152 results on '"Haycraft, Courtney J."'
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2. Rab35 Is Required for Embryonic Development and Kidney and Ureter Homeostasis through Regulation of Epithelial Cell Junctions
3. The Use of Bone Wax to Position and Secure the Kidney for Intravital Analysis in Mice Using an Abdominal Imaging Window: PUB252
4. Rab35 is required for embryonic development and kidney and ureter homeostasis through regulation of epithelial cell junctions
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. Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypes
12. A transgenic Alx4‐CreER mouse to analyze anterior limb and nephric duct development.
13. Telomerase immortalization of principal cells from mouse collecting duct
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. Development of the post-natal growth plate requires intraflagellar transport proteins
17. Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737orpk mutant mice
18. Chapter 11 Cilia Involvement in Patterning and Maintenance of the Skeleton
19. Loss of Primary Cilia Upregulates Renal Hypertrophic Signaling and Promotes Cystogenesis
20. ABbs5mouse model reveals pituitary cilia contributions to developmental abnormalities
21. Identification of CHE-13, a novel intraflagellar transport protein required for cilia formation
22. Transcriptomic characterization of signaling pathways associated with osteoblastic differentiation of MC-3T3E1 cells
23. Addition of an N-Terminal SNAP-Tag Induces a Novel Hypomorphic Pkd1 Allele
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. Generation of a New Mouse Model Harboring the Polycystin-2 Loss-of-Function D511V Patient Variant
29. Centrobin-mediated Regulation of the Centrosomal Protein 4.1-associated Protein (CPAP) Level Limits Centriole Length during Elongation Stage
30. Deletion of airway cilia results in noninflammatory bronchiectasis and hyperreactive airways
31. 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
32. An inducible CiliaGFP mouse model for in vivo visualization and analysis of cilia in live tissue
33. Erratum to: the buccohypophyseal canal is an ancestral vertebrate trait maintained by modulation in sonic hedgehog signaling
34. The buccohypophyseal canal is an ancestral vertebrate trait maintained by modulation in sonic hedgehog signaling
35. Caenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory Cilia
36. A Disintegrin and Metalloenzyme (ADAM) 17 Activation Is Regulated by α5β1 Integrin in Kidney Mesangial Cells
37. NIP45 negatively regulates RANK ligand induced osteoclast differentiation
38. Primary cilia mediate mechanotransduction through control of ATP‐induced Ca2+signaling in compressed chondrocytes
39. 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
40. The Primary Cilium as a Complex Signaling Center
41. EGFR augments cell proliferation in polycystic kidney disease through activation of a novel ion channel
42. Primary cilia regulate Shh activity in the control of molar tooth number
43. Role for primary cilia in the regulation of mouse ovarian function
44. THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia
45. Altered Regulation of Ion Channel Activity by EGF in Polycystic Kidney Disease
46. Cytosolic Calcium‐Dependence of Elevated cAMP in Polycystic Kidney Disease
47. Intraflagellar transport is essential for endochondral bone formation
48. Caenorhabditis elegansDYF-2, an Orthologue of Human WDR19, Is a Component of the Intraflagellar Transport Machinery in Sensory Cilia
49. IFTA-2 is a conserved cilia protein involved in pathways regulating longevity and dauer formation inCaenorhabditis elegans
50. TheC. eleganshomologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception
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