Video Experimental Relacionado
Updated: May 6, 2026
08:57
Author Spotlight: Genetically Engineered Mouse Models and Pathological Characterization of Neurofibromatosis Type 1 Associated Tumors
Published on: May 17, 2024
3.1K
¿Cro-Magnon 1 tiene neurofibromatosis tipo 2? - Respuesta de los autores
Philippe Charlier1, Nadia Benmoussa2, Philippe Froesch3
1Section of Medical Anthropology, University of Versailles Saint-Quentin-en-Yvelines, 78180 Montigny-Le-Bretonneux, France; Centre d'Accueil et de Soins Hospitaliers and Institut de la Précarité et de l'Exclusion Sociale, Nanterre, France.
Lancet (London, England)
|August 29, 2018
Resumen
No abstract available in PubMed .
Videos de Conceptos Relacionados
01:20The Retinoblastoma Gene
3.7K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
3.7K
01:19Cushing Syndrome II: Pathophysiology
58
Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features...
58