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List of works by Moien Kanaan

A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss

scientific article

Collaborative genomics for human health and cooperation in the Mediterranean region

article

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

scientific article

Functional characterization of pendrin mutations found in the Israeli and Palestinian populations

scientific article

GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome

GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome

scientific article

Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East

scientific article published on 8 February 2002

Genomic advances for gene discovery in hereditary hearing loss

scientific article published on 07 September 2012

Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.

scientific article

Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.

scientific article

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

scientific article published on 24 August 2020

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families

scientific article

The DNA-binding domain of the Cys-3 regulatory protein of Neurospora crassa is bipartite

scientific article published on March 31, 1992

The cpc-2 gene of Neurospora crassa encodes a protein entirely composed of WD-repeat segments that is involved in general amino acid control and female fertility.

scientific article published on July 1995

Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.

scientific article

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