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Bruton's Tyrosine Kinase and Phospholipase Cγ2 Mediate Chemokine-Controlled B Cell Migration and Homing

Immunity (Cambridge, Mass.), 2007, Vol.26 (1), p.93-104

2007

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Effects of Childhood Multidisciplinary Care and Growth Hormone Treatment on Health Problems in Adults with Prader-Willi Syndrome

Journal of clinical medicine, 2021-07, Vol.10 (15), p.3250

2021

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What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of ‘Internal Medicine for Rare Genetic Syndromes’

Journal of clinical medicine, 2021-11, Vol.10 (22), p.5457

2021

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Tumor suppressor function of Bruton tyrosine kinase is independent of its catalytic activity

Blood, 2005-01, Vol.105 (1), p.259-265

2005

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Somatic thrombopoietin (THPO) gene mutations in childhood myeloid leukemias

International journal of hematology, 2015-07, Vol.102 (1), p.140-143

2015

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Hypertension with hidden causes: the cognitive and behavioral profile of an adult female with chronic stress and 16p11.2 microdeletion

Journal of hypertension, 2024-01, Vol.42 (1), p.179

2024

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Missed Diagnoses and Health Problems in Adults With Prader-Willi Syndrome: Recommendations for Screening and Treatment

The journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.1-e4687

2020

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MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations

Human mutation, 2014-02, Vol.35 (2), p.236-247

2014

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Brutons Tyrosine Kinase and Phospholipase C gamma 2 Mediate Chemokine-Controlled B Cell Migration and Homing

Immunity (Cambridge, Mass.), 2007-01, Vol.26 (1), p.93-104

2007

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Educational paper: Syndromic forms of primary immunodeficiency

European journal of pediatrics, 2011-03, Vol.170 (3), p.295-308

2011

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Educational paper

European journal of pediatrics, 2011-03, Vol.170 (3), p.295

2011

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Hematopoietic Stem Cell Transplantation in a Patient With ICF2 Syndrome Presenting With EBV-Induced Hemophagocytic Lymphohystiocytosis

Transplantation, 2016-07, Vol.100 (7), p.e35

2016

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Sex steroids influence pancreatic islet hypertrophy and subsequent autoimmune infiltration in nonobese diabetic (NOD) and NODscid mice

Laboratory investigation, 2001-02, Vol.81 (2), p.231-239

2001

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Development and Function of Immune Cells in an Adolescent Patient With a Deficiency in the Interleukin-10 Receptor

Journal of pediatric gastroenterology and nutrition, 2017-07, Vol.65 (1), p.e5

2017

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Development and Function of Immune Cells in an Adolescent Patient With a Deficiency in the Interleukin‐10 Receptor

Journal of pediatric gastroenterology and nutrition, 2017-07, Vol.65 (1), p.e5-e15

2017

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Syndromic forms of primary immunodeficiency

European journal of pediatrics, 2011, Vol.170 (3), p.295-308

2011

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Constitutive activation of Bruton's tyrosine kinase induces the formation of autoreactive IgM plasma cells

European journal of immunology, 2010-09, Vol.40 (9), p.2643-2654

2010

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Correction: The ARID1B spectrum in 143 patients: fromnonsyndromic intellectual disability to Coffin–Siris syndrome

Genetics in medicine, 2019-09, Vol.21 (9), p.2160-2161

2019

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What Every Internist Should Know About Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five-Year Experience of Internal Medicine for Complex Rare Genetic Syndromes

Journal of the Endocrine Society, 2021-05, Vol.5 (Supplement_1), p.A513-A514

2021

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Bruton's tyrosine kinase cooperates with the B cell linker protein SLP-65 as a tumor suppressor in Pre-B cells

The Journal of experimental medicine, 2003-07, Vol.198 (1), p.91-98

2003

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Hemophilia B in a female with intellectual disability caused by a deletion of Xq26.3q28 encompassing the F9

Molecular genetics & genomic medicine, 2018-11, Vol.6 (6), p.1220-1224

2018

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MYH9 -Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations: HUMAN MUTATION

Human mutation, 2014-02, Vol.35 (2), p.236-247

2014

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Involvement of SLP-65 and Btk in tumor suppression and malignant transformation of pre-B cells

Seminars in Immunology, 2006-02, Vol.18 (1), p.67-76

2006

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Malignant transformation of Slp65-deficient pre-B cells involves disruption of the Arf-Mdm2-p53 tumor suppressor pathway

Blood, 2010-02, Vol.115 (7), p.1385-1393

2010

Volltextzugriff (PDF)

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Bruton's Tyrosine Kinase and Phospholipase Cγ2 Mediate Chemokine-Controlled B Cell Migration and Homing

Effects of Childhood Multidisciplinary Care and Growth Hormone Treatment on Health Problems in Adults with Prader-Willi Syndrome

What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of ‘Internal Medicine for Rare Genetic Syndromes’

Tumor suppressor function of Bruton tyrosine kinase is independent of its catalytic activity

Somatic thrombopoietin (THPO) gene mutations in childhood myeloid leukemias

Hypertension with hidden causes: the cognitive and behavioral profile of an adult female with chronic stress and 16p11.2 microdeletion

ANKRD26-related thrombocytopenia and myeloid malignancies

Missed Diagnoses and Health Problems in Adults With Prader-Willi Syndrome: Recommendations for Screening and Treatment

MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations

Brutons Tyrosine Kinase and Phospholipase C gamma 2 Mediate Chemokine-Controlled B Cell Migration and Homing

Educational paper: Syndromic forms of primary immunodeficiency

Educational paper

Hematopoietic Stem Cell Transplantation in a Patient With ICF2 Syndrome Presenting With EBV-Induced Hemophagocytic Lymphohystiocytosis

Sex steroids influence pancreatic islet hypertrophy and subsequent autoimmune infiltration in nonobese diabetic (NOD) and NODscid mice

Development and Function of Immune Cells in an Adolescent Patient With a Deficiency in the Interleukin-10 Receptor

Development and Function of Immune Cells in an Adolescent Patient With a Deficiency in the Interleukin‐10 Receptor

Syndromic forms of primary immunodeficiency

Constitutive activation of Bruton's tyrosine kinase induces the formation of autoreactive IgM plasma cells

Correction: The ARID1B spectrum in 143 patients: fromnonsyndromic intellectual disability to Coffin–Siris syndrome

What Every Internist Should Know About Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five-Year Experience of Internal Medicine for Complex Rare Genetic Syndromes

Bruton's tyrosine kinase cooperates with the B cell linker protein SLP-65 as a tumor suppressor in Pre-B cells

Hemophilia B in a female with intellectual disability caused by a deletion of Xq26.3q28 encompassing the F9

MYH9 -Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations: HUMAN MUTATION

Involvement of SLP-65 and Btk in tumor suppression and malignant transformation of pre-B cells

Malignant transformation of Slp65-deficient pre-B cells involves disruption of the Arf-Mdm2-p53 tumor suppressor pathway

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