About: Fabio C. L. Almeida

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About: Fabio C. L. Almeida Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Fabio Almeida (es) Fabio Almeida (nl) Fabio Almeida (sl) Fabio Almeida (ast) Fabio C. L. Almeida (en) Фабио Алмейда (ru)
skos:prefLabel	Fabio Almeida (es) Fabio Almeida (nl) Fabio Almeida (sl) Fabio Almeida (ast) Fabio C. L. Almeida (en) Фабио Алмейда (ru)
name	Fabio Almeida (es) Fabio Almeida (nl) Fabio Almeida (sl) Fabio Almeida (ast) Fabio C. L. Almeida (en) Фабио Алмейда (ru)
Scopus author ID	wds:Q42665610-C2513AE0-E631-4BC4-96F3-C25C6FFF0853
Scopus author ID	7006537189
given name	wds:Q42665610-546D8B49-2A3D-4DF8-BD99-F97B61D5C89D
given name	Fabio
instance of	wds:Q42665610-A74F135A-947C-43A9-A639-4391CEDE3FA5
instance of	Homo sapiens
zbMATH author ID	wds:Q42665610-43C52712-B3DD-442B-99B9-6AD94301C3EF
zbMATH author ID	almeida.fabio-c-l
skos:altLabel	Almeida (en) Almeida F. C. L. (en) Almeida FCL (en) F C L Almeida (en) F. C. L. Almeida (en) Fabio Almeida (en) Fabio C L Almeida (en) Fabio Ceneviva Lacerda de Almeida (en)
occupation	wds:Q42665610-33C2E841-2889-43A1-B105-7CE3D6591E7F
employer	wds:Q42665610-FBC6FDD7-B030-44D0-AF63-E8E282011BBA
sex or gender	wds:Q42665610-C1D0E87A-557E-4D39-80F5-530FB9548A5A
maintained by WikiProject	wds:Q42665610-97F4E31D-A25E-4BA1-BD0D-709A14DD90A5
educated at	wds:Q42665610-8C8A92D3-B33B-4B45-90A3-99185B8CF67D
family name	wds:Q42665610-59B6A968-0F5A-41FD-8335-A6AC2ACED3A2
occupation	researcher
employer	Federal University of Rio de Janeiro
sex or gender	male
maintained by WikiProject	WikiProject Mathematics
educated at	University of São Paulo
family name	Almeida
ORCID iD	wds:Q42665610-69FEC8C8-9E3D-49B0-BF9E-906ED1B797C8
ORCID iD	https://orcid.org/0000-0001-6046-7006
ORCID iD	0000-0001-6046-7006
ResearcherID	wds:Q42665610-A13E9E47-6F4F-4812-915C-49E208548AF8
ResearcherID	O-4989-2018
Mendeley person ID	wds:Q42665610-FDEDFBF4-D292-4B01-B187-1DD9065A258D
Mendeley person ID	fabio-almeida1
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42665610
is author of	Structural basis for the interaction of human β-defensin 6 and its putative chemokine receptor CCR2 and breast cancer microvesicles Antibody Binding Modulates Conformational Exchange in Domain III of Dengue Virus E Protein fd coat protein structure in membrane environments: structural dynamics of the loop between the hydrophobic trans-membrane helix and the amphipathic in-plane helix From combinatorial peptide selection to drug prototype (I): targeting the vascular endothelial growth factor receptor pathway Structure of a membrane-binding domain from a non-enveloped animal virus: insights into the mechanism of membrane permeability and cellular entry. Structure of the Ebola fusion peptide in a membrane-mimetic environment and the interaction with lipid rafts Interaction of the Dengue virus fusion peptide with membranes assessed by NMR: The essential role of the envelope protein Trp101 for membrane fusion Correlation between conformation and antibody binding: NMR structure of cross-reactive peptides from T. cruzi, human and L. braziliensis Implications of protein conformational diversity for binding and development of new biological active compounds. Structural meta-analysis of regular human insulin in pharmaceutical formulations Understanding dengue virus capsid protein disordered N-Terminus and pep14-23-based inhibition Spectroscopic characterization of a truncated hemoglobin from the nitrogen-fixing bacterium Herbaspirillum seropedicae. Herpes simplex type 1 activates glycolysis through engagement of the enzyme 6-phosphofructo-1-kinase (PFK-1). Inhibition of energy-producing pathways of HepG2 cells by 3-bromopyruvate Solution NMR structures of the antimicrobial peptides phylloseptin-1, -2, and -3 and biological activity: the role of charges and hydrogen bonding interactions in stabilizing helix conformations Structure and Membrane Interactions of the Antibiotic Peptide Dermadistinctin K by Multidimensional Solution and Oriented 15N and 31P Solid-State NMR Spectroscopy Solution structure of Pisum sativum defensin 1 by high resolution NMR: plant defensins, identical backbone with different mechanisms of action Portrayal of complex dynamic properties of sugarcane defensin 5 by NMR: multiple motions associated with membrane interaction Production of the active antifungal Pisum sativum defensin 1 (Psd1) in Pichia pastoris: overcoming the inefficiency of the STE13 protease In-Cell NMR spectroscopy: inhibition of autologous protein expression reduces Escherichia coli lysis. NMR structure of PW2 bound to SDS micelles. A tryptophan-rich anticoccidial peptide selected from phage display libraries Effect of micelle interface on the binding of anticoccidial PW2 peptide Hydration and conformational equilibrium in yeast thioredoxin 1: implication for H(+) exchange Backbone dynamics of the antifungal Psd1 pea defensin and its correlation with membrane interaction by NMR spectroscopy. Novel Zn2+-binding Sites in Human Transthyretin: IMPLICATIONS FOR AMYLOIDOGENESIS AND RETINOL-BINDING PROTEIN RECOGNITION Solution and high-pressure NMR studies of the structure, dynamics, and stability of the cross-reactive allergenic cod parvalbumin Gad m 1 High-throughput screening of structural proteomics targets using NMR. Effectiveness of prophylactic retropharyngeal lymph node irradiation in patients with locally advanced head and neck cancer Feasibility of intensity-modulated and image-guided radiotherapy for functional organ preservation in locally advanced laryngeal cancer The bZIP region of the plant transcription factor opaque-2 forms stable homodimers in solution and retains its helical structure upon subunit dissociation High-risk (HPV16) human papillomavirus E7 oncoprotein is highly stable and extended, with conformational transitions that could explain its multiple cellular binding partners

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