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Indirect co-cultures of stem cells with chondrocytes for cartilage tissue engin...

Publicado em "Journal of Tissue Engineering and Regenerative Medicine", vol. 7, supp. 1 (2013) ; Mesenchymal Stem Cells (MSCs) have been recognized for their ability to differentiate into cells of different tissues such as bone, cartilage or adipose tissue, and therefore might be of interest for potential therapeutic strategies. These cells are induced to differentiate by growth factors supplementation in cult...

Tissue engineering as a remarkable tool for cartilage repair

Articular cartilage is a very specialized tissue with outstanding load-bearing capacity. It consists mainly of a dense extracellular matrix (ECM) with chondrocytes embedded on it. Cartilage has very low capacity of self-repair and regeneration after traumatic, degenerative or inflammatory injury. Current available surgical treatments for cartilage repair present several drawbacks, such as possible implant rejec...

Diagnóstico Citogenético em Líquidos Amnióticos Realizado entre 2000-2011 no Ce...

Introdução: O diagnóstico pré-natal citogenético efetuado em líquido amniótico é um método seguro e fiável para deteção de anomalias cromossómicas fetais, sendo habitualmente realizado a partir das 15 semanas de gestação. Obtêm-se resultados, em média, após 8-10 dias de cultura dos amniócitos. Objectivo: Apresentar a estatística dos resultados obtidos na análise citogenética de líquidos amnióticos realizada na ...

Diagnóstico Pré-natal de Síndrome de Wolf-Hirschhorn: a propósito de um caso

Introdução: O Síndrome de Wolf-Hirschhorn é uma patologia originada por uma deleção da região terminal do braço curto do cromossoma 4. O tamanho da deleção pode ser variável levando a um espectro alargado de manifestações clínicas. Em diagnóstico pré-natal (DPN), as alterações fetais mais frequentes incluem atraso do crescimento intra-uterino, lábio leporino e/ou fenda do palato e anomalias cardíacas. A prevalê...

Deleção cromossómica intersticial em 14q “de novo”: apresentação de um caso

Introdução: As deleções intersticiais são anomalias cromossómicas estruturais, desequilibradas, resultantes de dois pontos de quebra, frequentemente associadas a quadros clínicos anormais devido à perda de material genético ativo (eucromatina). As consequências fenotípicas dependem do segmento cromossómico perdido e do número de genes aí localizados. Material e Métodos: Os autores apresentam o caso de um indiv...

Clinical, cytogenetic and molecular findings of a “de novo” inv dup del (6q)

Introduction: Complex rearrangements resulting in inverted duplications contiguous to a terminal deletion (inv dup del) were first reported for the short arm of chromosome 8 in1976. Since then this type of structural anomaly has been described for an increasing number of chromosomes. In these rearrangements, the concomitant presence of a deletion and a duplication has important consequences in genotype-phenotyp...

Identification of a mosaic non-inherited small supernumerary ring chromosome 2:...

Introduction: The identification of supernumerary marker chromosomes (SMCs) derived from all the autosomes is currently possible, but rarely by conventional cytogenetics alone. Supernumerary ring chromosomes (SRCs) account for about 10% of these cases. SRCs derived from chromosome 2 are unusual, and there are only a few cases reported in the literature. The severity of the phenotype depends on the type of the m...

Interstitial deletion 15q21 and Prader-Willi like syndrome phenotype: Case report

Introduction: Chromosome 15q interstitial deletions not involving the Prader-Willi/Angelman region are uncommon and poorly characterized. Very few cases of different segmental losses involving the 15q21 region have been reported at cytogenetic level. All the described patients present with moderate to several mental retardation and characteristic facial dysmorphic features. Some authors compare the similarity b...

Influence of conditioned medium over the chondrogenic differentiation of adult ...

A- and B-modes echobiometry in cataractous and noncataractous eyes of English C...

A- and B-modes ultrasonographic changes in the thickness of various structures of the eyeball in male and female English Cocker Spaniel dogs with and without nondiabetic cataracts were evaluated. Sixteen dogs with cataracts (32 eyes) and seven normal dogs (14 eyes) older than eight years were selected. A- and B-modes ultrasonography was performed with a 10MHz transducer. Data was statistically evaluated by one ...