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Lysyl hydroxylase 2 is a specific telopeptide hydroxylase, while all three isoenzymes hydroxylate collagenous sequences.

Lysyl hydroxylase 3 (LH3) modifies proteins in the extracellular space, a novel mechanism for matrix remodeling.

Lysyl hydroxylase 3 (LH3) modifies proteins in the extracellular space, a novel mechanism for matrix remodeling

Lysyl hydroxylase 3 is secreted from cells by two pathways.

Lysyl hydroxylase 3 is secreted from cells by two pathways.

Lysyl hydroxylase 3 is secreted from cells by two pathways

Lysyl Hydroxylase 3 Modifies Lysine Residues to Facilitate Oligomerization of Mannan-Binding Lectin.

Lysyl hydroxylase 3 modifies lysine residues to facilitate oligomerization of mannan-binding lectin

Regulation of EBNA1 Protein Stability by PLOD1 Lysine Hydroxylase

Characterization of recombinant human prolyl 3-hydroxylase isoenzyme 2, an enzyme modifying the basement membrane collagen IV.

Type I and type V procollagen triple helix use different subsets of the molecular ensemble for lysine post-translational modifications in the rER

Premature aggregation of type IV collagen and early lethality in lysyl hydroxylase 3 null mice.

Missense mutations that cause Bruck syndrome affect enzymatic activity, folding and oligomerization of lysyl hydroxylase 2.

Dimerization of human lysyl hydroxylase 3 (LH3) is mediated by the amino acids 541-547.

Dimerization of human lysyl hydroxylase 3 (LH3) is mediated by the amino acids 541-547.

Dimerization of human lysyl hydroxylase 3 (LH3) is mediated by the amino acids 541-547

Dimerization of human lysyl hydroxylase 3 (LH3) is mediated by the amino acids 541-547

FK506 binding protein 10: a key actor of collagen crosslinking in clear cell renal cell carcinoma

Glycosylation catalyzed by lysyl hydroxylase 3 is essential for basement membranes.

Expanding the lysyl hydroxylase toolbox: New insights into the localization and activities of lysyl hydroxylase 3 (LH3).

A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene.

A connective tissue disorder caused by mutations of the lysyl hydroxylase 3 gene

Expanding the lysyl hydroxylase toolbox: new insights into the localization and activities of lysyl hydroxylase 3 (LH3)

Glycosylation catalyzed by lysyl hydroxylase 3 is essential for basement membranes

Tissue-specific changes in the hydroxylysine content and crosslinks of collagens and alterations in fibril morphology in lysyl hydroxylase 1 knock-out mice.

Tissue-specific changes in the hydroxylysine content and crosslinks of collagens and alterations in fibril morphology in lysyl hydroxylase 1 knock-out mice.

Tissue-specific changes in the hydroxylysine content and crosslinks of collagens and alterations in fibril morphology in lysyl hydroxylase 1 knock-out mice.

The glycosyltransferase activities of lysyl hydroxylase 3 (LH3) in the extracellular space are important for cell growth and viability.

The glycosyltransferase activities of lysyl hydroxylase 3 (LH3) in the extracellular space are important for cell growth and viability.

Reduction of lysyl hydroxylase 3 causes deleterious changes in the deposition and organization of extracellular matrix.

Reduction of lysyl hydroxylase 3 causes deleterious changes in the deposition and organization of extracellular matrix

The glycosyltransferase activities of lysyl hydroxylase 3 (LH3) in the extracellular space are important for cell growth and viability

Berberine Attenuates Cell Motility <em>via</em> Inhibiting Inflammation-Mediated Lysyl Hydroxylase-2 and Glycolysis

Characterization of collagenous peptides bound to lysyl hydroxylase isoforms.

The lysyl hydroxylase isoforms are widely expressed during mouse embryogenesis, but obtain tissue- and cell-specific patterns in the adult.

The lysyl hydroxylase isoforms are widely expressed during mouse embryogenesis, but obtain tissue- and cell-specific patterns in the adult.

The Activities of Lysyl Hydroxylase 3 (LH3) Regulate the Amount and Oligomerization Status of Adiponectin.

The Activities of Lysyl Hydroxylase 3 (LH3) Regulate the Amount and Oligomerization Status of Adiponectin.

Clioquinol inhibits dopamine-β-hydroxylase secretion and noradrenaline synthesis by affecting the redox status of ATOX1 and copper transport in human neuroblastoma SH-SY5Y cells.

The activities of lysyl hydroxylase 3 (LH3) regulate the amount and oligomerization status of adiponectin

The lysyl hydroxylase isoforms are widely expressed during mouse embryogenesis, but obtain tissue- and cell-specific patterns in the adult

Characterization of collagenous peptides bound to lysyl hydroxylase isoforms

Retrieval-independent localization of lysyl hydroxylase in the endoplasmic reticulum via a peptide fold in its iron-binding domain

Correction: Procollagen-lysine 2-oxoglutarate 5-dioxygenase 2 promotes hypoxia-induced glioma migration and invasion

Cells, Vol. 10, Pages 1008: Transcriptome Analysis of Hypoxic Lymphatic Endothelial Cells Indicates Their Potential to Contribute to Extracellular Matrix Rearrangement

PLOD1 acts as a tumor promoter in glioma via activation of the HSF1 signaling pathway

Biomolecules, Vol. 11, Pages 1842: Identification and Validation of PLOD2 as an Adverse Prognostic Biomarker for Oral Squamous Cell Carcinoma

The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation

Genes, Vol. 11, Pages 1518: Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G&gt;A) in Different Horse Breeds from Europe and the United States

Adipose-derived stromal cells improve functional recovery after spinal cord injury through TGF-β1/Smad3/PLOD2 pathway activation.