sr 95531 has been researched along with Autosomal Chromosome Disorders in 1 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Artigas, F; Bastlund, JF; Bussey, TJ; Celada, P; Didriksen, M; Fejgin, K; Heath, CJ; Kent, BA; Larsen, PH; Nielsen, J; Nielsen, V; Nilsson, SRO; Robbins, TW; Saksida, LM; Santana, N; Stensbøl, TB; Thelin, J | 1 |
1 other study(ies) available for sr 95531 and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
A mouse model of the 15q13.3 microdeletion syndrome shows prefrontal neurophysiological dysfunctions and attentional impairment.
Topics: Animals; Attention Deficit Disorder with Hyperactivity; Behavior, Animal; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 15; Disease Models, Animal; Evoked Potentials, Auditory; Extinction, Psychological; GABA Antagonists; Gene Deletion; Humans; Intellectual Disability; Interneurons; Male; Mice; Mice, Inbred C57BL; Prefrontal Cortex; Pyramidal Cells; Pyridazines; Reaction Time; Receptors, GABA-A; Reversal Learning; Schizophrenia; Schizophrenic Psychology; Seizures | 2016 |