Ken Kojima
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Ken Kojima has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Juichi Ito
Kyoto University
2 shared publications - Akiko T. Nishida
Department of Otolaryngology, Head and Neck Surgery, Kitano Hospital, Tazuke Kofukai Medical Research Institute, Osaka, Japan
1 shared publication Juichi Ito
1 shared publicationKazuhiro Kobuke
Department of Medical Chemistry, Graduate School of Medicine, Kyoto University, Kyoto, Japan
1 shared publicationKazuya Ono
1 shared publication- Kei Tashiro
Center for Molecular Biology and Genetics, Kyoto University, and Department of Genomic Medical Sciences, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan
1 shared publication
Latest Publications
- 31 December 2007
- Published by Elsevier in Neuroscience Research
- Vol. 58, S56
Hes5-expressing supporting cells in the mammalian cochlea possess a high proliferative potential
- 31 December 2007
- Published by Elsevier in Neuroscience Research
- Vol. 58, S56
Hes5-expressing supporting cells in the mammalian cochlea possess a high proliferative potential
- 1 January 2007
- Published by Taylor & Francis in Acta Oto-Laryngologica
- Vol. 127 (557) , 26-29
Severe acoustic trauma in adult rats induced by short duration high intensity sound
Short duration high intensity sound (SDHIS) induced severe functional damage in adult rats.Previous reports showed that SDHIS induced severe histological changes in the cochleae of guinea pigs. This study examined the hearing functions of rats exposed to SDHIS.Animals were exposed for 1 min to a 137 dB sound pressure level (SPL) broadband noise. Auditory functions of the experimental animals were assessed using an auditory brainstem response (ABR) measurement system at frequencies of 8, 16, and 32 kHz before and 14 days after exposure to SDHIS.After SDHIS, none of the experimental animals showed any response when stimulated by maximum SPLs at all frequencies of our ABR system.
- 1 January 2007
- Published by Taylor & Francis in Acta Oto-Laryngologica
- Vol. 127 (557) , 26-29
Severe acoustic trauma in adult rats induced by short duration high intensity sound
Short duration high intensity sound (SDHIS) induced severe functional damage in adult rats.Previous reports showed that SDHIS induced severe histological changes in the cochleae of guinea pigs. This study examined the hearing functions of rats exposed to SDHIS.Animals were exposed for 1 min to a 137 dB sound pressure level (SPL) broadband noise. Auditory functions of the experimental animals were assessed using an auditory brainstem response (ABR) measurement system at frequencies of 8, 16, and 32 kHz before and 14 days after exposure to SDHIS.After SDHIS, none of the experimental animals showed any response when stimulated by maximum SPLs at all frequencies of our ABR system.
- Open Access
- 20 October 2004
- Published by Wiley in Developmental Dynamics
- Vol. 231 (4) , 766-774
OC29 is preferentially expressed in the presumptive sensory organ region of the otocyst
The mammalian inner ear derives from the otocyst. Molecular mechanisms underlying inner ear development are largely unknown. We have isolated a secreted molecule, OC29, from a rat otocyst cDNA library by the signal sequence trap method. OC29 was revealed to be a rat homologue of human WFIKKN. OC29 is preferentially expressed in the developing inner ear and the dorsal neural tube. In the inner ear, the expression of OC29 is first detectable at embryonic day 11.5 (E11.5), broadly in the dorsolateral region of the otocyst, which gives rise to the vestibular organ. At E12.5, the expression of OC29 becomes restricted to the presumptive sensory region, mainly to the BMP4‐positive presumptive cristae, and expression becomes reduced at later stages. These results suggest that OC29 may have a role in the early development of the inner ear sensory organ, particularly in the formation of the cristae of the semicircular canals. Developmental Dynamics 231:766–774, 2004.
- 20 October 2004
- Published by Wiley in Developmental Dynamics
- Vol. 231 (4) , 766-774
Open AccessOC29 is preferentially expressed in the presumptive sensory organ region of the otocyst
The mammalian inner ear derives from the otocyst. Molecular mechanisms underlying inner ear development are largely unknown. We have isolated a secreted molecule, OC29, from a rat otocyst cDNA library by the signal sequence trap method. OC29 was revealed to be a rat homologue of human WFIKKN. OC29 is preferentially expressed in the developing inner ear and the dorsal neural tube. In the inner ear, the expression of OC29 is first detectable at embryonic day 11.5 (E11.5), broadly in the dorsolateral region of the otocyst, which gives rise to the vestibular organ. At E12.5, the expression of OC29 becomes restricted to the presumptive sensory region, mainly to the BMP4‐positive presumptive cristae, and expression becomes reduced at later stages. These results suggest that OC29 may have a role in the early development of the inner ear sensory organ, particularly in the formation of the cristae of the semicircular canals. Developmental Dynamics 231:766–774, 2004.