FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

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Thymic stromal cells: Roles in atrophy and age-associated dysfunction of the thymus.

P2860

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P2860

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

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http://www.wikidata.org/entity/Q48317693

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-hans

2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

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FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

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label

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

@en

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

@nl

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FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

@en

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

@nl

P1476

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

@en

P2093

Emilia Cirillo

http://www.w3.org/2001/XMLSchema#string

Vera Gallo

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P2860

New member of the winged-helix protein family disrupted in mouse and rat nude mutations

Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants

A forkhead-domain gene is mutated in a severe speech and language disorder

Foxn1 is required to maintain the postnatal thymic microenvironment in a dosage-sensitive manner

Positive and negative selection of the T cell repertoire: what thymocytes see (and don't see)

Postnatal tissue-specific disruption of transcription factor FoxN1 triggers acute thymic atrophy.

Thymopoiesis in mice depends on a Foxn1-positive thymic epithelial cell lineage.

Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population.

Transient activation of FOXN1 in keratinocytes induces a transcriptional programme that promotes terminal differentiation: contrasting roles of FOXN1 and Akt.

The nude gene and the skin.

P2888

s10875-017-0445-z

P304

751-758

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scholarly article

P356

10.1007/S10875-017-0445-Z

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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Claudio Pignata

Giuliana Giardino

P577

2017-09-21T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28932937

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FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

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P2860

P2860

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.

description

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P1433

P1476

P2093

P2860

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P356

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P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698