Publications by authors named "Andreas D Zimmer"

Claim this Profile
A
Autosomal Dominant Lamellar Ichthyosis Due to a Missense Variant in the Gene NKPD1.
Katalin Komlosi, Cristina Glocker, Hao-Hsiang Hsu-Rehder, Svenja Alter, Julia Kopp, Andreas David Zimmer

J Invest Dermatol· December 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutational Spectrum of the Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis.
Alrun Hotz, Julia Kopp, Emmanuelle Bourrat, Vinzenz Oji, Kira Süßmuth, Andreas D Zimmer

Genes (Basel)· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pathogenic variants in the SPTLC1 gene cause hyperkeratosis lenticularis perstans.
Sabine Jägle, Hao-Hsiang Hsu, Hazem A Juratli, Andreas D Zimmer, Amelie Prieschl

Br J Dermatol· January 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation.
Mariem Ennouri, Andreas D Zimmer, Emna Bahloul, Rim Chaabouni, Slaheddine Marrakchi

BMC Med Genomics· January 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis.
Katalin Komlosi, Olivier Claris, Sophie Collardeau-Frachon, Julia Kopp, Ingrid Hausser, Andreas D Zimmer

Front Genet· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Importance of Extended Analysis Using Current Molecular Genetic Methods Based on the Example of a Cohort of 228 Patients with Hereditary Breast and Ovarian Cancer Syndrome.
Luise D Resch, Alrun Hotz, Andreas D Zimmer, Katalin Komlosi, Nina Singh

Genes (Basel)· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in .
Svenja Alter, Andreas David Zimmer, Misun Park, Jianli Gong, Almuth Caliebe

J Med Genet· June 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Meta-Analysis of Mutations in or Identified in a Large Cohort of 224 Patients.
Alrun Hotz, Julia Kopp, Emmanuelle Bourrat, Vinzenz Oji, Katalin Komlosi, Andreas D Zimmer

Genes (Basel)· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Neonatal presentation of COG6-CDG with prominent skin phenotype.
Katalin Komlosi, Selina Gläser, Julia Kopp, Alrun Hotz, Svenja Alter, Andreas D Zimmer

JIMD Rep· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Severe metabolic alterations in liver cancer lead to ERK pathway activation and drug resistance.
Zeribe Chike Nwosu, Weronika Piorońska, Nadia Battello, Andreas David Zimmer, Bedair Dewidar

EBioMedicine· April 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4.
Nadja Ballin, Alrun Hotz, Emmanuelle Bourrat, Julia Küsel, Vinzenz Oji, Andreas D Zimmer

Hum Mutat· December 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation.
Steffen Hörer, Slaheddine Marrakchi, Franz P W Radner, Gerd Zolles, Lisa Heinz, Andreas D Zimmer

J Invest Dermatol· October 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Homozygous intronic MITF mutation causes severe Waardenburg syndrome type 2A.
Marc-Alexander Rauschendorf, Andreas D Zimmer, Astrid Laut, Philipp Demmer, Bernd Rösler

Pigment Cell Melanoma Res· January 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The PD-L1- and IL6-mediated dampening of the IL27/STAT1 anticancer responses are prevented by α-PD-L1 or α-IL6 antibodies.
Catherine Rolvering, Andreas D Zimmer, Aurélien Ginolhac, Christiane Margue, Mélanie Kirchmeyer

J Leukoc Biol· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis.
Alrun Hotz, Emmanuelle Bourrat, Julia Küsel, Vinzenz Oji, Svenja Alter, Andreas D Zimmer

Hum Mutat· October 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The loss of SMG1 causes defects in quality control pathways in Physcomitrella patens.
James P B Lloyd, Daniel Lang, Andreas D Zimmer, Barry Causier, Ralf Reski

Nucleic Acids Res· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Physcomitrella patens chromosome-scale assembly reveals moss genome structure and evolution.
Daniel Lang, Kristian K Ullrich, Florent Murat, Jörg Fuchs, Jerry Jenkins, Andreas D Zimmer

Plant J· February 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Q
Quinalizarin inhibits adipogenesis through down-regulation of transcription factors and microRNA modulation.
Lisa Schwind, Lisa Nalbach, Andreas D Zimmer, Katja B Kostelnik, Jennifer Menegatti

Biochim Biophys Acta Gen Subj· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans.
Lisa Heinz, Gwang-Jin Kim, Slaheddine Marrakchi, Julie Christiansen, Hamida Turki, Andreas D Zimmer

Am J Hum Genet· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Crosstalk between different family members: IL27 recapitulates IFNγ responses in HCC cells, but is inhibited by IL6-type cytokines.
Catherine Rolvering, Andreas D Zimmer, Ines Kozar, Heike M Hermanns, Elisabeth Letellier

Biochim Biophys Acta Mol Cell Res· March 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients.
Maritta Hellström Pigg, Anette Bygum, Agneta Gånemo, Marie Virtanen, Flemming Brandrup, Andreas D Zimmer

Acta Derm Venereol· November 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Phosphorylation of the pyruvate dehydrogenase complex precedes HIF-1-mediated effects and pyruvate dehydrogenase kinase 1 upregulation during the first hours of hypoxic treatment in hepatocellular carcinoma cells.
Andreas David Zimmer, Geoffroy Walbrecq, Ines Kozar, Iris Behrmann, Claude Haan

Hypoxia (Auckl)· August 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The role of HIF-1 in oncostatin M-dependent metabolic reprogramming of hepatic cells.
Nadia Battello, Andreas David Zimmer, Carole Goebel, Xiangyi Dong, Iris Behrmann

Cancer Metab· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CK2 phosphorylation of C/EBPδ regulates its transcription factor activity.
Lisa Schwind, Andreas D Zimmer, Claudia Götz, Mathias Montenarh

Int J Biochem Cell Biol· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Insights from the cold transcriptome of Physcomitrella patens: global specialization pattern of conserved transcriptional regulators and identification of orphan genes involved in cold acclimation.
Anna K Beike, Daniel Lang, Andreas D Zimmer, Florian Wüst, Danika Trautmann

New Phytol· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis