544 results on '"Bross, Peter"'
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2. A genome-wide CRISPR-Cas9 knockout screen identifies novel PARP inhibitor resistance genes in prostate cancer
3. Interaction of sortilin with apolipoprotein E3 enables neurons to use long-chain fatty acids as alternative metabolic fuel
4. The psychiatric risk gene BRD1 modulates mitochondrial bioenergetics by transcriptional regulation
5. HSP60 chaperone deficiency disrupts the mitochondrial matrix proteome and dysregulates cholesterol synthesis
6. An inventory of interactors of the human HSP60/HSP10 chaperonin in the mitochondrial matrix space
7. Potential complementation effects of two disease-associated mutations in tetrameric glutaryl-CoA dehydrogenase is due to inter subunit stability-activity counterbalance
8. Effects of a Mutation in the HSPE1 Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental Disorder.
9. Deficiency of the mitochondrial sulfide regulator ETHE1 disturbs cell growth, glutathione level and causes proteome alterations outside mitochondria
10. APD-Containing Cyclolipodepsipeptides Target Mitochondrial Function in Hypoxic Cancer Cells
11. Advancing Clinical Trial Design for Non-Muscle Invasive Bladder Cancer
12. Regulation of Type I Chaperonin Gene Expression
13. Molecular Structure of Chaperonins
14. Chaperoning Mechanisms: Folding Helpers, Folding Protectors, or Misfolding Blockers?
15. Historical Sketch of the Discovery and Recognition of the Function of Chaperonins
16. Sequence Variations in Proteins Affecting Chaperonin Dependence
17. Introduction
18. Human Diseases Caused by Genetic Mutations in the Hsp60/Hsp10 System
19. Evolutionary Origins and Family Relations
20. Molecular Investigations of Disease Mechanisms
21. Application of an Image Cytometry Protocol for Cellular and Mitochondrial Phenotyping on Fibroblasts from Patients with Inherited Disorders
22. A Cell Model for HSP60 Deficiencies: Modeling Different Levels of Chaperonopathies Leading to Oxidative Stress and Mitochondrial Dysfunction
23. Folding by Enclosure in the Chaperonin Cavity
24. Genetic Organization of Type I Chaperonin Genes
25. LEFT MAIN CORONARY ARTERY COMPRESSION BY AORTIC ABSCESS DIAGNOSED BY INTRAVASCULAR ULTRASOUND
26. Mitochondrial Hsp70 and the troubles of nomenclature: leaving behind tradition to gain intuitiveness and clarity
27. Regulation of biologic oncology products in the FDA׳s Center for Biologics Evaluation and Research
28. Outlook
29. Variations in Hsp60 and Hsp10 in Humans
30. Subcellular Localization
31. Type I Chaperonins Are Essential for Cell Viability
32. Digitale Konvergenz und Handlungskonsequenzen
33. Enhanced genome editing in mammalian cells with a modified dual-fluorescent surrogate system
34. Effects of a mutation in the HSPE1 gene encoding the mitochondrial co-chaperonin HSP10 and its potential association with a neurological and developmental disorder
35. Clinical characteristics and symptom duration among outpatients with COVID-19
36. Protein quality control in mitochondria and neurodegeneration in hereditary spastic paraplegia
37. Biochemical Characterisation of Mutations of Human Medium-Chain Acyl-CoA Dehydrogenase
38. Posttranslational Modifications
39. Do lamin A and lamin C have unique roles?
40. Paediatric Strategy Forum for medicinal product development of chimeric antigen receptor T-cells in children and adolescents with cancer
41. A cell model to study different degrees of Hsp60 deficiency in HEK293 cells
42. Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice
43. Human skeletal muscle CD90+ fibro-adipogenic progenitors are associated with muscle degeneration in type 2 diabetic patients
44. Energy metabolism adaptations and gene expression reprogramming in a cellular MAFLD model
45. Introduction
46. The Hsp60 Chaperonin
47. Application of an Image Cytometry Protocol for Cellular and Mitochondrial Phenotyping on Fibroblasts from Patients with Inherited Disorders
48. Metabolic profiling of heat or anoxic stress in mouse C2C12 myotubes using multinuclear magnetic resonance spectroscopy
49. Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia
50. Energy metabolism adaptations and gene expression reprogramming in a cellular MAFLD model
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