Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma ; volume:43 ; number:7 ; day:14 ; month:6 ; year:2023 ; pages:1611-1622 ; date:10.2023
Journal of clinical immunology ; 43, Heft 7 (14.6.2023), 1611-1622, 10.2023

Creator: Minskaia, Ekaterina
Maimaris, Jesmeen
Jenkins, Persephone
Albuquerque, Adriana S.
Hong, Ying
Eleftheriou, Despina
Gilmour, Kimberly C.
Grace, Richard
Moreira, Fernando
Grimbacher, Bodo
Morris, Emma C.
Burns, Siobhan O.

Contributor: SpringerLink (Online service)

DOI: 10.1007/s10875-023-01530-7

URN: urn:nbn:de:101:1-2023112714120112256068

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:25 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Minskaia, Ekaterina
Maimaris, Jesmeen
Jenkins, Persephone
Albuquerque, Adriana S.
Hong, Ying
Eleftheriou, Despina
Gilmour, Kimberly C.
Grace, Richard
Moreira, Fernando
Grimbacher, Bodo
Morris, Emma C.
Burns, Siobhan O.
SpringerLink (Online service)

Other Objects (12)

Autosomal dominant STAT6 gain of function causes severe atopy associated with lymphoma

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Hochschulschrift

Identifikation des genetischen Defekts in einer iranischen Familie mit chronischer mucocutaner Candidose

Immune checkpoint deficiencies and autoimmune lymphoproliferative syndromes

Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells

Evaluation and management of deficiency of adenosine deaminase 2 : : an international consensus statement

STAT1-Mutationen in einer Kohorte von 62 Patienten mit chronischer mukokutaner Kandidose

Immunological phenotype of LRBA-deficient mice

Inborn errors of immunity associated with defects of self‐tolerance checkpoints: the CD28 family

Klinische Erforschung der CTLA-4-Insuffizienz

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

“Immune TOR-opathies,” a novel disease entity in clinical immunology

Autosomal dominant STAT6 gain of function causes severe atopy associated with lymphoma

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Hochschulschrift

Identifikation des genetischen Defekts in einer iranischen Familie mit chronischer mucocutaner Candidose

Immune checkpoint deficiencies and autoimmune lymphoproliferative syndromes

Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells

Evaluation and management of deficiency of adenosine deaminase 2 : : an international consensus statement

STAT1-Mutationen in einer Kohorte von 62 Patienten mit chronischer mukokutaner Kandidose

Immunological phenotype of LRBA-deficient mice

Inborn errors of immunity associated with defects of self‐tolerance checkpoints: the CD28 family

Klinische Erforschung der CTLA-4-Insuffizienz

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

“Immune TOR-opathies,” a novel disease entity in clinical immunology

Autosomal dominant STAT6 gain of function causes severe atopy associated with lymphoma

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Hochschulschrift

Identifikation des genetischen Defekts in einer iranischen Familie mit chronischer mucocutaner Candidose

Immune checkpoint deficiencies and autoimmune lymphoproliferative syndromes

Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells

Evaluation and management of deficiency of adenosine deaminase 2 : : an international consensus statement

STAT1-Mutationen in einer Kohorte von 62 Patienten mit chronischer mukokutaner Kandidose

Immunological phenotype of LRBA-deficient mice

Inborn errors of immunity associated with defects of self‐tolerance checkpoints: the CD28 family

Klinische Erforschung der CTLA-4-Insuffizienz

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

“Immune TOR-opathies,” a novel disease entity in clinical immunology

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Autosomal dominant STAT6 gain of function causes severe atopy associated with lymphoma

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Identifikation des genetischen Defekts in einer iranischen Familie mit chronischer mucocutaner Candidose

Immune checkpoint deficiencies and autoimmune lymphoproliferative syndromes

Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells

Evaluation and management of deficiency of adenosine deaminase 2 : : an international consensus statement

STAT1-Mutationen in einer Kohorte von 62 Patienten mit chronischer mukokutaner Kandidose

Immunological phenotype of LRBA-deficient mice

Inborn errors of immunity associated with defects of self‐tolerance checkpoints: the CD28 family

Klinische Erforschung der CTLA-4-Insuffizienz

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

“Immune TOR-opathies,” a novel disease entity in clinical immunology

Autosomal dominant STAT6 gain of function causes severe atopy associated with lymphoma

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Identifikation des genetischen Defekts in einer iranischen Familie mit chronischer mucocutaner Candidose

Immune checkpoint deficiencies and autoimmune lymphoproliferative syndromes

Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells

Evaluation and management of deficiency of adenosine deaminase 2 : : an international consensus statement

STAT1-Mutationen in einer Kohorte von 62 Patienten mit chronischer mukokutaner Kandidose

Immunological phenotype of LRBA-deficient mice

Inborn errors of immunity associated with defects of self‐tolerance checkpoints: the CD28 family

Klinische Erforschung der CTLA-4-Insuffizienz

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

“Immune TOR-opathies,” a novel disease entity in clinical immunology

Autosomal dominant STAT6 gain of function causes severe atopy associated with lymphoma

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Identifikation des genetischen Defekts in einer iranischen Familie mit chronischer mucocutaner Candidose

Immune checkpoint deficiencies and autoimmune lymphoproliferative syndromes

Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells

Evaluation and management of deficiency of adenosine deaminase 2 : : an international consensus statement

STAT1-Mutationen in einer Kohorte von 62 Patienten mit chronischer mukokutaner Kandidose

Immunological phenotype of LRBA-deficient mice

Inborn errors of immunity associated with defects of self‐tolerance checkpoints: the CD28 family

Klinische Erforschung der CTLA-4-Insuffizienz

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

“Immune TOR-opathies,” a novel disease entity in clinical immunology

Related objects

Reset password