protein A review

This is a Validated Antibody Database (VAD) review about protein A , based on 96 published articles (read how Labome selects the articles), using protein A product in experiments. It is aimed to help Labome visitors find the most suited protein A . Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.

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 ...

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 to the paper

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 to the paper

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 to the paper

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 to the paper

Roche protein A-agarose was used for immunoprecipitation in order to study the circadian gene expression of Integration of microRNA miR-122 in hepatic to the paper

Santa Cruz protein A G beads were used in immunoprecipitation in order to identify Amino Enhancer of Split (AES) as an HDRP-interacting protein to the paper

InvitrogenInvitrogen protein A product

Invitrogen Dynabeads Protein A were used to perform ChIP assays in order to investigate the molecular mechanism of ethylene-mediated growth control in Arabidopsis to the paper

Invitrogen Protein A Dynabeads were used to perform ChIP assays in order to investigate the role of Lsd1 during blood cell maturation to the paper

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 to the paper

Invitrogen protein A magnetic Dynabeads were used to perform immunoprecipitation in order to study the recognition of CpG islands by KDM2B-PRC1 complex to the paper

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 to the paper

Pierce protein A/G Sepharose was used to perform immunoprecipitation in order to show that lysosome function and macrophage homeostasis were disrupted without ENT3 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

Invitrogen Dynabeads Protein A was used to conjugat the antibody in order to study the functions of MEN Epsilon/beta non-coding RNAs to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

Invitrogen protein A Dynabeads were used in immunoprecipitation in order to demonstrate that Myo1c in conjunction with Rictor participates in cortical actin remodeling events to the paper

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 to the paper

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 to the paper

Invitrogen protein A-agarose was used in immunoprecipitation in order to examine the associations between Pol II and HDV RNAs to the paper

Miltenyi Biotec

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 to the paper

Santa Cruz Biotechnology

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 to the paper

Santa Cruz protein A/G beads were used to perform immunoprecipitation in order to investigate the role of PVRL4 in tumor progression to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

Santa Cruz Biotechnology protein A-sepharose beads were used in coimmunoprecipitation in order to study the role of PAM in modulating KCC2 function to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

MilliporeSigma

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 to the paper

Sigma protein A-sepharose was used to perform co-IP in order to study the mechanism of immune evasion of cowpox virus to the paper

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 to the paper

Sigma monoclonal anti-Protein A was used to perform immunoprecipitation in order to show that yeast centrosome function could be modulated by phosphorylation to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

Sigma protein A-Sepharose bead was used in immunoprecipitation in order to examine the associations between Pol II and HDV RNAs to the paper

Bio-Rad

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 to the paper

GenScript

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 to the paper

GE Healthcare Life Biosciencesshown:30; total:35

protein A-Sepharose was used for western blotting, in order to study the role of Bub1 in the process of spindle assembly checkpoint to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

GE healthcare protein A Sepharose beads were used to perform immunoprecipitation in order to investigate the importance of acetylation in autophagy regulation to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

Amersham protein A-Sepharose bead was used to perform protein purification in order to study the roles of the PTPsigma during the neural regeneration to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

EMD MilliporeEMD Millipore protein A product

Millipore protein A agarose beads were used to perform immunoprecipitation in order to show that DNA demethylation could be regulated by IDM1 in Arabidopsis to the paper

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 to the paper

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 to the paper

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 to the paper

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 to the paper

Calbiochem Protein A-agarose beads were used for immunoprecipitation in order to investigate the effect of merlin on glial cell growth to the paper

Upstate Biotechnology protein A agarose was used in immunoprecipitation in order to identify the regions of the human genome that encode transcripts to the paper

Spherotech

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 to the paper

Repligen

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 to the paper

Articles Reviewed

Overlack K, Primorac I, Vleugel M, Krenn V, Maffini S, Hoffmann I, et al. A molecular basis for the differential roles of Bub1 and BubR1 in the spindle assembly checkpoint. elife. 2015;4:e05269 pubmed publisher
Chatterjee D, Cooley R, Boyd C, Mehl R, O Toole G, Sondermann H. Mechanistic insight into the conserved allosteric regulation of periplasmic proteolysis by the signaling molecule cyclic-di-GMP. elife. 2014;3:e03650 pubmed publisher
Murray S, Panis G, Fumeaux C, Viollier P, Howard M. Computational and genetic reduction of a cell cycle to its simplest, primordial components. PLoS Biol. 2013;11:e1001749 pubmed publisher
Yao P, Potdar A, Ray P, Eswarappa S, Flagg A, Willard B, et al. The HILDA complex coordinates a conditional switch in the 3'-untranslated region of the VEGFA mRNA. PLoS Biol. 2013;11:e1001635 pubmed publisher
Zhang M, Wu P, Kelly F, Nurse P, Hang H. Quantitative control of protein S-palmitoylation regulates meiotic entry in fission yeast. PLoS Biol. 2013;11:e1001597 pubmed publisher
Chang K, Zhong S, Weirauch M, Hon G, Pelizzola M, Li H, et al. Temporal transcriptional response to ethylene gas drives growth hormone cross-regulation in Arabidopsis. elife. 2013;2:e00675 pubmed publisher
Kerenyi M, Shao Z, Hsu Y, Guo G, Luc S, O Brien K, et al. Histone demethylase Lsd1 represses hematopoietic stem and progenitor cell signatures during blood cell maturation. elife. 2013;2:e00633 pubmed publisher
Pavlova N, Pallasch C, Elia A, Braun C, Westbrook T, Hemann M, et al. A role for PVRL4-driven cell-cell interactions in tumorigenesis. elife. 2013;2:e00358 pubmed publisher
Cao M, Mao Z, Kam C, Xiao N, Cao X, Shen C, et al. PICK1 and ICA69 control insulin granule trafficking and their deficiencies lead to impaired glucose tolerance. PLoS Biol. 2013;11:e1001541 pubmed publisher
Shimomura K, Kumar V, Koike N, Kim T, Chong J, Buhr E, et al. Usf1, a suppressor of the circadian Clock mutant, reveals the nature of the DNA-binding of the CLOCK:BMAL1 complex in mice. elife. 2013;2:e00426 pubmed publisher
Lee B, Moon J, Shu J, Yuan L, Newman Z, Schekman R, et al. UNC93B1 mediates differential trafficking of endosomal TLRs. elife. 2013;2:e00291 pubmed publisher
Bohne A, Schwarz C, Schottkowski M, Lidschreiber M, Piotrowski M, Zerges W, et al. Reciprocal regulation of protein synthesis and carbon metabolism for thylakoid membrane biogenesis. PLoS Biol. 2013;11:e1001482 pubmed publisher
Miller M, Unal E, Brar G, Amon A. Meiosis I chromosome segregation is established through regulation of microtubule-kinetochore interactions. elife. 2012;1:e00117 pubmed publisher
Farcas A, Blackledge N, Sudbery I, Long H, McGouran J, Rose N, et al. KDM2B links the Polycomb Repressive Complex 1 (PRC1) to recognition of CpG islands. elife. 2012;1:e00205 pubmed publisher
Kang S, Akerblad P, Kiviranta R, Gupta R, Kajimura S, Griffin M, et al. Regulation of early adipose commitment by Zfp521. PLoS Biol. 2012;10:e1001433 pubmed publisher
McCoy W, Wang X, Yokoyama W, Hansen T, Fremont D. Structural mechanism of ER retrieval of MHC class I by cowpox. PLoS Biol. 2012;10:e1001432 pubmed publisher
Imai K, Daido Y, Kusakabe T, Satou Y. Cis-acting transcriptional repression establishes a sharp boundary in chordate embryos. Science. 2012;337:964-7 pubmed publisher
Zalatan J, Coyle S, Rajan S, Sidhu S, Lim W. Conformational control of the Ste5 scaffold protein insulates against MAP kinase misactivation. Science. 2012;337:1218-22 pubmed publisher
Conrad T, Cavalli F, Vaquerizas J, Luscombe N, Akhtar A. Drosophila dosage compensation involves enhanced Pol II recruitment to male X-linked promoters. Science. 2012;337:742-6 pubmed publisher
Mayer A, Heidemann M, Lidschreiber M, Schreieck A, Sun M, Hintermair C, et al. CTD tyrosine phosphorylation impairs termination factor recruitment to RNA polymerase II. Science. 2012;336:1723-5 pubmed publisher
Chu H, Pazgier M, Jung G, Nuccio S, Castillo P, de Jong M, et al. Human ?-defensin 6 promotes mucosal innate immunity through self-assembled peptide nanonets. Science. 2012;337:477-81 pubmed publisher
Qian W, Miki D, Zhang H, Liu Y, Zhang X, Tang K, et al. A histone acetyltransferase regulates active DNA demethylation in Arabidopsis. Science. 2012;336:1445-8 pubmed publisher
Nancy P, Tagliani E, Tay C, Asp P, Levy D, Erlebacher A. Chemokine gene silencing in decidual stromal cells limits T cell access to the maternal-fetal interface. Science. 2012;336:1317-21 pubmed publisher
Song Y, Smith R, To B, Millar A, Imaizumi T. FKF1 conveys timing information for CONSTANS stabilization in photoperiodic flowering. Science. 2012;336:1045-9 pubmed publisher
Yi C, Ma M, Ran L, Zheng J, Tong J, Zhu J, et al. Function and molecular mechanism of acetylation in autophagy regulation. Science. 2012;336:474-7 pubmed publisher
McCloskey A, Taniguchi I, Shinmyozu K, Ohno M. hnRNP C tetramer measures RNA length to classify RNA polymerase II transcripts for export. Science. 2012;335:1643-6 pubmed publisher
Hsu C, Lin W, Seshasayee D, Chen Y, Ding X, Lin Z, et al. Equilibrative nucleoside transporter 3 deficiency perturbs lysosome function and macrophage homeostasis. Science. 2012;335:89-92 pubmed publisher
Fryer J, Yu P, Kang H, Mandel Brehm C, Carter A, Crespo Barreto J, et al. Exercise and genetic rescue of SCA1 via the transcriptional repressor Capicua. Science. 2011;334:690-3 pubmed publisher
Diskin R, Scheid J, Marcovecchio P, West A, Klein F, Gao H, et al. Increasing the potency and breadth of an HIV antibody by using structure-based rational design. Science. 2011;334:1289-93 pubmed publisher
Corti D, Voss J, Gamblin S, Codoni G, Macagno A, Jarrossay D, et al. A neutralizing antibody selected from plasma cells that binds to group 1 and group 2 influenza A hemagglutinins. Science. 2011;333:850-6 pubmed publisher
Wang L, Gural A, Sun X, Zhao X, Perna F, Huang G, et al. The leukemogenicity of AML1-ETO is dependent on site-specific lysine acetylation. Science. 2011;333:765-9 pubmed publisher
Long D, R schle M, Joukov V, Walter J. Mechanism of RAD51-dependent DNA interstrand cross-link repair. Science. 2011;333:84-7 pubmed publisher
Keck J, Jones M, Wong C, Binkley J, Chen D, Jaspersen S, et al. A cell cycle phosphoproteome of the yeast centrosome. Science. 2011;332:1557-61 pubmed publisher
Heallen T, Zhang M, Wang J, Bonilla Claudio M, Klysik E, Johnson R, et al. Hippo pathway inhibits Wnt signaling to restrain cardiomyocyte proliferation and heart size. Science. 2011;332:458-61 pubmed publisher
Rizzini L, Favory J, Cloix C, Faggionato D, O Hara A, Kaiserli E, et al. Perception of UV-B by the Arabidopsis UVR8 protein. Science. 2011;332:103-6 pubmed publisher
Coles C, Shen Y, Tenney A, Siebold C, Sutton G, Lu W, et al. Proteoglycan-specific molecular switch for RPTPÏƒ clustering and neuronal extension. Science. 2011;332:484-8 pubmed publisher
Shen Y, Tenney A, Busch S, Horn K, Cuascut F, Liu K, et al. PTPsigma is a receptor for chondroitin sulfate proteoglycan, an inhibitor of neural regeneration. Science. 2009;326:592-6 pubmed publisher
Pan F, Yu H, Dang E, Barbi J, Pan X, Grosso J, et al. Eos mediates Foxp3-dependent gene silencing in CD4+ regulatory T cells. Science. 2009;325:1142-6 pubmed publisher
Gatfield D, Le Martelot G, Vejnar C, Gerlach D, Schaad O, Fleury Olela F, et al. Integration of microRNA miR-122 in hepatic circadian gene expression. Genes Dev. 2009;23:1313-26 pubmed publisher
Colombo M, Bourhis J, Chamontin C, Soriano C, Villet S, Costanzo S, et al. The interaction between the measles virus nucleoprotein and the Interferon Regulator Factor 3 relies on a specific cellular environment. Virol J. 2009;6:59 pubmed publisher
Chen Y, Honeychurch K, Yang G, Byrd C, Harver C, Hruby D, et al. Vaccinia virus p37 interacts with host proteins associated with LE-derived transport vesicle biogenesis. Virol J. 2009;6:44 pubmed publisher
Varea O, Garrido J, Dopazo A, Mendez P, Garcia Segura L, Wandosell F. Estradiol activates beta-catenin dependent transcription in neurons. PLoS ONE. 2009;4:e5153 pubmed publisher
Hata K, Kaibuchi K, Inagaki S, Yamashita T. Unc5B associates with LARG to mediate the action of repulsive guidance molecule. J Cell Biol. 2009;184:737-50 pubmed publisher
Zampieri M, Passananti C, Calabrese R, Perilli M, Corbi N, De Cave F, et al. Parp1 localizes within the Dnmt1 promoter and protects its unmethylated state by its enzymatic activity. PLoS ONE. 2009;4:e4717 pubmed publisher
De Domenico I, Lo E, Ward D, Kaplan J. Hepcidin-induced internalization of ferroportin requires binding and cooperative interaction with Jak2. Proc Natl Acad Sci U S A. 2009;106:3800-5 pubmed publisher
Eagle R, Flack G, Warford A, MartÃnez Borra J, Jafferji I, Traherne J, et al. Cellular expression, trafficking, and function of two isoforms of human ULBP5/RAET1G. PLoS ONE. 2009;4:e4503 pubmed publisher
Harduf H, Goldman S, Shalev E. Progesterone receptor A and c-Met mediates spheroids-endometrium attachment. Reprod Biol Endocrinol. 2009;7:14 pubmed publisher
Sone M, Uchida A, Komatsu A, Suzuki E, Ibuki I, Asada M, et al. Loss of yata, a novel gene regulating the subcellular localization of APPL, induces deterioration of neural tissues and lifespan shortening. PLoS ONE. 2009;4:e4466 pubmed publisher
Ma L, Tsai M, Wang S, Lu B, Chen R, Yates J, et al. Requirement for Nudel and dynein for assembly of the lamin B spindle matrix. Nat Cell Biol. 2009;11:247-56 pubmed publisher
Qin S, Wang Q, Ray A, Wani G, Zhao Q, Bhaumik S, et al. Sem1p and Ubp6p orchestrate telomeric silencing by modulating histone H2B ubiquitination and H3 acetylation. Nucleic Acids Res. 2009;37:1843-53 pubmed publisher
Roger T, Froidevaux C, Le Roy D, Reymond M, Chanson A, Mauri D, et al. Protection from lethal gram-negative bacterial sepsis by targeting Toll-like receptor 4. Proc Natl Acad Sci U S A. 2009;106:2348-52 pubmed publisher
Castillo Acosta V, Ruiz Perez L, Yang W, Gonzalez Pacanowska D, Vidal A. Identification of a residue critical for the excision of 3'-blocking ends in apurinic/apyrimidinic endonucleases of the Xth family. Nucleic Acids Res. 2009;37:1829-42 pubmed publisher
Canettieri G, Coni S, Della Guardia M, Nocerino V, Antonucci L, Di Magno L, et al. The coactivator CRTC1 promotes cell proliferation and transformation via AP-1. Proc Natl Acad Sci U S A. 2009;106:1445-50 pubmed publisher
Nishitsuji K, Tomiyama T, Ishibashi K, Ito K, Teraoka R, Lambert M, et al. The E693Delta mutation in amyloid precursor protein increases intracellular accumulation of amyloid beta oligomers and causes endoplasmic reticulum stress-induced apoptosis in cultured cells. Am J Pathol. 2009;174:957-69 pubmed publisher
Chatoo W, Abdouh M, David J, Champagne M, Ferreira J, Rodier F, et al. The polycomb group gene Bmi1 regulates antioxidant defenses in neurons by repressing p53 pro-oxidant activity. J Neurosci. 2009;29:529-42 pubmed publisher
Fritz J, Strehblow A, Taschner A, Schopoff S, Pasierbek P, Jantsch M. RNA-regulated interaction of transportin-1 and exportin-5 with the double-stranded RNA-binding domain regulates nucleocytoplasmic shuttling of ADAR1. Mol Cell Biol. 2009;29:1487-97 pubmed publisher
Bari R, Zhang Y, Zhang F, Wang N, Stipp C, Zheng J, et al. Transmembrane interactions are needed for KAI1/CD82-mediated suppression of cancer invasion and metastasis. Am J Pathol. 2009;174:647-60 pubmed publisher
Sunwoo H, Dinger M, Wilusz J, Amaral P, Mattick J, Spector D. MEN epsilon/beta nuclear-retained non-coding RNAs are up-regulated upon muscle differentiation and are essential components of paraspeckles. Genome Res. 2009;19:347-59 pubmed publisher
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