This is a review about protein A , based on 95 published articles (read ), using
in experiments.
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synonym: protein A-sepharose, protein A–G beads, protein A/G Sepharose, immobilized protein A/G, protein A-Sepharose bead, Protein A- sepharose CL-4B Beads, Protein A/G PLUS-Agarose beads, protein A/G-Sepharose, protein A/G -Agarose, Protein A-Sepharose beads, protein A DynaBeads, protein A- or protein G-Sepharose beads, Protein A-Sepharose CL-4B, Protein A/G PLUS-Agarose, protein A-Sepharose-linked anti-FLAG-M2 antibodies, protein A affinity column, protein A Sepharose CL-4B, protein A agarose, Protein A, Protein A/G gel slurry, protein A beads, protein A-conjugated beads, protein A–agarose, prote ...
Millipore protein A agarose beads were used to perform immunoprecipitation in order to show that DNA demethylation could be regulated by IDM1 in Arabidopsis
Upstate Protein A/G agarose was used to perform ChIP assays in order to study the roles of the Eos during the Foxp3-dependent gene silencing
Upstate protein A- (for immunoprecipitation anti PARP-1) or G (for immunoprecipitation anti Dnmt1) agarose beads were used to pretreat the lysates in order to show that Parp1 and ADP-ribose polymers localize on the Dnmt1 promoter and Parp1 can protect its unmethylated state
Upstate protein A or G beads were used for chromatin immunoprecipitation in order to study the effect of the interaction of CRTC1 with AP-1 on cell proliferation and transformation
Upstate Salmon Sperm DNA-protein A/G beads were used to perform immunoprecipitation in order to illustrate that the Bmi1 functions on neurons oxidative metabolism are associated with repression of p53 pro-oxidant activity
Calbiochem Protein A-agarose beads were used for immunoprecipitation in order to investigate the effect of merlin on glial cell growth
Upstate Biotechnology protein A agarose was used in immunoprecipitation in order to identify the regions of the human genome that encode transcripts
Miltenyi Biotech Auburn microMACS protein A/G microbeads were used in immunoprecipitation in order to show that Wnt/catenin signaling, osteoblast function, and bone formation can be negatively regulated by the N-cadherin-axin-LRP5 interaction
Santa Cruz protein A/G agarose beads were used to perform immunoprecipitation in order to investigate the regulatory effect of HILDA complex on VEGF-A expression
Santa Cruz protein A/G beads were used to perform immunoprecipitation in order to investigate the role of PVRL4 in tumor progression
Santa Cruz Biotechnology protein A/G beads was used to carry out immunoprecipitation assays in order to investigate the regulatory role of Zfp521 in determining the switch between the adipogenic and osteogenic lineages
Santa Cruz protein A/G agarose was used to perform immunoprecipitation in order to show that acetylation of AML1-ETO fusion protein by p300 is critical for leukemogenesis
Santa Cruz Protein A/G Plus agarose was used to perform ChIP assays in order to study the role of Hippo signaling in controlling mammalian heart size
Santa Cruz Biotechnology protein A/G resin was used for immunoprecipitation in order to study the role for the binding and interaction of ferroportin with Jak2 in hepcidin-induced internalization of ferroportin
Santa Cruz Biotech protein A/G agarose beads were used to do immunoprecipitate in order to investigate the role of the progesterone receptor A and c-Met in spheroids-endometrium
Santa Cruz Biotechnologies protein A agarose beads were used to lysates for immunoprecipitation in order to study the functions of E3 Ubiquitin Ligase WWP1 to HER4
Santa Cruz Biotechnology protein A-sepharose beads were used in coimmunoprecipitation in order to study the role of PAM in modulating KCC2 function
Santa Cruz protein A-agarose was used for western blot in order to investigate the role of transcription factor Ets-1 in the regulation of Natriuretic Peptide Receptor-A gene expression
Santa Cruz Protein A/G PLUS-Agarose beads were used in immunoprecipitation in order to study the mechanism of induction of heterochromatin by the RNA-binding protein vigilin
Santa Cruz Biotechnology Protein A/G PLUS-Agarose was used in immunoprecipitation in order to study the role of MMP-2 inhibition in tumor cells by targeting angiogenic components of tumor growth
Santa Cruz Biotechnology protein A agarose was used for immunoprecipitation experiments in order to gain insight into the SUMOylation system encoded in the genome of C. reinhardtii, a single-cell alga and model plant cell system
Santa Cruz Biotechnology protein A/G plus-agarose beads were used for immunoprecipitation in order to study the effect of the interaction between UBE1L and the PML domain for ISG15ylation on PML/RARalpha
Santa Cruz Biotechnology protein A/G Plus agarose beads were used in immunoprecipitation in order to demonstrate that FUSE Binding Protein is a cellular factor required for efficient replication of Hepatitis C Virus
Santa Cruz protein A/G Agarose was used to preclear total cell extracts for immunoprecipitation and immunoblot analysis in order to study the functional association between NOX5 NADPH oxidase and c-Abl
Sigma protein A-agarose was used to pre-clear fragmented chromatin in order to study the modulation effect of USF1 in molecular and behavioral circadian rhythms in mammals
Sigma protein A-sepharose was used to perform co-IP in order to study the mechanism of immune evasion of cowpox virus
Sigma anti-Protein A was used to perform immunoprecipitation and western blot in order to show that CO protein stabilization was maintained by FKF1 for flower induction
Sigma monoclonal anti-Protein A was used to perform immunoprecipitation in order to show that yeast centrosome function could be modulated by phosphorylation
Sigma Protein A-Agarose solution was used to treat the N2a-m cells in order to study the role estradiol plays in activating the beta-Catenin dependent transcription in neurons
Sigma protein A-Sepharose was used for immunoprecipitation in order to investigate the role of Sem1p and Ubp6p in the regulation of maintain telomeric silencing
Sigma protein A-sepharose column was used to purify antiserum in order to identify novel role for D70 of APE1 in the repair of damaged 3-ends and discusses its possible implication in the process of catalysis
Sigma protein A was used to perform ChIP assays in order to find out the factors that regulate renal tubular cholesterol synthesis during renal ischemia
Sigma-Aldrich protein A-sepharose was used to obtain lysates in order to study the molecular antagonism of Treg and Th17 cell genetic programs and indicate the plasticity of T cell differentiation programs
Sigma protein A beads were used in immunoprecipitation assays in order to study the role for EspF in pedestal maturation and the disruption of paracellular permeability
Sigma protein A- or protein G-Sepharose beads were used in immunoprecipitation in order to demonstrate that Myo1c in conjunction with Rictor participates in cortical actin remodeling events
Sigma-Aldrich protein A/G-Sepharose was used to pull down antibody-histone-DNA complexes in ChIP assays in order to determine whether DNA methylation of the maspin promoter and histone H3 dimethylation are involved in the mechanism of down regulation of maspin synthesis in human corneal stromal fibroblasts and myofibroblasts
Sigma protein A-Sepharose bead was used in immunoprecipitation in order to examine the associations between Pol II and HDV RNAs
RepliGen protein A agarose was used to perform antibody purification by affinity chromatography in order to study the recognition of CpG islands by KDM2B-PRC1 complex
Invitrogen Dynabeads Protein A were used to perform ChIP assays in order to investigate the molecular mechanism of ethylene-mediated growth control in Arabidopsis
Invitrogen Protein A Dynabeads were used to perform ChIP assays in order to investigate the role of Lsd1 during blood cell maturation
ThermoFisher Pierce Protein A/G beads were used to perform immunoprecipitation in order to study the diffrent trafficking mechanisms of endosomal TLRs mediated by UNC93B1
Invitrogen protein A magnetic Dynabeads were used to perform immunoprecipitation in order to study the recognition of CpG islands by KDM2B-PRC1 complex
Invitrogen Dynabeads protein A was used to perform immunoprecipitation in order to show that a sharp boundary in chordate embryos was established by cis-acting transcriptional repression
Pierce protein A/G Sepharose was used to perform immunoprecipitation in order to show that lysosome function and macrophage homeostasis were disrupted without ENT3
Invitrogen protein A Dynabeads were used to perform ChIP assay in order to show that spinocerebellar ataxia type 1 could be improved by Capicua reduction through exercise or genetic manipulation
Pierce 96-well Reactibind Protein A-coated plate was used to immobilize protein in order to study the role of receptor protein tyrosine phosphatase sigma in sensory neuron extension
Pierce 96-well Reactibind Protein A-coated plate was used to perform cell-free binding assays in order to study the roles of the PTPsigma during the neural regeneration
Invitrogen protein A Dynabeads slurry (#100.02) was used to immunodeplete Nudel and NudE from egg extracts in order to study the roles for nudel and dynein in assembly of the lamin B spindle matrix
Invitrogen Dynabeads Protein A was used to conjugat the antibody in order to study the functions of MEN Epsilon/beta non-coding RNAs
Invitrogen protein A-agarose was used to culture the cells in order to indicate that SUMOylation is mediated through reduced CDK7-induced phosphorylation of SF-1
Pierce immobilized protein A/G was used to pull down immune complexes in order to study the mechanism by which A3G is incorporated into HBV nucleocapsids
Pierce Protein A/G gel slurry was used for ChIP analysis in order to study rapid alkylation-induced recruitment of DNA repair proteins to chromosomal DNA within synchronized populations of MMR proficient cells (HeLa MR) after MNNG treatment
PIERCE protein A-conjugated beads were used to preclear chromatin in ChIP assays in order to study the role for the effect of 1, 1-Bis (3-indolyl) 1- (p-substituted phenyl) methanes on c-Jun N-terminal kinase in inhibiting colon cancer cell and tumor growth
Invitrogen protein A Dynabeads were used in immunoprecipitation in order to demonstrate that Myo1c in conjunction with Rictor participates in cortical actin remodeling events
Pierce protein A/G agarose bead was used in ChIP assays in order to investigate how phytoestrogens such as genistein impact ER-regulated gene expression
Pierce Protein A was used for surface plasmon resonance (SPR) analysis in order to study influenza virus-like particle vaccines that are non-replicating particle-based vaccine candidates for influenza based upon a influenza A H5N1 clade 1 and 2 isolates
Invitrogen protein A-agarose was used in immunoprecipitation in order to examine the associations between Pol II and HDV RNAs
Genscript Protein A sepharose was used to perform immunoprecipitation in order to study the regulation mechanism of periplasmic proteolysis by the signaling molecule cyclic-di-GMP
Spherotech protein A coated polystyrene beads were used to perform scanning electron microscopy in order to show that mucosal innate immunity could be promoted by HD6 self-assembly
Roche protein-A agarose was used to perform ChIP assay in order to reduce an asymmetric cell cycle to its simplest, primordial components using mathematical modelling and forward genetics
Roche Protein A agarose was used to perform immunoprecipitation in order to investigate the regulatory role of Erf2 in protein palmitoylation and meiotic entry in Schizosaccharomyces pombe
Roche Protein A bead was used to perform ChIP assays in order to study the mechanisms of meiosis I chromosome segregation pattern in germ cell development
Roche Applied Science protein A-agarose was used to perform immunoprecipitation in order to reveal that UVR8 protein perceives UV-B by a tryptophan-based mechanism
Roche protein A-agarose was used for immunoprecipitation in order to study the circadian gene expression of Integration of microRNA miR-122 in hepatic
Santa Cruz protein A G beads were used in immunoprecipitation in order to identify Amino Enhancer of Split (AES) as an HDRP-interacting protein
GE Healthcare Protein A Sepharose was used to perform co-immunoprecipitation in order to study the role for PICK1 and ICA69 in regulating the formation and maturation of insulin granules
GE Healthcare protein A Sepharose was used to perform immunoprecipitation in order to study the dual roles of dihydrolipoamide acetyltransferase in gene expression and carbon metabolism
GE Healthcare rProtein A affinity column was used to perform Ste5 PH Domain-Specific Fab selection in order to show that MAPK misactivation could be insulated by Ste5 conformational changes
GE Healthcare protein A-Sepharose was used to perform ChIP assay in order to show that male X-linked promoters would recruit more Pol II for Drosophila dosage compensation
GE Healthcare Protein G and Protein A Sepharose 4 Fast Flow was used to perform ChIP assay in order to show that termination factor recruitment was affected by polymerase II CTD modification
GE Healthcare 50:50 slurry of protein A-and G-sepharose was used to perform ChIP assay in order to show that fetomaternal immune tolerance was regulated by chemokine gene silence in decidual stromal cells
GE healthcare protein A Sepharose beads were used to perform immunoprecipitation in order to investigate the importance of acetylation in autophagy regulation
GE Healthcare Protein A Sepharose beads were used to perform immunoprecipitation in order to show that RNA length could be recognized by hnRNP C tetramer
GE Healthcare protein A affinity chromatography was used to perform protein purification in order to show that HIV antibody potency and breadth could be improved through structure-based design
GE Healthcare Protein A chromatography was used to perform protein purification in order to show that novel neutralizing antibody could interact with hemagglutinins of group 1 and 2 influenza A viruses
GE Healthcare Protein A Sepharose was used to perform antibody purification in order to show that DNA ICL repair is mediated by RAD51 pathway and homologous recombination
Amersham protein A-Sepharose bead was used to perform protein purification in order to study the roles of the PTPsigma during the neural regeneration
GE Healthcare Protein A-Sepharose CL 4B was used for co-immunoprecipitation of proteins in order to study the important role for specific cellular environment in the interaction between the measles virus nucleoprotein and the interferon regulator factor 3
Amersham Biosciences protein A-Sepharose 4B was used to preabsorbe protein in order to study the interaction between the vaccinia virus p37 and host proteins associated with LE-derived transport vesicle biogenesis
GE Healthcare protein A Sepharose beads were used for immunoprecipitation in order to investigate the role of Unc5B and LARG in the regulation of repulsive guidance molecule
Amersham protein A sepaharose was used in immunoprecipitation in order to characterize the two isoforms of ULBP5/RAET1G and study their cellular expression and trafficking
GE Hitrap protein A column was used to purification in the immunohistochemistry in order to research the function of yata in regulating the subcellular localization of APPL, loss of yata induces deterioration of neural tissues and lifespan shortening
GE Healthcare protein A affinity chromatography was used to isolate nonimmune and anti-mTLR4-Fc antibodies in order to illustrate that Toll-like receptor 4 (TLR4) plays a fundamental role in the sensing of LPS from Gram-negative bacteria
Pharmacia protein A Sepharose was used for immunoprecipitation in order to study the effect of E693deletemutation in amyloid precursor protein on intracellular accumulation of amyloid beta oligomers and its role in causing endoplasmic reticulum stress-induced apoptosis in cultured cells
Amersham Biosciences protein A Sepharose was used in immunoprecipitation in order to study the effect of interaction of transportin-1 and exportin-5 with the double-stranded RNA-binding domain on nucleocytoplasmic shuttling of ADAR1
Amersham protein A- and G-Sepharose beads were used for immunoprecipitation in order to study the role for the transmembrane interaction in KAI1/CD82-mediated suppression of cancer invasion and metastasis
GE Healthcare protein A beads were used in immunoprecipitation in order to demonstrate that USP19 as the deubiquitinating enzyme stabilizes KPC1 to support cell proliferation
Amersham Biosciences nProtein A-Sepharose 4 FastFlow 0.5-ml column was used to purify monoclonal anti-K15M antibody in order to investigate the regulation of microRNA expression along with cell migration and invasion by K15M protein of Kaposi's sarcoma associated herpesvirus
GE Healthcare protein A-Sepharose CL-4B was used to perform immunoprecipitation in order to indicate that the two functions of herpes simplex virus 1 ICP0, the degradation of PML and the blocking of silencing by the CoREST/REST/HDAC complex, are interdependent
GE Healthcare protein A-Sepharose was used for immunoprecipitation in order to study the effect of simian virus 40 large T antigen on genome integrity and DNA damage response
Amersham Biosciences protein A/G Sepharose was used in immunoprecipitation and western blot to study the effect of the interaction of CAPERalpha with Rel-TAD on modulating lymphocyte transformation
GE Healthcare protein A-Sepharose beads were used in immunoprecipitation in order to investigate the binding of the Streptococcus gordonii DL1 surface protein Hsa to the host cell membrane glycoproteins CD11b, CD43, and CD50
GE Healthcare protein A Sepharose CL-4B was used in ChIP assays in order to provide a mechanistic suggestion for the increased risk of breast cancer and heart disease in AT carriers
GE Healthcare Protein A and G beads were used in immunoprecipitation in oeder to demonstrate that huntington's disease protein contributes to RNA-mediated gene silencing
Amersham protein A sepharose CL-4B was used to pre-clear lysates for immunoprecipitation in order to study the role of SUMO-conjugated proteins in different processes during P. falciparum blood stage development
Bio-Rad Affi-Prep protein A beads (#156-0005) was used in immunoprecipitation to study the roles for nudel and dynein in assembly of the lamin B spindle matrix
Debashree Chatterjee et al. (2014). "Mechanistic insight into the conserved allosteric regulation of periplasmic proteolysis by the signaling molecule cyclic-di-GMP".Sean M Murray et al. (2013). "Computational and genetic reduction of a cell cycle to its simplest, primordial components".Peng Yao et al. (2013). "The HILDA complex coordinates a conditional switch in the 3'-untranslated region of the VEGFA mRNA".Mingzi M Zhang et al. (2013). "Quantitative control of protein S-palmitoylation regulates meiotic entry in fission yeast".Katherine Noelani Chang et al. (2013). "Temporal transcriptional response to ethylene gas drives growth hormone cross-regulation in Arabidopsis".Marc A Kerenyi et al. (2013). "Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation".Natalya N Pavlova et al. (2013). "A role for PVRL4-driven cell-cell interactions in tumorigenesis".Mian Cao et al. (2013). "PICK1 and ICA69 control insulin granule trafficking and their deficiencies lead to impaired glucose tolerance".Kazuhiro Shimomura et al. (2013). "Usf1, a suppressor of the circadian Clock mutant, reveals the nature of the DNA-binding of the CLOCK:BMAL1 complex in mice".Bettina L Lee et al. (2013). "UNC93B1 mediates differential trafficking of endosomal TLRs".Alexandra Viola Bohne et al. (2013). "Reciprocal regulation of protein synthesis and carbon metabolism for thylakoid membrane biogenesis".Matthew P Miller et al. (2012). "Meiosis I chromosome segregation is established through regulation of microtubule-kinetochore interactions".Anca M Farcas et al. (2012). "KDM2B links the Polycomb Repressive Complex 1 (PRC1) to recognition of CpG islands".Sona Kang et al. (2012). "Regulation of early adipose commitment by Zfp521".William H McCoy et al. (2012). "Structural mechanism of ER retrieval of MHC class I by cowpox".Kaoru S Imai et al. (2012). "Cis-acting transcriptional repression establishes a sharp boundary in chordate embryos".Jesse G Zalatan et al. (2012). "Conformational control of the Ste5 scaffold protein insulates against MAP kinase misactivation".Thomas Conrad et al. (2012). "Drosophila dosage compensation involves enhanced Pol II recruitment to male X-linked promoters".Andreas Mayer et al. (2012). "CTD tyrosine phosphorylation impairs termination factor recruitment to RNA polymerase II".Hiutung Chu et al. (2012). "Human α-defensin 6 promotes mucosal innate immunity through self-assembled peptide nanonets".Weiqiang Qian et al. (2012). "A histone acetyltransferase regulates active DNA demethylation in Arabidopsis".Patrice Nancy et al. (2012). "Chemokine gene silencing in decidual stromal cells limits T cell access to the maternal-fetal interface".Young Hun Song et al. (2012). "FKF1 conveys timing information for CONSTANS stabilization in photoperiodic flowering".Cong Yi et al. (2012). "Function and molecular mechanism of acetylation in autophagy regulation".Asako McCloskey et al. (2012). "hnRNP C tetramer measures RNA length to classify RNA polymerase II transcripts for export".Chia Lin Hsu et al. (2012). "Equilibrative nucleoside transporter 3 deficiency perturbs lysosome function and macrophage homeostasis".John D Fryer et al. (2011). "Exercise and genetic rescue of SCA1 via the transcriptional repressor Capicua".Ron Diskin et al. (2011). "Increasing the potency and breadth of an HIV antibody by using structure-based rational design".Davide Corti et al. (2011). "A neutralizing antibody selected from plasma cells that binds to group 1 and group 2 influenza A hemagglutinins".Lan Wang et al. (2011). "The leukemogenicity of AML1-ETO is dependent on site-specific lysine acetylation".David T Long et al. (2011). "Mechanism of RAD51-dependent DNA interstrand cross-link repair".Jamie M Keck et al. (2011). "A cell cycle phosphoproteome of the yeast centrosome".Todd Heallen et al. (2011). "Hippo pathway inhibits Wnt signaling to restrain cardiomyocyte proliferation and heart size".Luca Rizzini et al. (2011). "Perception of UV-B by the Arabidopsis UVR8 protein".Charlotte H Coles et al. (2011). "Proteoglycan-specific molecular switch for RPTPσ clustering and neuronal extension".Yingjie Shen et al. (2009). "PTPsigma is a receptor for chondroitin sulfate proteoglycan, an inhibitor of neural regeneration".Fan Pan et al. (2009). "Eos mediates Foxp3-dependent gene silencing in CD4+ regulatory T cells".David Gatfield et al. (2009). "Integration of microRNA miR-122 in hepatic circadian gene expression".Matteo Colombo et al. (2009). "The interaction between the measles virus nucleoprotein and the Interferon Regulator Factor 3 relies on a specific cellular environment".Yali Chen et al. (2009). "Vaccinia virus p37 interacts with host proteins associated with LE-derived transport vesicle biogenesis".Olga Varea et al. (2009). "Estradiol activates beta-catenin dependent transcription in neurons".Katsuhiko Hata et al. (2009). "Unc5B associates with LARG to mediate the action of repulsive guidance molecule".Michele Zampieri et al. (2009). "Parp1 localizes within the Dnmt1 promoter and protects its unmethylated state by its enzymatic activity".Ivana De Domenico et al. (2009). "Hepcidin-induced internalization of ferroportin requires binding and cooperative interaction with Jak2".Robert A Eagle et al. (2009). "Cellular expression, trafficking, and function of two isoforms of human ULBP5/RAET1G".Haggar Harduf et al. (2009). "Progesterone receptor A and c-Met mediates spheroids-endometrium attachment".Masaki Sone et al. (2009). "Loss of yata, a novel gene regulating the subcellular localization of APPL, induces deterioration of neural tissues and lifespan shortening".Li Ma et al. (2009). "Requirement for Nudel and dynein for assembly of the lamin B spindle matrix".Song Qin et al. (2009). "Sem1p and Ubp6p orchestrate telomeric silencing by modulating histone H2B ubiquitination and H3 acetylation".Thierry Roger et al. (2009). "Protection from lethal gram-negative bacterial sepsis by targeting Toll-like receptor 4".Victor M Castillo-Acosta et al. (2009). "Identification of a residue critical for the excision of 3'-blocking ends in apurinic/apyrimidinic endonucleases of the Xth family".Gianluca Canettieri et al. (2009). "The coactivator CRTC1 promotes cell proliferation and transformation via AP-1".Kazuchika Nishitsuji et al. (2009). "The E693Delta mutation in amyloid precursor protein increases intracellular accumulation of amyloid beta oligomers and causes endoplasmic reticulum stress-induced apoptosis in cultured cells".Wassim Chatoo et al. (2009). "The polycomb group gene Bmi1 regulates antioxidant defenses in neurons by repressing p53 pro-oxidant activity".Jutta Fritz et al. (2009). "RNA-regulated interaction of transportin-1 and exportin-5 with the double-stranded RNA-binding domain regulates nucleocytoplasmic shuttling of ADAR1".Rafijul Bari et al. (2009). "Transmembrane interactions are needed for KAI1/CD82-mediated suppression of cancer invasion and metastasis".Hongjae Sunwoo et al. (2009). "MEN epsilon/beta nuclear-retained non-coding RNAs are up-regulated upon muscle differentiation and are essential components of paraspeckles".S Sean Houshmandi et al. (2009). "The neurofibromatosis 2 protein, merlin, regulates glial cell growth in an ErbB2- and Src-dependent manner".Masayo Naito et al. (2009). "Renal ischemia-induced cholesterol loading: transcription factor recruitment and chromatin remodeling along the HMG CoA reductase gene".Eric Hay et al. (2009). "N-cadherin interacts with axin and LRP5 to negatively regulate Wnt/beta-catenin signaling, osteoblast function, and bone formation".Shu Mang Feng et al. (2009). "The E3 ubiquitin ligase WWP1 selectively targets HER4 and its proteolytically derived signaling isoforms for degradation".Yu Lu et al. (2009). "USP19 deubiquitinating enzyme supports cell proliferation by stabilizing KPC1, a ubiquitin ligase for p27Kip1".Wei Hsiung Yang et al. (2009). "SUMOylation inhibits SF-1 activity by reducing CDK7-mediated serine 203 phosphorylation".Yuan Hau Tsai et al. (2009). "The M type K15 protein of Kaposi's sarcoma-associated herpesvirus regulates microRNA expression via its SH2-binding motif to induce cell migration and invasion".Haidong Gu et al. (2009). "The two functions of herpes simplex virus 1 ICP0, inhibition of silencing by the CoREST/REST/HDAC complex and degradation of PML, are executed in tandem".Jennifer Hein et al. (2009). "Simian virus 40 large T antigen disrupts genome integrity and activates a DNA damage response via Bub1 binding".Nicole Garbarini et al. (2008). "The RCC1 domain of protein associated with Myc (PAM) interacts with and regulates KCC2".Jui Dutta et al. (2008). "CAPERalpha is a novel Rel-TAD-interacting factor that inhibits lymphocyte transformation by the potent Rel/NF-kappaB oncoprotein v-Rel".Yumiko Urano-Tashiro et al. (2008). "Binding of the Streptococcus gordonii DL1 surface protein Hsa to the host cell membrane glycoproteins CD11b, CD43, and CD50".Denis A Smirnov et al. (2008). "ATM gene mutations result in both recessive and dominant expression phenotypes of genes and microRNAs".Jeffrey N Savas et al. (2008). "Huntington's disease protein contributes to RNA-mediated gene silencing through association with Argonaute and P bodies".Prerna Kumar et al. (2009). "Regulation of natriuretic peptide receptor-A gene expression and stimulation of its guanylate cyclase activity by transcription factor Ets-1".Jing Zhou et al. (2008). "On the mechanism of induction of heterochromatin by the RNA-binding protein vigilin".Xuexian O Yang et al. (2008). "Molecular antagonism and plasticity of regulatory and inflammatory T cell programs".Chandramu Chetty et al. (2008). "Tissue inhibitor of metalloproteinase 3 suppresses tumor angiogenesis in matrix metalloproteinase 2-down-regulated lung cancer".Janneth Peralta-Ramirez et al. (2008). "EspF Interacts with nucleation-promoting factors to recruit junctional proteins into pedestals for pedestal maturation and disruption of paracellular permeability".Neha Issar et al. (2008). "Identification of a novel post-translational modification in Plasmodium falciparum: protein sumoylation in different cellular compartments".E Lecona et al. (2008). "Upregulation of annexin A1 expression by butyrate in human colon adenocarcinoma cells: role of p53, NF-Y, and p38 mitogen-activated protein kinase".Ying Wang et al. (2008). "The small ubiquitin-like modifier (SUMO) and SUMO-conjugating system of Chlamydomonas reinhardtii".Zheng Lian et al. (2008). "A genomic analysis of RNA polymerase II modification and chromatin architecture related to 3' end RNA polyadenylation".David H Nguyen et al. (2008). "Reverse transcriptase- and RNA packaging signal-dependent incorporation of APOBEC3G into hepatitis B virus nucleocapsids".Allen G Schroering et al. (2008). "Rapid induction of chromatin-associated DNA mismatch repair proteins after MNNG treatment".Ping Lei et al. (2008). "1,1-Bis(3'-indolyl)-1-(p-substituted phenyl)methanes inhibit colon cancer cell and tumor growth through activation of c-jun N-terminal kinase".Pawan Gulati et al. (2008). "Amino acids activate mTOR complex 1 via Ca2+/CaM signaling to hVps34".Xiaoguang Zhang et al. (2008). "Histone deacetylase-related protein inhibits AES-mediated neuronal cell death by direct interaction".G Nana Hagan et al. (2008). "A Rictor-Myo1c complex participates in dynamic cortical actin events in 3T3-L1 adipocytes".Sumit J Shah et al. (2008). "UBE1L represses PML/RAR{alpha} by targeting the PML domain for ISG15ylation".Zhengbin Zhang et al. (2008). "The FUSE binding protein is a cellular factor required for efficient replication of hepatitis C virus".Christoph Jochum et al. (2008). "Development and in vitro characterization of canine CD40-Ig".Mark A Horswill et al. (2008). "Epigenetic silencing of maspin expression occurs early in the conversion of keratocytes to fibroblasts".Edmund C Chang et al. (2008). "Estrogen Receptors alpha and beta as determinants of gene expression: influence of ligand, dose, and chromatin binding".Rick A Bright et al. (2008). "Cross-clade protective immune responses to influenza viruses with H5N1 HA and NA elicited by an influenza virus-like particle".Linda Yu et al. (2008). "Differential expression of receptor tyrosine kinases (RTKs) and IGF-I pathway activation in human uterine leiomyomas".Amina El Jamali et al. (2008). "Novel redox-dependent regulation of NOX5 by the tyrosine kinase c-Abl".Jinhong Chang et al. (2008). "Transcription of hepatitis delta virus RNA by RNA polymerase II".