Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Constanze Krohs"'
Autor:
Mor Bordeynik-Cohen, Michal Sperber, Lena Ebbers, Naama Messika-Gold, Constanze Krohs, Tal Koffler-Brill, Yael Noy, Ran Elkon, Hans Gerd Nothwang, Karen B. Avraham
Publikováno v:
RNA Biology, Vol 20, Iss 1, Pp 629-640 (2023)
The peripheral and central auditory subsystems together form a complex sensory network that allows an organism to hear. The genetic programs of the two subsystems must therefore be tightly coordinated during development. Yet, their interactions and c
Externí odkaz:
https://doaj.org/article/52292a900357441c8821cdf77955ae5d
Autor:
Haydn M. Prosser, Yvette Dörflinger, Lena Ebbers, Simone Hoppe, Constanze Krohs, Faiza Altaf, Christoph Körber, Hans Gerd Nothwang, Giulia Hollje
Publikováno v:
J Neurosci
A point mutation in miR-96 causes non-syndromic progressive peripheral hearing loss and alters structure and physiology of the central auditory system. To gain further insight into the functions of microRNAs (miRNAs) within the central auditory syste
Autor:
Mor Bordeynik-Cohen, Constanze Krohs, Karen B. Avraham, Hans Gerd Nothwang, Naama Messika-Gold, Ran Elkon
Publikováno v:
Cell and Tissue Research
The auditory system comprises the auditory periphery, engaged in sound transduction and the central auditory system, implicated in auditory information processing and perception. Recently, evidence mounted that the mammalian peripheral and central au
Autor:
Hans Gerd Nothwang, Pascal Fieth, Karen B. Avraham, Alexander K. Hartmann, Constanze Krohs, Elena Rosengauer, Felix Felmy, Karen P. Steel, Tina Schlüter, Christina Berger, Kathy Ushakov
Publikováno v:
Human Molecular Genetics. 27:860-874
The peripheral deafness gene Mir96 is expressed in both the cochlea and central auditory circuits. To investigate whether it plays a role in the auditory system beyond the cochlea, we characterized homozygous Dmdo/Dmdo mice with a point mutation in m