27 results on '"Pannetier, Solange"'
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2. Activation of RSK by UV-light: phosphorylation dynamics and involvement of the MAPK pathway
3. Unusual splice-site mutations in the RSK2 gene and suggestion of genetic heterogeneity in Coffin-Lowry syndrome
4. Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin-Lowry syndrome
5. A second family with XLRH displays the mutation S244L in the CLCN5 gene
6. Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations
7. Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome
8. Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome
9. Erratum to: Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome
10. RSK2 Is a Modulator of Craniofacial Development
11. Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin–Lowry syndrome
12. Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2
13. RSK2 Signaling in Medial Habenula Contributes to Acute Morphine Analgesia
14. RSK2 signaling in brain habenula contributes to place aversion learning
15. Erratum to: Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome
16. Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome
17. Coffin–Lowry syndrome
18. Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardation
19. Mitogen-Regulated RSK2-CBP Interaction Controls Their Kinase and Acetylase Activities
20. Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome
21. Coffin-Lowry syndrome: Current status
22. Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues
23. A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation
24. Germline mosaicism in Coffin-Lowry syndrome
25. Coffin–Lowry syndrome.
26. Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP).
27. Coffin-Lowry syndrome.
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