Publications by authors named "Helmut Fuchs"

Claim this Profile
A
A fin-loop-like structure in GPX4 underlies neuroprotection from ferroptosis.
Svenja M Lorenz, Adam Wahida, Mark J Bostock, Tobias Seibt, André Santos Dias Mourão, Helmut Fuchs

Cell· December 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
New treatment for pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: first proof-of-principle of upstream enzyme inhibition in the mouse.
Clara D M van Karnebeek, Valérie Gailus-Durner, Udo F Engelke, Claudia Seisenberger, Susan Marschall, Helmut Fuchs

Brain Commun· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolization.
René Winkler, Gemma Comas-Armangué, David Corujo, Adrián Sanz-Moreno, Julia Calzada-Wack, Helmut Fuchs

Sci Adv· October 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism.
Jean-Pierre Gillet, Louise Gerard, Wilfred Vieira, Marie Fourrez, Florence Gaudray, Helmut Fuchs

iScience· October 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Neuropathy-associated Tecpr2 mutation knock-in mice reveal endolysosomal loss of function phenotypes in neurons and microglia.
Debjani Bhattacharya, Patricia da Silva-Buttkus, Karsten Nalbach, Lizhen Cheng, Lillian Garrett, Helmut Fuchs

Cell Death Dis· October 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
NRAC controls CD36-mediated fatty acid uptake in adipocytes and lipid clearance in vivo.
Inderjeet Singh, Yasuhiro Onogi, Filipe Menezes, Dina Khasanova, Lingru Kang, Helmut Fuchs

EMBO J· September 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Structure Elucidation for MALDI Mass Spectrometry Imaging Using Infrared Ion Spectroscopy.
Jelle L Schuurman, Lara van Tetering, Kas J Houthuijs, Pieter Kooijman, Valerie Gailus-Durner, Helmut Fuchs

Anal Chem· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Towards a kingdom of reproductive life - the core sperm proteome.
Taylor Pini, Brett Nixon, Timothy L Karr, Raffaele Teperino, Adrián Sanz-Moreno, Helmut Fuchs

Reproduction· June 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Ocular Phenotyping of Knockout Mice Identifies Genes Associated With Late Adult Retinal Phenotypes.
Abraham Hang, Andy Shao, Michael Shea, Michel J Roux, Denise M Imai-Leonard, Helmut Fuchs

Invest Ophthalmol Vis Sci· June 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Systematic Ocular Phenotyping of Knockout Mouse Lines Identifies Genes Associated With Age-Related Corneal Dystrophies.
Andrew Briere, Peter Vo, Benjamin Yang, David Adams, Takanori Amano, Helmut Fuchs

Invest Ophthalmol Vis Sci· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome.
Shiyu Luo, Valérie Gailus-Durner, Bobbi McGivern, Qifei Li, Jessica Kottmeier, Helmut Fuchs

Eur J Hum Genet· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita.
Adrián Sanz-Moreno, Lore Becker, Kan Xie, Patricia da Silva-Buttkus, Nathalia R V Dragano, Helmut Fuchs

Sci Adv· April 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Systematic ocular phenotyping of 8,707 knockout mouse lines identifies genes associated with abnormal corneal phenotypes.
Peter Vo, Denise M Imai-Leonard, Benjamin Yang, Andrew Briere, Andy Shao, Helmut Fuchs

BMC Genomics· January 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
X
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes.
Tim P Hasenbein, Sarah Hoelzl, Zachary D Smith, Chiara Gerhardinger, Marion O C Gonner, Helmut Fuchs

Nat Commun· December 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Examining the liver-pancreas crosstalk reveals a role for the molybdenum cofactor in β-cell regeneration.
Christos Karampelias, Bianca Băloiu, Birgit Rathkolb, Patricia da Silva-Buttkus, Etty Bachar-Wikström, Helmut Fuchs

Life Sci Alliance· November 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Opa1 processing is dispensable in mouse development but is protective in mitochondrial cardiomyopathy.
Sofia Ahola, Lilli A Pazurek, Fiona Mayer, Philipp Lampe, Steffen Hermans, Helmut Fuchs

Sci Adv· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Comparative Phenotyping of Mice Reveals Canonical and Noncanonical Physiological Functions of TRα and TRβ.
Georg Sebastian Hönes, Daniela Geist, Christina Wenzek, Paul Thomas Pfluger, Timo Dirk Müller, Helmut Fuchs

Endocrinology· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Canonical and Noncanonical Contribution of Thyroid Hormone Receptor Isoforms Alpha and Beta to Cardiac Hypertrophy and Heart Rate in Male Mice.
Daniela Geist, Georg Sebastian Hönes, Susanne Camilla Grund, Janina Pape, Devon Siemes, Helmut Fuchs

Thyroid· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain.
Lillian Garrett, Dietrich Trümbach, Donghyung Lee, Silvia Mandillo, Rodney Samaco, Helmut Fuchs

Neurosci Appl· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
TRPS1 maintains luminal progenitors in the mammary gland by repressing SRF/MRTF activity.
Marie Tollot-Wegner, Marco Jessen, KyungMok Kim, Adrián Sanz-Moreno, Nadine Spielmann, Helmut Fuchs

Breast Cancer Res· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A brain-enriched circular RNA controls excitatory neurotransmission and restricts sensitivity to aversive stimuli.
Sebastian A Giusti, Natalia S Pino, Camila Pannunzio, Mora B Ogando, Natalia G Armando, Helmut Fuchs

Sci Adv· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, Julia Calzada-Wack, Yong Li, Helmut Fuchs

Kidney Int· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
LncRNA U90926 is dispensable for the development of obesity-associated phenotypes in vivo.
Bristy Sabikunnahar, Sydney Caldwell, Stella Varnum, Tyler Hogan, Karolyn G Lahue, Helmut Fuchs

Physiol Rep· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Single-cell, whole-embryo phenotyping of mammalian developmental disorders.
Xingfan Huang, Jana Henck, Chengxiang Qiu, Varun K A Sreenivasan, Saranya Balachandran, Helmut Fuchs

Nature· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease.
Daniel G Calame, Tianyu Guo, Chen Wang, Lillian Garrett, Angad Jolly, Helmut Fuchs

Am J Hum Genet· August 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis