38 results on '"Henke, Katrin"'
Search Results
2. Who Let the Dogs Out? Unmasking the Neglected: A Semi-Systematic Review on the Enduring Impact of Toxocariasis, a Prevalent Zoonotic Infection
3. The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish
4. Genetically engineered zebrafish as models of skeletal development and regeneration
5. Case report: Probable toxocariasis in a Swiss adult patient with hypereosinophilic syndrome and multiorgan involvement
6. Stroke-heart syndrome: A case report and mini literature review
7. The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish
8. Zebrafish mutants reveal unexpected role of Lrp5 in osteoclast regulation
9. Resolving primary pathomechanisms driving idiopathic-like spinal curvature using a new katnb1 scoliosis model
10. Latent developmental potential to form limb-like skeletal structures in zebrafish
11. Notochordal Signals Establish Phylogenetic Identity of the Teleost Spine
12. SCO-Spondin Defects and Neuroinflammation Are Conserved Mechanisms Driving Spinal Deformity across Genetic Models of Idiopathic Scoliosis
13. Correction: Unique and non-redundant function of csf1r paralogues in regulation and evolution of post-embryonic development of the zebrafish
14. celsr1a is essential for tissue homeostasis and onset of aging phenotypes in the zebrafish
15. Unique and non-redundant function of csf1r paralogues in regulation and evolution of post-embryonic development of the zebrafish
16. Author response: celsr1a is essential for tissue homeostasis and onset of aging phenotypes in the zebrafish
17. Celsr1a is essential for tissue homeostasis and onset of aging phenotypes in the zebrafish
18. Clearance by Microglia Depends on Packaging of Phagosomes into a Unique Cellular Compartment
19. Cyclin-dependent kinase 21 is a novel regulator of proliferation and meiosis in the male germline of zebrafish
20. SCO-Spondin Defects and Neuroinflammation Identified as Conserved Mechanisms Driving Severe Spine Deformity Across Genetic Models of Idiopathic Scoliosis
21. Latent Developmental Potential to Form Limb-Like Skeletal Structures in Zebrafish
22. Latent developmental potential to form limb-like skeletal structures in zebrafish
23. Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies
24. Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies
25. Genetic Screen for Postembryonic Development in the Zebrafish (Danio rerio): Dominant Mutations Affecting Adult Form
26. Utility of quantitative micro-computed tomographic analysis in zebrafish to define gene function during skeletogenesis
27. Identification of G protein-coupled receptor 137B (GPR137b) function in mouse and zebrafish osteoclasts
28. Colony-stimulating factor 1 receptor a (Csf1ra)-deficient zebrafish as a model of unbalanced bone remodeling
29. Chloride channel voltage-sensitive 7 (CLCN7) loss-of-function zebrafish as a genetic model of osteoclast-rich osteopetrosis
30. The SLC7A7 Transporter Identifies Microglial Precursors prior to Entry into the Brain
31. A Genetic Model to Understand Integration During Skull Development and Etiology of Craniofacial Disorders
32. Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number
33. Identification of Mutations in Zebrafish Using Next‐Generation Sequencing
34. Perspectives for identification of mutations in the zebrafish: Making use of next-generation sequencing technologies for forward genetic approaches
35. Novel Microcephalic Primordial Dwarfism Disorder Associated with Variants in the Centrosomal Protein Ninein
36. Efficient Mapping and Cloning of Mutations in Zebrafish by Low-Coverage Whole-Genome Sequencing
37. Microglia in the developing brain: from immunity to behaviour
38. Isolation and characterization of molecules involved in macrophage migration to and colonization of the zebrafish brain
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