FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

Gallo, Vera; Cirillo, Emilia; Giardino, Giuliana; Pignata, Claudio

Gallo, Vera; Cirillo, Emilia; Giardino, Giuliana; Pignata, Claudio.

Gallo V; Department of Translational Medical Sciences, Section of Pediatrics, Federico II University, Via S. Pansini, 5, 80131, Naples, Italy.
Cirillo E; Department of Translational Medical Sciences, Section of Pediatrics, Federico II University, Via S. Pansini, 5, 80131, Naples, Italy.
Giardino G; Department of Translational Medical Sciences, Section of Pediatrics, Federico II University, Via S. Pansini, 5, 80131, Naples, Italy.
Pignata C; Department of Translational Medical Sciences, Section of Pediatrics, Federico II University, Via S. Pansini, 5, 80131, Naples, Italy. pignata@unina.it.

J Clin Immunol ; 37(8): 751-758, 2017 Nov.

Article en En | MEDLINE | ID: mdl-28932937

Asunto(s)

Factores de Transcripción Forkhead/deficiencia; Folículo Piloso/fisiología; Uñas/patología; Inmunodeficiencia Combinada Grave/genética; Piel/metabolismo; Linfocitos T/fisiología; Timo/fisiología; Alopecia; Animales; Diferenciación Celular; Represión Epigenética; Factores de Transcripción Forkhead/metabolismo; Enfermedades Genéticas Ligadas al Cromosoma X; Humanos; Ratones; Ratones Desnudos; Fenotipo

Palabras clave

Athymia; FOXN1; Nude SCID phenotype; Nude mouse; Severe combined immunodeficiency; T cell development; Thymus transplantation

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Piel / Timo / Linfocitos T / Inmunodeficiencia Combinada Grave / Folículo Piloso / Factores de Transcripción Forkhead / Uñas Límite: Animals / Humans Idioma: En Año: 2017 Tipo del documento: Article

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