Results 181 to 190 of about 47,347 (285)

Evolutionary constraints impose multiple checkpoints that block mammalian sensory hair cell regeneration. [PDF]

Front Cell Dev Biol
Zhang X, Su Z, Guan D, Liu X, Xie H.
europepmc   +1 more source

Cochlea [PDF]

, 2020
openaire   +1 more source

Cilia in Nervous System Development, Function, and Disease

MedComm – Future Medicine, Volume 5, Issue 2, June 2026.
Cilia are evolutionarily conserved organelles that function as essential sensory and motility platforms in the nervous system. This review outlines key cilia‐dependent signaling pathways and their roles in neural development and function. Furthermore, it highlights how ciliary dysfunction can lead to a variety of neurological disorders, known as ...
Qingchao Li, Anqi Zhang, Ting Song
wiley   +1 more source

Transcriptomic characters of cochlear vascular cells with pericyte-driven angiogenetic activity. [PDF]

Angiogenesis
Wang P, Zhang Y, Hou Z, Zhang J, Sharma K, Shi X.   +5 more
europepmc   +1 more source

MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular Tachycardia

Molecular Genetics &Genomic Medicine, Volume 14, Issue 6, June 2026.
A novel homozygous frameshift variant in the MYO6 gene (c.2496_2497delAC; p.H833Qfs*5) was identified in a neonate presenting with bilateral congenital sensorineural hearing loss, paroxysmal supraventricular tachycardia (SVT), and prolonged QT interval.
Samira Kalayinia, Tannaz Masoumi, Amirreza Taherkhani, Nejat Mahdieh, Mohammadrafie Khorgami, Majid Maleki   +5 more
wiley   +1 more source

Live imaging and multimodal profiling reveal transdifferentiation of a cochlear supporting cell subpopulation upon Notch inhibition. [PDF]

Sci Adv
Khalaily L, Kasirer S, Domb R, Zhou M, Shao B, Taiber S, Elkon R, Tao L, Sprinzak D, Avraham KB.   +9 more
europepmc   +1 more source

Functional reassessment of extended splice region variants in MYO7A with hearing loss and Usher syndrome

The Journal of Pathology, Volume 269, Issue 2, Page 222-231, June 2026.
Abstract MYO7A is a causal gene, underlying Usher syndrome type 1B (USH1B) and both autosomal recessive (DFNB2) and dominant (DFNA11) non‐syndromic hearing loss. Despite the large number of reported MYO7A variants (over 2,200), variants located in an extended splice region remain difficult to interpret and are often classified as variants of uncertain ...
Tao Shi, Yu Huang, Xiaohuan Su, Lisheng Yu, Yixin Zhao, Jing Cheng   +5 more
wiley   +1 more source

Deep learning for discriminating cochlear malformations on temporal bone CT. [PDF]

Braz J Otorhinolaryngol
Li Z, Zhou L, Bin X, Liu B, Tang A, Tan S.   +5 more
europepmc   +1 more source

Feasibility of Minimally Invasive Robot‐Assisted Retrofacial Access to the Stapedius Muscle for Applications in Objective Cochlear Implant Fitting: A Cadaveric Study

The International Journal of Medical Robotics and Computer Assisted Surgery, Volume 22, Issue 3, June 2026.
ABSTRACT Background Accurate setting of maximum comfort levels (MCL) during cochlear implant (CI) fitting is essential but subjective, especially in non‐cooperative patients. The stapedius reflex (SR) correlates with the MCL and offers an objective measure.
Dirk Arnold, Francesca Maule, Pablo Galeazzi, Mohannad Al‐Qubaj, Orlando Guntinas‐Lichius   +4 more
wiley   +1 more source

Conditional knockout of Dkk3 drives Lgr5+ progenitor reprogramming into hair cells in the mouse cochlea. [PDF]

Theranostics
Xiao H, Wang X, Ye Z, Tan X, Ma Y, Ma X, Tong W, Zhang L, Lin Y, Tang X, Zhang H, Wan J, Zhang Q, Chai R, Zhang S.   +14 more
europepmc   +1 more source