Germ cells and transgenesis in chickens

JY Han - Comparative immunology, microbiology and infectious …, 2009 - Elsevier
Chickens have proven to be useful organisms for transgenic research. This work provides
enormous benefits in advancing animal biotechnology and aids in the development of …

Genome analysis reveals insights into physiology and longevity of the Brandt's bat Myotis brandtii

I Seim, X Fang, Z Xiong, AV Lobanov, Z Huang… - Nature …, 2013 - nature.com
Bats account for one-fifth of mammalian species, are the only mammals with powered flight,
and are among the few animals that echolocate. The insect-eating Brandt's bat (Myotis …

Actin in hair cells and hearing loss

MC Drummond, IA Belyantseva, KH Friderici… - Hearing research, 2012 - Elsevier
Hereditary deafness is genetically heterogeneous such that mutations of many different
genes can cause hearing loss. This review focuses on the evidence and implications that …

Cochlear transcript diversity and its role in auditory functions implied by an otoferlin short isoform

H Liu, H Liu, L Wang, L Song, G Jiang, Q Lu… - Nature …, 2023 - nature.com
Isoforms of a gene may contribute to diverse biological functions. In the cochlea, the
repertoire of alternative isoforms remains unexplored. We integrated single-cell short-read …

High-resolution transcriptional dissection of in vivo Atoh1-mediated hair cell conversion in mature cochleae identifies Isl1 as a co-reprogramming factor

T Yamashita, F Zheng, D Finkelstein, Z Kellard… - PLoS …, 2018 - journals.plos.org
In vivo direct conversion of differentiated cells holds promise for regenerative medicine;
however, improving the conversion efficiency and producing functional target cells remain …

Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42

G Borck, AU Rehman, K Lee, HM Pogoda… - The American Journal of …, 2011 - cell.com
By using homozygosity mapping in a consanguineous Pakistani family, we detected linkage
of nonsyndromic hearing loss to a 7.6 Mb region on chromosome 3q13. 31-q21. 1 within the …

Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35

RWJ Collin, E Kalay, M Tariq, T Peters… - The American Journal of …, 2008 - cell.com
In a large consanguineous family of Turkish origin, genome-wide homozygosity mapping
revealed a locus for recessive nonsyndromic hearing impairment on chromosome 14q24. 3 …

Ion channel gene expression in the inner ear

IS Gabashvili, BHA Sokolowski, CC Morton… - Journal of the …, 2007 - Springer
The ion channel genome is still being defined despite numerous publications on the subject.
The ion channel transcriptome is even more difficult to assess. Using high-throughput …

Discovery and characterization of medaka miRNA genes by next generation sequencing platform

SC Li, WC Chan, MR Ho, KW Tsai, LY Hu, CH Lai… - BMC genomics, 2010 - Springer
Background MicroRNAs (miRNAs) are endogenous non-protein-coding RNA genes which
exist in a wide variety of organisms, including animals, plants, virus and even unicellular …

ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells

EL Morozko, A Nishio, NJ Ingham… - Human molecular …, 2015 - academic.oup.com
In the mammalian inner ear, bicellular and tricellular tight junctions (tTJs) seal the
paracellular space between epithelial cells. Tricellulin and immunoglobulin-like (Ig-like) …