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25 in total

1. Inactivation of skeletal-muscle UDP-glucose pyrophosphorylase by reaction with carboxylate-directed reagents.

Authors: M Signorini; C Ferrari; E Mariotti; F Dallocchio; C M Bergamini
Journal: Biochem J Date: 1989-12-15 Impact factor: 3.857

2. Development of a novel method for analyzing collagen O-glycosylations by hydrazide chemistry.

Authors: Yuki Taga; Masashi Kusubata; Kiyoko Ogawa-Goto; Shunji Hattori
Journal: Mol Cell Proteomics Date: 2012-01-13 Impact factor: 5.911

3. Serum enzymes of collagen synthesis and type III procollagen aminopropeptide in Nigerian patients with sickle cell disease.

Authors: D M Bolarin
Journal: J Natl Med Assoc Date: 1986-07 Impact factor: 1.798

4. Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.

Authors: Yasemin Alanay; Hrispima Avaygan; Natalia Camacho; G Eda Utine; Koray Boduroglu; Dilek Aktas; Mehmet Alikasifoglu; Ergul Tuncbilek; Diclehan Orhan; Filiz Tiker Bakar; Bernard Zabel; Andrea Superti-Furga; Leena Bruckner-Tuderman; Cindy J R Curry; Shawna Pyott; Peter H Byers; David R Eyre; Dustin Baldridge; Brendan Lee; Amy E Merrill; Elaine C Davis; Daniel H Cohn; Nurten Akarsu; Deborah Krakow
Journal: Am J Hum Genet Date: 2010-04-01 Impact factor: 11.025

5. Prolonged exercise causes an increase in the activity of galactosylhydroxylysyl glucosyltransferase and in the concentration of type III procollagen aminopropeptide in human serum.

Authors: T E Takala; J Vuori; H Anttinen; K Väänänen; R Myllylä
Journal: Pflugers Arch Date: 1986-11 Impact factor: 3.657

Collagen glycosyltransferases.

1. Inactivation of skeletal-muscle UDP-glucose pyrophosphorylase by reaction with carboxylate-directed reagents.

2. Development of a novel method for analyzing collagen O-glycosylations by hydrazide chemistry.

3. Serum enzymes of collagen synthesis and type III procollagen aminopropeptide in Nigerian patients with sickle cell disease.

4. Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.

5. Prolonged exercise causes an increase in the activity of galactosylhydroxylysyl glucosyltransferase and in the concentration of type III procollagen aminopropeptide in human serum.

6. Immunological characterization of lysyl hydroxylase, an enzyme of collagen synthesis.

7. Regulation of collagen post-translational modification in transformed human and chick-embryo cells.

8. Core glycosylation of collagen is initiated by two beta(1-O)galactosyltransferases.

9. A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase gene.

Review 10. Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta.