proline and Osteogenesis Imperfecta

proline has been researched along with Osteogenesis Imperfecta in 26 studies

Research

Studies (26)

TimeframeStudies, this research(%)All Research%
pre-199012 (46.15)18.7374
1990's4 (15.38)18.2507
2000's5 (19.23)29.6817
2010's5 (19.23)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Banerjee, S; Erel-Göktepe, I; Onat, B; Tunçer, S; Ulusan, S1
Aglan, M; Besio, R; Biggiogera, M; Cipolla, L; Forlino, A; Garibaldi, N; Leoni, L; Mottes, M; Otaify, GA; Rossi, A; Sabbioneda, S; Temtamy, SA1
Bank, RA; Gjaltema, RA1
Cobben, JM; Dalton, A; Elting, MW; Fratantoni, SA; Högler, W; Huizer, M; Jimenez, CR; McKeown, C; Meijers-Heijboer, H; Morsman, AC; Nesbitt, IM; Nikkels, PG; Pals, G; Piersma, SR; Shaw, NJ; Sistermans, EA; van Dijk, FS; van Roij, MH; Verbeke, JI; Wijnaendts, LC; Zwikstra, EH1
Angle, B; Burton, BK; Byers, PH; Christiansen, HE; Dineen, R; Eyre, DR; Harris, C; Kim, K; Leistritz, DF; McCarthy, KJ; Pepin, MG; Pyott, SM; Russell, DW; Schwarze, U; Steiner, RD; Sussman, MD; Weis, M1
Amor, IM; Eyre, DR; Glorieux, FH; Gruenwald, K; Morello, R; Rauch, F; Roughley, P; Weis, M1
Galicka, A; Gindzieński, A; Wołczyński, S1
SUMMER, GK1
Klein, TE; Radmer, RJ1
Miltyk, W; Palka, J; Phang, JM; Surazynski, A1
Krane, SM1
Bateman, JF; Chan, D; Cole, WG; Mascara, T1
Turakainen, H1
Larjava, H; Penttinen, R; Saarni, H; Turakainen, H1
Bodo, M; Brenner, RE; Karbowski, A; Lehmann, HW; Müller, PK; Rimek, D; Vetter, U; Wörsdörfer, O1
Burrill, MJ; D'Avis, P; Fedarko, NS; Fergusson, V; Frazier, CR; Shapiro, JR; Sponseller, PD; Tayback, M1
Gay, S; Lemmen, C; Meigel, WN; Müller, PK1
Gold, RJ; Goldman, H; Lancaster, G; Scriver, CR; Wong, I1
Brenner, RE; Bushart, GB; Mörike, M; Teller, WM; Vetter, U1
Byers, PH; Starman, BJ; Wenstrup, RJ; Willing, MC1
Ott, R; Pesch, HJ; Pontz, BF; Stöss, H1
Beck, O; Hirthe, D; Kaiser, G; Kyselka, R; Lindenhayn, K; Mühlbach, R; Schramm, G1
Bleckmann, H; Buddecke, E; Kresse, H; Wollensak, J1
Eastoe, JE; Martens, P; Thomas, NR1
Casteleyn, PP; Moyson, F; Wittek, F1
Patton, WC; Summer, GK1

Reviews

3 review(s) available for proline and Osteogenesis Imperfecta

ArticleYear
Molecular insights into prolyl and lysyl hydroxylation of fibrillar collagens in health and disease.
    Critical reviews in biochemistry and molecular biology, 2017, Volume: 52, Issue:1

    Topics: Animals; Arthrogryposis; Connective Tissue Diseases; Ehlers-Danlos Syndrome; Fibrillar Collagens; Glycosylation; Humans; Hydroxylation; Hydroxylysine; Hydroxyproline; Lysine; Osteogenesis Imperfecta; Proline; Protein Folding

2017
Prolidase-dependent regulation of collagen biosynthesis.
    Amino acids, 2008, Volume: 35, Issue:4

    Topics: Collagen; Cytosol; Dipeptidases; Fibrosis; Gene Expression Regulation, Enzymologic; Humans; Integrin beta1; Ions; Lipids; Models, Biological; Models, Chemical; Models, Genetic; NF-kappa B; Osteogenesis Imperfecta; Proline

2008
The importance of proline residues in the structure, stability and susceptibility to proteolytic degradation of collagens.
    Amino acids, 2008, Volume: 35, Issue:4

    Topics: Amino Acid Sequence; Animals; Collagen; Glycine; Humans; Hydroxyproline; Mice; Models, Biological; Models, Genetic; Molecular Sequence Data; Mutation; Osteogenesis Imperfecta; Proline; Proteins

2008

Other Studies

23 other study(ies) available for proline and Osteogenesis Imperfecta

ArticleYear
Biodegradable polymer promotes osteogenic differentiation in immortalized and primary osteoblast-like cells.
    Biomedical materials (Bristol, England), 2019, 04-29, Volume: 14, Issue:4

    Topics: Biocompatible Materials; Bone and Bones; Bone Regeneration; Bone Substitutes; Cations; Cell Differentiation; Cell Line, Tumor; Cell Survival; Collagen; Collagen Type I; Collagen Type I, alpha 1 Chain; Extracellular Matrix; Humans; Osteoblasts; Osteogenesis; Osteogenesis Imperfecta; Polymers; Proline

2019
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate.
    Disease models & mechanisms, 2019, 06-20, Volume: 12, Issue:6

    Topics: Apoptosis; Autophagy; Cell Survival; Cells, Cultured; Collagen; Fibroblasts; Homeostasis; Humans; Hydroxylation; Mutation; Osteogenesis Imperfecta; Phenylbutyrates; Proline; Stress, Physiological; Unfolded Protein Response

2019
PPIB mutations cause severe osteogenesis imperfecta.
    American journal of human genetics, 2009, Volume: 85, Issue:4

    Topics: Catalysis; Collagen; Cyclophilins; DNA Mutational Analysis; Family Health; Female; Fibroblasts; Humans; Mutation; Osteogenesis Imperfecta; Pregnancy; Procollagen-Proline Dioxygenase; Proline; Protein Structure, Tertiary

2009
Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes.
    Human molecular genetics, 2011, Apr-15, Volume: 20, Issue:8

    Topics: Adolescent; Amino Acid Sequence; Base Sequence; Cells, Cultured; Child; Collagen Type I; Cyclophilins; Extracellular Matrix Proteins; Femur; Fibroblasts; Humans; Hydroxylation; Infant; Infant, Newborn; Membrane Glycoproteins; Molecular Chaperones; Molecular Sequence Data; Osteogenesis Imperfecta; Pedigree; Phenotype; Procollagen; Procollagen-Proline Dioxygenase; Proline; Proline-Rich Protein Domains; Prolyl Hydroxylases; Protein Disulfide-Isomerases; Protein Processing, Post-Translational; Protein Stability; Proteoglycans; Radiography; Ribs; Sequence Deletion; Skull

2011
Severe osteogenesis imperfecta caused by a small in-frame deletion in CRTAP.
    American journal of medical genetics. Part A, 2011, Volume: 155A, Issue:11

    Topics: Blotting, Western; Child, Preschool; Cyclophilins; Exons; Extracellular Matrix Proteins; Female; Fetus; Fluorescent Antibody Technique; Fractures, Bone; Homozygote; Humans; Hydroxylation; Infant; Infant, Newborn; Membrane Glycoproteins; Molecular Chaperones; Osteogenesis Imperfecta; Pedigree; Pregnancy; Pregnancy Trimester, Third; Primary Cell Culture; Proline; Prolyl Hydroxylases; Proteoglycans; Scoliosis; Sequence Deletion

2011
Studies on type I collagen in skin fibroblasts cultured from twins with lethal osteogenesis imperfecta.
    Acta biochimica Polonica, 2003, Volume: 50, Issue:2

    Topics: Aspartic Acid; Base Sequence; Cells, Cultured; Collagen Type I; Cyanogen Bromide; DNA, Complementary; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Histidine; Humans; Infant; Osteogenesis Imperfecta; Peptide Fragments; Point Mutation; Procollagen; Proline; Skin; Trypsin; Twins

2003
Oral proline tolerance in osteogenesis imperfecta.
    Science (New York, N.Y.), 1961, Nov-10, Volume: 134, Issue:3489

    Topics: Collagen; Diet; Humans; Nutrition Assessment; Osteogenesis Imperfecta; Proline

1961
Severity of osteogenesis imperfecta and structure of a collagen-like peptide modeling a lethal mutation site.
    Biochemistry, 2004, May-11, Volume: 43, Issue:18

    Topics: Amino Acid Sequence; Amino Acid Substitution; Collagen; Collagen Type I; Computer Simulation; Genes, Lethal; Glycine; Humans; Hydrogen Bonding; Hydrogen-Ion Concentration; Hydroxyproline; Models, Molecular; Molecular Sequence Data; Osteogenesis Imperfecta; Peptides; Predictive Value of Tests; Proline; Severity of Illness Index

2004
Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta.
    The Biochemical journal, 1984, Jan-01, Volume: 217, Issue:1

    Topics: Cells, Cultured; Chromatography, High Pressure Liquid; Collagen; Cyanogen Bromide; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Humans; Infant, Newborn; Lysine; Osteogenesis Imperfecta; Peptide Fragments; Procollagen; Proline; Protein Biosynthesis; Skin

1984
Altered glycosaminoglycan production in cultured osteogenesis-imperfecta skin fibroblasts.
    The Biochemical journal, 1983, Jul-01, Volume: 213, Issue:1

    Topics: Age Factors; Cells, Cultured; Child; Collagen; Female; Fibroblasts; Glucosamine; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant, Newborn; Male; Middle Aged; Molecular Weight; Osteogenesis Imperfecta; Proline; Protein Biosynthesis; Skin

1983
Synthesis of hyaluronic acid and collagen in skin fibroblasts cultured from patients with osteogenesis imperfecta.
    Biochimica et biophysica acta, 1980, Apr-03, Volume: 628, Issue:4

    Topics: Adolescent; Adult; Cells, Cultured; Child; Collagen; Female; Fibroblasts; Glucuronosyltransferase; Glycosyltransferases; Humans; Hyaluronan Synthases; Hyaluronic Acid; Infant; Male; Membrane Proteins; Osteogenesis Imperfecta; Pregnancy; Proline; Skin; Transferases; Xenopus Proteins

1980
Hydroxylation of collagen type I: evidence that both lysyl and prolyl residues are overhydroxylated in osteogenesis imperfecta.
    European journal of clinical investigation, 1995, Volume: 25, Issue:5

    Topics: Adolescent; Adult; Body Height; Cells, Cultured; Child; Child, Preschool; Collagen; Female; Fibroblasts; Fractures, Bone; Humans; Hydroxylation; Hydroxylysine; Hydroxyproline; Infant; Lysine; Male; Middle Aged; Osteogenesis Imperfecta; Phenotype; Pregnancy; Proline

1995
Cell proliferation of human fibroblasts and osteoblasts in osteogenesis imperfecta: influence of age.
    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 1995, Volume: 10, Issue:11

    Topics: Aging; Cell Division; Cells, Cultured; Collagen; Humans; Osteoblasts; Osteoclasts; Osteogenesis Imperfecta; Proline; Protein Biosynthesis

1995
Disturbance in the regulation of the type of collagen synthesized in a form of osteogenesis imperfecta.
    European journal of biochemistry, 1975, Nov-01, Volume: 59, Issue:1

    Topics: Cells, Cultured; Collagen; Fibroblasts; Fluorescent Antibody Technique; Glycine; Humans; Osteogenesis Imperfecta; Peptide Fragments; Proline; Skin

1975
Dominantly inherited osteogenesis imperfecta in man: an examination of collagen biosynthesis.
    Pediatric research, 1975, Volume: 9, Issue:2

    Topics: Adolescent; Adult; Carbon Radioisotopes; Child; Child, Preschool; Chromatography, Gel; Chromatography, Ion Exchange; Collagen; Dextrans; Fibroblasts; Galactose; Genes, Dominant; Glucose; Humans; Hydroxylation; Hydroxyproline; In Vitro Techniques; Infant; Lysine; Middle Aged; Osteogenesis Imperfecta; Peptide Biosynthesis; Proline

1975
Collagen metabolism in cultured osteoblasts from osteogenesis imperfecta patients.
    The Biochemical journal, 1992, Aug-15, Volume: 286 ( Pt 1)

    Topics: Adolescent; Adult; Cells, Cultured; Child; Child, Preschool; Collagen; Electrophoresis, Polyacrylamide Gel; Female; Fibroblasts; Fractures, Bone; Humans; Macromolecular Substances; Male; Osteoblasts; Osteogenesis Imperfecta; Procollagen; Proline; Reference Values; Skin; Tritium

1992
Distinct biochemical phenotypes predict clinical severity in nonlethal variants of osteogenesis imperfecta.
    American journal of human genetics, 1990, Volume: 46, Issue:5

    Topics: Cells, Cultured; Collagen; Fibroblasts; Genetic Variation; Humans; Macromolecular Substances; Molecular Weight; Osteogenesis Imperfecta; Phenotype; Procollagen; Proline; Protein Conformation; Skin

1990
Heterogeneity of osteogenesis imperfecta. Biochemical and morphological findings in a case of type III according to Sillence.
    European journal of pediatrics, 1986, Volume: 145, Issue:1-2

    Topics: Amino Acids; Bone and Bones; Cartilage; Chromatography, Ion Exchange; Collagen; Endoplasmic Reticulum; Humans; Hydroxylation; Hydroxylysine; Infant; Male; Mitochondrial Swelling; Osteoblasts; Osteogenesis Imperfecta; Proline; Skin

1986
[The significance of the excretion of amino acids and acid mucopolysaccharides in the urine in orthopedic diseases].
    Beitrage zur Orthopadie und Traumatologie, 1969, Volume: 16, Issue:10

    Topics: Adolescent; Adult; Amino Acids; Bone Diseases; Chromatography, Paper; Collagen; Glycosaminoglycans; Humans; Hydroxyproline; Osteitis Deformans; Osteogenesis Imperfecta; Osteomalacia; Osteoporosis; Proline; Scheuermann Disease

1969
[Glycosaminoglycan and collagen analyses in osteogenesis imperfecta].
    Zeitschrift fur Kinderheilkunde, 1971, Volume: 110, Issue:1

    Topics: Acetone; Aorta; Autoanalysis; Bone and Bones; Cartilage; Cartilage, Articular; Child, Preschool; Chondroitin; Collagen; Femur; Glycosaminoglycans; Hexosamines; Humans; Hydroxyproline; Intervertebral Disc; Keratins; Lysine; Male; Methods; Microscopy, Electron; Osteogenesis Imperfecta; Proline; Sclera; Skin

1971
The amino-acid composition of human hard tissue collagens in osteogenesis imperfecta and dentinogenesis imperfecta.
    Calcified tissue research, 1973, May-09, Volume: 12, Issue:2

    Topics: Alanine; Amino Acids; Bone and Bones; Child; Collagen; Dentin; Dentinogenesis Imperfecta; Glycine; Humans; Hydroxylysine; Hydroxyproline; Infant, Newborn; Male; Molar; Osteogenesis Imperfecta; Proline; Skull

1973
[Osteogenesis imperfecta. Current status].
    Acta paediatrica Belgica, 1971, Volume: 25, Issue:6

    Topics: Amino Acid Metabolism, Inborn Errors; Humans; Osteogenesis Imperfecta; Proline

1971
Intravenous proline tolerance in osteogenesis imperfecta.
    Metabolism: clinical and experimental, 1968, Volume: 17, Issue:1

    Topics: Adolescent; Adult; Child; Child, Preschool; Collagen; Humans; Osteogenesis Imperfecta; Proline; Time Factors

1968