155 results on '"Haycraft, Courtney"'
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2. Rab35 Is Required for Embryonic Development and Kidney and Ureter Homeostasis through Regulation of Epithelial Cell Junctions
3. Rab35 is required for embryonic development and kidney and ureter homeostasis through regulation of epithelial cell junctions
4. The Use of Bone Wax to Position and Secure the Kidney for Intravital Analysis in Mice Using an Abdominal Imaging Window: PUB252
5. Development of Sterile Ovules on Bisexual Cones of Gnetum gnemon (Gnetaceae)
6. A kidney resident macrophage subset is a candidate biomarker for renal cystic disease in preclinical models
7. Title spot
8. Fibulin-1 is required for bone formation and Bmp-2-mediated induction of Osterix
9. ATXN10 Is Required for Embryonic Heart Development and Maintenance of Epithelial Cell Phenotypes in the Adult Kidney and Pancreas
10. Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypes
11. MKP-1 regulates cytokine mRNA stability through selectively modulation subcellular translocation of AUF1
12. Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypes
13. A transgenic Alx4‐CreER mouse to analyze anterior limb and nephric duct development.
14. A transgenic Alx4‐CreER mouse to analyze anterior limb and nephric duct development
15. A mouse model of BBS identifies developmental and homeostatic effects of BBS5 mutation and identifies novel pituitary abnormalities
16. Telomerase immortalization of principal cells from mouse collecting duct
17. Development of the post-natal growth plate requires intraflagellar transport proteins
18. Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737orpk mutant mice
19. ABbs5mouse model reveals pituitary cilia contributions to developmental abnormalities
20. Chapter 11 Cilia Involvement in Patterning and Maintenance of the Skeleton
21. Loss of Primary Cilia Upregulates Renal Hypertrophic Signaling and Promotes Cystogenesis
22. Identification of CHE-13, a novel intraflagellar transport protein required for cilia formation
23. Transcriptomic characterization of signaling pathways associated with osteoblastic differentiation of MC-3T3E1 cells
24. A Novel Mouse Model for Cilia‐Associated Cardiovascular Anomalies with a High Penetrance of Total Anomalous Pulmonary Venous Return
25. Transcriptomic characterization of signaling pathways associated with osteoblastic differentiation of MC-3T3E1 cells
26. Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene
27. A Novel Mouse Model for Cilia‐Associated Cardiovascular Anomalies with a High Penetrance of Total Anomalous Pulmonary Venous Return.
28. Centrobin-mediated Regulation of the Centrosomal Protein 4.1-associated Protein (CPAP) Level Limits Centriole Length during Elongation Stage
29. Deletion of airway cilia results in noninflammatory bronchiectasis and hyperreactive airways
30. An inducible CiliaGFP mouse model for in vivo visualization and analysis of cilia in live tissue
31. Erratum to: the buccohypophyseal canal is an ancestral vertebrate trait maintained by modulation in sonic hedgehog signaling
32. The buccohypophyseal canal is an ancestral vertebrate trait maintained by modulation in sonic hedgehog signaling
33. A Disintegrin and Metalloenzyme (ADAM) 17 Activation Is Regulated by α5β1 Integrin in Kidney Mesangial Cells
34. NIP45 negatively regulates RANK ligand induced osteoclast differentiation
35. Primary cilia mediate mechanotransduction through control of ATP‐induced Ca2+signaling in compressed chondrocytes
36. GMAP210 and IFT88 are present in the spermatid golgi apparatus and participate in the development of the acrosome-acroplaxome complex, head-tail coupling apparatus and tail
37. The Primary Cilium as a Complex Signaling Center
38. EGFR augments cell proliferation in polycystic kidney disease through activation of a novel ion channel
39. Primary cilia regulate Shh activity in the control of molar tooth number
40. Role for primary cilia in the regulation of mouse ovarian function
41. THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia
42. Altered Regulation of Ion Channel Activity by EGF in Polycystic Kidney Disease
43. Cytosolic Calcium‐Dependence of Elevated cAMP in Polycystic Kidney Disease
44. Intraflagellar transport is essential for endochondral bone formation
45. Caenorhabditis elegansDYF-2, an Orthologue of Human WDR19, Is a Component of the Intraflagellar Transport Machinery in Sensory Cilia
46. IFTA-2 is a conserved cilia protein involved in pathways regulating longevity and dauer formation inCaenorhabditis elegans
47. TheC. eleganshomologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception
48. Gli2 and Gli3 Localize to Cilia and Require the Intraflagellar Transport Protein Polaris for Processing and Function
49. Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis
50. XBX-1 Encodes a Dynein Light Intermediate Chain Required for Retrograde Intraflagellar Transport and Cilia Assembly inCaenorhabditis elegans
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