Results 111 to 120 of about 5,521 (170)

Genome-wide CRISPR screening identifies cellular factors controlling nonviral genome editing efficiency. [PDF]

Nat Commun
Saxena S, Kabra M, Abdeen AA, Tabima DM, Sinha D, Rawding PA, Zhu M, Xie R, Kulkarni T, Hanstad GM, Fernandez Zepeda MA, Gamm DM, Pattnaik BR, Gong S, Saha K.   +14 more
europepmc   +1 more source

Clinical and Genetic Characterization of Gap Junction Protein β-6 Variants in Non-Syndromic Hearing Loss: A Case Report with Familial Evaluation and <i>In Silico</i> Analyses. [PDF]

Iran J Med Sci
Zahedi Abghari F, Mohseni M, Esmaeilzadeh E, Ghasemi H, Khorram Khorshid HR, Najafipour R.   +5 more
europepmc   +1 more source

Prenatal Diagnosis of Keratitis-Ichthyosis-Deafness Syndrome With Dandy Walker Malformation: A Case Report. [PDF]

Case Rep Obstet Gynecol
Bourdil L, Georgia Blume C.
europepmc   +1 more source

Disparities in deafness gene mutations between Han and Li ethnic newborns in Hainan, China: insights from a combined screening program. [PDF]

BMC Med Genomics
Qi X, Wang D, Liu S, Jiao B, Tian X, Dai P, Su Y.   +6 more
europepmc   +1 more source

Multi-omics single-cell dissection of malignant epithelial heterogeneity identifies GJB2 as an EMT-driving biomarker in triple-negative breast cancer. [PDF]

BMC Med Genomics
Xu H, Zhang C, Zhang X, Zhang S, Zhou G.
europepmc   +1 more source

In silico MicroRNAs target identification within the GJB2 Gene

International Journal of Biosciences (IJB), 2014
openaire   +1 more source

Comprehensive genotype-phenotype correlation analysis in 11 509 neonates carrying common deafness-associated pathogenic variants. [PDF]

J Med Genet
Li J, Zhan Z, Zhang X, Wu B, Liu W.
europepmc   +1 more source

Connexin 26 in Hearing Health and Disease: StructuralFoundations, Mutation Mechanisms, and Therapeutic Perspectives. [PDF]

Int J Mol Sci
Qiu W, Schneider K, Guo Y.
europepmc   +1 more source

Recent Progress in Mechanism-Based Therapies for <i>GJB2</i>-Related Hearing Loss. [PDF]

Int J Mol Sci
Liu C, Wang X, Sun Y.
europepmc   +1 more source

Exploring the Clinical and Psychosocial Impact of Genetic Diagnosis in Congenital Hearing Loss: A Comparative Study Between Syndromic and Non-Syndromic Conditions. [PDF]

Children (Basel)
Orzan E, Ceretta C, Bresciani G, Fantoni M, Michieletto P, Di Cesare T, Marchi R, Bonati MT, Feresin A.   +8 more
europepmc   +1 more source