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25 results on '"Casey, A R"'

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1. Disentangling top-down drivers of mortality underlying diel population dynamics of Prochlorococcus in the North Pacific Subtropical Gyre.

2. Complex marine microbial communities partition metabolism of scarce resources over the diel cycle.

4. Altered gene expression in slc4a11−/− mouse cornea highlights SLC4A11 roles.

5. r-Process elements from magnetorotational hypernovae.

6. Standardization of prey immunomarking: does a positive test always indicate predation?

7. The tidal remnant of an unusually metal-poor globular cluster.

8. Application and evaluation of a high-resolution mass spectrometry screening method for veterinary drug residues in incurred fish and imported aquaculture samples.

9. Past, present, and future of the satellite-based automatic identification system: areas of applications (2004-2016).

10. Extremely metal-poor stars from the cosmic dawn in the bulge of the Milky Way.

12. Towards Versatile Document Analysis Systems.

13. Measurement of Intracellular pH.

14. Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of C0L8A2 mutations in Fuchs endothelial corneal dystrophy.

15. A single low-energy, iron-poor supernova as the source of metals in the star SMSS J031300.36−670839.3.

16. Comparison of Amoxicillin/Clavulanic Acid High Dose with Cefdinir in the Treatment of Acute Otitis Media.

17. Frequency of False Positive Amphetamine Screens due to Bupropion Using the Syva Emit II Immunoassay.

18. Sensors and regulators of intracellular pH.

19. Design and Implementation of a Testbed for IEEE 802.15.4 (Zigbee) Performance Measurements.

20. Acellular Pertussis Vaccine Safety and Efficacy in Children, Adolescents and Adults.

21. Intrathecal drug therapy using the Codman Model 3000 Constant Flow Implantable Infusion Pumps: experience with 17 cases.

22. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

23. Giant adrenal myelolipomas: CT and MRI findings.

24. Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies.

25. Bicarbonate transporters in corals point towards a key step in the evolution of cnidarian calcification.

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