| scholarly article | Q13442814 |
| P50 | author | Ulrich Karl Lämmli | Q13365499 |
| P2093 | author name string | Zhao K | |
| Gonzalez E | |||
| Käs E | |||
| P2860 | cites work | A tissue-specific MAR/SAR DNA-binding protein with unusual binding site recognition | Q24321970 |
| Characterization of SAF-A, a novel nuclear DNA binding protein from HeLa cells with high affinity for nuclear matrix/scaffold attachment DNA elements | Q24337072 | ||
| Alternative processing of mRNAs encoding mammalian chromosomal high-mobility-group proteins HMG-I and HMG-Y | Q24633159 | ||
| Cloning of cDNAs coding for human HMG I and HMG Y proteins: both are capable of binding to the octamer sequence motif | Q24635381 | ||
| Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
| Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells | Q27860607 | ||
| Use of T7 RNA polymerase to direct expression of cloned genes | Q27860692 | ||
| CpG islands in vertebrate genomes | Q27861045 | ||
| Phosphorylation by cdc2 kinase modulates DNA binding activity of high mobility group I nonhistone chromatin protein | Q28242474 | ||
| The A.T-DNA-binding domain of mammalian high mobility group I chromosomal proteins. A novel peptide motif for recognizing DNA structure | Q28259556 | ||
| Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA | Q28265233 | ||
| Identification of sites on chromosomal protein HMG-I phosphorylated by casein kinase II | Q28280083 | ||
| The human chromosomal protein HMG I contains two identical palindrome amino acid sequences | Q28301791 | ||
| DBP, a liver-enriched transcriptional activator, is expressed late in ontogeny and its tissue specificity is determined posttranscriptionally | Q28580942 | ||
| How eukaryotic transcriptional activators work | Q29618289 | ||
| Hoechst 33258, distamycin A, and high mobility group protein I (HMG-I) compete for binding to mouse satellite DNA. | Q33190480 | ||
| Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions | Q33589210 | ||
| Chromatin structure of transcriptionally competent and repressed genes | Q33923306 | ||
| In vivo topoisomerase II cleavage of the Drosophila histone and satellite III repeats: DNA sequence and structural characteristics | Q33937443 | ||
| A model for chromatin opening: stimulation of topoisomerase II and restriction enzyme cleavage of chromatin by distamycin | Q34040750 | ||
| Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites | Q34161702 | ||
| Organization of the higher-order chromatin loop: specific DNA attachment sites on nuclear scaffold | Q34245431 | ||
| Posttranscriptional gene regulation and specific binding of the nonhistone protein HMG-I by the 3' untranslated region of bovine interleukin 2 cDNA. | Q34346833 | ||
| Scaffold-associated regions: cis-acting determinants of chromatin structural loops and functional domains | Q35230857 | ||
| A mammalian high mobility group protein recognizes any stretch of six A.T base pairs in duplex DNA. | Q35592304 | ||
| Electrophoretic separation of a class of nucleosomes enriched in HMG 14 and 17 and actively transcribed globin genes | Q35620064 | ||
| The interaction of high mobility proteins HMG14 and 17 with nucleosomes | Q35621795 | ||
| Chromatin changes during the cell cycle | Q35673451 | ||
| The matrix attachment regions of the chicken lysozyme gene co-map with the boundaries of the chromatin domain. | Q35978428 | ||
| Protein motifs that recognize structural features of DNA | Q36395443 | ||
| Complete murine cDNA sequence, genomic structure, and tissue expression of the high mobility group protein HMG-I(Y). | Q36438182 | ||
| Formation and characterization of soluble complexes of histone H1 with supercoiled DNA. | Q36480809 | ||
| Chromatin as an essential part of the transcriptional mechanim | Q36740976 | ||
| The repressor MDBP-2 is a member of the histone H1 family that binds preferentially in vitro and in vivo to methylated nonspecific DNA sequences | Q37241962 | ||
| Phosphorylation of the DNA-binding domain of nonhistone high-mobility group I protein by cdc2 kinase: reduction of binding affinity | Q37413109 | ||
| Histone H1 and the conformation of transcriptionally active chromatin | Q37713429 | ||
| Nucleosomes: regulators of transcription | Q37793913 | ||
| Nucleosome core displacement in vitro via a metastable transcription factor-nucleosome complex | Q38323699 | ||
| The high mobility group protein HMG I(Y) is required for NF-kappa B-dependent virus induction of the human IFN-beta gene | Q38324299 | ||
| Specific inhibition of DNA binding to nuclear scaffolds and histone H1 by distamycin. The role of oligo(dA).oligo(dT) tracts | Q38342812 | ||
| Binding of matrix attachment regions to lamin B1 | Q38508299 | ||
| A matrix/scaffold attachment region binding protein: Identification, purification, and mode of binding | Q38509426 | ||
| The chicken lysozyme 5' matrix attachment region increases transcription from a heterologous promoter in heterologous cells and dampens position effects on the expression of transfected genes | Q38509923 | ||
| The enhancer of the immunoglobulin heavy chain locus is flanked by presumptive chromosomal loop anchorage elements | Q38511602 | ||
| Assembly and propagation of repressed and depressed chromosomal states | Q39497132 | ||
| Studies on the association of the high mobility group non-histone chromatin proteins with isolated nucleosomes | Q40501035 | ||
| Analysis of the high mobility group proteins associated with salt-soluble nucleosomes | Q40574638 | ||
| Nuclear scaffold attachment sites in the human globin gene complexes. | Q41094015 | ||
| Cis-acting sequences regulating expression of the human alpha-globin cluster lie within constitutively open chromatin | Q41623472 | ||
| Scaffold-attached regions from the human interferon beta domain can be used to enhance the stable expression of genes under the control of various promoters | Q41695784 | ||
| Immunoglobulin kappa gene expression after stable integration. II. Role of the intronic MAR and enhancer in transgenic mice | Q41758301 | ||
| Immunoglobulin kappa gene expression after stable integration. I. Role of the intronic MAR and enhancer in plasmacytoma cells | Q41758304 | ||
| Role of nucleosomal cores and histone H1 in regulation of transcription by RNA polymerase II | Q42467327 | ||
| Sequence-specific antirepression of histone H1-mediated inhibition of basal RNA polymerase II transcription | Q42472464 | ||
| Expression of mRNAs encoding mammalian chromosomal proteins HMG-I and HMG-Y during cellular proliferation | Q42833075 | ||
| Differentiation-dependent chromatin alterations precede and accompany transcription of immunoglobulin light chain genes | Q44801601 | ||
| Purification and postsynthetic modifications of Friend erythroleukemic cell high mobility group protein HMG-I. | Q46146440 | ||
| Curvature of mouse satellite DNA and condensation of heterochromatin | Q48338279 | ||
| Chromosome assembly in vitro: Topoisomerase II is required for condensation | Q50801821 | ||
| Presence of histone H1 on an active Balbiani ring gene. | Q52450643 | ||
| Bent DNA is a structural feature of scaffold-attached regions in Drosophila melanogaster interphase nuclei. | Q52453005 | ||
| Nucleosome disruption at the yeast PHO5 promoter upon PHO5 induction occurs in the absence of DNA replication | Q52478184 | ||
| A protein binds to a satellite DNA repeat at three specific sites that would be brought into mutual proximity by DNA folding in the nucleosome. | Q53910276 | ||
| Salt-dependent co-operative interaction of histone H1 with linear DNA. | Q54432523 | ||
| Alternative chromatin structure at CpG islands | Q57259142 | ||
| Highly preferential nucleation of histone H1 assembly on scaffold-associated regions | Q57279041 | ||
| DNA topoisomerase II is required for condensation and separation of mitotic chromosomes in S. pombe | Q58457397 | ||
| Acid blobs and negative noodles | Q59070926 | ||
| A nuclear DNA attachment element mediates elevated and position-independent gene activity | Q59073618 | ||
| Chromatin fractionation procedure that yields nucleosomes containing near-stoichiometric amounts of high mobility group nonhistone chromosomal proteins | Q66921122 | ||
| Influence of DNA-binding drugs on chromatin condensation | Q68962610 | ||
| RAP-1 factor is necessary for DNA loop formation in vitro at the silent mating type locus HML | Q69502449 | ||
| Electrophoretic analyses of nucleosomes and other protein-DNA complexes | Q69705433 | ||
| Chromatin domain surrounding the human interferon-beta gene as defined by scaffold-attached regions | Q69838088 | ||
| Enrichment of transcribed and newly replicated DNA in soluble chromatin released from nuclei by mild micrococcal nuclease digestion | Q70812839 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 11 | |
| P304 | page(s) | 3237-3247 | |
| P577 | publication date | 1993-08-01 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | SAR-dependent mobilization of histone H1 by HMG-I/Y in vitro: HMG-I/Y is enriched in H1-depleted chromatin | |
| P478 | volume | 12 |
| Q36666659 | A Striking Similarity in the Organization of the E-Selectin and Bate Interferon gene Promoters |
| Q48086666 | A novel AT-rich DNA binding protein that combines an HMG I-like DNA binding domain with a putative transcription domain |
| Q40400623 | A plant scaffold attached region detected close to a T-DNA integration site is active in mammalian cells |
| Q36135924 | A retrospective study of high mobility group protein I(Y) as progression marker for prostate cancer determined by in situ hybridization |
| Q36561509 | A soluble transcription factor, Oct-1, is also found in the insoluble nuclear matrix and possesses silencing activity in its alanine-rich domain |
| Q38335226 | A/T-rich sequences act as quantitative enhancers of gene expression in transgenic tobacco and potato plants |
| Q38499008 | AHM1, a novel type of nuclear matrix-localized, MAR binding protein with a single AT hook and a J domain-homologous region |
| Q42724399 | An episomally replicating vector binds to the nuclear matrix protein SAF-A in vivo |
| Q42535738 | Assembly of two transgenes in an artificial chromatin domain gives highly coordinated expression in tobacco |
| Q42983240 | Calcium-dependent ADP-ribosylation of high-mobility-group I (HMGI) proteins |
| Q28776777 | Chicken MAR-binding protein ARBP is homologous to rat methyl-CpG-binding protein MeCP2 |
| Q42660513 | Chromosomal location and expression of the single-copy gene encoding high-mobility-group protein HMG-I/Y in Arabidopsis thaliana |
| Q38319579 | Cis-regulation of microRNA expression by scaffold/matrix-attachment regions |
| Q34634739 | Competition between HMG-I(Y), HMG-1 and histone H1 on four-way junction DNA. |
| Q36247428 | Construction and analysis of cells lacking the HMGA gene family. |
| Q40806429 | Contrasting effects of alpha and beta globin regulatory elements on chromatin structure may be related to their different chromosomal environments |
| Q38299243 | DNA binding mediated by the wheat HMGa protein: a novel instance of selectivity against alternating GC sequence |
| Q36484524 | Determinants of histone H1 mobility and chromatin binding in living cells. |
| Q40794274 | Differential repression of transcription factor binding by histone H1 is regulated by the core histone amino termini. |
| Q36036028 | Enhancer blocking activity located near the 3' end of the sea urchin early H2A histone gene. |
| Q39981740 | Fission yeast Sap1 protein is essential for chromosome stability |
| Q35727029 | Flanking nuclear matrix attachment regions synergize with the T cell receptor delta enhancer to promote V(D)J recombination |
| Q35217751 | From DNA structure to gene expression: mediators of nuclear compartmentalization and dynamics. |
| Q38475033 | Functional characterization of a tobacco matrix attachment region-mediated enhancement of transgene expression |
| Q37304075 | Functional equivalence of HMGA- and histone H1-like domains in a bacterial transcriptional factor |
| Q24651778 | Functional interaction between the POU domain protein Tst-1/Oct-6 and the high-mobility-group protein HMG-I/Y |
| Q36857307 | Functional interplay between histone H1 and HMG proteins in chromatin |
| Q24678821 | Functional roles of the transcription factor Oct-2A and the high mobility group protein I/Y in HLA-DRA gene expression |
| Q90006561 | Genome reading by the NF-κB transcription factors |
| Q72550950 | HMG protein binding to an A/T-rich positive regulatory region of the pea plastocyanin gene promoter |
| Q33964722 | HMG-I/Y, a new c-Myc target gene and potential oncogene |
| Q38264460 | HMGA proteins as modulators of chromatin structure during transcriptional activation. |
| Q48439630 | HMGA regulates the global chromatin state and neurogenic potential in neocortical precursor cells |
| Q33654752 | HMGA1 down-regulation is crucial for chromatin composition and a gene expression profile permitting myogenic differentiation |
| Q37119968 | HMGA1 is a molecular determinant of chemoresistance to gemcitabine in pancreatic adenocarcinoma |
| Q35763527 | HMGI(Y) expression in human uterine leiomyomata. Involvement of another high-mobility group architectural factor in a benign neoplasm |
| Q34721443 | High mobility group A: a novel biomarker and therapeutic target in pancreatic adenocarcinoma |
| Q37472409 | High mobility group I(Y)-like DNA-binding domains on a bacterial transcription factor |
| Q52552686 | High mobility group proteins cHMG1a, cHMG1b, and cHMGI are distinctly distributed in chromosomes and differentially expressed during ecdysone dependent cell differentiation. |
| Q34096006 | High-Mobility Group A (HMGA) Proteins and Breast Cancer. |
| Q38358283 | High-level transgene expression in plant cells: effects of a strong scaffold attachment region from tobacco. |
| Q41823823 | Hitting the bull's eye: targeting HMGA1 in cancer stem cells |
| Q50783241 | Identification of a novel plant MAR DNA binding protein localized on chromosomal surfaces. |
| Q33615450 | Identification of target genes for wild type and truncated HMGA2 in mesenchymal stem-like cells |
| Q33888626 | In vivo analysis of scaffold-associated regions in Drosophila: a synthetic high-affinity SAR binding protein suppresses position effect variegation |
| Q40015832 | Inhibition of HMGI-C protein synthesis suppresses retrovirally induced neoplastic transformation of rat thyroid cells |
| Q36446490 | Interaction between HMGA1a and the origin recognition complex creates site-specific replication origins |
| Q40022546 | Intra- and intermolecular cooperative binding of high-mobility-group protein I(Y) to the beta-interferon promoter |
| Q38352827 | Involvement of a high-mobility-group protein in the transcriptional activity of herpes simplex virus latency-active promoter 2. |
| Q39543718 | Kinetic analysis of high-mobility-group proteins HMG-1 and HMG-I/Y binding to cholesterol-tagged DNA on a supported lipid monolayer |
| Q52606640 | Lessons from the Crypt: HMGA1-Amping up Wnt for Stem Cells and Tumor Progression. |
| Q26799760 | MECP2 disorders: from the clinic to mice and back |
| Q33957193 | Maintaining genome stability in the nervous system |
| Q42814852 | Mapping of replication initiation sites in the mouse ribosomal gene cluster |
| Q33975148 | Matrix attachment region-dependent function of the immunoglobulin mu enhancer involves histone acetylation at a distance without changes in enhancer occupancy |
| Q38494026 | Matrix attachment regions enhance transcription of a downstream transgene and the accessibility of its promoter region to micrococcal nuclease |
| Q42275940 | Modification of position-effect variegation by competition for binding to Drosophila satellites |
| Q28478713 | Molecular and cellular characterization of an AT-hook protein from Leishmania |
| Q35986499 | Nuclear assembly is independent of linker histones. |
| Q37596093 | Nuclear functions of the HMG proteins |
| Q35209320 | Nuclear matrix attachment regions antagonize methylation-dependent repression of long-range enhancer-promoter interactions |
| Q38300450 | Nucleolin is a matrix attachment region DNA-binding protein that specifically recognizes a region with high base-unpairing potential |
| Q38311597 | PF1: an A-T hook-containing DNA binding protein from rice that interacts with a functionally defined d(AT)-rich element in the oat phytochrome A3 gene promoter |
| Q48926254 | Prediction of transgene integration by noninvasive bioluminescent screening of microinjected bovine embryos |
| Q42150259 | Prothymosin alpha is a chromatin-remodelling protein in mammalian cells |
| Q34606817 | Real time imaging of transcriptional activity in live mouse preimplantation embryos using a secreted luciferase |
| Q35196112 | Rearrangement of chromatin domains during development in Xenopus |
| Q40892666 | Recent advances in transgenic technology |
| Q34997657 | Recombination and transcription of the endogenous Ig heavy chain locus is effected by the Ig heavy chain intronic enhancer core region in the absence of the matrix attachment regions |
| Q33689010 | Regulation of DNA-dependent activities by the functional motifs of the high-mobility-group chromosomal proteins |
| Q38308113 | SAF-Box, a conserved protein domain that specifically recognizes scaffold attachment region DNA. |
| Q34888570 | SARs stimulate but do not confer position independent gene expression |
| Q27932431 | ScII: an abundant chromosome scaffold protein is a member of a family of putative ATPases with an unusual predicted tertiary structure. |
| Q36657097 | Scaffold attachment regions stimulate HSP70.1 expression in mouse preimplantation embryos but not in differentiated tissues |
| Q24537237 | Scaffold/matrix attachment region elements interact with a p300-scaffold attachment factor A complex and are bound by acetylated nucleosomes. |
| Q39445206 | Specific binding of high-mobility-group I (HMGI) protein and histone H1 to the upstream AT-rich region of the murine beta interferon promoter: HMGI protein acts as a potential antirepressor of the promoter |
| Q30326729 | Structural changes induced by binding of the high-mobility group I protein to a mouse satellite DNA sequence |
| Q34784740 | Synthesis of signals for de novo DNA methylation in Neurospora crassa |
| Q36893657 | TGF-beta and IL-6 signals modulate chromatin binding and promoter occupancy by acetylated FOXP3. |
| Q36159491 | The Architectural Chromatin Factor High Mobility Group A1 Enhances DNA Ligase IV Activity Influencing DNA Repair |
| Q52548786 | The C-terminal DNA-binding domain of Chironomus BR gene products shows preferential affinity for (dA.dT)-rich sequences. |
| Q34085807 | The HMG I proteins: dynamic roles in gene activation, development, and tumorigenesis |
| Q92543231 | The High Mobility Group A1 (HMGA1) Chromatin Architectural Factor Modulates Nuclear Stiffness in Breast Cancer Cells |
| Q33613335 | The High Mobility Group A1 (HMGA1) Transcriptome in Cancer and Development |
| Q37583383 | The amino terminus of Epstein-Barr Virus (EBV) nuclear antigen 1 contains AT hooks that facilitate the replication and partitioning of latent EBV genomes by tethering them to cellular chromosomes |
| Q38502867 | The beta-phaseolin 5' matrix attachment region acts as an enhancer facilitator |
| Q38505789 | The effect of matrix attached regions (MAR) and specialized chromatin structure (SCS) on the expression of gene constructs in cultured cells and in transgenic mice |
| Q35937688 | The expression of the high mobility group I(Y) mRNA in thyroid cancers: useful tool of differential diagnosis of thyroid nodules |
| Q34233434 | The forkhead transcription factor FoxI1 remains bound to condensed mitotic chromosomes and stably remodels chromatin structure |
| Q37672837 | The high mobility group A1 gene: transforming inflammatory signals into cancer? |
| Q35504403 | The high mobility group A1 molecular switch: turning on cancer - can we turn it off? |
| Q24532883 | The novel SAR-binding domain of scaffold attachment factor A (SAF-A) is a target in apoptotic nuclear breakdown. |
| Q28507683 | The preferential binding of histone H1 to DNA scaffold-associated regions is determined by its C-terminal domain |
| Q38496808 | The role of cell differentiation state and HMG-I/Y in the expression of transgenes flanked by matrix attachment regions. |
| Q33337226 | Transcription profiling of lung adenocarcinomas of c-myc-transgenic mice: identification of the c-myc regulatory gene network |
| Q34041282 | Use of matrix attachment regions (MARs) to minimize transgene silencing. |
| Q79822258 | [Molecular-genetic mechanisms of developing the brain based on an embryonic Xenopus model] |
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