glycine has been researched along with Collagen Diseases in 7 studies
Collagen Diseases: Historically, a heterogeneous group of acute and chronic diseases, including rheumatoid arthritis, systemic lupus erythematosus, progressive systemic sclerosis, dermatomyositis, etc. This classification was based on the notion that collagen was equivalent to connective tissue, but with the present recognition of the different types of collagen and the aggregates derived from them as distinct entities, the term collagen diseases now pertains exclusively to those inherited conditions in which the primary defect is at the gene level and affects collagen biosynthesis, post-translational modification, or extracellular processing directly. (From Cecil Textbook of Medicine, 19th ed, p1494)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (28.57) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Pace, RA | 1 |
| Peat, RA | 1 |
| Baker, NL | 1 |
| Zamurs, L | 1 |
| Mörgelin, M | 1 |
| Irving, M | 1 |
| Adams, NE | 1 |
| Bateman, JF | 1 |
| Mowat, D | 1 |
| Smith, NJ | 1 |
| Lamont, PJ | 1 |
| Moore, SA | 1 |
| Mathews, KD | 1 |
| North, KN | 1 |
| Lamandé, SR | 1 |
| Hwang, ES | 1 |
| Brodsky, B | 3 |
| Buevich, AV | 1 |
| Silva, T | 1 |
| Baum, J | 1 |
| Persikov, AV | 1 |
| Pillitteri, RJ | 1 |
| Amin, P | 1 |
| Schwarze, U | 1 |
| Byers, PH | 1 |
| Bonaventure, J | 1 |
| Cohen-Solal, L | 1 |
| Ritvaniemi, P | 1 |
| Van Maldergem, L | 1 |
| Kadhom, N | 1 |
| Delezoide, AL | 1 |
| Maroteaux, P | 1 |
| Prockop, DJ | 2 |
| Ala-Kokko, L | 1 |
| Morejón Sobrón, E | 1 |
7 other studies available for glycine and Collagen Diseases
| Article | Year |
|---|---|
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity.
Topics: Amino Acid Sequence; Cells, Cultured; Collagen Diseases; Collagen Type VI; Connective Tissue; Diseas | 2008 |
Folding delay and structural perturbations caused by type IV collagen natural interruptions and nearby Gly missense mutations.
Topics: Amino Acid Substitution; Collagen Diseases; Collagen Type IV; Glycine; Humans; Mutation, Missense; P | 2012 |
Transformation of the mechanism of triple-helix peptide folding in the absence of a C-terminal nucleation domain and its implications for mutations in collagen disorders.
Topics: Amino Acid Sequence; Circular Dichroism; Collagen; Collagen Diseases; Glycine; Humans; Magnetic Reso | 2004 |
Stability related bias in residues replacing glycines within the collagen triple helix (Gly-Xaa-Yaa) in inherited connective tissue disorders.
Topics: Amino Acid Substitution; Amino Acids; Collagen; Collagen Diseases; Collagen Type I; Collagen Type I, | 2004 |
Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationships.
Topics: Amino Acid Sequence; Aspartic Acid; Base Sequence; Bone Diseases, Developmental; Cartilage; Cells, C | 1995 |
The intracellular biosynthesis of collagen. Some possible implications for diseases of bone and other connective tissues.
Topics: Animals; Ascorbic Acid; Bone Diseases; Carbon Isotopes; Cartilage; Chemical Phenomena; Chemistry; Ch | 1969 |
[New therapeutic trends in osteoarticular diseases and collagen diseases based on the biochemistry of those tissues].
Topics: Amino Acids; Collagen Diseases; Glycine; Humans; Joint Diseases; Lidocaine | 1966 |