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| 1 | Cytotoxicity of Captafol in Mammalian Cells显示文摘The cytotoxicity of captafol, a phthalimide-derived fungicide, was evaluated in IB-RS-2 cells. Captafol at 0. 12-1 .0μg/ml blocks the cell multiplication. This effect is concentrationdependent, only partially rcversible and the degree of inhibition increases with time. The synthesis of DNA and RNA is inhibited in parallel by increasing concentrations of the | M. A. LA R. RODRIGUES AND M. D’ANGELO (Instituto Biologico, Caixa Postal 7119, 01064-970, Sao Paulo, SP Brazil) | 1994 | Biomedical and Environmental Sciences1994，7，3： | 2 |
| 2 | Peripheral Blood Mononuclear Cells Immunophenotyping in Pulmonary Tuberculosis Patients before and after Treatment显示文摘 | Warly Barcelos Olindo Assis Martins‐Filho Tania Mara Pinto Dabés Guimar?es Márcio Hamilton Prostzner Oliveira Silvana Spíndola‐de‐Miranda Beatriz Nascimento Carvalho Vicente de Paulo Coelho Peixoto Toledo | 2006 | Microbiology and Immunology2006，，： | 1 |
| 3 | Is there a correlation between structure and anticoagulant action of sulfated galactans and sulfated fucans显示文摘 | Mariana SP Fabio RM Paulo ASM | 2002 | Glycoblology2002，12，10： | 1 |
| 4 | Oxygen therapy,continuous positive airway pressure or noninvasive believe positive pressure ventilation in the treatment of acute cardiogenic pulmonary edema显示文摘 | PAULO S BRAZIL SP | 2001 | Arq Bras Cardio12001，76，5： | 1 |
| 5 | Oxygen therapy,Continuous positive airway pressure,or noninvasive bilevel positive pressure ventilation in the treatment of acute cardiogenic pulmonary edema 显示文摘 | Paulo S Brazil SP | 2001 | Arq Bras Cardiol2001，76，： | 1 |
| 6 | Long-long limb Roux-en-Y gastric by-pass is more efficacious in treatment of type 2 diabetes and lipid dis-orders in super-obese patients 显示文摘 | Jose SP Carlos AS Paulo BP | 2008 | Surg Obes Relat Dis2008，4，4： | 1 |
| 7 | Oral graft vs host disease:An immune system disorder in hematopoietic cell transplantation显示文摘Graft vs host disease(GVHD) is a complication of patients who are treated by hematopoietic cell transplantation.National Institutes of Health in 2005 by Working Group on Diagnosis and Staging Consensus Development Project on Criteria for Clinical Trials in Chronic GVHD(cGVHD) established 2 principal categories of oral GVHD, acute and chronic. The oral mucosa may be the first site of manifestation of the disease. Clinical diagnosis needs to be confirmed by a biopsy of oral mucosa and minor salivary glands. Microscopic results have played a major role in the diagnosis and management of acute and chronic oral GVHD. Development of second malignancies is the greatest risk of oral cGVHD patients, mostly regarding squamous cell carcinoma. The focus of oral GVHD therapy is to improve symptoms and maintain oral function. The aim of this review article is to update the information on the oral GVHD in its clinical, microscopic features and their complications. | Paulo Sérgio da Silva Santos Cassia Maria Fischer Rubira Héliton Spíndola Antunes Fabio Luiz Coracin Cristiane Miranda França | 2015 | World Journal of Stomatology2015，4，2： | 1 |
| 8 | Protein-losing enteropathy after the Fontan operation显示文摘 | Preto R Paulo SP Brazil SP | 2006 | Arq Bras Cardiol2006，87，： | 1 |
| 9 | Use of hybrid chitosan membranes and human mesenchymal stem cells from the Wharton jelly of umbilical cord for promoting nerve regeneration in an axonotmesis rat model显示文摘Many studies have been dedicated to the development of scaffolds for improving post-traumatic nerve regeneration. The goal of this study was to assess the effect on nerve regeneration, associating a hybrid chitosan membrane with non-differentiated human mesenchymal stem cells isolated from Wharton's jelly of umbilical cord, in peripheral nerve reconstruction after crush injury. Chromosome analysis on human mesenchymal stem cell line from Wharton's jelly was carried out and no structural alterations were found in metaphase. Chitosan membranes were previously tested in vitro, to assess their ability in supporting human mesenchymal stem cell survival, expansion, and differentiation. For the in vivo testing, Sasco Sprague adult rats were divided in 4 groups of 6 or 7 animals each:Group 1, sciatic axonotmesis injury without any other intervention (Group 1-Crush); Group 2, the axonotmesis lesion of 3 mm was infiltrated with a suspension of 1 250-1 500 human mesenchymal stem cells (total volume of 50 μL) (Group 2-CrushCell); Group 3, axonotmesis lesion of 3 mm was enwrapped with a chitosan type III membrane covered with a monolayer of non-differentiated human mesenchymal stem cells (Group 3-CrushChitIIICell) and Group 4, axonotmesis lesion of 3 mm was enwrapped with a chitosan type III membrane (Group 4-CrushChitIII). Motor and sensory functional recovery was evaluated throughout a healing period of 12 weeks using sciatic functional index, static sciatic index, extensor postural thrust, and withdrawal reflex latency. Stereological analysis was carried out on regenerated nerve fibers. Results showed that infiltration of human mesenchymal stem cells, or the combination of chitosan membrane enwrapment and human mesenchymal stem cell enrichment after nerve crush injury provide a slight advantage to post-traumatic nerve regeneration. Results obtained with chitosan type III membrane alone confirmed that they significantly improve post-traumatic axonal regrowth and may represent a very promising clinical tool in peripheral nerve reconstructive surgery. Yet, umbilical cord human mesenchymal stem cells, that can be expanded in culture and induced toform several different types of cells, may prove, in future experiments, to be a new source of cells for cell therapy, including targets such as peripheral nerve and muscle. | Andrea Gärtner Tiago Pereira Maria Joāo Simōes Paulo AS Armada-da-Silva Miguel L França Rosa Sousa Simone Bompasso Stefania Raimondo Yuki Shirosaki Yuri Nakamura Satoshi Hayakawa Akiyoshi Osakah Beatriz Porto Ana Lúcia Luís Artur SP Varejāo Ana Colette Maurício | 2012 | Neural Regeneration Research2012，7，29： | 1 |
| 10 | Structure and anticoagulant activity of a fucosylated chondroitin sulfate from echinoderm显示文摘 | PAULO ASM MARIANA SP MAURO SGP | 1996 | Biol Chem1996，271，23： | 1 |
| 11 | Oxygen therapy, continuous positive airway pressure,or noninvasive bilevel positive pressure ventilation in the treatment of acute cardiogenic pulmonary edema 显示文摘 | Paulo S Brazil SP | 2001 | Arq Bras Cardiol2001，76，5： | 1 |
| 12 | 食物中添加ι-卡尼汀对大鼠肝代谢ι-丙氨酸的作用(英文) | Vilma A F G GAZOLA, Gisele LOPES, Daniel M LIMEIRA, Ricardo GALLETTO, Sebastiao GAZOLA, Rui CURI, Roberto B BAZOTTE (State University of Maringa, SUM, Department of Pharmacy and Pharmacology, Maringa, PR, 87020-900 University of Sao Paulo, Sao Paulo, SP, 05508-900, Brazil) | 2002 | Acta Pharmacologica Sinica2002，23，4： | 0 |
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