asparagine has been researched along with Microcephaly in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 4 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Cheng, G; Cui, S; Dong, Y; Du, K; Li, H; Li, Y; Liu, L; Ren, C; Wang, H; Wang, J; Xia, L; Xu, Y; Yang, B; Zhang, X; Zhu, C | 1 |
| Bloom, LB; Chang, MC; Collins Ruff, K; Franz, DN; Kilberg, MS; McKenna, R; Merritt, ME; Qian, Z; Staklinski, SJ; Yu, F | 1 |
| Bekri, S; Guerrot, AM; Kilberg, MS; Lecoquierre, F; Snanoudj, S; Staklinski, SJ; Vanhulle, C | 1 |
| Chang, MC; Kilberg, MS; Malut, VR; Merritt, ME; Pierre, GL; Staklinski, SJ | 1 |
| de Koning, TJ | 1 |
| Cheng, ML; Deng, YQ; Hu, B; Huang, XY; Ji, X; Li, C; Li, G; Li, XF; Liu, ZY; Qin, CF; Shi, PY; Shi, W; Wang, HJ; Wang, X; Wu, M; Xie, DY; Xu, YP; Xu, Z; Ye, Q; Yu, JY; Yuan, L; Zhang, F; Zhu, XL | 1 |
1 review(s) available for asparagine and Microcephaly
| Article | Year |
|---|---|
Amino acid synthesis deficiencies.
Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Asparagine; Brain Diseases; Central Nervous System; Fetal Growth Retardation; Glutamine; High-Throughput Nucleotide Sequencing; Humans; Ichthyosis; Limb Deformities, Congenital; Metabolic Diseases; Mice; Microcephaly; Proline; Serine | 2017 |
5 other study(ies) available for asparagine and Microcephaly
| Article | Year |
|---|---|
An intractable epilepsy phenotype of ASNS novel mutation in two patients with asparagine synthetase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartate-Ammonia Ligase; Drug Resistant Epilepsy; Humans; Intellectual Disability; Microcephaly; Mutation; Neurodegenerative Diseases; Phenotype | 2022 |
Cellular and molecular characterization of two novel asparagine synthetase gene mutations linked to asparagine synthetase deficiency.
Topics: Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartate-Ammonia Ligase; Atrophy; Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor; Child; HEK293 Cells; Humans; Intellectual Disability; Microcephaly; Mutation; Neurodegenerative Diseases | 2022 |
Analysis of Enzyme Activity and Cellular Function for the N80S and S480F Asparagine Synthetase Variants Expressed in a Child with Asparagine Synthetase Deficiency.
Topics: Asparagine; Aspartate-Ammonia Ligase; Atrophy; Child; Humans; Intellectual Disability; Microcephaly; Nervous System Malformations; Seizures | 2022 |
Metabolomic Profiling of Asparagine Deprivation in Asparagine Synthetase Deficiency Patient-Derived Cells.
Topics: Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartate-Ammonia Ligase; Aspartic Acid; Atrophy; Humans; Intellectual Disability; Microcephaly | 2023 |
A single mutation in the prM protein of Zika virus contributes to fetal microcephaly.
Topics: Americas; Amino Acid Substitution; Animals; Asparagine; Cell Line, Tumor; Cricetinae; Disease Outbreaks; Humans; Incidence; Mice; Microcephaly; Mutation; Neural Stem Cells; Polynesia; Serine; Viral Envelope Proteins; Zika Virus; Zika Virus Infection | 2017 |