| Year |
Citation |
Score |
| 2022 |
Heffer A, Gilels FA, Kiernan AE. Deletion of during cochlear maturation leads to rapid supporting cell death and profound deafness. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 36418183 DOI: 10.1523/JNEUROSCI.1090-22.2022 |
0.524 |
|
| 2022 |
Gilels FA, Wang J, Bullen A, White PM, Kiernan AE. Deletion of the Notch ligand Jagged1 during cochlear maturation leads to inner hair cell defects and hearing loss. Cell Death & Disease. 13: 971. PMID 36400760 DOI: 10.1038/s41419-022-05380-w |
0.543 |
|
| 2020 |
Brown RM, Nelson JC, Zhang H, Kiernan AE, Groves AK. Notch-mediated lateral induction is necessary to maintain vestibular prosensory identity during inner ear development. Developmental Biology. PMID 32147304 DOI: 10.1016/j.ydbio.2020.02.015 |
0.4 |
|
| 2019 |
Steevens AR, Glatzer JC, Kellogg CC, Low WC, Santi PA, Kiernan AE. SOX2 is required for inner ear growth and cochlear nonsensory formation prior to sensory development. Development (Cambridge, England). PMID 31152002 DOI: 10.1242/dev.170522 |
0.397 |
|
| 2018 |
Rausch RL, Libby RT, Kiernan AE. Trabecular meshwork morphogenesis: A comparative analysis of wildtype and anterior segment dysgenesis mouse models. Experimental Eye Research. PMID 29452107 DOI: 10.1016/J.Exer.2018.02.011 |
0.345 |
|
| 2018 |
Johnson KR, Gagnon LH, Tian C, Longo-Guess CM, Low BE, Wiles MV, Kiernan AE. Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice. Genetics. PMID 29301908 DOI: 10.1534/genetics.117.300447 |
0.314 |
|
| 2017 |
Sun W, Zhang H, Wang H, Chiu YG, Ritchlin CT, Kiernan A, Boyce BF, Xing L. Targeting Notch-activated M1 Macrophages Attenuates Joint Tissue Damage in a Mouse Model of Inflammatory Arthritis. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 28256007 DOI: 10.1002/Jbmr.3117 |
0.335 |
|
| 2014 |
Savoy-Burke G, Gilels FA, Pan W, Pratt D, Que J, Gan L, White PM, Kiernan AE. Activated notch causes deafness by promoting a supporting cell phenotype in developing auditory hair cells. Plos One. 9: e108160. PMID 25264928 DOI: 10.1371/Journal.Pone.0108160 |
0.524 |
|
| 2013 |
Pan W, Jin Y, Chen J, Rottier RJ, Steel KP, Kiernan AE. Ectopic expression of activated notch or SOX2 reveals similar and unique roles in the development of the sensory cell progenitors in the mammalian inner ear. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 16146-57. PMID 24107947 DOI: 10.1523/Jneurosci.3150-12.2013 |
0.526 |
|
| 2013 |
Kiernan AE. Notch signaling during cell fate determination in the inner ear. Seminars in Cell & Developmental Biology. 24: 470-9. PMID 23578865 DOI: 10.1016/j.semcdb.2013.04.002 |
0.526 |
|
| 2013 |
Liu K, Jiang M, Lu Y, Chen H, Sun J, Wu S, Ku WY, Nakagawa H, Kita Y, Natsugoe S, Peters JH, Rustgi A, Onaitis MW, Kiernan A, Chen X, et al. Sox2 cooperates with inflammation-mediated Stat3 activation in the malignant transformation of foregut basal progenitor cells. Cell Stem Cell. 12: 304-15. PMID 23472872 DOI: 10.1016/J.Stem.2013.01.007 |
0.466 |
|
| 2010 |
Pan W, Jin Y, Stanger B, Kiernan AE. Notch signaling is required for the generation of hair cells and supporting cells in the mammalian inner ear. Proceedings of the National Academy of Sciences of the United States of America. 107: 15798-803. PMID 20733081 DOI: 10.1073/Pnas.1003089107 |
0.535 |
|
| 2006 |
Kiernan AE, Xu J, Gridley T. The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear. Plos Genetics. 2: e4. PMID 16410827 DOI: 10.1371/Journal.Pgen.0020004 |
0.526 |
|
| 2005 |
Kiernan AE, Cordes R, Kopan R, Gossler A, Gridley T. The Notch ligands DLL1 and JAG2 act synergistically to regulate hair cell development in the mammalian inner ear. Development (Cambridge, England). 132: 4353-62. PMID 16141228 DOI: 10.1242/Dev.02002 |
0.536 |
|
| 2005 |
Kiernan AE, Pelling AL, Leung KKH, Tang ASP, Bell DM, Tease C, Lovell-Badge R, Steel KP, Cheah KSE. Sox2 is required for sensory organ development in the mammalian inner ear Nature. 434: 1031-1035. PMID 15846349 DOI: 10.1038/Nature03487 |
0.513 |
|
| 2003 |
Hulander M, Kiernan AE, Blomqvist SR, Carlsson P, Samuelsson EJ, Johansson BR, Steel KP, Enerbäck S. Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice. Development (Cambridge, England). 130: 2013-25. PMID 12642503 |
0.32 |
|
| 2001 |
Kiernan AE, Ahituv N, Fuchs H, Balling R, Avraham KB, Steel KP, Hrabé de Angelis M. The Notch ligand Jagged1 is required for inner ear sensory development. Proceedings of the National Academy of Sciences of the United States of America. 98: 3873-8. PMID 11259677 DOI: 10.1073/Pnas.071496998 |
0.516 |
|
| 2001 |
Tsai H, Hardisty RE, Rhodes C, Kiernan AE, Roby P, Tymowska-Lalanne Z, Mburu P, Rastan S, Hunter AJ, Brown SD, Steel KP. The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti. Human Molecular Genetics. 10: 507-12. PMID 11181574 DOI: 10.1093/hmg/10.5.507 |
0.329 |
|
| 1999 |
Kiernan AE, Zalzman M, Fuchs H, Hrabe de Angelis M, Balling R, Steel KP, Avraham KB. Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival. Journal of Neurocytology. 28: 969-85. PMID 10900098 DOI: 10.1023/A:1007090626294 |
0.403 |
|
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