proline has been researched along with Abnormalities, Teeth in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Duan, X; Mao, T; Wang, W; Xue, Y | 1 |
| Dressler, P; Hartmann, J; Meyer-Marcotty, P; Stellzig-Eisenhauer, A; Weisschuh, N | 1 |
| Abate-Shen, C; Bendall, AJ; Greenfield, N; Hu, G; Logan, M; Nelson, C; Seidman, CE; Seidman, JG; Stein, S; Vastardis, H; Wang, Z; Zhang, H | 1 |
3 other study(ies) available for proline and Abnormalities, Teeth
| Article | Year |
|---|---|
Report of two Chinese patients suffering from CLCN7-related osteopetrosis and root dysplasia.
Topics: Adult; Arginine; Bone Density; China; Chloride Channels; Dentofacial Deformities; Genes, Recessive; Genetic Variation; Heterozygote; Homozygote; Humans; Leucine; Male; Osteomyelitis; Osteopetrosis; Osteosclerosis; Phenotype; Point Mutation; Proline; Tooth Abnormalities; Tooth Root; Tooth, Unerupted; Tryptophan | 2012 |
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 |
Haploinsufficiency of MSX1: a mechanism for selective tooth agenesis.
Topics: Amino Acid Substitution; Animals; Arginine; Binding Sites; Chickens; DNA; Extremities; Homeodomain Proteins; Humans; Mice; MSX1 Transcription Factor; Proline; Tooth Abnormalities; Transcription Factors | 1998 |