نتایج جستجو برای: transcription factor brn4

تعداد نتایج: 980024  

Journal: :مجله علوم اعصاب شفای خاتم 0
yasaman behmanesh islamic azad university, mashhad branch, mashhad, iran nafise bahrami islamic azad university, mashhad branch, mashhad, iran zahra ghane islamic azad university, mashhad branch, mashhad, iran

adult neurogenesis is a process of producing nerve cells from their progenitor that occurs in some areas in the brain such as the hypothalamus. low activity in this area plays a role in neural degeneration and diseases such as multiple sclerosis, epilepsy and depression. ms is a neurodegenerative disease with a permanent disability that the main reason for it is axonal degeneration and neuronal...

Nafise Bahrami, Yasaman Behmanesh, Zahra Ghane,

Adult neurogenesis is a process of producing nerve cells from their progenitor that occurs in some areas in the brain such as the hypothalamus. Low activity in this area plays a role in neural degeneration and diseases such as multiple sclerosis, epilepsy and depression. MS is a neurodegenerative disease with a permanent disability that the main reason for it is axonal degeneration and neuronal...

2014
Yoshinobu Kidokoro Keiko Karasawa Osamu Minowa Yoshinobu Sugitani Tetsuo Noda Katsuhisa Ikeda Kazusaku Kamiya Eliana Scemes

Brn4, which encodes a POU transcription factor, is the gene responsible for DFN3, an X chromosome-linked, non-syndromic type of hearing loss. Brn4-deficient mice have a low endocochlear potential (EP), hearing loss, and ultrastructural alterations in spiral ligament fibrocytes, however the molecular pathology through which Brn4 deficiency causes low EP is still unclear. Mutations in the Gjb2 an...

Journal: :Human molecular genetics 2000
D Phippard Y Boyd V Reed G Fisher W K Masson E P Evans J C Saunders E B Crenshaw

We have demonstrated that the phenotype of the mouse mutant sex-linked fidget ( slf ) is caused by developmental malformations of the inner ear that result in hearing loss and vestibular dysfunction. Recently, pilot mapping experiments suggested that the mouse Brn4 / Pou3f4 gene co-segregated with the slf locus on the mouse X chromosome. These mapping data, in conjunction with the observation t...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1999
D Phippard L Lu D Lee J C Saunders E B Crenshaw

Targeted mutagenesis in mice demonstrates that the POU-domain gene Brn4/Pou3f4 plays a crucial role in the patterning of the mesenchymal compartment of the inner ear. Brn4 is expressed extensively throughout the condensing mesenchyme of the developing inner ear. Mutant animals displayed behavioral anomalies that resulted from functional deficits in both the auditory and vestibular systems, incl...

Journal: :Archives of otolaryngology--head & neck surgery 2005
Steven E Sobol Xiuyin Teng E Bryan Crenshaw

OBJECTIVE To examine the developmental time course of the mutant phenotype and cellular mechanisms that result in malformations of the superior semicircular canal (SSCC) in Brn4 knockout mice. Mutations in the Brn4/Pou3f4 gene result in characteristic inner ear abnormalities in mutant mouse pedigrees, and the findings in these mice are similar to those in human X-linked deafness type III. DES...

Journal: :iranian journal of biotechnology 2015
ghazale khaksar badredin ebrahim sayed tabatabaei ahmad arzani cyrus ghobadi esmaeil ebrahimie

background: pomegranate fruit (punica granatum l.) is a rich source of anthocyanin pigments resulting in vibrant colours and anti-oxidant contents. although the intensity and pattern of anthocyanin biosynthesis in fruit are strongly influenced by r2r3-myb transcription factors, little is known about the regulation and role of myb in anthocyanin pathway of pomegranate.objectives: the present stu...

Journal: :gene, cell and tissue 0
marijana tadic university hospital center “dr. dragisa misovic”, belgrade, serbia; university hospital center “dr. dragisa misovic”, belgrade, serbia. tel: +38-1658107085, fax: +38-1112411464 cesare cuspidi italian auxologico institute, clinical research unit, university of milan-bicocca, meda, italy

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