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1.
Plants (Basel) ; 13(1)2023 Dec 26.
Artigo em Inglês | MEDLINE | ID: mdl-38202386

RESUMO

Pea (Pisum sativum L.), like most legumes, forms mutualistic symbioses with nodule bacteria and arbuscular mycorrhizal (AM) fungi. The positive effect of inoculation is partially determined by the plant genotype; thus, pea varieties with high and low symbiotic responsivity have been described, but the molecular genetic basis of this trait remains unknown. Here, we compare the symbiotically responsive breeding line 'Triumph' of grain pea with its parental cultivars 'Vendevil' (a donor of high symbiotic responsivity) and 'Classic' (a donor of agriculturally valuable traits) using genome and transcriptome sequencing. We show that 'Triumph' inherited one-fourth of its genome from 'Vendevil', including the genes related to AM and nodule formation, and reveal that under combined inoculation with nodule bacteria and AM fungi, 'Triumph' and 'Vendevil', in contrast to 'Classic', demonstrate similar up-regulation of the genes related to solute transport, hormonal regulation and flavonoid biosynthesis in their roots. We also identify the gene PsGLP2, whose expression pattern distinguishing 'Triumph' and 'Vendevil' from 'Classic' correlates with difference within the promoter region sequence, making it a promising marker for the symbiotic responsivity trait. The results of this study may be helpful for future molecular breeding programs aimed at creation of symbiotically responsive cultivars of pea.

2.
Microbiol Resour Announc ; 11(4): e0102321, 2022 Apr 21.
Artigo em Inglês | MEDLINE | ID: mdl-35297685

RESUMO

Rhizobium ruizarguesonis (Rhizobium leguminosarum) strain 1TK341 was isolated from pink nodules of fixation-negative mutant line P61 of pea (Pisum sativum L.) grown in soil. Here, we report the draft genome sequence of the strain.

3.
Microbiol Resour Announc ; 10(11)2021 Mar 18.
Artigo em Inglês | MEDLINE | ID: mdl-33737366

RESUMO

Plants can form various beneficial associations with soil microorganisms, such as associations with plant growth-promoting bacteria (PGPB). In this work, we report the full-genome sequence of the component of Mysorin biopreparation, identified as Microbacterium hominis, consisting of a single 3.5-Mbp circular chromosome.

4.
Niger J Clin Pract ; 23(12): 1767-1771, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33355833

RESUMO

Alveolar bone loss subsequent to long-term edentulism and trauma may be severe and treatment plan is always an esthetic and functional challenge. Implant supported hybrid prosthesis is widely regarded as an effective treatment option for patients with excessive and irregular bone loss. However, implant placement is occasionally impossible without surgical procedures in such cases. This case report presents rehabilitation of 19-year-old maxillary anterior edentulous male patient with maxillary anterior bone defect and excessive cross-bite anterior closure with multidisciplinary approach. The patient was rehabilitated with implant supported hybrid prosthesis with Malo Bridge design following autogeneous iliac bone augmentation, teeth leveling with orthodontic treatment, and surgical placement of three implants. Esthetics, pleasing phonetics and function were achieved as desired with this treatment option and no complications were observed.


Assuntos
Perda do Osso Alveolar , Aumento do Rebordo Alveolar , Implantes Dentários , Arcada Edêntula , Procedimentos de Cirurgia Plástica , Adulto , Perda do Osso Alveolar/cirurgia , Transplante Ósseo , Prótese Dentária Fixada por Implante , Humanos , Arcada Edêntula/cirurgia , Masculino , Maxila/cirurgia , Resultado do Tratamento , Adulto Jovem
5.
Niger J Clin Pract ; 23(9): 1328-1331, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32913176

RESUMO

It is possible to rehabilitate fully edentulous patients with implantsupported fixed or removable prostheses; however, implantsupported fixed prostheses are the gold standard for patients who not prefer to use removable dentures. This case report, prosthetic rehabilitation of a completely edentulous young patient with an implantsupported fixed hybrid prosthesis using the "Malo Bridge" technique is described. A 18 years old male patient was referred to the clinic with complaints of tooth loss, aesthetics, function, and phonetic. A total of 5 implants were placed in both the jaws. Considering that screw holes may cause aesthetic problems due to the Class III occlusion, these problems have been solved with the implant-supported hybrid prosthesis called Malo bridge. With the Malo Bridge design, the patient's aesthetic, functional and phonetic loss was eliminated, patient comfort and quality of life were improved, and patient expectations were met. It is a viable treatment option to rehabilitate completely edentulous jaws with a cross relationship and increase interarch distance using Malo Bridge to support a fixed prosthesis.


Assuntos
Implantes Dentários , Prótese Dentária Fixada por Implante , Arcada Edêntula/reabilitação , Maxila/cirurgia , Qualidade de Vida , Perda de Dente/psicologia , Adolescente , Planejamento de Prótese Dentária , Retenção de Dentadura/instrumentação , Humanos , Arcada Edêntula/cirurgia , Masculino , Fonética , Radiografia Panorâmica , Resultado do Tratamento
6.
J. pediatr. (Rio J.) ; 83(4): 335-342, July-Aug. 2007. tab
Artigo em Português | LILACS | ID: lil-459889

RESUMO

OBJETIVO: Investigar os fatores de risco associados à hipertensão arterial primária em adolescentes. MÉTODOS: Estudo caso-controle de base ambulatorial com adolescentes, de 12 a 20 anos incompletos, todos provenientes do Núcleo de Estudos da Saúde do Adolescente da Universidade Estadual do Rio de Janeiro. O estado nutricional foi avaliado através do índice de massa corporal. Obteve-se ainda a medida da circunferência abdominal, estatura, história familiar de hipertensão arterial, peso ao nascer e desenvolvimento puberal. A análise foi elaborada através de regressão logística não condicional. RESULTADOS: Participaram 91 casos e 182 controles. O índice de massa corporal mostrou-se associado à hipertensão. A estatura mostrou associação positiva com hipertensão apenas em meninas. Não se evidenciou associação entre desenvolvimento puberal e peso ao nascer com hipertensão arterial na adolescência. Por outro lado, a história familiar, principalmente quando ambos os pais são hipertensos, apresentou forte associação, tanto em meninos (OR = 13,32; IC95 por cento 2,25-78,94), como em meninas (OR = 11,35; IC95 por cento 1,42-90,21). CONCLUSÕES: Em nosso estudo, sobrepeso, obesidade e história familiar de hipertensão (pai e mãe hipertensos) foram os principais fatores de risco para o desenvolvimento de hipertensão arterial em adolescentes.


OBJECTIVE: To investigate the risk factors associated with essential arterial hypertension in adolescents. METHODS: A case-control, outpatients-based study of adolescents, aged 11 to 19 years, all treated at the Center for Studies into Adolescent Health (Núcleo de Estudos da Saúde do Adolescente) at Universidade Estadual do Rio de Janeiro. Nutritional status was assessed by means of body mass index. Data were also obtained on waist circumference, height, family history of arterial hypertension, birth weight and pubertal development. The analysis was performed using unconditional logistic regression. RESULTS: The study investigated 91 cases and 182 controls. Body mass index was associated with hypertension. Height had a positive association with hypertension only among the girls. There was no evidence of an association between pubertal development or birth weight with arterial hypertension in adolescence. In contrast, family history, particularly when both parents had hypertension, exhibited a robust association, both among the boys (OR = 13.32; 95 percentCI 2.25-78.94), and the girls (OR = 11.35; 95 percentCI 1.42-90.21). CONCLUSIONS: In our study, overweight, obesity and family history of hypertension (father and mother with hypertension) were the principal risk factors for arterial hypertension in adolescents.


Assuntos
Adolescente , Adulto , Criança , Feminino , Humanos , Masculino , Hipertensão/epidemiologia , Obesidade/epidemiologia , Índice de Massa Corporal , Brasil/epidemiologia , Estudos de Casos e Controles , Estudos Transversais , Hipertensão/diagnóstico , Hipertensão/etiologia , Obesidade/complicações , Obesidade/diagnóstico , Pais , Fatores de Risco , Fatores Socioeconômicos
7.
J Pediatr (Rio J) ; 83(4): 335-42, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17627321

RESUMO

OBJECTIVE: To investigate the risk factors associated with essential arterial hypertension in adolescents. METHOD: A case-control, outpatient-based study of adolescents aged 11 to 19 years treated at the Center for Studies into Adolescent Health (Núcleo de Estudos da Saúde do Adolescente) at the Universidade Estadual do Rio de Janeiro. Nutritional status was assessed by means of body mass index. Data were also obtained on waist circumference, height, family history of arterial hypertension, birth weight and pubertal development. The analysis was performed using unconditional logistic regression. RESULTS: The study investigated 91 cases and 182 controls. Body mass index was associated with hypertension. Height had a positive association with hypertension only among the girls. There was no evidence of an association between pubertal development or birth weight with arterial hypertension in adolescence. In contrast, family history, particularly when both parents had hypertension, exhibited a robust association, both among the boys (OR = 13.32; 95%CI 2.25-78.94), and the girls (OR = 11.35; 95%CI 1.42-90.21). CONCLUSIONS: In our study, overweight, obesity and family history of hypertension (father and mother with hypertension) were the principal risk factors for arterial hypertension in adolescents.


Assuntos
Hipertensão/epidemiologia , Obesidade/epidemiologia , Adolescente , Adulto , Índice de Massa Corporal , Brasil/epidemiologia , Estudos de Casos e Controles , Criança , Estudos Transversais , Feminino , Humanos , Hipertensão/diagnóstico , Hipertensão/etiologia , Masculino , Obesidade/complicações , Obesidade/diagnóstico , Pais , Fatores de Risco , Fatores Socioeconômicos
8.
J Neurol Sci ; 214(1-2): 49-56, 2003 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-12972388

RESUMO

The human T-cell lymphotropic virus type 1 (HTLV-I) causes a neurological disease known as HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP) in a minority of infected individuals. Although other neurological outcomes have been described their prevalence is presently unknown. To evaluate the frequency and characteristics of neurological involvement in a population of HTLV-I-infected blood donors we investigated 196 HTLV-I positive and 196 negative blood donors from a blood center of Rio de Janeiro, Brazil. Individuals with abnormalities at the neurological examination were examined by three neurologists, and when pertinent, additional neurological investigations were performed. Descriptive analysis, Student's t-test and chi2 test were employed for statistical analysis. Neurological abnormalities were found in 71 (36.2%) of the HTLV-I positive blood donors and in only 29 (14.8%) of the HTLV-I negative donors (OR = 2.54, 95% CI = 1.67-3.59, p = 0.000002). Cases of myelopathy, motor neuron disease and myopathy were only found in the HTLV-I positive group. In addition, peripheral neuropathy (PN) was significantly more frequent in the positive group (p = 0.015). In summary, our data suggest that HTLV-I-infected individuals exhibit a wide variety of neurological manifestations apart from the classical picture of HAM/TSP.


Assuntos
Doadores de Sangue , Sistema Nervoso/fisiopatologia , Paraparesia Espástica Tropical/fisiopatologia , Adulto , Brasil , Feminino , Vírus Linfotrópico T Tipo 1 Humano/isolamento & purificação , Humanos , Masculino , Pessoa de Meia-Idade , Doença dos Neurônios Motores/epidemiologia , Doença dos Neurônios Motores/fisiopatologia , Doenças Musculares/epidemiologia , Doenças Musculares/fisiopatologia , Sistema Nervoso/patologia , Sistema Nervoso/virologia , Exame Neurológico , Paraparesia Espástica Tropical/sangue , Paraparesia Espástica Tropical/epidemiologia , Nervos Periféricos/patologia , Nervos Periféricos/fisiopatologia , Doenças do Sistema Nervoso Periférico/epidemiologia , Doenças do Sistema Nervoso Periférico/fisiopatologia , Prevalência
9.
Int J Cancer ; 101(1): 69-73, 2002 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-12209590

RESUMO

Somatic mutations in the TP53 gene are the most frequently observed genetic alterations in human malignancies, including breast cancer, which is one of the leading causes of death among women in Brazil. In our study, we determined the frequency and the pattern of TP53 mutations in malignant breast tumors from 120 patients living in Rio de Janeiro, Brazil. TP53 mutations were found in 20% of the tumors, which contained a diversity of mutation types: missense (62.5%), nonsense (8.3%), silent (4.2%), intronic (12.5%), insertion (4.2%) and deletion (8.3%). Of a total of 15 missense mutations, 4 were observed at Arg248 and 2 at Cys242, which are directly involved in DNA binding and in zinc binding, respectively. A subgroup of 51 patients was analyzed with respect to the relation between the presence of TP53 mutations and classical risk factors and with tumor and patient characteristics. For this analysis, we used logistic regression and, in order to obtain more precise confidence intervals, they were recalculated using a bootstrap resampling technique. Our results demonstrate that these mutations are not statistically associated with the risk factors or the patients' characteristics. However, the presence of TP53 mutations is strongly associated with the aggressiveness of the tumors, measured by Elston classification (OR = 11.97 and 95% CI of 2.24-307.05). This finding is in agreement with previous studies, which report the presence of TP53 mutations in tumors with poor prognosis. This correlation between tumor aggressiveness and TP53 mutations could be a crucial variable for the treatment and prognosis of breast cancer.


Assuntos
Neoplasias da Mama/genética , Neoplasias da Mama/patologia , Predisposição Genética para Doença/genética , Mutação/genética , Proteína Supressora de Tumor p53/genética , Adulto , Idoso , Consumo de Bebidas Alcoólicas , Brasil/epidemiologia , Neoplasias da Mama/epidemiologia , DNA de Neoplasias/genética , Feminino , Humanos , Pessoa de Meia-Idade , Razão de Chances , Reação em Cadeia da Polimerase , Polimorfismo Conformacional de Fita Simples , Fumar
10.
Cad. saúde pública ; 12(1): 53-9, jan.-mar. 1996. tab
Artigo em Inglês | LILACS | ID: lil-173602

RESUMO

Realizou-se um estudo ecológico com base em dados de 10 capitais brasileiras e, através de análise de regressäo linear, examinou-se a associaçäo entre dieta e as taxas de mortalidade para as principais localizaçöes de câncer, entre adultos com 30 anos ou mais. As taxas de mortalidade ajustadas por idade variavam de 2,4 a 3,3 vezes entre as capitais. Consumo de energia associou-se positivamente com câncer de colon, pulmäo e esôfago (p menor ou igual 0,02 em cada associaçäo). Mortalidade por câncer de colon associou-se positivamente com o consumo de gordura, ovos, álcool, mate, cereais e vegetais (p menor ou igual 0,01); câncer de pulmäo associou-se ao consumo de mate e cereias (p menor ou igual 0,05); câncer de estômago associou-se positivamente com ovos (p=0,04) e, negativamente , com o consumo de fibras, frutas e vitaminas A e C (p menor ou igual 0,05). Câncer de esôfago foi positivamente associado com consumo de gordura e mate (p menor ou igual 0,05) e, negativamente, com vitamina A (p=0,02); câncer de próstata associou-se negativamente com vitamina C (p=0,007). Câncer de mama näo se associou a nenhum dos fatores estudados. A importante variaçäo nas taxas de mortalidade por câncer no Brasil podem ser parcialmente associadas as variaçöes em componentes da dietas ou a fatores a ale associados.


Assuntos
Inquéritos sobre Dietas , Neoplasias/mortalidade , Ecologia , Neoplasias/epidemiologia
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