serine has been researched along with Child Development Deviations 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 |
|---|---|---|
| "The observed constellation of microcephaly, deafness, cryptorchidism, developmental delay, hypertension, and bilateral pheochromocytoma in association with a VHL mutation A451G in a patient with negative family history has not previously been described in the literature." | 1.32 | Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene. ( Assadi, F; Brackbill, EL, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ali, Z | 1 |
| Zulfiqar, S | 1 |
| Klar, J | 1 |
| Wikström, J | 1 |
| Ullah, F | 1 |
| Khan, A | 1 |
| Abdullah, U | 1 |
| Baig, S | 1 |
| Dahl, N | 1 |
| Damseh, N | 1 |
| Simonin, A | 1 |
| Jalas, C | 1 |
| Picoraro, JA | 1 |
| Shaag, A | 1 |
| Cho, MT | 1 |
| Yaacov, B | 1 |
| Neidich, J | 1 |
| Al-Ashhab, M | 1 |
| Juusola, J | 1 |
| Bale, S | 1 |
| Telegrafi, A | 1 |
| Retterer, K | 1 |
| Pappas, JG | 1 |
| Moran, E | 1 |
| Cappell, J | 1 |
| Anyane Yeboa, K | 1 |
| Abu-Libdeh, B | 1 |
| Hediger, MA | 1 |
| Chung, WK | 1 |
| Elpeleg, O | 1 |
| Edvardson, S | 1 |
| Assadi, F | 1 |
| Brackbill, EL | 1 |
| de Koning, TJ | 1 |
| Klomp, LW | 1 |
1 review available for serine and Child Development Deviations
| Article | Year |
|---|---|
Serine-deficiency syndromes.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic, Inborn; Carbohydrate | 2004 |
3 other studies available for serine and Child Development Deviations
| Article | Year |
|---|---|
Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features.
Topics: Adult; Aged; Amino Acid Sequence; Atrophy; Base Sequence; Binding Sites; Brain; Cerebellar Ataxia; C | 2017 |
Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination.
Topics: Adolescent; Amino Acid Transport System ASC; Biological Transport; Child; Child, Preschool; Developm | 2015 |
Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene.
Topics: Adrenal Gland Neoplasms; Amino Acid Substitution; Child; Cryptorchidism; Developmental Disabilities; | 2003 |