Donna Fekete

Dr. Donna Fekete

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Research Focus & Metrics

Academic Career Length

46Years (1981-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 1996
Verified
Book Chapter
Closed access
BMBruce A. Morgan
Bruce A. Morgan
DFDonna Fekete
Donna Fekete

1 February 2002 in Current Opinion in Neurobiology
Verified
Journal Article
Closed access
DFDonna Fekete
Donna Fekete
DWDoris K Wu
Doris K Wu

15 January 2012 in Development
Verified
Journal Article
Closed access
PDF file
AGAndrew Groves
Andrew Groves
DFDonna Fekete
Donna Fekete
The inner ear is one of the most morphologically elaborate tissues in vertebrates, containing a group of mechanosensitive sensory organs that mediate hearing and balance. These organs are arranged precisely in space and contain intricately patterned sensory epithelia. Here, we review recent studies of inner ear development and patterning which reveal that multiple stages of ear development – ranging from its early induction from the embryonic ectoderm to the establishment of the three cardinal axes and the fine-grained arrangement of sensory cells – are orchestrated by gradients of signaling molecules.

1 November 1984 in Journal of Comparative Neurology
Verified
Journal Article
Closed access
PDF file
DFDonna Fekete
Donna Fekete
ERE. M. Rouiller
E. M. Rouiller
MLM. C. Liberman
M. C. Liberman
DRDavid Ryugo
David Ryugo

1 October 1998 in Journal of Neuroscience
Verified
Journal Article
Open access
PDF file
DFDonna Fekete
Donna Fekete
SMShanthini Muthukumar
Shanthini Muthukumar
 Domna  Karagogeos Domna Karagogeos
Domna Karagogeos
Sensory organs of the vertebrate inner ear contain two major cell types: hair cells (HCs) and supporting cells (SCs). To study the lineage relationships between these two populations, replication-defective retroviral vectors encoding marker genes were delivered to the otic vesicle of the chicken embryo. The resulting labeled clones were analyzed in the hearing organ of the chicken, called the basilar papilla (BP), after cellular differentiation. BPs were allowed to develop for 2 weeks after delivery of the retrovirus, were removed, and were processed histochemically as whole mounts to identify clones of cells. Clusters of labeled cells were evident in the sensory epithelium, the nonsensory epithelium, and in adjacent tissues. Labeled cell types included HCs, two morphologically distinct types of SCs, homogene cells, border cells, hyaline cells, ganglion cells, and connective tissue cells. Each clone was sectioned and cell-type identification was performed on sensory clones expressing retrovirally transduced β-galactosidase. Cell composition was determined for 41 sensory clones, most of which contained both HCs and SCs. Clones containing one HC and one SC were observed, suggesting that a common progenitor exists that can remain bipotential up to its final mitotic division. The possibility that these two cell types may also arise from a mitotic precursor during HC regeneration in the mature basilar papilla is consistent with their developmental history.

20 September 1982 in Journal of Comparative Neurology
Verified
Journal Article
Closed access
PDF file
DRDavid Ryugo
David Ryugo
DFDonna Fekete
Donna Fekete