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1. A Upf3b-mutant mouse model with behavioral and neurogenesis defects

2. RNA variant assessment using transactivation and transdifferentiation

3. Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants

4. Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variants

5. Missense variant contribution to USP9X-female syndrome

7. Identification of High Affinity Binding Sites for LexA which Define New DNA Damage-inducible Genes in Escherichia coli

8. Properties of Acinetobacter calcoaceticus recA and its contribution to intracellular gene conversion

9. RNA variant assessment using transactivation and transdifferentiation.

10. Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment.

11. Endogenous protein interactomes resolved through immunoprecipitation-coupled quantitative proteomics in cell lines.

12. Locking down SOS Mutagenesis Repression in a Dynamic Pathogen.

13. Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants.

14. The DUB Club: Deubiquitinating Enzymes and Neurodevelopmental Disorders.

15. Vav Proteins in Development of the Brain: A Potential Relationship to the Pathogenesis of Congenital Zika Syndrome?

16. Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells.

17. Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variants.

18. Development of Novel Follicular Thyroid Cancer Models Which Progress to Poorly Differentiated and Anaplastic Thyroid Cancer.

19. Abnormal Behavior and Cortical Connectivity Deficits in Mice Lacking Usp9x.

20. Missense variant contribution to USP9X-female syndrome.

21. A synonymous UPF3B variant causing a speech disorder implicates NMD as a regulator of neurodevelopmental disorder gene networks.

22. Usp9X Controls Ankyrin-Repeat Domain Protein Homeostasis during Dendritic Spine Development.

23. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.

24. Robust imaging and gene delivery to study human lymphoblastoid cell lines.

25. PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy.

26. Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitors.

27. Structural alterations in tumor-draining lymph nodes before papillary thyroid carcinoma metastasis.

28. Viperin is an important host restriction factor in control of Zika virus infection.

29. USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitors.

30. Immune Suppression Mediated by Myeloid and Lymphoid Derived Immune Cells in the Tumor Microenvironment Facilitates Progression of Thyroid Cancers Driven by Hras G12V and Pten Loss.

31. Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice.

32. Fibroblast-Mediated Collagen Remodeling Within the Tumor Microenvironment Facilitates Progression of Thyroid Cancers Driven by BrafV600E and Pten Loss.

33. Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems.

34. THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability.

35. HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.

36. La FAM fatale: USP9X in development and disease.

37. Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder.

38. Control of human PLP1 expression through transcriptional regulatory elements and alternatively spliced exons in intron 1.

39. Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth.

40. The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth.

41. Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis.

42. A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability.

44. USP9X enhances the polarity and self-renewal of embryonic stem cell-derived neural progenitors.

45. Sensitivity of an Acinetobacter baylyi mpl mutant to DNA damage.

46. A constitutively expressed, truncated umuDC operon regulates the recA-dependent DNA damage induction of a gene in Acinetobacter baylyi strain ADP1.

47. The FAM deubiquitylating enzyme localizes to multiple points of protein trafficking in epithelia, where it associates with E-cadherin and beta-catenin.

48. The expression of the Acinetobacter calcoaceticus recA gene increases in response to DNA damage independently of RecA and of development of competence for natural transformation.

49. Nucleotide sequences transferred by gene conversion in the bacterium Acinetobacter calcoaceticus.

50. Properties of Acinetobacter calcoaceticus recA and its contribution to intracellular gene conversion.

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