Bibliografias temáticas / Gd00

Literatura científica selecionada sobre o tema "Gd00"

Autor: Grafiati
Publicado: 26 de julho de 2024

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Artigos de revistas sobre o assunto "Gd00"

1

Stenhouse, Claire, Peter Tennant, W. Colin Duncan e Cheryl J. Ashworth. "Doppler ultrasound can be used to monitor umbilical arterial blood flow in lightly sedated pigs at multiple gestational ages". Reproduction, Fertility and Development 30, n.º 11 (2018): 1402. http://dx.doi.org/10.1071/rd17298.

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Doppler ultrasound was performed under moderate sedation (ketamine and azaperone) for 30 min to monitor umbilical arterial (UA) blood flow in one uterine horn of Large White × Landrace gilts (n = 23) at Gestational Days (GD) 30, 45, 60 and 90. Gilts were scanned before they were killed to examine relationships between litter size, sex ratio and five UA parameters (peak systolic velocity (PSV), end diastolic velocity (EDV), A/B (PSV to EDV) ratio, fetal heart rate (FHR) and resistance index (RI)). In gilts in which scans were obtained from all fetuses in the scanned horn, relationships between UA parameters, and fetal weight and sex were examined. A subset of gilts were sedated, scanned and recovered (SSR) earlier in gestation (GD30 or GD45) to assess the effects of sedation on later fetal development by comparison with control litters (no previous sedation). Temporal changes were observed in all UA parameters (P ≤ 0.001). At GD60 and GD90, FHR decreased with increasing duration of sedation (P ≤ 0.001). Sex ratio and fetal weight affected UA blood flow, whereas litter size and fetal sex did not. SSR at GD30 and GD45 was associated with decreased fetal weight at GD60 (P ≤ 0.001) and GD90 (P = 0.06) respectively, compared with controls. These results suggest maternal sedation during gestation affects fetal development, which should be investigated further. Measuring UA blood flow in growth-restricted porcine fetuses throughout gestation may be feasible.
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Stenhouse, Claire, Charis O. Hogg e Cheryl J. Ashworth. "Association of foetal size and sex with porcine foeto-maternal interface integrin expression". Reproduction 157, n.º 4 (abril de 2019): 317–28. http://dx.doi.org/10.1530/rep-18-0520.

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Integrins regulate adhesion at the foeto-maternal interface by interacting with secreted phosphoprotein 1 (SPP1) and fibronectin (FN). It is hypothesised that impaired foetal growth of ‘runt’ piglets is linked to altered integrin signalling at the foeto-maternal interface. Placental and endometrial samples associated with the lightest and closest to mean litter weight (CTMLW) (gestational day (GD18, 30, 45, 60 and 90), of both sex (GD30, 45, 60 and 90) (n = 5–8 litters/GD), Large White × Landrace conceptuses or foetuses were obtained. The mRNA expression of the integrin subunits (ITG) ITGA2, ITGAV, ITGB1, ITGB3, ITGB5, ITGB6, ITGB8, SPP1 and FN was quantified by qPCR. Temporal changes in mRNA expression were observed, with different profiles in the two tissues. Endometrial ITGB1 (P ≤ 0.05, GD45) and SPP1 (P ≤ 0.05, all GD combined and GD60) expression was decreased in samples supplying the lightest compared to the CTMLW foetuses. Placentas supplying female foetuses had decreased expression of ITGB6 (GD45, P ≤ 0.05) and FN (GD90, P ≤ 0.05) compared to those supplying male foetuses. Endometrial samples supplying females had increased ITGB3 (P ≤ 0.05, GD60) and FN (P ≤ 0.05, GD30) expression and decreased SPP1 (P ≤ 0.05, GD60) expression compared to male foetuses. Correlations between mean within-gilt mRNA expression and percentage prenatal survival, number of live foetuses or conceptuses and percentage male foetuses were observed. This study has highlighted novel and dynamic associations between foetal size, sex and integrin subunit mRNA expression at the porcine foeto-maternal interface. Further studies should be performed to improve the understanding of the mechanisms behind these novel findings.
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Stenhouse, Claire, Charis O. Hogg e Cheryl J. Ashworth. "Novel relationships between porcine fetal size, sex, and endometrial angiogenesis†". Biology of Reproduction 101, n.º 1 (23 de abril de 2019): 112–25. http://dx.doi.org/10.1093/biolre/ioz068.

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Abstract It is hypothesized that growth restriction occurs due to inadequate vascularization of the feto-maternal interface. Evidence exists for sexual dimorphism in placental function although associations between fetal sex and the endometrium remain poorly investigated. This study investigated the relationship between porcine fetal size, sex and endometrial angiogenesis at multiple gestational days (GD). Endometrial samples supplying the lightest and closest to mean litter weight (CTMLW), male and female Large White X Landrace conceptuses or fetuses were obtained at GD18, 30, 45, 60, and 90 (n = 5–9 litters/GD). Immunohistochemistry for CD31 revealed a greater number of blood vessels in endometrium supplying females compared to those supplying males at GD45. Endometrial samples supplying the lightest fetuses had fewer blood vessels (GD60) and uterine glands (GD90) compared to those supplying the CTMLW fetuses. Quantitative PCR revealed decreased CD31 (GD60), HPSE and VEGFA (GD90) expression, alongside increased HIF1A (GD45) expression in endometrial samples supplying the lightest compared to the CTMLW fetuses. At GD30, PTGFR, CD31, and VEGFA mRNA expression was increased in samples supplying female fetuses compared to those supplying male fetuses. Intriguingly, decreased expression of ACP5, CD31, HIF1A, and VEGFA mRNAs was observed at GD60 in endometrial samples supplying female fetuses compared to those supplying their male littermates. Endothelial cell branching assays demonstrated impaired endothelial cell branching in response to conditioned media from endometrial samples supplying the lightest and female fetuses compared with the CTMLW and male fetuses, respectively. This study has highlighted that endometrial tissues supplying the lightest and female fetuses have impaired angiogenesis when compared with the CTMLW and female fetuses respectively. Importantly, the relationship between fetal size, sex and endometrial vascularity is dynamic and dependent upon the GD investigated.
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4

Knapczyk-Stwora, Katarzyna, Malgorzata Durlej-Grzesiak, Renata E. Ciereszko, Marek Koziorowski e Maria Slomczynska. "Antiandrogen flutamide affects folliculogenesis during fetal development in pigs". REPRODUCTION 145, n.º 3 (março de 2013): 265–76. http://dx.doi.org/10.1530/rep-12-0236.

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Androgen deficiency during prenatal development may affect the expression of genes involved in the folliculogenesis regulation. In order to study the effect of antiandrogen on fetal ovarian development, pregnant gilts were injected with flutamide (for 7 days, 50 mg/kg body weight per day) or corn oil (control groups) starting on gestation days 43 (GD50), 83 (GD90), or 101 (GD108). The obtained fetal ovaries were fixed for histology and immunohistochemistry or frozen for real-time PCR. Morphological evaluation, TUNEL assay, and expression of selected factors (Ki-67, GATA binding transcription factor 4 (GATA4), E-Cadherin and tumor necrosis factor α (TNFα)) were performed. On GD90 and GD108, ovaries following flutamide administration showed a higher number of egg nests and lower number of follicles than those in respective control groups. An increased mRNA and protein expression of Ki-67 was observed in flutamide-treated groups compared with controls on GD50 and GD108 but decreased expression was found on GD90. In comparison to control groups a higher percentage of TUNEL-positive cells was shown after flutamide exposure on GD50 and GD90 and a lower percentage of apoptotic cells was observed on GD108. These data were consistent with changes in TNF (TNFα) mRNA expression, which increased on GD90 and decreased on GD108. E-cadherin mRNA and protein expression was upregulated on GD50 and downregulated on GD90 and GD108. In conclusion diminished androgen action in porcine fetal ovaries during mid- and late gestation leads to changes in the expression of genes crucial for follicle formation. Consequently, delayed folliculogenesis was observed on GD90 and GD108. It seems however that androgens exhibit diverse biological effects depending on the gestational period.
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Agoh, Charly Fernand, Mahaman Bachir Saley, Tacra Thierry Lekadou, Saraka Didier Martial Yao, Pierre-Marie Janvier Coffi, N’klo François Hala e Bi Tié Albert Goula. "Impacts of climate variability on the production of Dwarf x Tall and Tall x Tall coconut (Cocos nucifera L.) palm hybrids planted on the coast in Côte d'Ivoire". International Journal of Biological and Chemical Sciences 17, n.º 2 (31 de maio de 2023): 451–74. http://dx.doi.org/10.4314/ijbcs.v17i2.14.

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The Ivorian coast is the main coconut production area where agriculture is mainly rainfed. However, in this area, climate variability poses a great threat to the growth and sustainable development of agriculture. This study aimed at highlighting the impacts of climate variability on the production of the most popular Dwarf x Tall and Tall x Tall coconut palm hybrids in the world. It is based on the evaluation of the production of the hybrids from statistical tests (ANOVA, STUDENT's T-test at 5%) and the results of the standardized precipitation and evapotranspiration indices (SPEI) during the period of 2009 to 2018 of the study area. The results obtained revealed that the NJM×GOA+ hybrid was significantly differentiated by its good production potential of bunches (10 bunches), fruits (151 nuts) and copra (3.69 t). The maximum fruit production per year was observed in the Dwarf × Tall hybrids (101 nuts). The highest mass productions of copra per tree and copra per hectare were recorded in the Tall × Tall hybrids. The maximum productions of the ten hybrids were observed in 2012, 2015 and 2018 and the lowest in 2014 and 2017. Productions gradually increase or remain stable for consecutive wet years (2009 to 2011) prior to harvest. The onset of drought in one year (2012, 2013, 2015, 2016) and pronounced for two consecutive dry years (2012 to 2013 and 2015 to 2016) prior to harvest significantly decrease the level of production. These cumulative effects of drought are most pronounced in NRC×GRL+, NRM×GTN, NJM×GD001, NJM×GD002, and NJM×GD003 hybrids. NJM×GOA+, GVT×GTN, GSL×GTN, NRM×GVT, and NVS×GVT hybrids are developing abilities to express themselves better under this climate variability. They could be taken into account in the crop improvement program and proposed to growers to improve the yield of coconut trees under rainfed conditions.
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Kleinbussink, Chanta’l, Flora Kiss, Morton Frankson, Andrew Y. Finlay e Jui Vyas. "GD09 GD10 Impact of chronic conditions on the quality of life of patients and their family members". British Journal of Dermatology 191, Supplement_1 (28 de junho de 2024): i165. http://dx.doi.org/10.1093/bjd/ljae090.348.

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Abstract This study aimed to determine impact of chronic conditions on the quality of life (QoL) of patients and their family members. A cross-sectional correlational study was undertaken in the Bahamas and Wales, involving patients aged > 18 years with psoriasis, acne, eczema and hidradenitis suppurativa. Patients in both countries completed the Dermatology Life Quality Index (DLQI). In the Bahamas, children (aged 4–16 years) also completed the Children’s DLQI (CDLQI). Family members (> 18 years) completed the Family Reported Outcome Measure (FROM)-16 and the Family DLQI (FDLQI). Patients in the Bahamas with other chronic conditions (rheumatoid arthritis, diabetes mellitus and chronic kidney disease) completed the WHOQOL-BREF, and children (4–16 years) completed the KINDLR. Their family members (> 18 years) completed FROM-16. The 436 participants were from Wales (20%) and the Bahamas (80%). Of the 203 adult patients, 74% identified as Black, 21% as White and 5% as mix, multiple ethnic groups or other. Of 218 family members, 77% identified as Black, 19% as White, and 4% as mix, multiple ethnic groups or other. In Wales the mean DLQI score was 13.8 (SD 7.7, n = 44), indicating very large impact on QoL. Family members’ FROM-16 mean score was 8.7 (SD 6.7, n = 44), indicating moderate effect on QoL. The FDLQI mean score was 7.7 (SD 6.7, n = 44). DLQI and FDLQI scores [rsp = 0.61, P (two-tailed) = 0.01, n = 88] and DLQI and FROM-16 scores [rsp = 0.59, P (two-tailed) = 0.01, n = 88] were strongly positively correlated. FROM-16 and FDLQI scores were very strongly positively correlated [rsp = 0.74, P (two-tailed) = 0.01, n = 44]. In the Bahamas the mean DLQI score was 7.4 (SD 5, n = 34), indicating moderate impact on QoL. The FROM-16 mean score for family members of adult patients was 3.5 (SD 4.5, n = 45), indicating small effect on QoL. The FDLQI mean score was 3.0 (SD 3.7, n = 45). DLQI and FDLQI scores [rsp = 0.34, P (two-tailed) = 0.05, n = 68] were moderately positively correlated. FROM-16 and FDLQI scores were strongly positively correlated [rsp = 0.61, P (two-tailed) < 0.001, n = 45]. Children’s mean CDLQI score was 7 (SD 4.3, n = 11), indicating moderate effect on QoL. Their family members’ mean FROM-16 score was 3.1 (SD 2.4, n = 11), indicating small impact. The FDLQI mean score was 3.6 (SD 4.4, n = 11). The CDLQI and FDLQI [rsp = 0.60, P (two-tailed) = 0.05, n = 22] and CDLQI and FROM-16 personal/social domain scores [rsp = 0.67, P (two-tailed) = 0.03, n = 22] were strongly positively correlated. FROM-16 and FDLQI scores [rsp = 0.72, P (two-tailed) < 0.01, n = 11] were strongly positively correlated. The mean WHOQOL-BREF for other chronic conditions was 56.4 (SD 8.9, n = 125) and the mean KINDLR score was 74.5 (SD 12.5, n = 4). Their family members’ FROM-16 mean score was 6.3 (SD 5.5, n = 129), indicating small impact on QoL. The WHOQOL-BREF and FROM-16 scores [rsp = −0.28, P (two-tailed) = 0.001] were weakly negatively correlated. Validated QoL questionnaires can be used to measure impact on QoL in different countries. Family members experience a substantial impact on QoL. Skin disease can impact the QoL of family members just as much as family members of people with other noncutaneous chronic diseases. The data provide a challenge to clinicians to identify severely affected family members and assist them further.
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7

Strawn, Monica, Joao G. N. Moraes, Timothy J. Safranski e Susanta K. Behura. "Sexually Dimorphic Transcriptomic Changes of Developing Fetal Brain Reveal Signaling Pathways and Marker Genes of Brain Cells in Domestic Pigs". Cells 10, n.º 9 (16 de setembro de 2021): 2439. http://dx.doi.org/10.3390/cells10092439.

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In this study, transcriptomic changes of the developing brain of pig fetuses of both sexes were investigated on gestation days (GD) 45, 60 and 90. Pig fetal brain grows rapidly around GD60. Consequently, gene expression of the fetal brain was distinctly different on GD90 compared to that of GD45 and GD60. In addition, varying numbers of differentially expressed genes (DEGs) were identified in the male brain compared to the female brain during development. The sex of adjacent fetuses also influenced gene expression of the fetal brain. Extensive changes in gene expression at the exon-level were observed during brain development. Pathway enrichment analysis showed that the ionotropic glutamate receptor pathway and p53 pathway were enriched in the female brain, whereas specific receptor-mediated signaling pathways were enriched in the male brain. Marker genes of neurons and astrocytes were significantly differentially expressed between male and female brains during development. Furthermore, comparative analysis of gene expression patterns between fetal brain and placenta suggested that genes related to ion transportation may play a key role in the regulation of the brain-placental axis in pig. Collectively, the study suggests potential application of pig models to better understand influence of fetal sex on brain development.
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8

Iqbal, Majid, William Gibb e Stephen G. Matthews. "Corticosteroid Regulation of P-Glycoprotein in the Developing Blood-Brain Barrier". Endocrinology 152, n.º 3 (1 de março de 2011): 1067–79. http://dx.doi.org/10.1210/en.2010-1227.

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The early fetal brain is susceptible to teratogens in the maternal circulation, because brain microvessel expression of drug efflux transporter, P-glycoprotein (P-gp), is very low. However, there is a dramatic up-regulation of brain microvessel P-gp in late gestation. This study investigated the role of cortisol and dexamethasone in this up-regulation of fetal brain microvessel P-gp expression. Primary brain endothelial cell (BEC) cultures derived from gestational d (GD)40, GD50, GD65 (term, ∼68 d) and postnatal d 14 male guinea pigs were treated with varying doses (10−8 to 10−5m) of cortisol, dexamethasone, and aldosterone. After treatment, P-gp function was assessed using calcein-acetoxymethyl ester (P-gp substrate; 1 μm for 1 h) and measuring BEC accumulation of calcein. Corticosteroid treatment of BECs derived from postnatal d 14 resulted in increased P-gp activity. BECs derived from GD65 (near term) responded similarly, but these cells were extremely sensitive to the effects of mineralocorticoid receptor agonists (cortisol and aldosterone). BECs derived from GD50 displayed dose-dependent increases in P-gp function with dexamethasone (P < 0.05) and a trend towards increased function with cortisol. Cells derived from GD40 were unresponsive to all treatments. In conclusion, P-gp function in BECs is more responsive to glucocorticoids (GCs) in late gestation. Therefore, the late gestational surge in fetal plasma GCs, which parallels the increase in brain microvessel P-gp expression, may contribute to this P-gp up-regulation. Further, synthetic GCs (administered to pregnant women at risk of preterm delivery) may increase the protective capacity of the developing fetal blood-brain barrier, depending on the timing of GC exposure.
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Damani, Namiz, Adam Gold, S. Krishnakumar e Paul Devakar Yesudian. "GD04 Erythroderma: uncovering the culprit". British Journal of Dermatology 191, Supplement_1 (28 de junho de 2024): i162—i163. http://dx.doi.org/10.1093/bjd/ljae090.343.

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Abstract A middle-aged man presented to clinic in South India with a 1-year history of a widespread rash involving his whole body. There was no pre-existing skin condition. It appeared to be a possible inflammatory dermatosis and he was prescribed fixed-dose combination topical agents, including topical steroids (clobetasol propionate), topical antibiotics (gentamicin and neomycin), and a combination of an oral antifungal (terbinafine) and topical antifungals (clotrimazole and miconazole). On examination, there were numerous large, scaly plaques coalescing to an erythrodermic morphology. He was reviewed by two dermatologists, who commenced him on a reducing course of prednisolone. Due to nonresponse he was then started on ciclosporin 2.5 mg kg−1 per day. However, the condition continued to worsen. A skin biopsy was taken; this demonstrated hyperkeratosis with multiple fungal filaments consistent with extensive dermatophytosis. Over the past decade, there has been a significant increase in recalcitrant dermatophytosis seen in India. A recent multicentre study notes that the inaccessibility of adequate antifungal susceptibility testing results in excessively long treatment durations with poorly selected drugs and experimentation in medication dosage and frequency, which in turn contribute to drug resistance and the emergence of new strains (Ebert A, Monod M, Salamin K et al. Alarming India-wide phenomenon of antifungal resistance in dermatophytes: a multicentre study. Mycoses 2020; 63: 717–28). Trichophyton indotineae (previously known as Trichophyton mentagrophytes genotype VIII) is a newly identified dermatophyte species and has outpaced Trichophyton rubrum as the major causative agent of tinea cruris, tinea corporis and tinea faciei in India (Uhrlaß S, Verma SB, Gräser Y et al. Trichophyton indotineae – an emerging pathogen causing recalcitrant dermatophytoses in India and worldwide – a multidimensional perspective. J Fungi 2022; 8: 757). It has since spread to many countries globally. It is particularly problematic due to its resistance to terbinafine as a result of point mutations within the squalene epoxidase gene. Clinically, T. indotineae infections are extensive, involving multiple sites with symptoms of pain, pruritis and localized burning. Infection characteristically follows a chronic and relapsing clinical course, with an average duration of 9 months. The drug of choice is itraconazole 100 mg twice daily for 4–8 weeks, with fluconazole and griseofulvin as second-line options. Adequate hygiene measures are crucial to avert transmission and reinfection. This case highlights the issue of recalcitrant dermatophytosis in the subcontinent, emphasizing the need for improved antifungal susceptibility testing and judicious use of medications to curb drug resistance.
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Roselli, Charles E., Radhika C. Reddy, Charles T. Estill, Melissa Scheldrup, Mary Meaker, Fred Stormshak e Hernán J. Montilla. "Prenatal Influence of an Androgen Agonist and Antagonist on the Differentiation of the Ovine Sexually Dimorphic Nucleus in Male and Female Lamb Fetuses". Endocrinology 155, n.º 12 (1 de dezembro de 2014): 5000–5010. http://dx.doi.org/10.1210/en.2013-2176.

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The ovine sexually dimorphic nucleus (oSDN) is 2 times larger in rams than in ewes. Sexual differentiation of the oSDN is produced by testosterone exposure during the critical period occurring between gestational day (GD)60 and GD90 (term, 147 d). We tested the hypothesis that testosterone acts through the androgen receptor to control development of the male-typical oSDN. In experiment 1, pregnant ewes received injections of vehicle, androgen receptor antagonist flutamide, or nonaromatizable androgen dihydrotestosterone (DHT) propionate during the critical period. Fetuses were delivered at GD135. Both antagonist and agonist treatments significantly reduced mean oSDN volume in males but had no effects in females. Experiment 2, we analyzed the effect of treatments on the fetal hypothalamic-pituitary-gonadal axis to determine whether compensatory changes in hormone secretion occurred that could explain the effect of DHT. Pregnant ewes were injected with vehicle, flutamide, or DHT propionate from GD60 to GD84, and fetuses were delivered on GD85. Flutamide significantly increased LH and testosterone in males, whereas DHT significantly decreased both hormones. In females, LH was unaffected by flutamide but significantly reduced by DHT exposure. DHT significantly decreased pituitary gonadotropin and hypothalamic kisspeptin mRNA expression in males and females. These results suggest that androgen receptor mediates the effect of testosterone on oSDN masculinization, because this process was blocked by the androgen receptor antagonist flutamide in eugonadal males. In contrast, the reduction of oSDN volume observed after DHT exposure appears to be mediated by a negative feedback mechanism exerted on the hypothalamus to reduce LH and testosterone secretion. The reduced androgen exposure most likely accounted for the decreased oSDN volume. We conclude that, during the critical period, the male reproductive axis in long gestation species, such as sheep, is sufficiently developed to react to perturbations in serum androgens and mitigate disruptions in brain masculinization.
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Livros sobre o assunto "Gd00"

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Kasahara, K., ed. Recent Plate Movements and Deformation. Washington, D. C.: American Geophysical Union, 2013. http://dx.doi.org/10.1029/gd020.

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Stein, Seth, e Jeffrey T. Freymueller, eds. Plate Boundary Zones. Washington, D. C.: American Geophysical Union, 2002. http://dx.doi.org/10.1029/gd030.

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Transportation Safety Board of Canada. Runway excursion, Calm Air International Ltd., Hawker Siddeley HS 748-2A C-GD0P, Thompson, Manitoba, 20 January 1994. Hull, Quebec: Transportation Safety Board of Canada, 1994.

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4

NA. Advertising: Principles& Ebiz Mrkt Gd01 Pkg. Addison Wesley Longman, 2000.

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5

Pearson. Backpack Literature&pearson Gd08 MLA Upd Pk. Pearson, 2009.

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Pearson. Quick Access& Mycomplab W/Ebk&pearson Gd08. Pearson, 2009.

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Pearson. Writers Guide Research& Pearsn Gd08 MLA Upd. Prentice Hall, 2009.

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Pearson. Longman Writer& Mycomplab W/Ebk&pearsn Gd08. Pearson, 2009.

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Westwood College GD100: Introduction to Graphic Design. Thomson Customer Publishing, 2003.

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10

NA. Fundmtls Nursg: Concp& Clin& Drug Gd07& Fluids. Addison Wesley Longman, 2006.

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Capítulos de livros sobre o assunto "Gd00"

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Sheahan, Timothy, Damon Deming, Eric Donaldson, Raymond Pickles e Ralph Baric. "Resurrection of an “Extinct” SARS-CoV Isolate GD03 from LATE 2003". In Advances in Experimental Medicine and Biology, 547–50. Boston, MA: Springer US, 2006. http://dx.doi.org/10.1007/978-0-387-33012-9_100.

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Liu, X. Y., J. A. Barclay, M. Földeàki, B. R. Gopal, R. Chahine e T. K. Bose. "Magnetic Properties of Amorphous Gd70(Fe, Ni)30 and Dy70(Fe, Ni)30 Alloys". In Advances in Cryogenic Engineering Materials, 431–38. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4757-9059-7_57.

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Trabalhos de conferências sobre o assunto "Gd00"

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Aguilar-Reyes, E., C. León-Patiño e K. Rangel-Arreola. "Elaboration of Solid Nano-Structured Electrolytes of Ce0?85??Gd0?15M?O2?d (x = 0, 0.03, 0.05; M = Sm, La) and Measurement of Ionic Conductivity at Intermediate Temperatures". In MS&T19. TMS, 2019. http://dx.doi.org/10.7449/2019mst/2019/mst_2019_690_699.

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Aguilar-Reyes, E., C. León-Patiño e K. Rangel-Arreola. "Elaboration of Solid Nano-Structured Electrolytes of Ce0?85??Gd0?15M?O2?d (x = 0, 0.03, 0.05; M = Sm, La) and Measurement of Ionic Conductivity at Intermediate Temperatures". In MS&T19. TMS, 2019. http://dx.doi.org/10.7449/2019/mst_2019_690_699.

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