Publications by authors named "Katrin Junger"

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DLG1 functions upstream of SDCCAG3 and IFT20 to control ciliary targeting of polycystin-2.
Csenge K Rezi, Mariam G Aslanyan, Gaurav D Diwan, Tao Cheng, Mohamed Chamlali, Katrin Junger

EMBO Rep· July 2024

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DLG1 functions upstream of SDCCAG3 and IFT20 to control ciliary targeting of polycystin-2.
Csenge K Rezi, Mariam G Aslanyan, Gaurav D Diwan, Tao Cheng, Mohamed Chamlali, Katrin Junger

bioRxiv· March 2024

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Interactome Analysis Reveals a Link of the Novel ALMS1-CEP70 Complex to Centrosomal Clusters.
Franziska Woerz, Felix Hoffmann, Shibu Antony, Sylvia Bolz, Mohamed Ali Jarboui, Katrin Junger

Mol Cell Proteomics· January 2024

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Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG Tags.
Tina Beyer, Tiago Martins, Jeshmi Jeyabalan Srikaran, Marian Seda, Emma Peskett, Katrin Junger

Methods Mol Biol· November 2023

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Paralog-specific TTC30 regulation of Sonic hedgehog signaling.
Felix Hoffmann, Sylvia Bolz, Katrin Junger, Franziska Klose, Isabel F Stehle

Front Mol Biosci· November 2023

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Defective airway intraflagellar transport underlies a combined motile and primary ciliopathy syndrome caused by IFT74 mutations.
Mahmoud R Fassad, Nisreen Rumman, Katrin Junger, Mitali P Patel, James Thompson

Hum Mol Genet· October 2023

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Gene augmentation of LCA5-associated Leber congenital amaurosis ameliorates bulge region defects of the photoreceptor ciliary axoneme.
Siebren Faber, Olivier Mercey, Katrin Junger, Alejandro Garanto, Helen May-Simera

JCI Insight· May 2023

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PDE6D Mediates Trafficking of Prenylated Proteins NIM1K and UBL3 to Primary Cilia.
Siebren Faber, Stef J F Letteboer, Katrin Junger, Rossano Butcher, Trinadh V Satish Tammana

Cells· January 2023

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A targeted multi-proteomics approach generates a blueprint of the ciliary ubiquitinome.
Mariam G Aslanyan, Cenna Doornbos, Gaurav D Diwan, Zeinab Anvarian, Tina Beyer, Katrin Junger

Front Cell Dev Biol· January 2023

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Intronic enhancers of the human gene predominantly regulate its expression in brain in vivo.
Fubo Cheng, Wenxu Zheng, Chang Liu, Peter Antony Barbuti, Libo Yu-Taeger, Katrin Junger

Sci Adv· November 2022

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Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease.
Marilena Elpidorou, James A Poulter, Katarzyna Szymanska, Wia Baron, Katrin Junger

Eur J Hum Genet· July 2022

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TTC30A and TTC30B Redundancy Protects IFT Complex B Integrity and Its Pivotal Role in Ciliogenesis.
Felix Hoffmann, Sylvia Bolz, Katrin Junger, Franziska Klose, Timm Schubert

Genes (Basel)· July 2022

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Proteasuria in nephrotic syndrome-quantification and proteomic profiling.
Matthias Wörn, Bernhard N Bohnert, Fawza Alenazi, Karsten Boldt, Franziska Klose, Katrin Junger

J Proteomics· January 2021

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CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.
Gerard W Dougherty, Katsutoshi Mizuno, Tabea Nöthe-Menchen, Yayoi Ikawa, Karsten Boldt, Katrin Junger

Nat Commun· November 2020

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Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathy.
Markus Burkard, Susanne Kohl, Timm Krätzig, Naoyuki Tanimoto, Christina Brennenstuhl, Katrin Junger

J Clin Invest· December 2018

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CRISPR/Cas9-mediated Genomic Editing of Cluap1/IFT38 Reveals a New Role in Actin Arrangement.
Tina Beyer, Sylvia Bolz, Katrin Junger, Nicola Horn, Muhammad Moniruzzaman

Mol Cell Proteomics· July 2018

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