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GIPC3 gene

Known as: GAIP C-TERMINUS-INTERACTING PROTEIN 3, GIPC PDZ DOMAIN-CONTAINING FAMILY, MEMBER 3, GIPC PDZ domain containing family member 3 
National Institutes of Health

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Related topics

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DEAFNESS, AUTOSOMAL RECESSIVE 15

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort
Hearing loss or hearing impairment is a clinically and genetically heterogeneous disorder. More than 117 genes were discovered to… 
2018
2018
A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing.
2017
2017
Survival of BRCA2-Deficient Cells Is Promoted by GIPC3, a Novel Genetic Interactor of BRCA2
BRCA2 loss-of-heterozygosity (LOH) is frequently observed in BRCA2-mutated tumors, but its biallelic loss causes embryonic… 
2014
2014
A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family
With homozygosity mapping we have identified two large homozygous regions on chromosome 3q13.11–q13.31 and chromosome 19p13.3–q31… 
2013
2013
Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family.
Review
2013
Review
2013
Great challenges in molecular medicine: toward personalized medicine
  • M. Katoh
  • Front. Cell Dev. Biol.
  • 2013
  • Corpus ID: 2400595
GENE HUNTING, SIGNALING NETWORK, AND MOLECULAR MEDICINE In the 20th century, most researchers investigated WNT signaling in cell… 
2012
2012
Challenges in Whole Exome Sequencing: An Example from Hereditary Deafness
Whole exome sequencing provides unprecedented opportunities to identify causative DNA variants in rare Mendelian disorders… 
2012
2012
Molecular characterization and ligand binding specificity of the PDZ domain-containing protein GIPC3 from Schistosoma japonicum
BackgroundSchistosomiasis is a serious global health problem that afflicts more than 230 million people in 77 countries. Long… 
2011
2011
High-Frequency Sensorineural Hearing Loss and Its Underlying Genetics (Hfhl1 and Hfhl2) in NIH Swiss Mice
Studies using inbred strains of mice have been invaluable for identifying alleles that adversely affect hearing. However, the… 
2002
2002
Molecular cloning and characterization of mouse Gipc3.
GIPC1/GIPC interacts with GTPase-activating protein RGS-GAIP, transmembrane protein M-SemF, receptor tyrosine kinase TrkA… 
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