588 results on '"Cruts Marc"'
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2. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood
3. Frontotemporal dementia and its subtypes: a genome-wide association study
4. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
5. Clinical variability and onset age modifiers in an extended Belgian GRN founder family
6. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood
7. Modifiers of GRN-Associated Frontotemporal Lobar Degeneration
8. Data Mining: Applying the AD&FTD Mutation Database to Progranulin
9. List of Contributors
10. Frontotemporal dementia
11. Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation
12. Chromosome 17-linked Frontotemporal dementia with Ubiquitin-Positive, Tau-Negative Inclusions
13. Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth
14. The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS
15. Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
16. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
17. TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
18. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
19. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia
20. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
21. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
22. Geneticsof frontotemporal dementia and related disorders
23. Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins
24. Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
25. Reduced secretion and altered proteolytic processing caused by missense mutations in progranulin
26. hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations
27. The genetics and neuropathology of frontotemporal lobar degeneration
28. Call for participation in the neurogenetics consortium within the Human Variome Project
29. Cholesterol and triglycerides moderate the effect of apolipoprotein e on memory functioning in older adults
30. Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample
31. A Major Genetic Factor at Chromosome 9p Implicated in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Degeneration (FTLD)
32. Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort
33. A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
34. Diagnostic accuracy of the Preclinical AD Scale (PAS) in cognitively mildly impaired subjects
35. Dose dependent effect of APOE ɛ4 on behavioral symptoms in frontal lobe dementia
36. Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion
37. The gene encoding nicastrin, a major [gamma]-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample. (Report)
38. Locus-specific mutation databases for neurodegenerative brain diseases
39. Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
40. Apolipoprotein E genotype and progression of Alzheimer’s disease: the Rotterdam Study
41. Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNA
42. Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar Degeneration
43. TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
44. Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update
45. Identification of 2 Loci at Chromosomes 9 and 14 in a Multiplex Family With Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
46. Chromosome 17-linked Frontotemporal dementia with Ubiquitin-Positive, Tau-Negative Inclusions
47. Molecular Pathogenesis of Frontotemporal Lobar Degeneration: Basic Science Seminar in Neurology
48. Alzheimer and Parkinson Diagnoses in Progranulin Null Mutation Carriers in an Extended Founder Family
49. Progranulin Null Mutations in Both Sporadic and Familial Frontotemporal Dementia
50. Mutations Other Than Null Mutations Producing a Pathogenic Loss of Progranulin in Frontotemporal Dementia
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