q24672647 | ||
| Evolution, biogenesis, expression, and target predictions of a substantially expanded set of Drosophila microRNAs | Q24684603 | ||
| MicroRNAs: Key Regulators in the Central Nervous System and Their Implication in Neurological Diseases | Q26744819 | ||
| Mechanisms underlying structural variant formation in genomic disorders | Q26765934 | ||
| The involvement of microRNAs in neurodegenerative diseases | Q26858788 | ||
| VMD: visual molecular dynamics | Q27860554 | ||
| SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling | Q27860614 | ||
| The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling | Q27860637 | ||
| edgeR: a Bioconductor package for differential expression analysis of digital gene expression data | Q27860819 | ||
| Type 3 adenylyl cyclase: a key enzyme mediating the cAMP signaling in neuronal cilia | Q28073873 | ||
| Nuclear organization and 3D chromatin architecture in cognition and neuropsychiatric disorders | Q28077403 | ||
| miRBase: annotating high confidence microRNAs using deep sequencing data | Q28660701 | ||
| Functional characterization of the human mariner transposon Hsmar2 | Q28680786 | ||
| Transposable elements and the evolution of regulatory networks | Q28756349 | ||
| Sequence Relationships among C. elegans, D. melanogaster and Human microRNAs Highlight the Extensive Conservation of microRNAs in Biology | Q29013737 | ||
| BEDTools: a flexible suite of utilities for comparing genomic features | Q29547332 | ||
| The role of site accessibility in microRNA target recognition | Q29547436 | ||
| SeaView version 4: A multiplatform graphical user interface for sequence alignment and phylogenetic tree building | Q29547665 | ||
| Extensive promoter-centered chromatin interactions provide a topological basis for transcription regulation | Q29615949 | ||
| Biology of mammalian L1 retrotransposons | Q29618630 | ||
| Systematic analysis of microRNA targeting impacted by small insertions and deletions in human genome | Q31104377 | ||
| Distinct modes of regulation by chromatin encoded through nucleosome positioning signals | Q33383211 | ||
| De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. | Q33398247 | ||
| Predicting nucleosome positioning using a duration Hidden Markov Model | Q33615372 | ||
| Steroids as external temporal codes act via microRNAs and cooperate with cytokines in differential neurogenesis | Q33728146 | ||
| Heat shock improves Sca-1+ stem cell survival and directs ischemic cardiomyocytes toward a prosurvival phenotype via exosomal transfer: a critical role for HSF1/miR-34a/HSP70 pathway | Q33918205 | ||
| Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s). | Q33919755 | ||
| The Drosophila agnostic Locus: Involvement in the Formation of Cognitive Defects in Williams Syndrome | Q33970330 | ||
| Cruciform structures are a common DNA feature important for regulating biological processes. | Q33982201 | ||
| Spontaneous and ethyl methanesulfonate-induced mutations controlling viability in Drosophila melanogaster. II. Homozygous effect of polygenic mutations | Q33992507 | ||
| Chromosomal sites necessary for normal levels of meiotic recombination in Drosophila melanogaster. I. Evidence for and mapping of the sites | Q33994137 | ||
| An initial map of insertion and deletion (INDEL) variation in the human genome. | Q33998460 | ||
| Physical properties of naked DNA influence nucleosome positioning and correlate with transcription start and termination sites in yeast | Q34043829 | ||
| Small insertions and deletions (INDELs) in human genomes | Q34139307 | ||
| Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes | Q34388540 | ||
| Williams syndrome as a model for elucidation of the pathway genes - the brain - cognitive functions: genetics and epigenetics | Q34417419 | ||
| Databases on transcriptional regulation: TRANSFAC, TRRD and COMPEL | Q34650759 | ||
| Gene expression variation in Drosophila melanogaster due to rare transposable element insertion alleles of large effect. | Q34864384 | ||
| Localization of mariner DNA transposons in the human genome by PRINS | Q35024648 | ||
| LIMK1 and CLIP-115: linking cytoskeletal defects to Williams syndrome | Q35639950 | ||
| Hormonal activation of let-7-C microRNAs via EcR is required for adult Drosophila melanogaster morphology and function | Q35893637 | ||
| Structural Basis for Elastic Mechanical Properties of the DNA Double Helix | Q35982816 | ||
| Su(UR)ES: a gene suppressing DNA underreplication in intercalary and pericentric heterochromatin of Drosophila melanogaster polytene chromosomes | Q36495183 | ||
| Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion | Q36586599 | ||
| How to judge animal models of Parkinson's disease in terms of neuroprotection. | Q36611524 | ||
| Non-B DNA conformations, mutagenesis and disease | Q36817656 | ||
| Discovery of the role of non-B DNA structures in mutagenesis and human genomic disorders | Q37152813 | ||
| Disorders of the genome architecture: a review | Q37223724 | ||
| Interplay between RNA interference and heat shock response systems in Drosophila melanogaster. | Q37385787 | ||
| Breakpoints of gross deletions coincide with non-B DNA conformations | Q37557324 | ||
| Dissecting the chromatin interactome of microRNA genes. | Q37631820 | ||
| Chromatin connectivity maps reveal dynamic promoter-enhancer long-range associations | Q37638159 | ||
| The central role of RNA in human development and cognition | Q37873983 | ||
| Neurodegeneration as an RNA disorder | Q38051910 | ||
| The p53/miR-34 axis in development and disease | Q38210767 | ||
| Enhancer function: mechanistic and genome-wide insights come together | Q38226378 | ||
| Palindrome analyser - A new web-based server for predicting and evaluating inverted repeats in nucleotide sequences | Q38290997 | ||
| Preferential binding of p53 tumor suppressor to p21 promoter sites that contain inverted repeats capable of forming cruciform structure | Q39077494 | ||
| ConSite: web-based prediction of regulatory elements using cross-species comparison | Q41010589 | ||
| Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans. | Q42150838 | ||
| Specific microRNAs regulate heat stress responses in Caenorhabditis elegans | Q43179779 | ||
| Non-coding RNA as a trigger of neuropathologic disorder phenotypes in transgenic Drosophila | Q44926381 | ||
| Architecture of the X chromosome, expression of LIM kinase 1, and recombination in the agnostic mutants of Drosophila: a model of human Williams syndrome | Q45039791 | ||
| Abnormal spine morphology and enhanced LTP in LIMK-1 knockout mice | Q48545185 | ||
| [Influence of limk1 Gene Polymorphism on Learning Acquisition and Memory Formation with pCREB Distribution and Aggregate Formation in Neuromuscular Junctions in Drosophila melanogaster]. | Q50567937 | ||
| The effect of ts mutations in the agnostic gene controlling calmodulin functions and learning capacity on the ectopic conjugation of polytene chromosomes in Drosophila | Q52238666 | ||
| Behavioral effects of temperature sensitive mutations affecting metabolism of cAMP in Drosophila melanogaster. | Q52293846 | ||
| [Systemic regulation of genetic and cytogenetic processes by a signal cascade of actin remodeling: locus agnostic in Drosophila] | Q52693413 | ||
| De novo copy number variants associated with intellectual disability have a paternal origin and age bias. | Q53089589 | ||
| Williams-Beuren syndrome: a model of recurrent genomic mutation | Q73130939 | ||
| P4510 | describes a project that uses | edgeR | Q113334690 |
| P921 | main subject | Williams-Beuren syndrome | Q558077 |
| microRNA | Q310899 | ||
| Drosophila | Q312154 | ||
| P304 | page(s) | 123 | |
| P577 | publication date | 2017-09-20 | |
| P1433 | published in | Frontiers in Genetics | Q2499875 |
| P1476 | title | Drosophila Model for the Analysis of Genesis of LIM-kinase 1-Dependent Williams-Beuren Syndrome Cognitive Phenotypes: INDELs, Transposable Elements of the Tc1/Mariner Superfamily and MicroRNAs | |
| P478 | volume | 8 |
Search more.