9 results on '"Segura K"'
Search Results
2. A Small Mission Concept to the Sun-Earth Lagrangian L5 Point for Innovative Solar, Heliospheric and Space Weather Science
- Author
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Lavraud, B, Liu, Y, Segura, K, He, J, Qin, G, Temmer, M, Vial, J.-C, Xiong, M, Davies, J. A, Rouillard, A. P, and Gopalswamy, N
- Subjects
Astronomy ,Astrophysics - Abstract
We present a concept for a small mission to the Sun-Earth Lagrangian L5 point for innovative solar, heliospheric and space weather science. The proposed INvestigation of Solar-Terrestrial Activity aNd Transients (INSTANT) mission is designed to identify how solar coronal magnetic fields drive eruptions, mass transport and particle acceleration that impact the Earth and the heliosphere. INSTANT is the first mission designed to (1) obtain measurements of coronal magnetic fields from space and (2) determine coronal mass ejection (CME) kinematics with unparalleled accuracy. Thanks to innovative instrumentation at a vantage point that provides the most suitable perspective view of the Sun-Earth system, INSTANT would uniquely track the whole chain of fundamental processes driving space weather at Earth. We present the science requirements, payload and mission profile that fulfill ambitious science objectives within small mission programmatic boundary conditions.
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- 2016
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3. Differentiating Among Type 1, Type 2 Diabetes, and MODY: Raising Awareness About the Clinical Implementation of Genetic Testing in Latin America
- Author
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Lam-Chung César Ernesto, MD, Elizondo Ochoa Álvaro, MD, Segura Kato Yayoi, MSc, Silva-Serrano Juanita, MD, Tusié Luna María Teresa, MD, PhD, and Paloma Almeda-Valdes, MD, PhD
- Subjects
diabetes mellitus ,maturity onset ,maturity-onset diabetes of the young ,type 2 ,glucokinase ,Diseases of the endocrine glands. Clinical endocrinology ,RC648-665 - Abstract
Objective: To describe a case of maturity-onset diabetes of the young (MODY) to highlight the importance of a correct diabetes diagnosis. Methods: We describe a Mexican family misdiagnosed with T1D and T2D. Results: A 36-year-old woman with diabetes and adverse outcomes during 2 pregnancies had been diagnosed with T2D 10 years ago. Genetic testing was performed due to clinical and family history, which showed a pathogenic heterozygous variant c.544G>T (p.Val182Leu) in the GCK gene. This mutation was also confirmed in most of the family members who had been diagnosed with diabetes. Conclusion: This case highlights the need for a correct diabetes classification. Reassessment of diabetes etiology is justified, especially in individuals with unclear clinical presentation or when family history is suggestive.
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- 2021
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4. Functional synthetic Antennapedia genes and the dual roles of YPWM motif and linker size in transcriptional activation and repression
- Author
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Papadopoulos, D. K., primary, Resendez-Perez, D., additional, Cardenas-Chavez, D. L., additional, Villanueva-Segura, K., additional, Canales-del-Castillo, R., additional, Felix, D. A., additional, Funfschilling, R., additional, and Gehring, W. J., additional
- Published
- 2011
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5. A low pre-existing anti-NS1 humoral immunity to DENV is associated with microcephaly development after gestational ZIKV exposure.
- Author
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Castro-Trujillo S, Mejía WR, Segura K, Castro-Meneses J, Vega R, Salgado D, Fonseca CE, Ortiz ÁM, Perdomo-Celis F, Bosch I, and Narváez CF
- Subjects
- Humans, Female, Pregnancy, Adult, Male, Colombia epidemiology, Young Adult, Infant, Child, Preschool, Adolescent, Zika Virus Infection immunology, Zika Virus Infection complications, Microcephaly immunology, Microcephaly virology, Antibodies, Viral blood, Zika Virus immunology, Viral Nonstructural Proteins immunology, Immunity, Humoral, Dengue Virus immunology, Immunoglobulin M blood, Immunoglobulin G blood, Pregnancy Complications, Infectious immunology, Pregnancy Complications, Infectious virology
- Abstract
Background: Gestational Zika virus (ZIKV) infection is associated with the development of congenital Zika syndrome (CZS), which includes microcephaly and fetal demise. The magnitude and quality of orthoflavivirus-specific humoral immunity have been previously linked to the development of CZS. However, the role of ZIKV NS1-specific humoral immunity in mothers and children with prenatal ZIKV exposure and CZS remains undefined. In addition, considering that most of the at-risk population lives in dengue virus (DENV)-endemic areas, it is not clear what is the association between pre-existing DENV NS1-specific humoral immunity and CZS., Methods: Here, we studied 328 mothers and children with a clinical diagnosis and seropositivity for ZIKV infection during pregnancy, included during the 2015-2016 ZIKV epidemic in Colombia. We also performed clinical evaluation and pediatric neurological follow-up. The relative levels of circulating NS1-specific IgM and IgG against ZIKV and DENV were evaluated in mothers and children, and the association with the development of microcephaly was analyzed., Results: DENV and ZIKV IgG-NS1 antibodies in pregnant women were placentally transferred, and this passage and its duration in children depended on the maternal levels of the antibodies. We reported that higher concentrations of pre-existing DENV, but not ZIKV IgG-NS1 antibodies, were associated with a reduced risk of CZS-related microcephaly. Also, we observed that the IgM-NS1 response in infants is long-term and has a minor association with poor outcomes., Conclusions: The development of microcephaly in children prenatally exposed to ZIKV is associated with low plasma levels of placentally transferred, pre-existing DENV IgG-NS1 antibodies. These data are compatible with a protective role of anti-NS1 IgG antibodies against ZIKV infection during pregnancy and highlight the promising role of NS1 as an orthoflavivirus vaccine target in high-risk populations., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2025 Castro-Trujillo et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
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- 2025
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6. Cytokine profiles and their correlation with clinical and blood parameters in rheumatoid arthritis and systemic lupus erythematosus.
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Duarte-Delgado NP, Segura K, Gómez O, Pulido S, Tovar-Sánchez C, Bello-Gualtero JM, Fernández-Ávila DG, Amado-Garzón SB, Romero-Sanchez C, Cacciatore S, and Rodríguez C LS
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- Humans, Female, Male, Adult, Middle Aged, Biomarkers blood, Case-Control Studies, Aged, Arthritis, Rheumatoid blood, Lupus Erythematosus, Systemic blood, Cytokines blood
- Abstract
The abnormal biological activity of cytokines and their imbalance are implicated in developing rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). Cytokine levels were measured in RA and SLE patients and compared to healthy controls using the Wilcoxon rank sum test and Kruskal-Wallis test. The relationship between cytokine levels and blood and clinical parameters was assessed using Spearman's correlation test. Compared to healthy controls, both RA and SLE patients exhibited elevated levels of GM-CSF, CX3CL1, IFN-α2, IL-12p70, IL-17A, TNF-α, IL-1β, and IFN-γ, which is evidence of their shared inflammatory signature. IL-2 levels were elevated exclusively in RA patients, while MCP-1 and IL-10 were uniquely increased in SLE patients. Notably, TNF-α showed the most significant increase in SLE patients. IL-4 was elevated in SLE patients with nephritis, correlating with IL-6, IL-10, sCD40L, and IL-8, suggesting B cell involvement in lupus nephritis. The negative correlation between CX3CL1 and TNF-α with HDL in RA and SLE respectively, highlights the potential association of these inflammatory markers with cardiovascular risk. These findings underscore the complex cytokine interplay in RA and SLE. CX3CL1 emerges as a potential therapeutic target for RA, while TNF-α and IL-4 show promise as therapeutic targets for SLE., (© 2024. The Author(s).)
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- 2024
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7. Multiplex PCR for simultaneous genotyping of kdr mutations V410L, V1016I and F1534C in Aedes aegypti (L.).
- Author
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Villanueva-Segura K, Ponce-Garcia G, Lopez-Monroy B, Mora-Jasso E, Perales L, Gonzalez-Santillan FJ, Ontiveros-Zapata K, Davila-Barboza JA, and Flores AE
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- Animals, Genes, Insect, Genotyping Techniques methods, Insect Proteins genetics, Mosquito Vectors genetics, Mutation, Pyrethrins, Aedes genetics, Insecticide Resistance genetics, Multiplex Polymerase Chain Reaction methods, Voltage-Gated Sodium Channels genetics
- Abstract
Background: Knockdown resistance (kdr) is the main mechanism that confers resistance to pyrethroids and DDT. This is a product of non-synonymous mutations in the voltage-gated sodium channel (vgsc) gene, and these mutations produce a change of a single amino acid which reduces the affinity of the target site for the insecticide molecule. In Mexico, V410L, V1016I and F1534C mutations are common in pyrethroid-resistant Aedes aegypti (L.) populations., Methods: A multiplex PCR was developed to detect the V410L, V1016I and F1534C mutations in Ae. aegypti. The validation of the technique was carried out by DNA sequencing using field populations previously characterized for the three mutations through allele-specific PCR (AS-PCR) and with different levels of genotypic frequencies., Results: The standardized protocol for multiplex end-point PCR was highly effective in detecting 15 genotypes considering the three mutations V410L, V1106I and F1534C, in 12 field populations of Ae. aegypti from Mexico. A complete concordance with AS-PCR and DNA sequencing was found for the simultaneous detection of the three kdr mutations., Conclusions: Our diagnostic method is highly effective for the simultaneous detection of V410L, V1016I and F1534C, when they co-occur. This technique represents a viable alternative to complement and strengthen current monitoring and resistance management strategies against Ae. aegypti.
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- 2020
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8. Impact of deltamethrin selection on kdr mutations and insecticide detoxifying enzymes in Aedes aegypti from Mexico.
- Author
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Contreras-Perera Y, Ponce-Garcia G, Villanueva-Segura K, Lopez-Monroy B, Rodríguez-Sanchez IP, Lenhart A, Manrique-Saide P, and Flores AE
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- Aedes drug effects, Aedes genetics, Aedes metabolism, Animals, Esterases drug effects, Esterases metabolism, Genes, Insect, Glutathione Transferase drug effects, Glutathione Transferase metabolism, Insect Control, Insecticides pharmacology, Mosquito Vectors drug effects, Mosquito Vectors genetics, Mosquito Vectors metabolism, Mutation, Oxidoreductases drug effects, Oxidoreductases metabolism, Vascular Endothelial Growth Factor Receptor-2 drug effects, Insecticide Resistance genetics, Nitriles pharmacology, Pyrethrins pharmacology, Vascular Endothelial Growth Factor Receptor-2 genetics
- Abstract
Background: Insecticide resistance is a serious problem for vector control programmes worldwide. Resistance is commonly attributed to mutations at the insecticide's target site or increased activity of detoxification enzymes., Methods: We determined the knockdown concentration (KC
50 ) and lethal concentration (LC50 ) of deltamethrin in six natural populations of adult Aedes aegypti from southeastern Mexico. These populations were then selected over five generations using the LC50 from the preceding generation that underwent selection, and the heritability of deltamethrin resistance was quantified. For each generation, we also determined the frequency of the kdr alleles L410, I1016 and C1534, and the levels of activity of three enzyme families (α- and β-esterases, mixed-function oxidases and glutathione S-transferases (GST)) associated with insecticide detoxification., Results: There was an increase in KC50 and LC50 values in the subsequent generations of selection with deltamethrin (FS5 vs FS0 ). According to the resistance ratios (RRs), we detected increases in LC50 ranging from 1.5 to 5.6 times the values of the parental generation and in KC50 ranging from 1.3-3.8 times the values of the parental generation. Triple homozygous mutant individuals (tri-locus, LL/II/CC) were present in the parental generations and increased in frequency after selection. The frequency of L410 increased from 1.18-fold to 2.63-fold after selection with deltamethrin (FS5 vs FS0 ) in the populations analyzed; for I1016 an increase between 1.19-fold to 2.79-fold was observed, and C1534 was fixed in all populations after deltamethrin selection. Enzymatic activity varied significantly over the generations of selection. However, only α- esterase activity remained elevated in multiple populations after five generations of deltamethrin selection. We observed an increase in the mean activity levels of GSTs in two of the six populations analyzed., Conclusions: The high levels of resistance and their association with high frequencies of kdr mutations (V410L, V1016I and F1534C) obtained through artificial selection, suggest an important role of these mutations in conferring resistance to deltamethrin. We highlight the need to implement strategies that involve the monitoring of kdr frequencies in insecticide resistance monitoring and management programmes.- Published
- 2020
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9. Report of Chikungunya Virus in Wild Populations of Aedes aegypti in Guerrero State, Mexico.
- Author
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Ponce-García G, Flores-Suarez AE, Villanueva-Segura K, Lopez-Rodriguez M, Dzul F, Lopez-Monroy B, and Rodriguez-Sanchez I
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- Aedes growth & development, Animals, Female, Larva growth & development, Larva virology, Male, Mexico, Mosquito Vectors growth & development, Polymerase Chain Reaction, Aedes virology, Chikungunya virus isolation & purification, Mosquito Vectors virology
- Abstract
We detected vertical transmission of chikungunya virus (CHIKV) in wild populations of Aedes aegypti from San Marcos, Guerrero, Mexico, with real-time reverse transcriptase-polymerase chain reaction. A total of 20 pools (1-11 specimens/pool) of larvae, male, and female mosquitoes were tested. We report the detection of CHIKV in 2 of 11 larval pools, 4 of 5 male pools, and 1 of 4 female pools, from field-collected mosquitoes.
- Published
- 2018
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