Raimund Wagener

Kerpener Str. 62
Koeln, NW 50924, Germany

Last Updated: 09/26/2026

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Found 48 publications

Extracellular matrix abnormalities in Hutchinson-Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?

Extracellular matrix abnormalities in Hutchinson-Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?

Journal: Matrix biology plus

Published: April 10, 2026

Furin-like cleavage at the C1-C2 linker region of the ⍺3 chain is not required for collagen VI assembly.

Furin-like cleavage at the C1-C2 linker region of the ⍺3 chain is not required for collagen VI assembly.

Journal: Matrix biology : journal of the International Society for Matrix Biology

Published: June 24, 2025

ANTXR2 Deficiency Promotes Cellular Senescence and Chondroid Differentiation in Hyaline Fibromatosis Syndrome Fibroblasts.

ANTXR2 Deficiency Promotes Cellular Senescence and Chondroid Differentiation in Hyaline Fibromatosis Syndrome Fibroblasts.

Journal: The Journal of investigative dermatology

Published: November 14, 2024

Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930+189C>T.

Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930+189C>T.

Journal: Brain : a journal of neurology

Published: October 03, 2024

The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy.

The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy.

Journal: medRxiv : the preprint server for health sciences

Published: April 08, 2024

ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.

ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.

Journal: Scientific reports

Published: December 29, 2023

The UCMD-Causing COL6A1 (c.930 + 189C > T) Intron Mutation Leads to the Secretion and Aggregation of Single Mutated Collagen VI α1 Chains.

The UCMD-Causing COL6A1 (c.930 + 189C > T) Intron Mutation Leads to the Secretion and Aggregation of Single Mutated Collagen VI α1 Chains.

Journal: Human mutation

Published: May 15, 2023

The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal-Epidermal Junction of Mouse Skin.

The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal-Epidermal Junction of Mouse Skin.

Journal: International journal of molecular sciences

Published: March 03, 2023

Structure, evolution and expression of zebrafish cartilage oligomeric matrix protein (COMP, TSP5). CRISPR-Cas mutants show a dominant phenotype in myosepta.

Structure, evolution and expression of zebrafish cartilage oligomeric matrix protein (COMP, TSP5). CRISPR-Cas mutants show a dominant phenotype in myosepta.

Journal: Frontiers in endocrinology

Published: July 22, 2022

Lack of evidence for a role of anthrax toxin receptors as surface receptors for collagen VI and for its cleaved-off C5 domain/endotrophin.

Lack of evidence for a role of anthrax toxin receptors as surface receptors for collagen VI and for its cleaved-off C5 domain/endotrophin.

Journal: iScience

Published: February 16, 2022

LTBP1 promotes fibrillin incorporation into the extracellular matrix.

LTBP1 promotes fibrillin incorporation into the extracellular matrix.

Journal: Matrix biology : journal of the International Society for Matrix Biology

Published: December 21, 2021

Anchoring Cords: A Distinct Suprastructure in the Developing Skin.

Anchoring Cords: A Distinct Suprastructure in the Developing Skin.

Journal: The Journal of investigative dermatology

Published: December 06, 2021

Showing 1-12 of 48

Last Updated: 09/26/2026