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Keyword [Fragile]
Result: 141 - 160 | Page: 8 of 9
141. BDNF-TrkB Signaling Pathway Is Implicated In Dendritic Spine Development And Abnormal Behaviors In Fragile X Syndrome Mouse Model
142. CLSTN1 Overexpressing In Dendate Gyrus Rescues Hippocampus-dependent Memory Deficits In Fragile X Syndrome Mice
143. Correlation Between Fragile Intertrochanteric Fracture And Knee Joint Degeneration
144. Relationship Between Kv1.1 Expression And Neuronal Excitability In A Mouse Model Of Fragile X Syndrome
145. The Effect And Mechanisms Of Tanshinone ?A In Improving Cognitive Deficits Induced By Status Epilepticus
146. Study On Cognition,social And Maternal Behavior Of Fragile X Syndrome Rat Model
147. 7,8-Dihydroxyflavone Induces Synapse Expression Of AMPA Glua1 And Ameliorates Cognitive And Spine Abnormalities In A Mouse Model Of Fragile X Syndrome
148. Overexpression Of Kv1.1 In The Prefrontal Cortex On The Regulation Of Brain Excitability In Fragile X Syndrome
149. MiR-142 Regulates The Expressions Of PSD95 And Synapsin ? In Hippocampal Neurons Of APP/PS1 Mice Through FMRP To Affect The Abilities Of Learning And Memory
150. Expression Of FXR1 In Colon Cancer And Its Effect On Proliferation And Invasion Of Colon Cancer Cell
151. Molecular Mechanism Underlying Abnormal Social Preference Behavior In Mice Model Of Fragile X Syndrome
152. Clinical Study Of CTX And P1NP In Elderly Patients With OVCF
153. The role of astrocytes in Fragile X neurobiology
154. Activity analysis of the Fragile X mental retardation protein isoforms 1, 2 and 3: Recombinant bacterial expression and purification with subsequent quantitative analysis of binding to in vivo target G quadruplex forming ribonucleic acids and regulation o
155. Early Developmental Alterations in GABAergic Protein Expression in Fragile X Knockout Mice
156. Translation initiation and secondary structure of the fragile X mental retardation 1 mRNA
157. Mechanisms of common fragile site instability and cancer
158. MicroRNA-mediated regulation and the fragile X family of proteins
159. The loss of HNRNPA0 alters the selection of myeloid cell fate and replication dynamics at human chromosomal common fragile sites
160. Brain Development in the Fmr1 KO Mouse Model of Fragile X Syndrom
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