proline has been researched along with Brittle Bone Disease in 26 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 12 (46.15) | 18.7374 |
1990's | 4 (15.38) | 18.2507 |
2000's | 5 (19.23) | 29.6817 |
2010's | 5 (19.23) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Banerjee, S; Erel-Göktepe, I; Onat, B; Tunçer, S; Ulusan, S | 1 |
Aglan, M; Besio, R; Biggiogera, M; Cipolla, L; Forlino, A; Garibaldi, N; Leoni, L; Mottes, M; Otaify, GA; Rossi, A; Sabbioneda, S; Temtamy, SA | 1 |
Bank, RA; Gjaltema, RA | 1 |
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, EH | 1 |
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, M | 1 |
Amor, IM; Eyre, DR; Glorieux, FH; Gruenwald, K; Morello, R; Rauch, F; Roughley, P; Weis, M | 1 |
Galicka, A; Gindzieński, A; Wołczyński, S | 1 |
SUMMER, GK | 1 |
Klein, TE; Radmer, RJ | 1 |
Miltyk, W; Palka, J; Phang, JM; Surazynski, A | 1 |
Krane, SM | 1 |
Bateman, JF; Chan, D; Cole, WG; Mascara, T | 1 |
Turakainen, H | 1 |
Larjava, H; Penttinen, R; Saarni, H; Turakainen, H | 1 |
Bodo, M; Brenner, RE; Karbowski, A; Lehmann, HW; Müller, PK; Rimek, D; Vetter, U; Wörsdörfer, O | 1 |
Burrill, MJ; D'Avis, P; Fedarko, NS; Fergusson, V; Frazier, CR; Shapiro, JR; Sponseller, PD; Tayback, M | 1 |
Gay, S; Lemmen, C; Meigel, WN; Müller, PK | 1 |
Gold, RJ; Goldman, H; Lancaster, G; Scriver, CR; Wong, I | 1 |
Brenner, RE; Bushart, GB; Mörike, M; Teller, WM; Vetter, U | 1 |
Byers, PH; Starman, BJ; Wenstrup, RJ; Willing, MC | 1 |
Ott, R; Pesch, HJ; Pontz, BF; Stöss, H | 1 |
Beck, O; Hirthe, D; Kaiser, G; Kyselka, R; Lindenhayn, K; Mühlbach, R; Schramm, G | 1 |
Bleckmann, H; Buddecke, E; Kresse, H; Wollensak, J | 1 |
Eastoe, JE; Martens, P; Thomas, NR | 1 |
Casteleyn, PP; Moyson, F; Wittek, F | 1 |
Patton, WC; Summer, GK | 1 |
3 review(s) available for proline and Brittle Bone Disease
Article | Year |
---|---|
Molecular insights into prolyl and lysyl hydroxylation of fibrillar collagens in health and disease.
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.
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.
Topics: Amino Acid Sequence; Animals; Collagen; Glycine; Humans; Hydroxyproline; Mice; Models, Biological; Models, Genetic; Molecular Sequence Data; Mutation; Osteogenesis Imperfecta; Proline; Proteins | 2008 |
23 other study(ies) available for proline and Brittle Bone Disease
Article | Year |
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Biodegradable polymer promotes osteogenic differentiation in immortalized and primary osteoblast-like cells.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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].
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].
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.
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].
Topics: Amino Acid Metabolism, Inborn Errors; Humans; Osteogenesis Imperfecta; Proline | 1971 |
Intravenous proline tolerance in osteogenesis imperfecta.
Topics: Adolescent; Adult; Child; Child, Preschool; Collagen; Humans; Osteogenesis Imperfecta; Proline; Time Factors | 1968 |