serine has been researched along with Congenital Foot Deformities in 4 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "[1996: Am J Med Genet 66:138-143] as Pfeiffer syndrome type III with normal thumbs." | 1.30 | Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type III. ( Bartlett, SP; Gripp, KW; Katowitz, JA; Markowitz, RI; McDonald-McGinn, DM; Muenke, M; Stolle, CA; Zackai, EH, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (75.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kozoriz, MG | 1 |
| Lai, S | 1 |
| Vega, JL | 1 |
| Sáez, JC | 1 |
| Sin, WC | 1 |
| Bechberger, JF | 1 |
| Naus, CC | 1 |
| Oldridge, M | 1 |
| Lunt, PW | 1 |
| Zackai, EH | 2 |
| McDonald-McGinn, DM | 2 |
| Muenke, M | 2 |
| Moloney, DM | 1 |
| Twigg, SR | 1 |
| Heath, JK | 1 |
| Howard, TD | 1 |
| Hoganson, G | 1 |
| Gagnon, DM | 1 |
| Jabs, EW | 1 |
| Wilkie, AO | 1 |
| Gripp, KW | 1 |
| Stolle, CA | 1 |
| Markowitz, RI | 1 |
| Bartlett, SP | 1 |
| Katowitz, JA | 1 |
| Passos-Bueno, MR | 1 |
| Richieri-Costa, A | 1 |
| Sertié, AL | 1 |
| Kneppers, A | 1 |
4 other studies available for serine and Congenital Foot Deformities
| Article | Year |
|---|---|
Cerebral ischemic injury is enhanced in a model of oculodentodigital dysplasia.
Topics: Animals; Astrocytes; Brain Infarction; Brain Ischemia; Cell Death; Cells, Cultured; Connexin 43; Cra | 2013 |
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2.
Topics: Adult; Child; Craniosynostoses; Dipeptides; Female; Foot Deformities, Congenital; Genotype; Hand Def | 1997 |
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type III.
Topics: Abnormalities, Multiple; Acrocephalosyndactylia; Amino Acid Substitution; Cysteine; Elbow; Eye Abnor | 1998 |
Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactyly.
Topics: Acrocephalosyndactylia; Child, Preschool; Foot Deformities, Congenital; Hand Deformities, Congenital | 1998 |