32 results on '"Wilson, Gabrielle R"'
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2. The emerging role of Rab GTPases in the pathogenesis of Parkinsonʼs disease
3. Molecular analysis of the PArkin co-regulated gene and association with male infertility
4. Developing bone marrow transplant and novel therapeutic vectors to treat Friedreich ataxia: OS6
5. DEVELOPING NOVEL THERAPIES AND BIOMARKERS FOR FRIEDREICH ATAXIA: O14
6. Familial early onset Parkinson's disease caused by a homozygous frameshift variant in PARK7: Clinical features and literature update
7. Genetic Analysis of RAB39B in an Early-Onset Parkinson's Disease Cohort
8. Distribution of Parkinson’s disease associated RAB39B in mouse brain tissue
9. Distribution of Parkinson’s disease associated RAB39B in mouse brain tissue
10. Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse
11. Experimental Autoimmune Anti–Glomerular Basement Membrane Glomerulonephritis: A Protective Role for IFN-γ
12. Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype
13. Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype
14. Generation of RAB39B knockout isogenic human embryonic stem cell lines to model RAB39B-mediated Parkinson's disease
15. Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype
16. 374. Developing Bone Marrow Transplant and Lentiviral Vectors to Treat Friedreich Ataxia
17. ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy
18. Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype.
19. 395. Developing Bone Marrow Transplant and Lentiviral Vectors for Friedreich Ataxia
20. Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology
21. Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency
22. The role of the Parkin Co-Regulated Gene (PACRG) in male infertility
23. Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome
24. ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible
25. Expression and localization of the Parkin Co-Regulated Gene in mouse CNS suggests a role in ependymal cilia function
26. Regional and cellular localisation of Parkin Co-Regulated Gene in developing and adult mouse brain
27. Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome.
28. Additional file 1 of Distribution of Parkinson’s disease associated RAB39B in mouse brain tissue
29. Additional file 1 of Distribution of Parkinson’s disease associated RAB39B in mouse brain tissue
30. IL-12p40 and IL-18 in crescentic glomerulonephritis: IL-12p40 is the key Th1-defining cytokine chain, whereas IL-18 promotes local inflammation and leukocyte recruitment.
31. Experimental autoimmune Goodpasture's disease: a pathogenetic role for both effector cells and antibody in injury.
32. Experimental autoimmune anti-glomerular basement membrane glomerulonephritis: a protective role for IFN-gamma.
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