Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 15 de 15
Filtrar
Más filtros












Base de datos
Intervalo de año de publicación
1.
J Periodontol ; 2024 Jun 17.
Artículo en Inglés | MEDLINE | ID: mdl-38884702

RESUMEN

BACKGROUND: To date, the clinical evidence regarding the effectiveness of alveolar ridge preservation (ARP) in restricting alveolar bone height and width change after extraction at periodontally compromised molar extraction sockets still remains controversial. This retrospective cohort study aims to evaluate the effect of ARP in molars extracted for periodontal reasons. METHODS: Retrospective data were collected from patient electronic records from January 2019 to December 2023. Patients with Stage III/IV periodontitis who underwent extraction of molars for periodontal reasons were screened for eligibility. The outcomes included the horizontal and vertical dimensions of alveolar bone. The need for additional augmentation procedure during implantation was also evaluated. A linear regression model was used to adjust for known confounders. RESULTS: A total of 80 sockets were included in this study, of which 27 sockets received ARP therapy after extraction while 53 sockets experienced natural healing (NH). ARP resulted in significantly less bone height change in the periodontally compromised molar sites compared to the NH group (p < 0.001). In sockets displaying a height disparity of >2 mm between the buccal and palatal/lingual walls, the ARP group exhibited advantageous outcomes in terms of ridge width change, surpassing the NH group (p = 0.004). Moreover, the percentage for additional augmentation was significantly reduced in the ARP compared to the NH group (p = 0.006). Age, sex, smoking, jaw, location, and buccal wall thickness did not show any significant effect on bone height change. CONCLUSION: ARP had benefits on limiting ridge resorption subsequent to molar extraction for periodontal reasons.

2.
Front Cell Infect Microbiol ; 12: 892610, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35846745

RESUMEN

Autophagy is an immune homeostasis process induced by multiple intracellular and extracellular signals. Inflammation is a protective response to harmful stimuli such as pathogen microbial infection and body tissue damage. Porphyromonas gingivalis infection elicits both autophagy and inflammation, and dysregulation of autophagy and inflammation promotes pathology. This review focuses on the interaction between autophagy and inflammation caused by Porphyromonas gingivalis infection, aiming to elaborate on the possible mechanism involved in the interaction.


Asunto(s)
Autofagia , Porphyromonas gingivalis , Autofagia/fisiología , Homeostasis , Humanos , Inflamación , Porphyromonas gingivalis/fisiología
3.
Br J Nutr ; 128(9): 1711-1719, 2022 11 14.
Artículo en Inglés | MEDLINE | ID: mdl-34789344

RESUMEN

A 30-d feeding trial was conducted to investigate effects of dietary eucommia ulmoides leaf extract (ELE) on growth performance, activities of digestive enzymes, antioxidant capacity, immunity, expression of inflammatory factors and feeding-related genes of large yellow croaker larvae. Five micro-diets were formulated with supplementation of 0 g kg-1 (the control), 5 g kg-1 (0·5 %), 10 g kg-1 (1·0 %) and 20 g kg-1 (2·0 %) of ELE, respectively. Results showed that the best growth performance was found in larvae fed the diet with 1·0 % ELE. Furthermore, ELE supplementation significantly increased the npy expression at 1·0 % dosage, while increased ghrelin in larvae at 0·5 % dosages. The activity of leucine aminopeptidase in larvae fed the diet with 1·0 % ELE was significantly higher than the control, while alkaline phosphatase was significantly upregulated in larvae fed the diet with 2·0 % ELE. A clear increase in total antioxidant capacity in larvae fed the diet with 1·0 % ELE was observed, whereas catalase activity was significantly higher in 1·0 % and 2·0 % ELE supplementation compared with the control. Larvae fed the diet with 1·0 % ELE had a significantly higher activities of lysozyme, total nitric oxide synthase and nitric oxide content than the control. Moreover, transcriptional levels of cox-2, il-1ß and il-6 were remarkably downregulated by the supplementation of 0·5-1·0 % ELE. This study demonstrated that the supplementation of 1·0 % ELE in diet could increase the growth performance of large yellow croaker larvae probably by promoting expression of feeding-related genes, enhancing antioxidant capacity and immunity and inhibiting expression of inflammatory factors.


Asunto(s)
Eucommiaceae , Perciformes , Animales , Antioxidantes/metabolismo , Eucommiaceae/metabolismo , Citocinas/metabolismo , Larva , Dieta , Extractos Vegetales/metabolismo , Alimentación Animal/análisis , Suplementos Dietéticos
4.
BMC Evol Biol ; 20(1): 25, 2020 02 11.
Artículo en Inglés | MEDLINE | ID: mdl-32046636

RESUMEN

BACKGROUND: Taste is fundamental to diet selection in vertebrates. Genetic basis of sweet taste receptor in the shaping of food habits has been extensively studied in mammals and birds, but scarcely studied in fishes. Grass carp is an excellent model for studying vegetarian adaptation, as it exhibits food habit transition from carnivory to herbivory. RESULTS: We identified six sweet taste receptors (gcT1R2A-F) in grass carp. The four gcT1R2s (gcT1R2C-F) have been suggested to be evolved from and paralogous to the two original gcT1R2s (gcT1R2A and gcT1R2B). All gcT1R2s were expressed in taste organs and mediated glucose-, fructose- or arginine-induced intracellular calcium signaling, revealing they were functional. In addition, grass carp was performed to prefer fructose to glucose under a behavioral experiment. Parallelly, compared with gcT1R2A-F/gcT1R3 co-transfected cells, gcT1R2C-F/gcT1R3 co-transfected cells showed a higher response to plant-specific fructose. Moreover, food habit transition from carnivory to herbivory in grass carp was accompanied by increased gene expression of certain gcT1R2s. CONCLUSIONS: We suggested that the gene expansion of T1R2s in grass carp was an adaptive strategy to accommodate the change in food environment. Moreover, the selected gene expression of gcT1R2s might drive the food habit transition from carnivory to herbivory in grass carp. This study provided some evolutional and physiological clues for the formation of herbivory in grass carp.


Asunto(s)
Adaptación Biológica/genética , Carpas/genética , Herbivoria/genética , Receptores Acoplados a Proteínas G/genética , Gusto/genética , Aclimatación/genética , Animales , Carpas/clasificación , Carpas/fisiología , Conducta Alimentaria , Proteínas de Peces/genética , Amplificación de Genes/fisiología , Expresión Génica , Mamíferos/genética , Papilas Gustativas/metabolismo
5.
Fish Physiol Biochem ; 42(4): 1093-105, 2016 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-26820140

RESUMEN

The aim of the present study was to explore the effect of waterborne zinc (control, 0.85, 2.20, 3.10 mg/l, respectively) exposure on lipid deposition and metabolism in the hepatopancreas and muscle of grass carp Ctenopharyngodon idella. The lipid content, Zn accumulation, and the activities and expression levels of several enzymes involved in lipid metabolism were determined in hepatopancreas and muscle. Waterborne Zn exposure reduced growth performance and increased Zn accumulation in both tested tissues. In hepatopancreas, Zn exposure increased lipid content, the activities of lipogenic enzymes, such as 6PGD, G6PD, ME, ICDH and FAS, as well as the mRNA expression level of G6PD, 6PGD, ICDH, FAS and SREBP-1. But the activity of CPT I and the mRNA expression of HSL, CPT Iα1a, CPT Iα2a and PPARα were down-regulated by Zn exposure. In contrast, in muscle, waterborne Zn exposure decreased lipid deposition, activities of 6GPD, ICDH and ME, as well as the mRNA expression level of G6PD, ICDH, ME, FAS and SREBP-1. However, the activity of CPT I as well as the mRNA expression level of PPARα, HSL, CPT Iα2a, CPT Iα1b and CPT Iß were up-regulated by Zn exposure. Our results indicate that waterborne Zn increases lipid content by up-regulating lipogenesis and down-regulating lipolysis in hepatopancreas. But, in muscle, waterborne Zn reduces lipid accumulation by up-regulating lipolysis and down-regulating lipogenesis. Differential patterns of lipid deposition, enzymatic activities and genes' expression indicate the tissue-specific regulatory mechanism in fish.


Asunto(s)
Carpas/metabolismo , Metabolismo de los Lípidos/efectos de los fármacos , Contaminantes Químicos del Agua/toxicidad , Zinc/toxicidad , Animales , Carpas/crecimiento & desarrollo , Hepatopáncreas/efectos de los fármacos , Hepatopáncreas/metabolismo , Metabolismo de los Lípidos/genética , Músculos/efectos de los fármacos , Músculos/metabolismo , Contaminantes Químicos del Agua/farmacocinética , Zinc/farmacocinética
6.
Fish Physiol Biochem ; 41(6): 1393-401, 2015 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-26170093

RESUMEN

The ontogeny and kinetics of carnitine palmitoyltransferase I (CPT I) were investigated in hepatopancreas and muscle throughout four developmental stages (newly hatched larvae, 1-month-old juvenile, 3-month-old, and 6-month-old, respectively) of grass carp Ctenopharyngodon idella. In hepatopancreas, the maximal velocity (Vmax) significantly increased from hatching to 1-month-old grass carp and then gradually declined at 6-month-old grass carp. In muscle, CPT I activity was the highest at 1-month-old grass carp, nearly twofold higher than that at hatching (P < 0.05). The Michaelis constant (Km) value was also the highest for 1-month-old in both tested tissues. Carnitine concentrations (FC, AC and TC) were the lowest for 3-month-old grass carp and remained relatively constant in both tissues from fish under the other developmental stages. The FC concentration in hepatopancreas and muscle at four developmental stages were less than the respective Km, indicating that grass carp required supplemental carnitine in their food to ensure that CPT I activity was not constrained by carnitine availability.


Asunto(s)
Carnitina O-Palmitoiltransferasa/metabolismo , Carpas/metabolismo , Hepatopáncreas/enzimología , Músculo Esquelético/enzimología , Animales , Carnitina/metabolismo , Cinética , Larva/metabolismo , Metabolismo de los Lípidos
7.
ACS Appl Mater Interfaces ; 7(20): 10952-6, 2015 May 27.
Artículo en Inglés | MEDLINE | ID: mdl-25923539

RESUMEN

A protective polydopamine (PDA) coating is applied to core-shell microcapsule surfaces by the polymerization of dopamine monomers. A neutral aqueous solution and the addition of an oxidant (i.e., ammonium persulfate) are crucial for microcapsule survival and the initiation of PDA polymerization, respectively. The resulting PDA coating is a dense and uniform layer approximately 50 nm thick. The PDA protective coating significantly increases capsule stability at an elevated temperature (180 °C) and in a variety of organic solvents and acidic/basic solutions that otherwise lead to deflation and loss of the core content of uncoated microcapsules.


Asunto(s)
Materiales Biomiméticos/química , Cápsulas/química , Materiales Biocompatibles Revestidos/química , Indoles/química , Polímeros/química , Solventes/química , Estabilidad de Medicamentos , Calor , Ensayo de Materiales , Tamaño de la Partícula , Porosidad
8.
Nat Commun ; 4: 1543, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23443571

RESUMEN

An important trend in electronics involves the development of materials, mechanical designs and manufacturing strategies that enable the use of unconventional substrates, such as polymer films, metal foils, paper sheets or rubber slabs. The last possibility is particularly challenging because the systems must accommodate not only bending but also stretching. Although several approaches are available for the electronics, a persistent difficulty is in power supplies that have similar mechanical properties, to allow their co-integration with the electronics. Here we introduce a set of materials and design concepts for a rechargeable lithium ion battery technology that exploits thin, low modulus silicone elastomers as substrates, with a segmented design in the active materials, and unusual 'self-similar' interconnect structures between them. The result enables reversible levels of stretchability up to 300%, while maintaining capacity densities of ~1.1 mAh cm(-2). Stretchable wireless power transmission systems provide the means to charge these types of batteries, without direct physical contact.

9.
Artículo en Inglés | MEDLINE | ID: mdl-22079418

RESUMEN

The peroxisome proliferator-activated receptors (PPARs) are ligand-dependent transcription factors belonging to the nuclear receptor family, and can regulate various genes involved in lipid metabolism. The aim of the present study was to investigate the tissue distribution patterns of PPARs and their ligand specificities in grass carp. We cloned three PPAR isotypes of the species and evaluated their organ distribution patterns using real-time PCR. Through analyzing the deduced amino acid sequences identities between the products cloned in grass carp and those described in other species, we concluded that the same type of PPAR amino acid sequences in different species were with high homology, and different subtypes of PPAR in the same species were with low homology. The mRNA constitutive expression level of PPARα predominated in the liver, but was weak in other tested tissues. PPARß was present in all tested organs, and particularly abundant in heart, liver and muscle. PPARγ was only detected in the liver, and to a lesser extent in brain, muscle and visceral adipose tissue. Grass carp were intraperitoneally injected with 50 mg kg(-1) body mass (bw) dose of clofibrate, 42 mg kg(-1) bw dose of 2-bromo palmitate and 1 mg kg(-1) bw dose of 15-deoxy-Δ(12,14) prostaglandin J2 (15d-PGJ2), respectively, and the relative changes of the mRNA abundance of PPARs in liver were analyzed by real-time PCR. Clofibrate was able to increase the expressions of both PPARα and ß, but was not able to for PPARγ. 2-bromo palmitate could affect the expressions of both PPARß and γ, but was not able to for PPARα. 15d-PGJ2 was able to induce PPARß expression, but PPARα and γ were not enhanced. Consequently, these results indicate that clofibrate, 2-bromo palmitate and 15d-PGJ2 could be applied as the activators of grass carp PPARs.


Asunto(s)
Carpas/genética , Proteínas de Peces/genética , Perfilación de la Expresión Génica , Receptores Activados del Proliferador del Peroxisoma/genética , Animales , Clofibrato/farmacología , Expresión Génica/efectos de los fármacos , Hígado/efectos de los fármacos , Hígado/metabolismo , PPAR alfa/clasificación , PPAR alfa/genética , PPAR gamma/clasificación , PPAR gamma/genética , PPAR-beta/clasificación , PPAR-beta/genética , Palmitatos/farmacología , Receptores Activados del Proliferador del Peroxisoma/clasificación , Filogenia , Prostaglandina D2/análogos & derivados , Prostaglandina D2/farmacología , ARN Mensajero/genética , ARN Mensajero/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
10.
Fish Shellfish Immunol ; 29(1): 117-25, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20211737

RESUMEN

Selenium-binding protein (SEBP) is believed to play crucial role in controlling the oxidation/reduction in the physiological processes. In this study, the cDNA of selenium-binding protein from abalone Haliotis discus hannai Ino (HdhSEBP) was cloned by homology cloning and rapid amplification of cDNA ends (RACE) technique. The full length of HdhSEBP cDNA was 2071 bp, consisting of a 5' untranslated region (UTR) of 55 bp, a 3' UTR of 522 bp, and an open reading frame (ORF) of 1494 bp. The deduced protein has 497 amino acid residues with a calculated molecular mass of 55.6 kDa and a predicted isoelectric point of 5.47. BLAST analysis reveals that HdhSEBP shares high identities with other known SEBPs from mammal, bird, fish and mollusk, etc. The mRNA expression patterns of HdhSEBP in hepatopancreas and haemocytes were measured by real-time PCR in abalone fed with nine different diets containing graded levels of selenium (0, 1 and 50 mg kg(-1)), iron (0, 65 and 1300 mg kg(-1)) and zinc (0, 35 and 700 mg kg(-1)) for 20 weeks, respectively. The results showed that the expression of the HdhSEBP mRNA increased and reached the maximum at optimal dietary selenium (1 mg kg(-1)), iron (65 mg kg(-1)) and zinc (35 mg kg(-1)), respectively. Deficient or excessive level of dietary selenium, iron or zinc, respectively, leaded to significant depression of HdhSEBP mRNA. It is concluded that the expression levels of HdhSEBP are affected by dietary selenium, iron or zinc.


Asunto(s)
Gastrópodos/inmunología , Proteínas de Unión al Selenio/inmunología , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Clonación Molecular , Gastrópodos/genética , Hemocitos/inmunología , Hepatopáncreas/inmunología , Hierro/inmunología , Datos de Secuencia Molecular , ARN/química , ARN/genética , Técnica del ADN Polimorfo Amplificado Aleatorio , Selenio/inmunología , Proteínas de Unión al Selenio/genética , Alineación de Secuencia , Zinc/inmunología
11.
Mar Pollut Bull ; 58(11): 1643-8, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19665739

RESUMEN

To investigate the role of detoxification-related liver genes in amnesic shellfish poisoning toxin metabolism, red sea bream Pagrus major were exposed to domoic acid (DA, 2mugg(-1) wet weight) for 24h. Hepatic mRNA expression levels of AHR, ARNT, CYP1 and GSTs were determined by semi-quantitative RT-PCR. The cytosolic factors aryl hydrocarbon receptor (AHR) and aryl hydrocarbon receptor nuclear translocator (ARNT) mRNA levels of DA exposure group were substantially enhanced by 113.3% and 90.9%, respectively. Consistent with this result, the phase I xenobiotic metabolizing enzyme (XME) cytochrome P-450 1A (CYP1A) was significantly induced. In contrast, the transcriptions of three major phase II XME glutathione S-transferases as well as heat shock protein 70 were not significantly affected by DA exposure. These results suggest a possible role of CYP1A after DA exposure in the toxin metabolism of marine fish, possibly through the AHR/ARNT signaling pathway.


Asunto(s)
Citocromo P-450 CYP1A1/metabolismo , Ácido Kaínico/análogos & derivados , Hígado/efectos de los fármacos , Toxinas Marinas/toxicidad , Dorada/metabolismo , Factores de Transcripción/metabolismo , Amnesia/inducido químicamente , Amnesia/metabolismo , Animales , Translocador Nuclear del Receptor de Aril Hidrocarburo/clasificación , Translocador Nuclear del Receptor de Aril Hidrocarburo/genética , Translocador Nuclear del Receptor de Aril Hidrocarburo/metabolismo , Clonación Molecular , Citocromo P-450 CYP1A1/clasificación , Citocromo P-450 CYP1A1/genética , Ácido Kaínico/toxicidad , Hígado/enzimología , Hígado/metabolismo , Filogenia , ARN Mensajero/metabolismo , Receptores de Hidrocarburo de Aril/metabolismo , Dorada/genética , Intoxicación por Mariscos , Transcripción Genética/efectos de los fármacos
12.
Biol Pharm Bull ; 32(4): 583-8, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19336888

RESUMEN

Cardiotoxin III (CTX III), a 60-amino acid basic polypeptide isolated from Naja venom, showed potential therapeutic activity toward cancer cells. Here we report that CTX III inhibited proliferation of human leukemia K562 cells by G2/M phase arresting and apoptosis which was associated with the activation of caspase-8 and cytochrome c release as well as the p38 and c-Jun N-terminal protein kinase (JNK) phosphorylation signaling pathway. We further demonstrated that daily administration of CTX III for 2 d to chicken chorioallantoic membrane (CAM) bearing tumours derived from the CAM at E10 administration of K562 cells resulted in inhibition of the tumours in vivo. Importantly, this in vivo inhibition was also associated with caspase-8 activation and cytochrome c release. Our results suggest that CTX III-induced apoptosis is mediated via the p38 and JNK pathway as well as the caspase-8-dependent Bid-Bax pathway in human K562 cells.


Asunto(s)
Apoptosis/efectos de los fármacos , Proteínas Cardiotóxicas de Elápidos/farmacología , Venenos Elapídicos/farmacología , Proteínas Quinasas JNK Activadas por Mitógenos/fisiología , Proteínas Quinasas p38 Activadas por Mitógenos/fisiología , Animales , Western Blotting , Caspasa 8/fisiología , Ciclo Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Embrión de Pollo , Membrana Corioalantoides/citología , Citocromos c/metabolismo , Humanos , Células K562 , Proteína Quinasa 1 Activada por Mitógenos/fisiología , Proteína Quinasa 3 Activada por Mitógenos/fisiología , Transducción de Señal/efectos de los fármacos , Ensayos Antitumor por Modelo de Xenoinjerto
13.
Acta Pharmacol Sin ; 27(2): 184-92, 2006 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-16412268

RESUMEN

AIM: To clone cDNAs of thrombin-like enzymes (TLEs) from venom gland of Deinagkistrodon acutus and analyze the mechanisms by which their structural diversity arose. METHODS: Reverse transcription-polymerase chain reaction and gene cloning techniques were used, and the cloned sequences were analyzed by using bioinformatics tools. RESULTS: Novel cDNAs of snake venom TLEs were cloned. The possibilities of post-transcriptional recombination and horizontal gene transfer are discussed. A phylogenetic tree was constructed. CONCLUSION: The cDNAs of snake venom TLEs exhibit great diversification. There are several types of structural variations. These variations may be attributable to certain mechanisms including recombination.


Asunto(s)
ADN Complementario/genética , Trombina/genética , Venenos de Víboras/química , Viperidae , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Clonación Molecular , Datos de Secuencia Molecular , Filogenia , Alineación de Secuencia , Homología de Secuencia , Trombina/aislamiento & purificación , Viperidae/genética
14.
Acta Pharmacol Sin ; 25(3): 372-7, 2004 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15000893

RESUMEN

AIM: To clone the cDNA of a new member of snake venom C-type lectin-like proteins, to study its structure-function relationships and to achieve its recombinant production. METHODS: PCR primers were designed based on the homology and cDNA was amplified by RT-PCR using total RNA from snake venom gland as the template. The PCR products were cloned into the plasmid pGEM-T and sequenced. The deduced protein sequence was analyzed with some bioinformatic programs. A recombinant expression plasmid was constructed using pBAD-TOPO as vector and transformed into E.coli TOP10 competent cells. RESULTS: A novel cDNA sequence encoding akitonin beta was found and accepted by GenBank (accession number AF387100). Akitonin beta consists of a typical carbohydrate recognition domain (CRD) of C-type lectins, and it is homologous with other snake venom C-type lectin-like proteins. It was predicted to be a platelet antagonist. Upon induction with arabinose rAkitonin beta expressing in E coli was achieved at a high level (superior to 150 mg/L). The recombinant fusion protein exhibited inhibitory activities on rat platelet aggregation in vitro. CONCLUSION: A new member of snake venom C-type lectin-like proteins was discovered and characterized, and an efficient recombinant expression system was established for its production.


Asunto(s)
Agkistrodon , Venenos de Crotálidos/química , Lectinas Tipo C/química , Proteínas Recombinantes de Fusión/biosíntesis , Secuencia de Aminoácidos , Animales , Secuencia de Bases , ADN Complementario , Escherichia coli/genética , Escherichia coli/metabolismo , Datos de Secuencia Molecular , Agregación Plaquetaria/efectos de los fármacos , Inhibidores de Agregación Plaquetaria/farmacología , Ratas , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/farmacología , Análisis de Secuencia
15.
Zhonghua Zheng Xing Wai Ke Za Zhi ; 19(5): 325-7, 2003 Sep.
Artículo en Chino | MEDLINE | ID: mdl-15179866

RESUMEN

OBJECTIVE: To investigate the causes of complications of polyacrylamide hydrogel injection for facial plasty and reliable treatments. METHODS: Eight patients were included in the study. Some of them were examined by MRI. All the patients received surgical treatments. RESULTS: The injected polyacrylamide hydrogel was found in the superficial layer of the superficial temporal fasica, the loose connective tissue below the deep temporal fascia, the subcutaneous tissue or the orbicularis muscle. Polyacrylamide hydrogel injected into the superficial layer of the superficial temporal fascia could spread to the face along the SMAS. Polyacrylamide hydrogel injected into the loose connective tissue below the deep temporal fascia could spread down to the cheek. The patients' symptoms were relieved with the operation. Satisfactory results were obtained. CONCLUSION: Polyacrylamide hydrogel injection does not adapt to facial plasty. The reliability of polyacrylamide hydrogel injection for facial plasty is in doubt.


Asunto(s)
Resinas Acrílicas/efectos adversos , Cara/cirugía , Cirugía Plástica/efectos adversos , Adulto , Femenino , Humanos , Inyecciones/efectos adversos , Inyecciones/métodos , Persona de Mediana Edad , Cirugía Plástica/métodos , Resultado del Tratamiento
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...