Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population.
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Insights on FoxN1 biological significance and usages of the "nude" mouse in studies of T-lymphopoiesisGenetics of SCIDWDR55 is a nucleolar modulator of ribosomal RNA synthesis, cell cycle progression, and teleost organ developmentDeclining expression of a single epithelial cell-autonomous gene accelerates age-related thymic involutionIntegrated weighted gene co-expression network analysis with an application to chronic fatigue syndrome.Postnatal tissue-specific disruption of transcription factor FoxN1 triggers acute thymic atrophy.Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice.First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases.Molecular evidence for a thymus-independent partial T cell development in a FOXN1-/- athymic human fetusIntergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.A deletion in FOXN1 is associated with a syndrome characterized by congenital hypotrichosis and short life expectancy in Birman cats.Overexpression of Foxn1 attenuates age-associated thymic involution and prevents the expansion of peripheral CD4 memory T cellsHuman FOXN1-deficiency is associated with αβ double-negative and FoxP3+ T-cell expansions that are distinctly modulated upon thymic transplantationFOXN1 deficient nude severe combined immunodeficiency.Foxn1-β5t transcriptional axis controls CD8+ T-cell production in the thymus.Thymus transplantation.Severe combined immunodeficiences: new and old scenarios.New genetic discoveries and primary immune deficiencies.FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program.FOXN1 in organ development and human diseases.Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.Severe combined immunodeficiency--an update.Development and developmental potential of cortical thymic epithelial cells.Ethylnitrosourea-induced thymus-defective mutants identify roles of KIAA1440, TRRAP, and SKIV2L2 in teleost organ development.MicroRNA-205 Maintains T Cell Development following Stress by Regulating Forkhead Box N1 and Selected Chemokines.A missense mutation in the extracellular domain of Fas: the most common change in Argentinean patients with autoimmune lymphoproliferative syndrome represents a founder effect.Recurrent anencephaly: a case report and examination of the VANGL1 and FOXN1 genes.Whole-exome sequencing for detecting inborn errors of immunity: overview and perspectives.FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.Formation of a functional thymus initiated by a postnatal epithelial progenitor cell.Foxn1 in Skin Development, Homeostasis and Wound Healing
P2860
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P2860
Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population.
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Ancestral founder mutation of ...... in southern Italy population.
@ast
Ancestral founder mutation of ...... in southern Italy population.
@en
Ancestral founder mutation of the nude
@nl
type
label
Ancestral founder mutation of ...... in southern Italy population.
@ast
Ancestral founder mutation of ...... in southern Italy population.
@en
Ancestral founder mutation of the nude
@nl
prefLabel
Ancestral founder mutation of ...... in southern Italy population.
@ast
Ancestral founder mutation of ...... in southern Italy population.
@en
Ancestral founder mutation of the nude
@nl
P2093
P2860
P1476
Ancestral founder mutation of ...... in southern Italy population.
@en
P2093
A M Christiano
A Martinez-Mir
E Matrecano
M V Ursini
R Busiello
P2860
P304
P356
10.1046/J.1529-8817.2004.00091.X
P407
P577
2004-05-01T00:00:00Z