BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Salazar-Silva R, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague E, Mingroni-Netto RC. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Hum Mol Genet 2021;29:3691-705. [PMID: 33326993 DOI: 10.1093/hmg/ddaa240] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
Number Citing Articles
1 Xiang P, Ge T, Zhou J, Zhang Y. Protective role of circRNA CCND1 in ulcerative colitis via miR-142-5p/NCOA3 axis. BMC Gastroenterol 2023;23:18. [PMID: 36658474 DOI: 10.1186/s12876-023-02641-6] [Reference Citation Analysis]
2 Nascimento LRD, Vieira-Silva GA, Kitajima JPFW, Batissoco AC, Lezirovitz K. New Insights into the Identity of the DFNA58 Gene. Genes (Basel) 2022;13. [PMID: 36553541 DOI: 10.3390/genes13122274] [Reference Citation Analysis]
3 Yin G, Qian F, Yao J, Wang Z, Wang X, Liu D, Wang C. ftr82 is necessary for hair cell morphogenesis and auditory function during zebrafish development. J Genet Genomics 2022:S1673-8527(22)00252-1. [PMID: 36464225 DOI: 10.1016/j.jgg.2022.11.008] [Reference Citation Analysis]
4 Yu X, Li S, Ding Y. Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNA(Ala) 5601C>T and tRNA(Leu(CUN)) 12311T>C mutations. J Clin Lab Anal 2022;36:e24298. [PMID: 35218233 DOI: 10.1002/jcla.24298] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Lezirovitz K, Mingroni-Netto RC. Genetic etiology of non-syndromic hearing loss in Latin America. Hum Genet 2021. [PMID: 34652575 DOI: 10.1007/s00439-021-02354-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Batissoco AC, Pedroso-Campos V, Pardono E, Sampaio-Silva J, Sonoda CY, Vieira-Silva GA, da Silva de Oliveira Longati EU, Mariano D, Hoshino ACH, Tsuji RK, Jesus-Santos R, Abath-Neto O, Bento RF, Oiticica J, Lezirovitz K. Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss. Hum Genet 2021. [PMID: 34599368 DOI: 10.1007/s00439-021-02372-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Tesolin P, Morgan A, Notarangelo M, Ortore RP, Concas MP, Notarangelo A, Girotto G. Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene. Genes (Basel) 2021;12:1043. [PMID: 34356059 DOI: 10.3390/genes12071043] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Zhang HL, Zhao B, Yang P, Du YQ, Han W, Xu J, Yin DM. Steroid Receptor Coactivator 3 Regulates Synaptic Plasticity and Hippocampus-dependent Memory. Neurosci Bull 2021. [PMID: 34228315 DOI: 10.1007/s12264-021-00741-5] [Reference Citation Analysis]