List of works - Dirk Hubmacher

ADAMTS proteins as modulators of microfibril formation and function

scientific article

Acromelic dysplasias: how rare musculoskeletal disorders reveal biological functions of extracellular matrix proteins

scientific article published on 02 September 2020

Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia--a novel mouse model providing insights into geleophysic dysplasia

scientific journal article

Classical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein function.

scientific article published on 22 July 2011

Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation

scientific journal article

Early fibrillin-1 assembly monitored through a modifiable recombinant cell approach

scientific article published on 7 March 2014

Effects of iron limitation on the respiratory chain and the membrane cytochrome pattern of the Euryarchaeon Halobacterium salinarum

scientific article published in December 2003

Fibrillin assembly requires fibronectin.

scientific article

Fibrillin-1 interactions with fibulins depend on the first hybrid domain and provide an adaptor function to tropoelastin.

scientific article

Fibrillin-3 expression in human development.

scientific article published on 21 October 2010

Fibrillins, fibulins, and matrix-associated glycoprotein modulate the kinetics and morphology of in vitro self-assembly of a recombinant elastin-like polypeptide.

scientific article published on November 2008

Fibrillins: from biogenesis of microfibrils to signaling functions.

scientific article published on January 2006

Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and function ⬇️

scientific article published on August 20, 2011

Heparin/heparan sulfate controls fibrillin-1, -2 and -3 self-interactions in microfibril assembly

scientific article

Homocysteine modifies structural and functional properties of fibronectin and interferes with the fibronectin-fibrillin-1 interaction.

scientific article

Human eye development is characterized by coordinated expression of fibrillin isoforms

scientific article

Iron-uptake in the Euryarchaeon Halobacterium salinarum.

scientific article published on 23 January 2007

The "other" 15-40%: The Role of Non-Collagenous Extracellular Matrix Proteins and Minor Collagens in Tendon

scientific article published on 26 August 2019

The biology of the extracellular matrix: novel insights

scientific article published on January 2013

Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease.

scientific article published on 08 February 2017

List of works by Dirk Hubmacher

ADAMTS proteins as modulators of microfibril formation and function

Acromelic dysplasias: how rare musculoskeletal disorders reveal biological functions of extracellular matrix proteins

Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia--a novel mouse model providing insights into geleophysic dysplasia

Classical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein function.

Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation

Early fibrillin-1 assembly monitored through a modifiable recombinant cell approach

Effects of iron limitation on the respiratory chain and the membrane cytochrome pattern of the Euryarchaeon Halobacterium salinarum

Fibrillin assembly requires fibronectin.

Fibrillin-1 interactions with fibulins depend on the first hybrid domain and provide an adaptor function to tropoelastin.

Fibrillin-3 expression in human development.

Fibrillins, fibulins, and matrix-associated glycoprotein modulate the kinetics and morphology of in vitro self-assembly of a recombinant elastin-like polypeptide.

Fibrillins: from biogenesis of microfibrils to signaling functions.

Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and function ⬇️

Heparin/heparan sulfate controls fibrillin-1, -2 and -3 self-interactions in microfibril assembly

Homocysteine modifies structural and functional properties of fibronectin and interferes with the fibronectin-fibrillin-1 interaction.

Human eye development is characterized by coordinated expression of fibrillin isoforms

Iron-uptake in the Euryarchaeon Halobacterium salinarum.

The "other" 15-40%: The Role of Non-Collagenous Extracellular Matrix Proteins and Minor Collagens in Tendon

The biology of the extracellular matrix: novel insights

Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease.