Robert Bruce Russell

Professor

Ruprecht Karls Universität Heidelberg

Germany

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Robert Bruce Russell is a Professor at Ruprecht Karls Universität Heidelberg, Germany. His research areas include ciliary biology, protein stability in disease contexts, mesenchymal cell identities, and the genomic landscape of lymphomas. He has published recent articles on topics such as the targeting mechanisms of polycystin-2, chemogenetic activation of signaling pathways, and the structural biology of intraflagellar transport complexes.

Articles (16)

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2022

Collaborators (15)

Esben Lorentzen

Aarhus University

DENMARK

Robert Bruce Russell

Research Interests

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Articles (16)

DLG1 functions upstream of SDCCAG3 and IFT20 to control ciliary targeting of polycystin-2

Reduced Protein Stability of 11 Pathogenic Missense STXBP1/MUNC18-1 Variants and Improved Disease Prediction

Emerging Trends in the Field of Inflammation and Proteinopathy in ALS/FTD Spectrum Disorder

Chemogenetic activation of G12 signaling enhances adipose tissue browning

A targeted multi-proteomics approach generates a blueprint of the ciliary ubiquitinome.

De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of <i>Bbs1</i>

Genomic landscape of follicular lymphoma across a wide spectrum of clinical behaviors.

Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B-cell lymphomas.

Biochemically validated structural model of the 15-subunit intraflagellar transport complex IFT-B

The S-palmitoylome and DHHC-PAT interactome of Drosophila melanogaster S2R+ cells indicate a high degree of conservation to mammalian palmitoylomes

Biochemically validated structural model of the 15-subunit intraflagellar transport complex IFT-B

The human signal peptidase complex acts as a quality control enzyme for membrane proteins

The human signal peptidase complex acts as a quality control enzyme for membrane proteins

Leveraging biochemical reactions to unravel functional impacts of cancer somatic variants affecting protein interaction interfaces.

Never-homozygous genetic variants in healthy populations are potential recessive disease candidates

PRECOGx: exploring GPCR signaling mechanisms with deep protein representations

Collaborators (15)

Esben Lorentzen

Eduardo Felipe Alves Fernandes

Lotte Pedersen

Emanuele Buratti

Stine Falsig Pedersen

Ruud Toonen

Guanming Wu

Fabiola De Marchi

Ivana Munitic

Jasna Kriz

Juro Sakai

Marius Ueffing

Philip Beales

Kristian Strømgaard

Simon Anders

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