Keywords: Otof; Otoferlin; Cdh23; Cadherin 23; Pcdh15; Protocadherin 15; Chiroptera; Echolocation; Convergent evolution;
مقالات ISI (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: ABR; auditory brainstem response; ANSD; auditory neuropathy spectrum disorder; CHD; calponin homology domain; DIAPH3; Diaphanous homolog 3; DPOAEs; distortion product otoacoustic emissions; GSDM; gasdermin; IHCs; inner hair cells; KO; knockout; OAEs; otoa
Keywords: Auditory nerve disease; Auditory neuropathy; Auditory neuropathy spectrum disorders; DPOAE; ABR; OTOF; OPA1;
Targeted next generation sequencing reveals OTOF mutations in auditory neuropathy spectrum disorder
Keywords: Auditory neuropathy spectrum disorder; Cochlear implantation; Deafness; OTOF; Targeted next generation sequencing;
Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling
Keywords: DOCs; double C2-like-domain-containing proteins; SLPs; synaptotagmin-like proteins; ERK; extracellular-signal-regulated kinase; pERK; phosphorylated ERK; MAPK; mitogen-activated protein kinase; DYSF; dysferlin; MYOF; myoferlin; OTOF; otoferlin; CAPN1; cal
A case of auditory neuropathy revealed by OTOF gene mutation analysis in a junior high school girl
Keywords: Auditory neuropathy; Auditory nerve disease; Auditory neuropathy spectrum disorders; OTOF; Speech discrimination;
Evidence for genotype–phenotype correlation for OTOF mutations
Keywords: Auditory neuropathy; Autosomal recessive; Hearing loss; OTOF
Identification of a novel splice site variant of OTOF in the Korean nonsyndromic hearing loss population with low prevalence of the OTOF mutations
Keywords: OTOF; DFNB9; Auditory neuropathy; Auditory dys-synchrony; Vertical transmission; Isoform
Identification of novel OTOF compound heterozygous mutations by targeted next-generation sequencing in a Chinese patient with auditory neuropathy spectrum disorder
Keywords: Auditory neuropathy; Auditory neuropathy spectrum disorders; Cochlear implantation; Congenital deafness; OTOF; Mutation
Screening of OTOF mutations in Iran: A novel mutation and review
Keywords: OTOF; ARNSHL; Hearing loss; Auditory neuropathy; Iranian population; Synaptopathy and deafness