proline has been researched along with Eye Abnormalities in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Billingsley, G; Glaser, T; Heon, E; Levin, A; Oliver, E; Priston, M; Ritch, R; Vincent, A; Walter, M | 1 |
| Fuse, N; Nishida, K; Takahashi, K; Yokokura, S | 1 |
| Dressler, P; Hartmann, J; Meyer-Marcotty, P; Stellzig-Eisenhauer, A; Weisschuh, N | 1 |
3 other study(ies) available for proline and Eye Abnormalities
| Article | Year |
|---|---|
Further support of the role of CYP1B1 in patients with Peters anomaly.
Topics: Arginine; Aryl Hydrocarbon Hydroxylases; Case-Control Studies; Child; Cytochrome P-450 CYP1B1; Cytochrome P-450 Enzyme System; Eye Abnormalities; Female; Glaucoma; Histidine; Humans; Methionine; Mutation, Missense; Proline; Threonine | 2006 |
Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome.
Topics: Abnormalities, Multiple; Adult; Alanine; Anterior Eye Segment; Asian People; Base Sequence; Child, Preschool; Eye Abnormalities; Female; Forkhead Transcription Factors; Frameshift Mutation; Gene Deletion; Genes, Dominant; Humans; Mutation, Missense; Pedigree; Phenotype; Proline; Protein Structure, Tertiary; Syndrome | 2007 |
Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation.
Topics: Adolescent; Cephalometry; Chromosomes, Human, Pair 13; Codon; Cranial Fossa, Posterior; Craniofacial Abnormalities; Cytosine; Eye Abnormalities; Facial Bones; Female; Forkhead Transcription Factors; Heterozygote; Homeobox Protein PITX2; Homeodomain Proteins; Humans; Leucine; Male; Malocclusion, Angle Class III; Maxilla; Middle Aged; Mutation, Missense; Proline; Sella Turcica; Syndrome; Thymine; Tooth Abnormalities; Transcription Factors; Young Adult | 2008 |