N-Acetyl-Cysteine: Modulating the Cysteine Redox Proteome in Neurodegenerative Diseases

M Martinez-Banaclocha - Antioxidants, 2022 - mdpi.com
In the last twenty years, significant progress in understanding the pathophysiology of age-
associated neurodegenerative diseases has been made. However, the prevention and …

Structural insights into the activation mechanisms of human HtrA serine proteases

D Zurawa-Janicka, T Wenta, M Jarzab… - Archives of biochemistry …, 2017 - Elsevier
Human HtrA1-4 proteins belong to the HtrA family of evolutionarily conserved serine
proteases and function as important modulators of many physiological processes, including …

Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL

H Nozaki, T Kato, M Nihonmatsu, Y Saito, I Mizuta… - Neurology, 2016 - AAN Enterprises
Objective: To elucidate the molecular mechanism of mutant HTRA1-dependent cerebral
small vessel disease in heterozygous individuals. Methods: We recruited 113 unrelated …

Determinants of amyloid fibril degradation by the PDZ protease HTRA1

S Poepsel, A Sprengel, B Sacca, F Kaschani… - Nature chemical …, 2015 - nature.com
Excessive aggregation of proteins has a major impact on cell fate and is a hallmark of
amyloid diseases in humans. To resolve insoluble deposits and to maintain protein …

Development of a therapeutic anti-HtrA1 antibody and the identification of DKK3 as a pharmacodynamic biomarker in geographic atrophy

I Tom, VC Pham, KJ Katschke Jr, W Li… - Proceedings of the …, 2020 - National Acad Sciences
Genetic polymorphisms in the region of the trimeric serine hydrolase high-temperature
requirement 1 (HTRA1) are associated with increased risk of age-related macular …

Biochemical mechanisms of aggregation in TGFBI-linked corneal dystrophies

NS Nielsen, ET Poulsen, MV Lukassen… - Progress in Retinal and …, 2020 - Elsevier
Transforming growth factor-β-induced protein (TGFBIp), an extracellular matrix protein, is the
second most abundant protein in the corneal stroma. In this review, we summarize the …

Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease

I Di Donato, S Bianchi, GN Gallus… - CNS neuroscience & …, 2017 - Wiley Online Library
Aims Cerebral small vessel disease (SVD) is the leading cause of vascular dementia.
Although the most of cases are sporadic, familial monogenic causes have been identified in …

[HTML][HTML] 10q26–The enigma in age-related macular degeneration

DA Merle, M Sen, A Armento, CM Stanton… - Progress in Retinal and …, 2023 - Elsevier
Despite comprehensive research efforts over the last decades, the pathomechanisms of age-
related macular degeneration (AMD) remain far from being understood. Large-scale …

HtrA4 is up-regulated during trophoblast syncytialization and BeWo cells fail to syncytialize without HtrA4

M Mansilla, Y Wang, R Lim, K Palmer, G Nie - Scientific Reports, 2021 - nature.com
The outer layer of the human placenta comprises syncytiotrophoblast, which forms through
fusion of cytotrophoblasts (syncytialization), and plays a critical role in maternal–fetal …

[HTML][HTML] N-Terminomics identifies HtrA1 cleavage of thrombospondin-1 with generation of a proangiogenic fragment in the polarized retinal pigment epithelial cell …

C Chen, E Melo, P Jakob, A Friedlein, B Elsässer… - Matrix Biology, 2018 - Elsevier
Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in
the elderly population. Variants in the HTRA1-ARMS2 locus have been linked to increased …