Author details

Full Name

Jeremie Poschmann

Affiliation

ORCID

Career Start Year

2006

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36635667	CD4 and CD8 regulatory T cell characterization in the rat using a unique transgenic Foxp3-EGFP model.		2023
37588598	Human granzyme B regulatory B cells prevent effector CD4+CD25- T cell proliferation through a mechanism dependent from lymphotoxin alpha.		2023
36717250	A cluster of broadly neutralizing IgG against BK polyomavirus in a repertoire dominated by IgM.		2023
34929443	Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 system.	Stem Cell Research	2022
35683619	Time-Limited Therapy with Belatacept in Kidney Transplant Recipients.	Journal of Clinical Medicine	2022
35486851	Monocyte Signature Associated with Herpes Simplex Virus Reactivation and Neurological Recovery after Brain Injury.	American Journal of Respiratory and Critical Care Medicine	2022
36056160	Author Correction: Histone acetylome-wide associations in immune cells from individuals with active Mycobacterium tuberculosis infection.	Nat Microbiol	2022
36399563	CLEC-1 is a death sensor that limits antigen cross-presentation by dendritic cells and represents a target for cancer immunotherapy.	Science advances	2022
36497174	Deciphering Transcriptional Networks during Human Cardiac Development.		2022
35102304	Histone acetylome-wide associations in immune cells from individuals with active Mycobacterium tuberculosis infection.	Nat Microbiol	2022
35051358	Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder.	Am J Hum Genet	2022
34685700	Alveolar Macrophages: Adaptation to Their Anatomic Niche during and after Inflammation.	Cells	2021
33811806	Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.	Am J Hum Genet	2021
34233909	Dendritic Cells Require TMEM176A/B Ion Channels for Optimal MHC Class II Antigen Presentation to Naive CD4<sup>+</sup> T Cells.	J Immunol	2021
33609296	Cystathionine-gamma-lyase overexpression in T cells enhances antitumor effect independently of cysteine autonomy.	Cancer Science	2021
32697326	Regulatory T Cells Expressing Tumor Necrosis Factor Receptor Type 2 Play a Major Role in CD4+ T-Cell Impairment During Sepsis.	Journal of Infectious Diseases	2020
32140157	Characterization of Rat ILCs Reveals ILC2 as the Dominant Intestinal Subset.	Frontiers in Immunology	2020
32424365	Alveolar macrophages are epigenetically altered after inflammation, leading to long-term lung immunoparalysis.	Nature Immunology	2020
31426802	Development and application of a transcriptional sensor for detection of heterologous acrylic acid production in E. coli.	Microbial Cell Factories	2019
31645609	Resistin expression in human monocytes is controlled by two linked promoter SNPs mediating NFKB p50/p50 binding and C-methylation.	Sci Rep	2019
30399125	23rd Nantes ActualitÃ©s Transplantation: "Genomics and Immunogenetics of Kidney and Inflammatory Diseases-Lessons for Transplantation".	Transplantation	2019
31220268	Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.	Hum Mol Genet	2019
30349106	A histone acetylome-wide association study of Alzheimer's disease identifies disease-associated H3K27ac differences in the entorhinal cortex.	Nat Neurosci	2018
27863250	Histone Acetylome-wide Association Study of Autism Spectrum Disorder.	Cell	2016
26893351	The transcription factor SOX6 contributes to the developmental origins of obesity by promoting adipogenesis.	Development	2016
26883533	Pitfalls of haplotype phasing from amplicon-based long-read sequencing.	Sci Rep	2016
26957309	Comprehensive benchmarking reveals H2BK20 acetylation as a distinctive signature of cell-state-specific enhancers and promoters.	Genome Res	2016
26605881	The PsychENCODE project.	Nat Neurosci	2015
25799442	Sensitive detection of chromatin-altering polymorphisms reveals autoimmune disease mechanisms.	Nat Methods	2015
25915184	ACSL1 Is Associated With Fetal Programming of Insulin Sensitivity and Cellular Lipid Content.	Mol Endocrinol	2015
24802670	MiR-135b is a direct PAX6 target and specifies human neuroectoderm by inhibiting TGF-Î²/BMP signaling.	EMBO J	2014
25382769	[Food consumption and dietary behaviour in haemophilia patients before and after a nutrition consultation].	Hamostaseologie	2014
23668784	A functional autophagy pathway is required for rapamycin-induced degradation of the Sgs1 helicase in Saccharomyces cerevisiae.	Biochemistry and Cell Biology	2013
21884683	RNA polymerase II degradation in response to rapamycin is not mediated through ubiquitylation.	Biochemical and Biophysical Research Communications	2011
21887235	The peptidyl prolyl isomerase Rrd1 regulates the elongation of RNA polymerase II during transcriptional stresses.	PLoS One	2011
21129186	Rrd1 isomerizes RNA polymerase II in response to rapamycin.	BMC Molecular Biology	2010
17078097	Deletion of the chromatin remodeling gene SPT10 sensitizes yeast cells to a subclass of DNA-damaging agents.	Environmental and Molecular Mutagenesis	2006