143 results on '"Schänzer, Anne"'
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2. Inhibition of autophagy prevents cardiac dysfunction at early stages of cardiomyopathy in Bag3-deficient hearts
3. Gadolinium contrast agents: dermal deposits and potential effects on epidermal small nerve fibers
4. Muscle diffusion MRI reveals autophagic buildup in a mouse model for Pompe disease
5. Correction: Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking
6. Molecular and cellular evidence for the impact of a hypertrophic cardiomyopathy-associated RAF1 variant on the structure and function of contractile machinery in bioartificial cardiac tissues
7. Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking
8. Rise and fall of peroxisomes during Alzheimer´s disease: a pilot study in human brains
9. A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function
10. Cardiomyocyte maturation alters molecular stress response capacities and determines cell survival upon mitochondrial dysfunction
11. Neuropathologie II: Erkrankungen des zentralen und peripheren Nervensystems: Ausblick auf neue Techniken in der Elektronenmikroskopie
12. Neuropathologie I: Muskuläre Erkrankungen
13. Cardiomyocyte hyperplasia and immaturity but not hypertrophy are characteristic features of patients with RASopathies
14. Skeletal muscle provides the immunological micro-milieu for specific plasma cells in anti-synthetase syndrome-associated myositis
15. Aluminium Chloride instead of Ferric chloride for inducing superior sagittal sinus thrombosis to reduce ferromagnetic artifacts on MRI-imaging in experimental models
16. Small fiber involvement is independent from clinical pain in late-onset Pompe disease
17. Characterization of the neuropathic pain component contributing to myalgia in patients with myotonic dystrophy type 1 and 2.
18. Differentiating idiopathic inflammatory myopathies by automated morphometric analysis of MHC‐1, MHC‐2 and ICAM‐1 in muscle tissue.
19. Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function
20. Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy.
21. A Homozygous NDUFS6 Variant Associated with Neuropathy and Optic Atrophy
22. Automated pipeline for nerve fiber selection and g-ratio calculation in optical microscopy: exploring staining protocol variations
23. A Homozygous NDUFS6Variant Associated with Neuropathy and Optic Atrophy
24. Synaptopodin-2 Isoforms Have Specific Binding Partners and Display Distinct, Muscle Cell Type-Specific Expression Patterns.
25. Distribution of ferritin complex in the adult brain and altered composition in neuroferritinopathy due to a novel variant in the ferritin heavy chain gene FTH1 (c.409_410del; p.H137Lfs*4).
26. Genetic Screening Reveals Heterogeneous Clinical Phenotypes in Patients with Dilated Cardiomyopathy and Troponin T2 Variants
27. Supplementary Figures 1-3 from Extracellular RNA Liberates Tumor Necrosis Factor-α to Promote Tumor Cell Trafficking and Progression
28. Data from Extracellular RNA Liberates Tumor Necrosis Factor-α to Promote Tumor Cell Trafficking and Progression
29. Supplementary Table 1 from Extracellular RNA Liberates Tumor Necrosis Factor-α to Promote Tumor Cell Trafficking and Progression
30. Muscle diffusion MRI reveals autophagic buildup in a mouse model for Pompe disease
31. Automated pipeline for nerve fiber selection and g-ratio calculation in optical microscopy: exploring staining protocol variations
32. Gadolinium contrast agents: dermal deposits and potential effects on epidermal small nerve fibers
33. Neuropathologie I: Muskuläre Erkrankungen
34. Dysregulation of Metabolism and Proteostasis in Skeletal Muscle of a Presymptomatic Pompe Mouse Model
35. Differential Effects of Mutations of Popeye Domain Containing Proteins on Heteromeric Interaction and Membrane Trafficking
36. Morphological and Molecular Patterns of Polymyositis With Mitochondrial Pathology and Inclusion Body Myositis
37. Proteomic and morphological insights and clinical presentation of two young patients with novel mutations of BVES (POPDC1)
38. Quantitative and qualitative evaluation of the hippocampal cytoarchitecture in adult cats with regard to the pathological diagnosis of hippocampal sclerosis
39. Higher expression of High-mobility Group AT Hook Protein 2 (HMGA2) in the border zone compared to the center zone of glioblastoma and a tendency that high HMGA2 expression in the border zone may have a poor impact on survival
40. Identification of a novel homozygous synthesis of cytochrome c oxidase 2 variant in siblings with early‐onset axonal Charcot‐Marie‐Tooth disease
41. Additional file 1 of Small fiber involvement is independent from clinical pain in late-onset Pompe disease
42. Additional file 4 of Small fiber involvement is independent from clinical pain in late-onset Pompe disease
43. Additional file 2 of Small fiber involvement is independent from clinical pain in late-onset Pompe disease
44. Additional file 3 of Small fiber involvement is independent from clinical pain in late-onset Pompe disease
45. Quantitative and qualitative evaluation of the hippocampal cytoarchitecture in adult cats with regard to the pathological diagnosis of hippocampal sclerosis
46. Alteration of myocardial structure and function in RAF1-associated Noonan syndrome: Insights from cardiac disease modeling based on patient-derived iPSCs
47. Cardiomyocyte Hyperplasia and Immaturity but not Hypertrophy are Characteristic Features of Patients with Rasopathies
48. Rubella vaccine–induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity
49. Morphological Characteristics of Idiopathic Inflammatory Myopathies in Juvenile Patients
50. Morphological Characteristics of Idiopathic Inflammatory Myopathies in Juvenile Patients.
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