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The Genetics and Epigenetics of 22q11.2 Deletion Syndrome

Frontiers in genetics, 2020-02, Vol.10, p.1365-1365

2020

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Regulation of TLR7/9 responses in plasmacytoid dendritic cells by BST2 and ILT7 receptor interaction

The Journal of experimental medicine, 2009-07, Vol.206 (7), p.1603-1614

2009

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Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome

The Journal of clinical investigation, 2023-07, Vol.133 (13)

2023

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CD2AP/SHIP1 complex positively regulates plasmacytoid dendritic cell receptor signaling by inhibiting the E3 ubiquitin ligase Cbl

The Journal of immunology (1950), 2012-07, Vol.189 (2), p.786-792

2012

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Death receptor 6 is a novel plasmacytoid dendritic cell-specific receptor and modulates type I interferon production

Protein & cell, 2016-04, Vol.7 (4), p.291-294

2016

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Plasmacytoid dendritic cells in antiviral immunity and autoimmunity

Science China. Life sciences, 2010-02, Vol.53 (2), p.172-182

2010

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Plasmacytoid dendritic cells in antiviral immunity and autoimmunity

Science China. Life sciences, 2010-02, Vol.53 (2), p.172-182

2010

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Abstract 6056: A next-gen anti-CD73 Antibody with potential to show better efficacy and safety profile than existing approach

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.6056-6056

2020

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Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome

The Journal of clinical investigation, 2023-07, Vol.133 (13)

2023

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MIR205HG Is a Long Noncoding RNA that Regulates Growth Hormone and Prolactin Production in the Anterior Pituitary

Developmental cell, 2019-05, Vol.49 (4), p.618-631.e5

2019

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Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome

The Journal of clinical investigation, 2022-11, Vol.132 (22), p.1-17

2022

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FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans

The Journal of clinical investigation, 2019-11, Vol.129 (11), p.4724-4738

2019

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Agonist antibody activates death receptor 6 downstream signaling involving TRADD recruitment

FEBS letters, 2014-01, Vol.588 (3), p.401-407

2014

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Characterization of the Thymic Hypoplasia in Mouse Models of 22q11.2 Deletion Syndrome (DiGeorge Syndrome)

The Journal of immunology (1950), 2018-05, Vol.200 (1_Supplement), p.166-166.19

2018

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22q11.2 Deletion Syndrome (DiGeorge) and Mutations in Forkhead Box N1 ( FOXN1 ) cause a Thymic Hypoplasia through distinct Developmental Processes

The Journal of immunology (1950), 2019-05, Vol.202 (1_Supplement), p.182-182.32

2019

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Signature Gene Expression Patterns Revealed in Hypoplastic Thymii from Mouse Models of DiGeorge-22q11.2 Deletion Syndrome

The Journal of immunology (1950), 2017-05, Vol.198 (1_Supplement), p.59-59.14

2017

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MIR205HG is a Long Noncoding RNA with Distinct Functions in the Thymus versus the Anterior Pituitary

The Journal of immunology (1950), 2018-05, Vol.200 (1_Supplement), p.165-165.11

2018

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Compound Heterozygous Mutations in Forkhead Box N1 ( FOXN1 ) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients

The Journal of immunology (1950), 2018-05, Vol.200 (1_Supplement), p.166-166.20

2018

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MicroRNA-205 Maintains T Cell Development following Stress by Regulating Forkhead Box N1 and Selected Chemokines

The Journal of biological chemistry, 2016-10, Vol.291 (44), p.23237-23247

2016

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Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development

The Journal of immunology (1950), 2017-05, Vol.198 (1_Supplement), p.59-59.3

2017

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A Long Noncoding RNA, lncRNA205, and an Embedded MicroRNA, MiR-205 have Overlapping and Distinct Contributions to Thymopoiesis and Development

The Journal of immunology (1950), 2017-05, Vol.198 (1_Supplement), p.60-60.22

2017

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Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome

The Journal of clinical investigation, 2023-07, Vol.132 (22)

2023

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基于广义弹性理论的微梁固有频率及模态的尺寸效应

Ying yong shu xue he li xue = Applied mathematics and mechanics, 2018, Vol.39 (9), p.999-1008

2018

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Preferential depletion of CD2 plasmacytoid dendritic cells in HIV-infected subjects

Cellular & molecular immunology, 2011-09, Vol.8 (5), p.441-444

2011

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Preferential depletion of CD2low plasmacytoid dendritic cells in HIV-infected subjects

Cellular & molecular immunology, 2011-09, Vol.8 (5), p.441-444

2011

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The Genetics and Epigenetics of 22q11.2 Deletion Syndrome

Regulation of TLR7/9 responses in plasmacytoid dendritic cells by BST2 and ILT7 receptor interaction

Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome

CD2AP/SHIP1 complex positively regulates plasmacytoid dendritic cell receptor signaling by inhibiting the E3 ubiquitin ligase Cbl

Death receptor 6 is a novel plasmacytoid dendritic cell-specific receptor and modulates type I interferon production

Plasmacytoid dendritic cells in antiviral immunity and autoimmunity

Plasmacytoid dendritic cells in antiviral immunity and autoimmunity

Abstract 6056: A next-gen anti-CD73 Antibody with potential to show better efficacy and safety profile than existing approach

Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome

MIR205HG Is a Long Noncoding RNA that Regulates Growth Hormone and Prolactin Production in the Anterior Pituitary

Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome

FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans

Agonist antibody activates death receptor 6 downstream signaling involving TRADD recruitment

Characterization of the Thymic Hypoplasia in Mouse Models of 22q11.2 Deletion Syndrome (DiGeorge Syndrome)

22q11.2 Deletion Syndrome (DiGeorge) and Mutations in Forkhead Box N1 ( FOXN1 ) cause a Thymic Hypoplasia through distinct Developmental Processes

Signature Gene Expression Patterns Revealed in Hypoplastic Thymii from Mouse Models of DiGeorge-22q11.2 Deletion Syndrome

MIR205HG is a Long Noncoding RNA with Distinct Functions in the Thymus versus the Anterior Pituitary

Compound Heterozygous Mutations in Forkhead Box N1 ( FOXN1 ) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients

MicroRNA-205 Maintains T Cell Development following Stress by Regulating Forkhead Box N1 and Selected Chemokines

Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development

A Long Noncoding RNA, lncRNA205, and an Embedded MicroRNA, MiR-205 have Overlapping and Distinct Contributions to Thymopoiesis and Development

Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome

基于广义弹性理论的微梁固有频率及模态的尺寸效应

Preferential depletion of CD2 plasmacytoid dendritic cells in HIV-infected subjects

Preferential depletion of CD2low plasmacytoid dendritic cells in HIV-infected subjects

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