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1. Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives

2. Bacterial Protein Homeostasis Disruption as a Therapeutic Intervention.

3. The EU-ToxRisk method documentation, data processing and chemical testing pipeline for the regulatory use of new approach methods.

4. Determination of benchmark concentrations and their statistical uncertainty for cytotoxicity test data and functional in vitro assays.

5. Prdm12 Directs Nociceptive Sensory Neuron Development by Regulating the Expression of the NGF Receptor TrkA.

8. In vitro acute and developmental neurotoxicity screening: an overview of cellular platforms and high-throughput technical possibilities.

9. Efficient Recombinase-Mediated Cassette Exchange in hPSCs to Study the Hepatocyte Lineage Reveals AAVS1 Locus-Mediated Transgene Inhibition.

10. Small heat shock proteins target mutant cystic fibrosis transmembrane conductance regulator for degradation via a small ubiquitin-like modifier-dependent pathway.

11. Serine/threonine phosphatase Stp1 mediates post-transcriptional regulation of hemolysin, autolysis, and virulence of group B Streptococcus.

12. Two paediatric cases of skin and soft-tissue infections due to clindamycin-resistant Staphylococcus aureus carrying a plasmid-encoded vga(A) allelic variant for a putative efflux pump.

13. Regulation of hemolysin expression and virulence of Staphylococcus aureus by a serine/threonine kinase and phosphatase.

14. Cysteine string protein promotes proteasomal degradation of the cystic fibrosis transmembrane conductance regulator (CFTR) by increasing its interaction with the C terminus of Hsp70-interacting protein and promoting CFTR ubiquitylation.

15. Contribution of the HEDJ/ERdj3 cysteine-rich domain to substrate interactions.

16. ADD66, a gene involved in the endoplasmic reticulum-associated degradation of alpha-1-antitrypsin-Z in yeast, facilitates proteasome activity and assembly.

17. Cysteine string protein monitors late steps in cystic fibrosis transmembrane conductance regulator biogenesis.

18. Accumulation of mutant alpha1-antitrypsin Z in the endoplasmic reticulum activates caspases-4 and -12, NFkappaB, and BAP31 but not the unfolded protein response.

19. Grp78, Grp94, and Grp170 interact with alpha1-antitrypsin mutants that are retained in the endoplasmic reticulum.

20. Complement: a critical test of its biological importance.

21. Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiency.

22. Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism.

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