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Journal articles on the topic 'GFOGER'

Author: Grafiati

Published: 4 June 2021

Last updated: 19 February 2022

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1

Pugh, Nicholas, Anna M. C. Simpson, Peter A. Smethurst, Philip G. de Groot, Nicolas Raynal, and Richard W. Farndale. "Synergism between platelet collagen receptors defined using receptor-specific collagen-mimetic peptide substrata in flowing blood." Blood 115, no. 24 (2010): 5069–79. http://dx.doi.org/10.1182/blood-2010-01-260778.

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AbstractExposed subendothelial collagen acts as a substrate for platelet adhesion and thrombus formation after vascular injury. Synthetic collagen-derived triple-helical peptides, designated collagen-related peptide (CRP), GFOGER, and VWF-III, can specifically engage the platelet collagen receptors, glycoprotein VI and integrin α2β1, and plasma von Willebrand factor (VWF), respectively. Hitherto, the role of these 3 collagen-binding axes has been studied indirectly. Use of these uniform peptide substrates, rather than collagen fibers, provides independent control of each axis. Here, we use con

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2

Zhang, Wan-Ming, Jarmo Käpylä, J. Santeri Puranen та ін. "α11β1Integrin Recognizes the GFOGER Sequence in Interstitial Collagens". Journal of Biological Chemistry 278, № 9 (2002): 7270–77. http://dx.doi.org/10.1074/jbc.m210313200.

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3

Elton, Catherine, Peter Smethurst, Paul Eggleton та Rich Farndalerd. "Physical and Functional Interaction Between Cell-Surface Calreticulin and the Collagen Receptors Integrin α2β1 and Glycoprotein VI in Human Platelets". Thrombosis and Haemostasis 88, № 10 (2002): 648–54. http://dx.doi.org/10.1055/s-0037-1613270.

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SummaryCalreticulin is an abundant protein in the endoplasmic reticulum of most cells. In this study, flow cytometry and immunoprecipitation from surface-biotinylated platelets each provided direct evidence that calreticulin is also expressed on the surface of human platelets. Anti-calreticulin antibodies caused platelet activation, inducing Fc RIIa-independent platelet aggregation. In addition, these antibodies inhibited platelet adhesion to the integrin α2β1-specific ligands, GFOGER-GPP and monomeric collagen I, and to the glycoprotein VI-specific ligand, CRP. Inhibition of platelet adhesion

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4

SLATTER, D. A., and R. W. FARNDALE. "Platelet Adhesion to Glycated GFOGER Peptide and Bovine Serum Albumin." Annals of the New York Academy of Sciences 1043, no. 1 (2005): 930. http://dx.doi.org/10.1196/annals.1333.144.

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5

Gigout, Anne, Mario Jolicoeur, Monica Nelea, Nicolas Raynal, Richard Farndale та Michael D. Buschmann. "Chondrocyte Aggregation in Suspension Culture Is GFOGER-GPP- and β1 Integrin-dependent". Journal of Biological Chemistry 283, № 46 (2008): 31522–30. http://dx.doi.org/10.1074/jbc.m804234200.

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6

Wojtowicz, Abigail M., Asha Shekaran, Megan E. Oest, et al. "Coating of biomaterial scaffolds with the collagen-mimetic peptide GFOGER for bone defect repair." Biomaterials 31, no. 9 (2010): 2574–82. http://dx.doi.org/10.1016/j.biomaterials.2009.12.008.

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7

Mhanna, Rami, Ece Öztürk, Queralt Vallmajo-Martin, Christopher Millan, Michael Müller, and Marcy Zenobi-Wong. "GFOGER-Modified MMP-Sensitive Polyethylene Glycol Hydrogels Induce Chondrogenic Differentiation of Human Mesenchymal Stem Cells." Tissue Engineering Part A 20, no. 7-8 (2014): 1165–74. http://dx.doi.org/10.1089/ten.tea.2013.0519.

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8

Kunicki, Thomas J., Daniel Diaz, Shirley A. Williams, Richard W. Farndale та Diane J. Nugent. "The Integrin α2 Dimorphism E534K Modulates Platelet Binding to Decorin but Not Collagen I",. Blood 118, № 21 (2011): 3256. http://dx.doi.org/10.1182/blood.v118.21.3256.3256.

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Abstract Abstract 3256 Background. Integrin a2b1-mediated adhesion to collagens supports cellular attachment, while decorin binding by a2b1 often attenuates adhesion. Collagen I binds to the a2 I-domain via the triple-helical sequence GFOGER, but the decorin binding site is not within the a2 I-domain and has not yet been identified. A single nucleotide polymorphism in the a2 gene ITGA2 (rs1801106) (G1600A) resulting in the amino acid substitution glutamate-534 to lysine-534 (E534K) is the basis for one of the most important human platelet alloantigen (HPA) systems, HPA-5, yet HPA-5 alleles do

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9

Lahti, Matti, Jyrki Heino та Jarmo Käpylä. "Leukocyte integrins αLβ2, αMβ2 and αXβ2 as collagen receptors—Receptor activation and recognition of GFOGER motif". International Journal of Biochemistry & Cell Biology 45, № 7 (2013): 1204–11. http://dx.doi.org/10.1016/j.biocel.2013.03.016.

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10

Farndale, Richard W., Pia R. Siljander, David J. Onley, Pavithra Sundaresan, C. Graham Knight, and Michael J. Barnes. "Collagen-platelet interactions: recognition and signalling." Biochemical Society Symposia 70 (September 1, 2003): 81–94. http://dx.doi.org/10.1042/bss0700081.

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The collagen-platelet interaction is central to haemostasis and may be a critical determinant of arterial thrombosis, where subendothelium is exposed after rupture of atherosclerotic plaque. Recent research has capitalized on the cloning of an important signalling receptor for collagen, glycoprotein VI, which is expressed only on platelets, and on the use of collagen-mimetic peptides as specific tools for both glycoprotein VI and integrin α2ϐ1. We have identified sequences, GPO and GFOGER (where O denotes hydroxyproline), within collagen that are recognized by the collagen receptors glycoprote

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11

Dobler, D., N. Ahmed, L. Song, K. E. Eboigbodin, and P. J. Thornalley. "Increased Dicarbonyl Metabolism in Endothelial Cells in Hyperglycemia Induces Anoikis and Impairs Angiogenesis by RGD and GFOGER Motif Modification." Diabetes 55, no. 7 (2006): 1961–69. http://dx.doi.org/10.2337/db05-1634.

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12

Carafoli, Federico, Samir W. Hamaia, Dominique Bihan, Erhard Hohenester та Richard W. Farndale. "An Activating Mutation Reveals a Second Binding Mode of the Integrin α2 I Domain to the GFOGER Motif in Collagens". PLoS ONE 8, № 7 (2013): e69833. http://dx.doi.org/10.1371/journal.pone.0069833.

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13

Knight, C. Graham, Laurence F. Morton, Anthony R. Peachey, Danny S. Tuckwell, Richard W. Farndale та Michael J. Barnes. "The Collagen-binding A-domains of Integrins α1β1and α2β1Recognize the Same Specific Amino Acid Sequence, GFOGER, in Native (Triple-helical) Collagens". Journal of Biological Chemistry 275, № 1 (2000): 35–40. http://dx.doi.org/10.1074/jbc.275.1.35.

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14

Consonni, Alessandra, Lina Cipolla, Gianni Guidetti та ін. "Role and regulation of phosphatidylinositol 3-kinase β in platelet integrin α2β1 signaling". Blood 119, № 3 (2012): 847–56. http://dx.doi.org/10.1182/blood-2011-07-364992.

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Abstract Integrin α2β1–mediated adhesion of human platelets to monomeric type I collagen or to the GFOGER peptide caused a time-dependent activation of PI3K and Akt phosphorylation. This process was abrogated by pharmacologic inhibition of PI3Kβ, but not of PI3Kγ or PI3Kα. Moreover, Akt phosphorylation was undetectable in murine platelets expressing a kinase-dead mutant of PI3Kβ (PI3KβKD), but occurred normally in PI3KγKD platelets. Integrin α2β1 failed to stimulate PI3Kβ in platelets from phospholipase Cγ2 (PLCγ2)–knockout mice, and we found that intracellular Ca2+ linked PLCγ2 to PI3Kβ activ

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15

Siljander, Pia R. M., Imke C. A. Munnix, Peter A. Smethurst, et al. "Platelet receptor interplay regulates collagen-induced thrombus formation in flowing human blood." Blood 103, no. 4 (2004): 1333–41. http://dx.doi.org/10.1182/blood-2003-03-0889.

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Abstract The platelet glycoproteins (GPs) Ib, integrin α2β1, and GPVI are considered central to thrombus formation. Recently, their relative importance has been re-evaluated based on data from murine knockout models. To examine their relationship during human thrombus formation on collagen type I fibers at high shear (1000 s–1), we tested a novel antibody against GPVI, an immunoglobulin single-chain variable fragment, 10B12, together with specific antagonists for GPIbα (12G1 Fab2) and α2β1 (6F1 mAb or GFOGER-GPP peptide). GPVI was found to be crucial for aggregate formation, Ca2+ signaling, an

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16

Knight, C. G., L. F. Morton, A. R. Peachey, D. S. Tuckwell, R. W. Farndale та M. J. Barnes. "THE COLLAGEN SEQUENCE, GFOGER, IS A BINDING SITE FOR INTEGRIN α1 AND α2 A-DOMAINS AND FULLY MEDIATES α2β1-DEPENDENT CELL-RECOGNITION BY COLLAGEN". Biochemical Society Transactions 27, № 5 (1999): A144. http://dx.doi.org/10.1042/bst027a144b.

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17

Attwood, Simon, Anna Simpson, Samir Hamaia, et al. "Measurement of the Interaction Between Recombinant I-domain from Integrin alpha 2 beta 1 and a Triple Helical Collagen Peptide with the GFOGER Binding Motif Using Molecular Force Spectroscopy." International Journal of Molecular Sciences 14, no. 2 (2013): 2832–45. http://dx.doi.org/10.3390/ijms14022832.

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18

Tasneem, Subia, Monika Pawlikowska, Dominique Bihan, Richard W. Farndale, and Catherine P. M. Hayward. "Interaction of Multimerin 1 with Collagens: Role in Platelet Adhesion." Blood 118, no. 21 (2011): 2207. http://dx.doi.org/10.1182/blood.v118.21.2207.2207.

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Abstract Abstract 2207 Multimerin 1 (MMRN1) is a large, homopolymeric adhesive protein stored in platelets and endothelium that binds to activated platelets, endothelial cells and the extracellular matrix after agonist stimulation. MMRN1 supports platelet adhesion by von Willebrand factor (VWF) dependent and independent mechanisms, and also increases platelet adhesion to Horm collagen. Mice deficient in Mmrn1/Snca (α-synuclein) showed defective platelet adhesion to collagen in vitro and in vivo which was corrected by MMRN1. The ability of MMRN1 to support platelet adhesion in vivo and enhance

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19

Choi, Sungwook, Seth E. Snyder, David T. Moore, Gaston Vilaire, Joel S. Bennett та William F. DeGrado. "The Development of Small Molecule Inhibitors of Collagen Binding to the Integrin α2β1 as Antithrombotic Drugs." Blood 106, № 11 (2005): 3677. http://dx.doi.org/10.1182/blood.v106.11.3677.3677.

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Abstract Platelets tether to collagen in the subendothelial matrix that is exposed by vascular damage. Collagen is a particularly important matrix component in this context, not only because it is a substrate for platelet adhesion, but because it is an agonist for platelet aggregation and secretion as well. There are two platelet collagen receptors, the immunoglobulin gene superfamily member GPVI and the integrin α2Β1. Both are involved in adhesion to exposed collagen and generate downstream activating signals. α2Β1 is widely expressed and has been implicated in hemostasis and thrombosis, as w

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20

Blaudeck, Natascha, Georg A. Sprenger, Roland Freudl, and Thomas Wiegert. "Specificity of Signal Peptide Recognition in Tat-Dependent Bacterial Protein Translocation." Journal of Bacteriology 183, no. 2 (2001): 604–10. http://dx.doi.org/10.1128/jb.183.2.604-610.2001.

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ABSTRACT The bacterial twin arginine translocation (Tat) pathway translocates across the cytoplasmic membrane folded proteins which, in most cases, contain a tightly bound cofactor. Specific amino-terminal signal peptides that exhibit a conserved amino acid consensus motif, S/T-R-R-X-F-L-K, direct these proteins to the Tat translocon. The glucose-fructose oxidoreductase (GFOR) ofZymomonas mobilis is a periplasmic enzyme with tightly bound NADP as a cofactor. It is synthesized as a cytoplasmic precursor with an amino-terminal signal peptide that shows all of the characteristics of a typical twi

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21

FOX, JACOB, and JÁNOS PACH. "Applications of a New Separator Theorem for String Graphs." Combinatorics, Probability and Computing 23, no. 1 (2013): 66–74. http://dx.doi.org/10.1017/s0963548313000412.

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An intersection graph of curves in the plane is called astring graph. Matoušek almost completely settled a conjecture of the authors by showing that every string graph withmedges admits a vertex separator of size$O(\sqrt{m}\log m)$. In the present note, this bound is combined with a result of the authors, according to which every dense string graph contains a large complete balanced bipartite graph. Three applications are given concerning string graphsGwithnvertices: (i) ifKt⊈Gfor somet, then the chromatic number ofGis at most (logn)O(logt); (ii) ifKt,t⊈G, thenGhas at mostt(logt)O(1)nedges,; a

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22

Obaid, Evelyn E. "On a variation of Sands' method." International Journal of Mathematics and Mathematical Sciences 9, no. 3 (1986): 597–604. http://dx.doi.org/10.1155/s0161171286000753.

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A subset of a finite additive abelian groupGis aZ-set if for alla∈G,na∈Gfor alln∈Z. The groupGis called Z-good if in every factorizationG=A⊕B, whereAandBareZ-sets at least one factor is periodic. OtherwiseGis called Z-bad.The purpose of this paper is to investigate factorizations of finite ablian groups which arise from a variation of Sands' method. A necessary condition is given for a factorizationG=A⊕B, whereAandBareZ-sets, to be obtained by this variation. An example is provided to show that this condition is not sufficient. It is also shown that in general all factorizationsG=A⊕B, wher

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23

Kustiawan, Erfan, Dyah Laksito Rukmi, Shokhirul Imam, and Sandi Owen Permadi. "Studi Intensitas Pencahayaan Terhadap Puncak Produksi Ayam Petelur Fase Layer di UD. Mahakarya Farm Banyuwangi." Jurnal Ilmu Peternakan Terapan 3, no. 1 (2019): 14–18. http://dx.doi.org/10.25047/jipt.v3i1.1552.

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The objective of this case study was to evaluate good lighting levels in laying hens. The data were collected for three months at UD. Mahakarya Farm Banyuwangi. A total of 4.400 heads of layer chicken were used in this study. The lighting intensityused were 15 lux in cage A and 10 lux in cage B. The average of egg production were75.91% and 73.57% for cage A (15 lux) and cage B (10 lux), respectively. The average of egg weight were 59.37 g and 59.23 gfor cage A (15 lux) and cage B (10 lux), respectively. The results of this study presented that layer chicken aged 25 weeks produced better produc

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24

Kustiawan, Erfan, Dyah Laksito Rukmi, Shokhirul Imam, and Sandi Owen Permadi. "Studi Intensitas Pencahayaan Terhadap Puncak Produksi Ayam Petelur Fase Layer di UD. Mahakarya Farm Banyuwangi." Jurnal Ilmu Peternakan Terapan 3, no. 1 (2019): 14–18. http://dx.doi.org/10.25047/jupiter.v3i1.1552.

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The objective of this case study was to evaluate good lighting levels in laying hens. The data were collected for three months at UD. Mahakarya Farm Banyuwangi. A total of 4.400 heads of layer chicken were used in this study. The lighting intensityused were 15 lux in cage A and 10 lux in cage B. The average of egg production were75.91% and 73.57% for cage A (15 lux) and cage B (10 lux), respectively. The average of egg weight were 59.37 g and 59.23 gfor cage A (15 lux) and cage B (10 lux), respectively. The results of this study presented that layer chicken aged 25 weeks produced better produc

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25

Prowse, Terry D., Frederick J. Wrona, James D. Reist, John E. Hobbie, Lucie M. J. Lévesque, and Warwick F. Vincent. "General Features of the Arctic Relevant to Climate Change in Freshwater Ecosystems." AMBIO: A Journal of the Human Environment 35, no. 7 (2006): 330–38. http://dx.doi.org/10.1579/0044-7447(2006)35[330:gfotar]2.0.co;2.

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26

Ma, Pengfei, Ren Xin, and Jitao Yao. "Assessment of failure mode and seismic performance of damaged masonry structures retrofitted with grout-injected ferrocement overlay reinforcement (GFOR)." Construction and Building Materials 305 (October 2021): 124778. http://dx.doi.org/10.1016/j.conbuildmat.2021.124778.

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27

Pedruzzi, Israel, Eduardo A. Borges da Silva, and Alírio E. Rodrigues. "Production of lactobionic acid and sorbitol from lactose/fructose substrate using GFOR/GL enzymes from Zymomonas mobilis cells: A kinetic study." Enzyme and Microbial Technology 49, no. 2 (2011): 183–91. http://dx.doi.org/10.1016/j.enzmictec.2011.04.017.

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28

Tanase, Corneliu, Sanda Cosarca, Felicia Toma, et al. "Antibacterial Activities of Spruce Bark (Picea abies L.) Extract and Its Components Against Human Pathogens." Revista de Chimie 69, no. 6 (2018): 1462–67. http://dx.doi.org/10.37358/rc.18.6.6347.

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Spruce is a used material in the wood industry and bark is regarded as a by-product. The aim of this study was to provide information about natural bioactive compounds from spruce (Picea abies L.) bark with potential therapeutic applications such as antibacterial activity against human pathogens. Spruce bark extract was obtained by the conventional aqueous extraction (EAM), and second with ultrasounds (USM). It was determined the total polyphenols by spectrophotometric methods and individual polyphenols by high-performance liquid chromatography (HPLC). For the determination of minimum inhibito

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29

Berberi, Antoine, Malkan Abdrashidova Amkhadova, Antoine Samarani, and Georges Aoun. "PHYSICOCHEMICAL CHARACTERIZATION: COMPARATIVE EVALUATION OF ALLOGRAFT BIOMATERIALS AND AUTOGENOUS BONE." Russian Journal of Dentistry 21, no. 5 (2017): 233–37. http://dx.doi.org/10.18821/1728-2802-2017-21-5-233-237.

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Objectives: bone substitutes used in oral surgery include allografts, xenografts and synthetic materials that are frequently used to compensate bone loss or to reinforce repaired bone by encouraging new bone ingrowth into the defect site. The aim of this study was to evaluate a number ofphysical and chemical properties in a variety of allografts biomaterials used in oral surgery and to compare them with those of autogenous bone. Materials and methods: autogenous bone andfive different allograft biomaterials were studied by high-resolution X-ray diffractometry, atomic absorption spectrometry, l

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30

Júnior, João B. Severo, José C. Pinto, Helen C. Ferraz, and Tito L. M. Alves. "Analysis of experimental errors in bioprocesses. 1. Production of lactobionic acid and sorbitol using the GFOR (glucose-fructose oxidoreductase) enzyme from permeabilized cells of Zymomonas mobilis." Journal of Industrial Microbiology & Biotechnology 38, no. 9 (2011): 1575–85. http://dx.doi.org/10.1007/s10295-011-0948-1.

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31

Wiegert, Thomas, Hermann Sahm, and Georg A. Sprenger. "Expression of the Zymomonas Mobilis Gfo Gene for NADP-Containing Glucose: Fructose Oxidoreductase (GFOR) in Escherichia Coli- Formation of Enzymatically Active Pregfor but Lack of Processing Into a Stable Periplasmic Protein." European Journal of Biochemistry 244, no. 1 (1997): 107–12. http://dx.doi.org/10.1111/j.1432-1033.1997.00107.x.

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32

Lee, Dong-Young Donna, Igla Muskaj, and William Savage. "Platelet Proteins Cause Allergic Transfusion Reactions through an Immunoglobulin-Dependent Mechanism." Blood 128, no. 22 (2016): 91. http://dx.doi.org/10.1182/blood.v128.22.91.91.

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Abstract Background: A general understanding of allergic transfusion reaction (ATR) mechanisms remains elusive. Various hypotheses invoke proteins, small molecules, mitochondria, or microparticles that may be plasma or platelet derived and suggest antibody dependent or independent mechanisms. There has been no systematic comparison of these proposed mechanisms. The aim of this study is to characterize the mechanistic determinants of ATRs. Methods: Basophil enriched cell suspensions were collected from healthy donors (n=8). Basophil histamine release was measured in response to platelet-derived

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33

Mansour, Ali, Walaa Darwiche, Linda Yaker, et al. "GFOGER Peptide Modifies the Protein Content of Extracellular Vesicles and Inhibits Vascular Calcification." Frontiers in Cell and Developmental Biology 8 (November 30, 2020). http://dx.doi.org/10.3389/fcell.2020.589761.

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ObjectiveVascular calcification (VC) is an active process during which vascular smooth muscle cells (VSMCs) undergo an osteogenic switch and release extracellular vesicles (EVs). In turn, the EVs serve as calcification foci via interaction with type 1 collagen (COL1). We recently showed that a specific, six-amino-acid repeat (GFOGER) in the sequence of COL1 was involved in the latter’s interaction with integrins expressed on EVs. Our main objective was to test the GFOGER ability to inhibit VC.ApproachWe synthesized the GFOGER peptide and tested its ability to inhibit the inorganic phosphate (P

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34

Clark, Amy Y., Karen E. Martin, José R. García, et al. "Integrin-specific hydrogels modulate transplanted human bone marrow-derived mesenchymal stem cell survival, engraftment, and reparative activities." Nature Communications 11, no. 1 (2020). http://dx.doi.org/10.1038/s41467-019-14000-9.

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AbstractStem cell therapies are limited by poor cell survival and engraftment. A hurdle to the use of materials for cell delivery is the lack of understanding of material properties that govern transplanted stem cell functionality. Here, we show that synthetic hydrogels presenting integrin-specific peptides enhance the survival, persistence, and osteo-reparative functions of human bone marrow-derived mesenchymal stem cells (hMSCs) transplanted in murine bone defects. Integrin-specific hydrogels regulate hMSC adhesion, paracrine signaling, and osteoblastic differentiation in vitro. Hydrogels pr

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35

Koivunen, Jarkko, Hongmin Tu, Antti Kemppainen та ін. "Integrin α11β1 is a receptor for collagen XIII". Cell and Tissue Research, 11 грудня 2020. http://dx.doi.org/10.1007/s00441-020-03300-y.

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AbstractCollagen XIII is a conserved transmembrane collagen mainly expressed in mesenchymal tissues. Previously, we have shown that collagen XIII modulates tissue development and homeostasis. Integrins are a family of receptors that mediate signals from the environment into the cells and vice versa. Integrin α11β1 is a collagen receptor known to recognize the GFOGER (O=hydroxyproline) sequence in collagens. Interestingly, collagen XIII and integrin α11β1 both have a role in the regulation of bone homeostasis. To study whether α11β1 is a receptor for collagen XIII, we utilized C2C12 cells trans

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36

Lahti, Matti, Jyrki Heino та Jarmo Käpylä. "Leukocyte Integrins α L β 2 , α M β 2 and α X β 2 as Collagen Receptors ‐ Receptor Activation and Recognition of GFOGER Motif". FASEB Journal 29, S1 (2015). http://dx.doi.org/10.1096/fasebj.29.1_supplement.lb167.

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37

"Gforge Hevesy Medal 1986." Journal of Radioanalytical and Nuclear Chemistry Letters 106, no. 2 (1986): 65. http://dx.doi.org/10.1007/bf02162550.

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38

"EURECO–GFOE 2008: Call for Sessions/Symposia." Bulletin of the Ecological Society of America 89, no. 1 (2008): 77–78. http://dx.doi.org/10.1890/0012-9623(2008)89[77:ecfs]2.0.co;2.

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39

"Immobilization of Zymomonas mobilis In situ in Flexible Polyurethane and Potential for Bioconversion in Sodium Maltobionate." Biointerface Research in Applied Chemistry 12, no. 1 (2021): 279–91. http://dx.doi.org/10.33263/briac121.279291.

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Maltobionic acid and its salts are produced by the action of the periplasmic enzymatic complex glucose-fructose oxidoreductase (GFOR), and glicono-δ-lactonase (GL) from Zymomonas mobilis and, for such, cell immobilization is outstanding. Thus, the objective of this work was to immobilize, in situ, Z. mobilis cells containing GFOR/GL in flexible polyurethane foam (PU) in order to produce maltobionic acid. In the immobilization, concentrations of polyurethane and biomass support constituents varied, and the visual aspect of the material immobilized was assessed, its enzymatic activity, immobiliz

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40

Henz, Fabiane, Leonardo Fin, and Carlos Leandro Tiggemann. "ASSOCIAÇÃO ENTRE A FORÇA MUSCULAR E A CAPACIDADE CARDIORRESPIRATÓRIA COM A FADIGA DE MULHERES." Arquivos de Ciências da Saúde da UNIPAR 25, no. 1 (2021). http://dx.doi.org/10.25110/arqsaude.v25i1.2021.7834.

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A prática de exercícios físicos é um importante componente na prevenção e tratamento de doenças crônicas não transmissíveis, além disso, parece ser um importante componente na diminuição das sensações de fadiga. O objetivo do presente estudo foi comparar os níveis de fadiga entre mulheres sedentárias, praticantes de treinamento de força e treinamento aeróbico, bem como, verificar a associação entre os níveis de força muscular e capacidade cardiorrespiratória com a sensação de fadiga. Procedimentos metodológicos: a amostra foi constituída de 45 mulheres saudáveis, sendo 15 sedentárias (GSED), 1

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