Recent Publications
Recent Publications
- Notch1 is required to maintain supporting cell identity and vestibular function during maturation of the mammalian balance organs.; bioRxiv : the preprint server for biology. 2024 Jun 21.
- Corrigendum: Increased central auditory gain in 5xFAD Alzheimer's disease mice as an early biomarker candidate for Alzheimer's disease diagnosis.; Frontiers in neuroscience; Vol 17, pp. 1250244. 2023 Jul 18.
- Increased central auditory gain in 5xFAD Alzheimer's disease mice as an early biomarker candidate for Alzheimer's disease diagnosis.; Frontiers in neuroscience; Vol 17, pp. 1106570. 2023 May 26.
- Deletion of Notch1 during cochlear maturation leads to rapid supporting cell death and profound deafness.; The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022 Jan 23.
- Deletion of the Notch ligand Jagged1 during cochlear maturation leads to inner hair cell defects and hearing loss.; Cell death & disease; Vol 13(11), pp. 971. 2022 Jan 18.
- Notch-mediated lateral induction is necessary to maintain vestibular prosensory identity during inner ear development.; Developmental biology; Vol 462(1). 2020 Jun 01.
- SOX2 is required for inner ear growth and cochlear nonsensory formation prior to sensory development.; Development (Cambridge, England). 2019 May 31.
- Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice.; Genetics; Vol 208(3). 2018 Mar.
- Trabecular meshwork morphogenesis: A comparative analysis of wildtype and anterior segment dysgenesis mouse models.; Experimental eye research. 2018 Feb 13.
- Ciliary margin-derived BMP4 does not have a major role in ocular development.; PloS one; Vol 13(5). 2018.
- SOX2 is required for inner ear neurogenesis.; Scientific reports; Vol 7(1). 2017 Jun 22.
- Using genetic mouse models to gain insight into glaucoma: Past results and future possibilities.; Experimental eye research; Vol 141. 2015 Dec.
- LMO4 functions as a negative regulator of sensory organ formation in the mammalian cochlea.; The Journal of neuroscience : the official journal of the Society for Neuroscience; Vol 34(30). 2014 Jul 23.
- Activated notch causes deafness by promoting a supporting cell phenotype in developing auditory hair cells.; PloS one; Vol 9(9). 2014.
- 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; Vol 33(41). 2013 Oct 9.
- Notch2 regulates BMP signaling and epithelial morphogenesis in the ciliary body of the mouse eye.; Proceedings of the National Academy of Sciences of the United States of America; Vol 110(22). 2013 May 28.
- Notch signaling during cell fate determination in the inner ear.; Seminars in cell & developmental biology; Vol 24(5). 2013 May.
- Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defects.; PloS one; Vol 7(11). 2012.
- 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; Vol 107(36). 2010 Sep 7.
- Genetic background modifies inner ear and eye phenotypes of jag1 heterozygous mice.; Genetics; Vol 177(1). 2007 Sep.
- The paintfill method as a tool for analyzing the three-dimensional structure of the inner ear.; Brain research; Vol 1091(1). 2006 May 26.
- The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear.; PLoS genetics; Vol 2(1). 2006 Jan.
- The Notch ligands DLL1 and JAG2 act synergistically to regulate hair cell development in the mammalian inner ear.; Development (Cambridge, England); Vol 132(19). 2005 Oct.
- Sox2 is required for sensory organ development in the mammalian inner ear.; Nature; Vol 434(7036). 2005 Apr 21.
- Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice.; Development (Cambridge, England); Vol 130(9). 2003 May.
- ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.; Mammalian genome : official journal of the International Mammalian Genome Society; Vol 13(3). 2002 Mar.
- The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects.; Developmental biology; Vol 234(1). 2001 Jun 01.
- The Notch ligand Jagged1 is required for inner ear sensory development.; Proceedings of the National Academy of Sciences of the United States of America; Vol 98(7). 2001 Mar 27.
- The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.; Human molecular genetics; Vol 10(5). 2001 Mar 01.
- Molecular genetics of pattern formation in the inner ear: do compartment boundaries play a role?; Proceedings of the National Academy of Sciences of the United States of America; Vol 97(22). 2000 Oct 24.
- Mouse homologues for human deafness.; Advances in oto-rhino-laryngology; Vol 56. 2000.
- Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.; Journal of neurocytology; Vol 28(10-11). 1999 Oct.
- The expression domain of two related homeobox genes defines a compartment in the chicken inner ear that may be involved in semicircular canal formation.; Developmental biology; Vol 191(2). 1997 Nov 15.
- In vivo gene transfer into the embryonic inner ear using retroviral vectors.; Audiology & neuro-otology; Vol 2(1-2). 1997 Jan.