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Relevant bibliographies by topics / GRPEL1

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Academic literature on the topic 'GRPEL1'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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Journal articles on the topic "GRPEL1"

1

Srivastava, Shubhi, Mohammad Azharuddin Savanur, Devanjan Sinha, et al. "Regulation of mitochondrial protein import by the nucleotide exchange factors GrpEL1 and GrpEL2 in human cells." Journal of Biological Chemistry 292, no. 44 (2017): 18075–90. http://dx.doi.org/10.1074/jbc.m117.788463.

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Chen, Pingbo, Beibei Wang, Qingqing Mo, et al. "The LIV-1-GRPEL1 axis adjusts cell fate during anti-mitotic agent-damaged mitosis." EBioMedicine 49 (November 2019): 26–39. http://dx.doi.org/10.1016/j.ebiom.2019.09.054.

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Paixão, Gustavo, Sofia Botelho Fontela, Jorge Marques, Alexandra Esteves, Rui Charneca, and Rita Payan-Carreira. "Long-Term Immunocastration Protocols Successfully Reduce Testicles’ Size in Bísaro Pigs." Animals 11, no. 3 (2021): 632. http://dx.doi.org/10.3390/ani11030632.

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This study aimed to find a suitable immunocastration protocol for male Bísaro pigs (BP) due to the breed and production system particularities. Twenty-five male BP were treated with Improvac® according to three protocols: using two (GrpE2 and L2) or three vaccinations (GrpL3) and starting at 9 (GrpE2) or 13 weeks old (GrpL2 and L3). Eleven animals were kept as intact males (GrpC). Scrotal measurements and the morphometry of the testes and epididymides collected at slaughter were used to survey the effectiveness of the immunocastration compared with the age-matched intact controls. Animals in g

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Lebacq-Verheyden, A. M., P. G. Kasprzyk, M. G. Raum, K. Van Wyke Coelingh, J. A. Lebacq, and J. F. Battey. "Posttranslational processing of endogenous and of baculovirus-expressed human gastrin-releasing peptide precursor." Molecular and Cellular Biology 8, no. 8 (1988): 3129–35. http://dx.doi.org/10.1128/mcb.8.8.3129.

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The 27-amino-acid gastrin-releasing peptide (GRP1-27) is a neuropeptide and growth factor that is synthesized by various neural and neuroendocrine cells. The major pro-GRP hormone (isoform I) contains both GRP1-27 and a novel C-terminal extension peptide termed pro-GRP31-125. In order to define potentially active neuropeptides that could be generated from this novel protein domain, we analyzed the posttranslational processing of endogenous human pro-GRP1-125 in a small-cell lung cancer cell line. Because such studies are much easier in an overexpression system, we investigated at the same time

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Lebacq-Verheyden, A. M., P. G. Kasprzyk, M. G. Raum, K. Van Wyke Coelingh, J. A. Lebacq, and J. F. Battey. "Posttranslational processing of endogenous and of baculovirus-expressed human gastrin-releasing peptide precursor." Molecular and Cellular Biology 8, no. 8 (1988): 3129–35. http://dx.doi.org/10.1128/mcb.8.8.3129-3135.1988.

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The 27-amino-acid gastrin-releasing peptide (GRP1-27) is a neuropeptide and growth factor that is synthesized by various neural and neuroendocrine cells. The major pro-GRP hormone (isoform I) contains both GRP1-27 and a novel C-terminal extension peptide termed pro-GRP31-125. In order to define potentially active neuropeptides that could be generated from this novel protein domain, we analyzed the posttranslational processing of endogenous human pro-GRP1-125 in a small-cell lung cancer cell line. Because such studies are much easier in an overexpression system, we investigated at the same time

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Tawab, Faiza, Iqbal Munir, Zeeshan Nasim, et al. "Identification and characterization of a novel multi-stress responsive gene in Arabidopsis." PLOS ONE 15, no. 12 (2020): e0244030. http://dx.doi.org/10.1371/journal.pone.0244030.

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Abiotic stresses especially salinity, drought and high temperature result in considerable reduction of crop productivity. In this study, we identified AT4G18280 annotated as a glycine-rich cell wall protein-like (hereafter refer to as GRPL1) protein as a potential multistress-responsive gene. Analysis of public transcriptome data and GUS assay of pGRPL1::GUS showed a strong induction of GRPL1 under drought, salinity and heat stresses. Transgenic plants overexpressing GRPL1-3HA showed significantly higher germination, root elongation and survival rate under salt stress. Moreover, the 35S::GRPL1

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Milella, Michele, Sabina Chiaretti, Maria R. Ricciardi, et al. "Comparative Gene Profiling of Acute Myeloid Leukemia (AML) and Malignant Melanoma (MEL) Cell Lines Exposed to the MEK Inhibitor PD0325901 Reveals Common Effectors of the MEK/ERK Kinase Module." Blood 110, no. 11 (2007): 3470. http://dx.doi.org/10.1182/blood.v110.11.3470.3470.

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Abstract The MEK/ERK kinase module is frequently deregulated in human malignancies, including AML and MEL, and represents a promising therapeutic target. We have recently demonstrated that PD0325901, a selective MEK inhibitor, potently inhibits the growth of both AML and MEL cell lines (IC50 5–20 nM), through a combination of inhibition of cell cycle progression and induction of apoptosis. In order to identify functionally relevant targets of the activity of the MEK/ERK kinase module, we compared the gene expression profiles of the PD0325901-sensitive cell lines OCI-AML3 (AML, harboring a NPM

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Milella, Michele, Maria Rosaria Ricciardi, Paola Bergamo, et al. "Development of Mek inhibition (MEK-I)-Based Therapeutic Strategies in Acute Myeloid Leukemia (AML)." Blood 112, no. 11 (2008): 860. http://dx.doi.org/10.1182/blood.v112.11.860.860.

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Abstract In hematologic malignancies, constitutive activation of the Raf/MEK/ERK pathway is frequently observed, conveys a poor prognosis, and constitutes a promising target for therapeutic intervention. Indeed, we have recently demonstrated that selective MEK-I potently inhibit the growth of AML cell lines and ex vivo-cultured primary AML blasts (Blood2006, 108:254). However, these effects are mostly related to the inhibition of cell cycle progression, while apoptosis induction requires higher concentrations of the inhibitors and longer times of exposure. Thus, we investigated MEK-I-induced c

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Mehl, Andrew F., Kelby Okada, Shirley M. Dehn, and Sarah Kurian. "Probing the stability and mechanism for folding of the GrpE1-112 tetrameric deletion mutant of the GrpE protein from E. coli." Biochemical and Biophysical Research Communications 420, no. 3 (2012): 635–38. http://dx.doi.org/10.1016/j.bbrc.2012.03.052.

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Lamba, Jatinder, Lata Chauhan, Christophe Echeverri, et al. "High-Throughput, High-Content siRNA/Drug Modifier Screen for Validation of Transcriptional Profiles Predictive of Cytarabine Response in AML." Blood 124, no. 21 (2014): 3615. http://dx.doi.org/10.1182/blood.v124.21.3615.3615.

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Abstract Cytarabine is the backbone of modern AML chemotherapy. However, extensive inter-patient variation in treatment response, development of resistance, and severe toxicity remain as major hurdles to effective cytarabine chemotherapy. Although the genes involved in cytarabine’s activation/inactivation and transport are well defined, we still lack in understanding of the PD genes of relevance. So far several efforts have been made to identify cytarabine response genes have some of these utilized transcriptional profiling to identify gene expression signatures that differentiate sensitive an

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Dissertations / Theses on the topic "GRPEL1"

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Yan, Junxia. "Combined linkage analysis and exome sequencing identifies novel genes for familial goiter." Kyoto University, 2014. http://hdl.handle.net/2433/188654.

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Hage, Aziz El. "Protéines chaperons intervenant dans l'assemblage des ribosomes chez Escherichia coli." Paris 7, 2004. http://www.theses.fr/2004PA077059.

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Linke, Katrin. "Characterization of the DnaK-DnaJ-GrpE system under oxidative heat stress." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=974431346.

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Emond, Audrey. "Étude du rôle du general receptor for phosphoinositides 1 (GRP1) dans l'adipogenèse." Mémoire, Université de Sherbrooke, 2011. http://savoirs.usherbrooke.ca/handle/11143/4075.

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Many studies have shown that peroxisome-proliferator-activated receptor [gamma] (PPAR[gamma]) plays an important role in adipose tissue formation by activating genes implicated in adipogenesis. PPAR[gamma] heterodimerizes with retinoid X receptor [alpha] (RXR[alpha]), in the presence of ligand, on PPAR response elements (PPREs) in the promoter of target genes involved in adipocyte differentiation. General receptor for phosphoinositides 1 (GRP1) is a corepressor of thyroid hormone receptors (TRs), a nuclear receptor like PPAR[gamma]. GRP1 decreases TRs' transcriptional activity by lowering dime

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Cronin, Thomas Charles. "Structural Determinants of Phosphoinositide Recognition by Grp1 Family Pleckstrin Homology Domains: a Dissertation." eScholarship@UMMS, 2005. http://escholarship.umassmed.edu/gsbs_diss/165.

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Pleckstrin homology (PH) domains, which play an essential role in membrane trafficking and signal transduction, recognize phosphoinositides with a diverse range of affinities and specificities. The PH domains of the Grp1 family of Arf GTPase exchange factors recognize a select group of phosphoinositides with dramatic differences in specificity, despite 90% sequence identity. The work described in this thesis has focused on the structural basis for these differences. The structure of the Grp1 PH domain revealed structural determinants for phosphoinositide recognition. Through a wide range of cr

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Naylor, Dean Jason. "The Mammalian mitochondrial Hsp70 chaperone system, new GrpE-like members and novel organellar substrates." Title page, contents and summary only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09phn331.pdf.

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Bibliography: leaves 104-136. The DnaK (Hsp70), DnaJ and GrpE heat shock proteins of Escherichia coli work synergistically in a diverse number of vital cellular processes including the folding of nascent polypeptides, assembly and disassembly of multimeric proteins, refolding of malfolded proteins, degredation of unstable and non-native polypeptides, regulation of the stress response and the mediation of protein translocation across membranes. In this study Dna-K-affinity purification was employed to identify a mammalian mitrochondrial GrpE homologue (mt-GrpE#1) for the first time. The results

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Barthel, Sandra [Verfasser]. "Physiologische Veränderungen bei der Thylakoidmembranbiogenese und die Funktionsweise des Nukleotidaustauschfaktors GrpE in Cyanobakterien / Sandra Barthel." Mainz : Universitätsbibliothek Mainz, 2011. http://d-nb.info/1031783741/34.

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DE, CROUY CHANEL AXELLE. "Interaction entre les machines chaperons dnak/dnaj/grpe et groel/groes et leurs proteines substrats." Paris 7, 1997. http://www.theses.fr/1997PA077103.

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Les molecules chaperons forment une classe de proteine qui fixent selectivement les polypeptides naissants, non replies, mal replies, ou agreges, en reconnaissant des regions hydrophobes exposees par les proteines depliees. Cette propriete est la base de l'implication des machines chaperons (dnak/dnaj/grpe) et (groel/groes) dans des processus cellulaires tels que le repliement, l'adressage, la renaturation des proteines, et le controle des interactions proteine-proteine. Les chaperons fonctionnent en collaboration avec leur cochaperon. Nous avons etudie l'interaction entre les machines chapero

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Sand, Olivier. "Rôle des protéines de choc thermique DnaK, DnaJ et GrpE dans la transcription tardive du bactériophage Mu." Doctoral thesis, Universite Libre de Bruxelles, 1995. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/212581.

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Akhrymuk, Alena [Verfasser]. "Studies on the interaction between the molecular chaperone DnaK and Nucleotide exchange factor GrpE from Thermus thermophilus / Alena Akhrymuk." Dortmund : Universitätsbibliothek Technische Universität Dortmund, 2004. http://d-nb.info/1011532042/34.

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Books on the topic "GRPEL1"

1

Programa de Fortalecimento Institucional para a Igualdade de Gênero e Raça, Erradicação da Pobreza e Geração de Emprego (GRPE). Gênero, raça, pobreza e emprego : GRPE no Brasil. OIT - Secretaria Internacional do Trabalho, 2006.

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Kingsbury, Roy. Greek Grammar (GRPL). Longman, 1995.

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Kingsbury, Roy, and Kingsbury. Grammar Plus, Level 1 (GRPL). Addison Wesley Publishing Company, 1996.

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Book chapters on the topic "GRPEL1"

1

Wloka, Dieter W. "Off-Line Programmierung mit GRPAL." In Robotersysteme 2. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-93511-4_12.

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Powell, Gavin, Matthew Roberts, and Dafni Stampouli. "Improvements to the GRP1 Combination Rule." In Advances in Intelligent and Soft Computing. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29461-7_34.

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Bracher, Andreas, and Jacob Verghese. "GrpE, Hsp110/Grp170, HspBP1/Sil1 and BAG Domain Proteins: Nucleotide Exchange Factors for Hsp70 Molecular Chaperones." In Subcellular Biochemistry. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-11731-7_1.

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4

Liberek, K., D. Skowyra, J. Marszalek, et al. "Bacteriophage λ DNA Replication and the Role of the Universally Conserved dnaK, dnaJ and grpE Heat Shock Proteins." In DNA Replication: The Regulatory Mechanisms. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76988-7_32.

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Emond, A., and MF Langlois. "The Implication of GRP1, a Novel PPARg Coregulator, in Adipogenesis." In Posters I. Endocrine Society, 2010. http://dx.doi.org/10.1210/endo-meetings.2010.part1.p1.p1-38.

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Klarlund, Jes K., and Michael P. Czech. "[30] Isolation and properties of GRP1, an ADP-ribosylation factor (ARF)-guanine nucleotide exchange protein regulated by phosphatidylinositol 3,4,5-triphosphate." In Methods in Enzymology. Elsevier, 2001. http://dx.doi.org/10.1016/s0076-6879(01)29089-2.

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Conference papers on the topic "GRPEL1"

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Gatos, Basilis, Nikolaos Stamatopoulos, Georgios Louloudis, et al. "GRPOLY-DB: An old Greek polytonic document image database." In 2015 13th International Conference on Document Analysis and Recognition (ICDAR). IEEE, 2015. http://dx.doi.org/10.1109/icdar.2015.7333841.

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