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This resource contains materials from an advanced courses in the field of mitochondrial biology and genetics.

Genomes and annotation Issues • Mass spectrometry in proteomics • Use of proteomics for functional analysis of signaling pathways

This resource contains materials from advanced courses of embryology.

This resource contains materials from advanced courses of cytogenetics and it is especially focused on Comparative Genomic Hybridisation (CGH).

Conceptos básicos sobre el genoma. tipos del ADN, estucura del genoma. El gen: concepto y estructura, intrones y exones. Tipos de gen. Patrones de herencia

En este documento, se revisan los aspecto básicos de genética humana: estructura del ADN, el código genético, cómo el genoma codifica y dirige la síntesis de proteínas. Diferencias interindividuales y variabilidad genética

This resource contains materials from advanced courses of cytogenetics and it is especially focused on. basic principle on nuclei architecture.

Haemophilia A (X-linked): Factor VIII deficiency •Classic mutations in F8 that cause structural change in FVIII molecule or produce a truncated protein lacking essential functional domains •Mutations in proteins that interact intracellularly in the correct folding and trafficking of FVIII pro...

De basis van de humane genetica voor de leek. Een introductie wb nucleotiden, genen, chromosomen, alsook promoters en transcriptiefactoren. De impact van de omgeving op onze genen: de concepten van polygene-multifactoriele kenmerken.

Mitochondrial disorders are clinical phenotypes associated with abnormalities of oxidative phosphorylation (OXPHOS), the terminal component of mitochondrial energy metabolism. OXPHOS is carried out in the inner mitochondrial membrane by the four enzymatic complexes of the respiratory chain (compl...