Jacek Puchalka

Dr. Von Haunersches Kinderspital
Munich, BY 80337, Germany

Last Updated: 09/26/2026

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Found 28 publications

Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.

Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.

Journal: Nature communications

Published: April 22, 2020

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.

Journal: Nature communications

Published: January 14, 2019

miR-181a/b-1 controls thymic selection of Treg cells and tunes their suppressive capacity.

miR-181a/b-1 controls thymic selection of Treg cells and tunes their suppressive capacity.

Journal: PLoS biology

Published: May 18, 2018

miR-191 modulates B-cell development and targets transcription factors E2A, Foxp1, and Egr1.

miR-191 modulates B-cell development and targets transcription factors E2A, Foxp1, and Egr1.

Journal: European journal of immunology

Published: April 24, 2018

Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention.

Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention.

Journal: World journal of gastrointestinal pathophysiology

Published: November 22, 2016

Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes.

Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes.

Journal: Nature genetics

Published: August 16, 2016

Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome.

Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome.

Journal: Journal of clinical immunology

Published: June 08, 2016

A human immunodeficiency syndrome caused by mutations in CARMIL2.

A human immunodeficiency syndrome caused by mutations in CARMIL2.

Journal: Nature communications

Published: April 18, 2016

Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations.

Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations.

Journal: The Journal of allergy and clinical immunology

Published: April 13, 2016

Characterizing the optimal flux space of genome-scale metabolic reconstructions through modified latin-hypercube sampling.

Characterizing the optimal flux space of genome-scale metabolic reconstructions through modified latin-hypercube sampling.

Journal: Molecular bioSystems

Published: January 29, 2016

Genotypic and phenotypic analyses of a Pseudomonas aeruginosa chronic bronchiectasis isolate reveal differences from cystic fibrosis and laboratory strains.

Genotypic and phenotypic analyses of a Pseudomonas aeruginosa chronic bronchiectasis isolate reveal differences from cystic fibrosis and laboratory strains.

Journal: BMC genomics

Published: May 21, 2015

Limited niche availability suppresses murine intrathymic dendritic-cell development from noncommitted progenitors.

Limited niche availability suppresses murine intrathymic dendritic-cell development from noncommitted progenitors.

Journal: Blood

Published: November 21, 2014

Showing 1-12 of 28

Last Updated: 09/26/2026