Pages that link to "Q30716775"

The following pages link to Tissue specificity of a new splice form of the human lysyl hydroxylase 2 gene (Q30716775):

Displaying 35 items.

• Lysyl hydroxylase 3 is a multifunctional protein possessing collagen glucosyltransferase activity. (Q27876225) (← links)
• The third activity for lysyl hydroxylase 3: galactosylation of hydroxylysyl residues in collagens in vitro. (Q27919632) (← links)
• Identification and characterization of a third human, rat, and mouse collagen prolyl 4-hydroxylase isoenzyme (Q28577338) (← links)
• Complete exon-intron organization of the gene for human lysyl hydroxylase 3 (LH3). (Q33891121) (← links)
• Fox-2 protein regulates the alternative splicing of scleroderma-associated lysyl hydroxylase 2 messenger RNA (Q34043151) (← links)
• Characterization of three fragments that constitute the monomers of the human lysyl hydroxylase isoenzymes 1-3. The 30-kDa N-terminal fragment is not required for lysyl hydroxylase activity (Q34123986) (← links)
• Identification of PLOD2 as telopeptide lysyl hydroxylase, an important enzyme in fibrosis (Q34535766) (← links)
• Mechano-regulation of collagen biosynthesis in periodontal ligament (Q34620621) (← links)
• Lysyl hydroxylase 2 induces a collagen cross-link switch in tumor stroma (Q35183870) (← links)
• Genomic structure and embryonic expression of zebrafish lysyl hydroxylase 1 and lysyl hydroxylase 2. (Q35688590) (← links)
• A scalable lysyl hydroxylase 2 expression system and luciferase-based enzymatic activity assay. (Q36285050) (← links)
• Lysine post-translational modifications of collagen (Q36404717) (← links)
• Expanding the lysyl hydroxylase toolbox: new insights into the localization and activities of lysyl hydroxylase 3 (LH3). (Q36828014) (← links)
• Disentangling mechanisms involved in collagen pyridinoline cross-linking: The immunophilin FKBP65 is critical for dimerization of lysyl hydroxylase 2 (Q37065130) (← links)
• Collagen cross-links as a determinant of bone quality: a possible explanation for bone fragility in aging, osteoporosis, and diabetes mellitus (Q37598559) (← links)
• Molecular properties and fibril ultrastructure of types II and XI collagens in cartilage of mice expressing exclusively the α1(IIA) collagen isoform (Q37691905) (← links)
• Effects of Collagen Crosslinking on Bone Material Properties in Health and Disease (Q38384409) (← links)
• Missense mutations that cause Bruck syndrome affect enzymatic activity, folding, and oligomerization of lysyl hydroxylase 2 (Q39798194) (← links)
• Reduction of lysyl hydroxylase 3 causes deleterious changes in the deposition and organization of extracellular matrix. (Q39810232) (← links)
• The glycosyltransferase activities of lysyl hydroxylase 3 (LH3) in the extracellular space are important for cell growth and viability (Q40009117) (← links)
• The post-translational phenotype of collagen synthesized by SAOS-2 osteosarcoma cells (Q40167208) (← links)
• Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 gene. (Q40482578) (← links)
• Lysyl hydroxylase-2b directs collagen cross-linking pathways in MC3T3-E1 cells (Q40539802) (← links)
• Characterization of collagenous peptides bound to lysyl hydroxylase isoforms. (Q42629745) (← links)
• Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome--osteogenesis imperfecta phenotypic spectrum. (Q43581213) (← links)
• The kyphoscoliotic type of Ehlers-Danlos syndrome (type VI): differential effects on the hydroxylation of lysine in collagens I and II revealed by analysis of cross-linked telopeptides from urine (Q44070464) (← links)
• Lysine hydroxylation of collagen in a fibroblast cell culture system (Q44450984) (← links)
• Identification, expression, and tissue distribution of the three rat lysyl hydroxylase isoforms (Q44523748) (← links)
• TIA nuclear proteins regulate the alternate splicing of lysyl hydroxylase 2. (Q46182214) (← links)
• Novel Mutations in PLOD2 Cause Rare Bruck Syndrome (Q49607993) (← links)
• Deletion of cysteine 369 in lysyl hydroxylase 1 eliminates enzyme activity and causes Ehlers-Danlos syndrome type VI. (Q52576719) (← links)
• Identification of Exonic Cis-Elements Regulating the Alternative Splicing of Scleroderma-Associated Lysyl Hydroxylase 2 mRNA (Q54643277) (← links)
• Mutational analysis of 12 patients with the phenotype of Ehlers-Danlos syndrome type VIB shows no linkage to the zinc transporter gene SLC39A13. (Q55136708) (← links)
• Recent examples of α-ketoglutarate-dependent mononuclear non-haem iron enzymes in natural product biosyntheses (Q57169314) (← links)
• Functional diversity of lysyl hydroxylase 2 in collagen synthesis of human dermal fibroblasts (Q64377540) (← links)