MIZ-1 ACTIVATES GENE EXPRESSION VIA A NOVEL CONSENSUS DNA BINDING MOTIF.


Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation.

Autosomal recessive non-syndromic hearing loss is one of the most common monogenic diseases.It is characterized by high allelic and locus heterogeneities that make a precise diagnosis difficult.In this study, whole-exome sequencing was HEATHER performed for an affected patient allowing us to identify a new frameshift mutation (c.804delG) in the Imm

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Regional risk factors associated with adverse outcomes of COVID-19 infection among the older adult: A systematic review and meta-analysis

The rapid global spread of Coronavirus Disease 2019 (COVID-19) has resulted in millions of Reach-In Refrigerators infections and deaths, particularly impacting older adults.This study systematically analyzes risk factors reported in different geographical regions such as Asia and Europe that are associated with adverse outcomes in older adults with

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