proline and Brittle Bone Disease

proline has been researched along with Brittle Bone Disease in 26 studies

Research

Studies (26)

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

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

Reviews

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. 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 Brittle Bone Disease

Article	Year
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