I. Buers

发表

GFP-tagged proteins visualized by freeze-fracture immuno-electron microscopy: a new tool in cellular and molecular medicine

S. Lorkowski, H. Robenek, I. Buers, 2008, Journal of cellular and molecular medicine.

Adipophilin-enriched domains in the ER membrane are sites of lipid droplet biogenesis

H. Robenek, I. Buers, Oliver Hofnagel, 2006, Journal of Cell Science.

MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum.

Y. Crow, G. Rice, I. Buers, 2017, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

Cytokine & Growth Factor Reviews

I. Buers, F. Rutsch, Y. Nitschke, 2016 .

Novel interferonopathies associated with mutations in RIG-I like receptors.

I. Buers, F. Rutsch, Y. Nitschke, 2016, Cytokine & growth factor reviews.

SR-PSOX at sites predisposed to atherosclerotic lesion formation mediates monocyte-endothelial cell adhesion.

H. Robenek, I. Buers, Oliver Hofnagel, 2011, Atherosclerosis.

Lipid Droplets Gain PAT Family Proteins by Interaction with Specialized Plasma Membrane Domains*

S. Lorkowski, H. Robenek, I. Buers, 2005, Journal of Biological Chemistry.

Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.

G. Zampino, A. Angius, L. Crisponi, 2016, American journal of human genetics.

Topography of Lipid Droplet-Associated Proteins: Insights from Freeze-Fracture Replica Immunogold Labeling

H. Robenek, I. Buers, Oliver Hofnagel, 2010, Journal of lipids.

Compartmentalization of proteins in lipid droplet biogenesis.

H. Robenek, I. Buers, Oliver Hofnagel, 2009, Biochimica et biophysica acta.

ENPP1-Fc prevents neointima formation in generalized arterial calcification of infancy through the generation of AMP

Kristina W. Kintziger, Yan Yan, I. Buers, 2018, Experimental & Molecular Medicine.

Postprandial triglyceride-rich lipoproteins regulate perilipin-2 and perilipin-3 lipid-droplet-associated proteins in macrophages.

H. Robenek, I. Buers, S. López, 2015, The Journal of nutritional biochemistry.

Butyrophilin controls milk fat globule secretion

S. Lorkowski, H. Robenek, I. Buers, 2006, Proceedings of the National Academy of Sciences.

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism

M. Baumgartner, T. Suormala, G. Nürnberg, 2009, Nature Genetics.

Lmbrd1 expression is essential for the initiation of gastrulation

P. Pennekamp, B. Skryabin, I. Buers, 2016, Journal of cellular and molecular medicine.

TIP47, a Lipid Cargo Protein Involved in Macrophage Triglyceride Metabolism

S. Lorkowski, H. Robenek, I. Buers, 2009, Arteriosclerosis, thrombosis, and vascular biology.

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

E. Shoubridge, M. Baumgartner, T. Suormala, 2012, Nature Genetics.

CRLF1 and CLCF1 in Development, Health and Disease

L. Crisponi, I. Buers, F. Rutsch, 2022, International journal of molecular sciences.

Effects of Different Variants in the ENPP1 Gene on the Functional Properties of Ectonucleotide Pyrophosphatase/Phosphodiesterase Family Member 1

I. Buers, F. Rutsch, W. Höhne, 2016, Human mutation.

ENPP1-Fc prevents neointima formation in generalized arterial calcification of infancy through the generation of AMP

Kristina W. Kintziger, Yan Yan, I. Buers, 2018, Experimental & Molecular Medicine.

Hereditary Disorders of Cardiovascular Calcification

I. Buers, F. Rutsch, Y. Nitschke, 2020, Arteriosclerosis, thrombosis, and vascular biology.

Efficient non-viral transfection of THP-1 cells.

Stefan Lorkowski, S. Lorkowski, H. Robenek, 2009, Journal of immunological methods.

A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome.

R. Hennekam, Y. Crow, P. Nürnberg, 2015, American journal of human genetics.

Lipid droplet associated proteins: an emerging role in atherogenesis.

H. Robenek, I. Buers, Oliver Hofnagel, 2011, Histology and histopathology.

Expression of perilipin isoforms in cell types involved in atherogenesis.

S. Lorkowski, H. Robenek, I. Buers, 2007, Atherosclerosis.

Improved protocol for efficient nonviral transfection of premature THP-1 macrophages.

S. Lorkowski, H. Robenek, I. Buers, 2011, Cold Spring Harbor protocols.

Protocol Improved Protocol for Ef fi cient Nonviral Transfection of Premature THP-1 Macrophages

S. Lorkowski, H. Robenek, I. Buers, 2011 .

Expanding the Mutational Spectrum of CRLF1 in Crisponi/CISS1 Syndrome

G. Usala, B. Kamien, A. Zankl, 2014, Human mutation.

Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual.

H. Omran, A. Röpke, L. Crisponi, 2020, Stem cell research.

Crisponi/cold‐induced sweating syndrome: Differential diagnosis, pathogenesis and treatment concepts

G. Zampino, L. Crisponi, I. Buers, 2019, Clinical genetics.

Exome sequencing in Crisponi/cold‐induced sweating syndrome–like individuals reveals unpredicted alternative diagnoses

F. Muntoni, F. Cucca, A. Fry, 2019, Clinical genetics.

Mutations in CRLF1 cause familial achalasia

A. Busch, I. Buers, I. Kurth, 2017, Clinical genetics.

Title : Exome sequencing in Crisponi / CISS-like individuals reveals unpredicted alternative diagnoses

F. Muntoni, F. Cucca, A. Fry, 2019 .

Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.

G. Zampino, A. Angius, L. Crisponi, 2018, American journal of human genetics.

The freeze-fracture replica immunolabeling technique for the study of lipid droplet biogenesis and function

H. Robenek, I. Buers, N. Severs, 2008 .

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

E. Shoubridge, M. Baumgartner, T. Suormala, 2012, Nature Genetics.

Butyrophilin controls milk fat globule secretion

S. Lorkowski, H. Robenek, I. Buers, 2006, Proceedings of the National Academy of Sciences.