Characterization of a partial cDNA for lysyl hydroxylase from human skin fibroblasts; lysyl hydroxylase mRNAs are regulated differently by minoxidil derivatives and hydralazine.

Structure-activity relationship of minoxidil analogs as inhibitors of lysyl hydroxylase in cultured fibroblasts.

Abnormal properties of collagen lysyl hydroxylase from skin fibroblasts of siblings with hydroxylysine-deficient collagen.

Hydroxylation of lysyl residues in lysine-rich and arginine-rich histones by lysyl hydroxylase in vitro.

Inherited human collagen lysyl hydroxylase deficiency: ascorbic acid response.

TGF-ß induces Lysyl hydroxylase 2b in human synovial osteoarthritic fibroblasts through ALK5 signaling.

Purification and enzymatic properties of lysyl hydroxylase from fetal porcine skin.

Minoxidil specifically decreases the expression of lysine hydroxylase in cultured human skin fibroblasts.

Glomerular protocollagen lysyl-hydroxylase activity in streptozotocin diabetes.

Procollagen Lysyl Hydroxylase 2 Expression Is Regulated by an Alternative Downstream Transforming Growth Factor β-1 Activation Mechanism.

Lysyl hydroxylase 2 induces a collagen cross-link switch in tumor stroma.

Prolyl and lysyl hydroxylase activation and cofactor specificity in young and senescent WI-38 fibroblast cultures.

Deregulation of the lysyl hydroxylase matrix cross-linking system in experimental and clinical bronchopulmonary dysplasia.

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

FKBP65-dependent peptidyl-prolyl isomerase activity potentiates the lysyl hydroxylase 2-driven collagen cross-link switch.

In vitro inhibition of chick embryo lysyl hydroxylase by homogentisic acid. A proposed connective tissue defect in alkaptonuria.

Partial purification and characterization of chick-embryo prolyl 3-hydroxylase.

Origin and content of methionyl-lysyl-bradykinin, lysyl-bradykinin and bradykinin in human urine.

Disentangling mechanisms involved in collagen pyridinoline cross-linking: The immunophilin FKBP65 is critical for dimerization of lysyl hydroxylase 2.

Human skin aryl hydrocarbon hydroxylase. Induction by coal tar.

Multiple mRNAs of monkey tyrosine hydroxylase.

A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers-Danlos syndrome type VI.

Lysyl Hydroxylase 3 Localizes to Epidermal Basement Membrane and Is Reduced in Patients with Recessive Dystrophic Epidermolysis Bullosa.

Purification of lysyl oxidase from piglet skin by selective interaction with Sephacryl S-200.

Phenylalanine hydroxylase activity in fibroblasts.

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Structure-activity relationship of minoxidil analogs as inhibitors of lysyl hydroxylase in cultured fibroblasts.

Abnormal properties of collagen lysyl hydroxylase from skin fibroblasts of siblings with hydroxylysine-deficient collagen.

Hydroxylation of lysyl residues in lysine-rich and arginine-rich histones by lysyl hydroxylase in vitro.

Inherited human collagen lysyl hydroxylase deficiency: ascorbic acid response.

TGF-ß induces Lysyl hydroxylase 2b in human synovial osteoarthritic fibroblasts through ALK5 signaling.

Purification and enzymatic properties of lysyl hydroxylase from fetal porcine skin.

Minoxidil specifically decreases the expression of lysine hydroxylase in cultured human skin fibroblasts.

Glomerular protocollagen lysyl-hydroxylase activity in streptozotocin diabetes.

Procollagen Lysyl Hydroxylase 2 Expression Is Regulated by an Alternative Downstream Transforming Growth Factor β-1 Activation Mechanism.

Lysyl hydroxylase 2 induces a collagen cross-link switch in tumor stroma.

Prolyl and lysyl hydroxylase activation and cofactor specificity in young and senescent WI-38 fibroblast cultures.

Deregulation of the lysyl hydroxylase matrix cross-linking system in experimental and clinical bronchopulmonary dysplasia.

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

FKBP65-dependent peptidyl-prolyl isomerase activity potentiates the lysyl hydroxylase 2-driven collagen cross-link switch.

In vitro inhibition of chick embryo lysyl hydroxylase by homogentisic acid. A proposed connective tissue defect in alkaptonuria.

Partial purification and characterization of chick-embryo prolyl 3-hydroxylase.

Origin and content of methionyl-lysyl-bradykinin, lysyl-bradykinin and bradykinin in human urine.

Disentangling mechanisms involved in collagen pyridinoline cross-linking: The immunophilin FKBP65 is critical for dimerization of lysyl hydroxylase 2.

Human skin aryl hydrocarbon hydroxylase. Induction by coal tar.

Multiple mRNAs of monkey tyrosine hydroxylase.

A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers-Danlos syndrome type VI.

Lysyl Hydroxylase 3 Localizes to Epidermal Basement Membrane and Is Reduced in Patients with Recessive Dystrophic Epidermolysis Bullosa.

Purification of lysyl oxidase from piglet skin by selective interaction with Sephacryl S-200.

Phenylalanine hydroxylase activity in fibroblasts.

Characterization of a partial cDNA for lysyl hydroxylase from human skin fibroblasts; lysyl hydroxylase mRNAs are regulated differently by minoxidil derivatives and hydralazine.

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