Novel CRISPR/Cas12a-based genetic diagnostic approach for SLC26A4 mutation-related hereditary hearing loss

Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

(2020) Mengnan Li et al.   Nature Communications

Development and clinical application of a novel CRISPR-Cas12a based assay for the detection of African swine fever virus

(2020) Xiaoying Wang et al.   BMC MICROBIOLOGY

Detection of unamplified target genes via CRISPR–Cas9 immobilized on a graphene field-effect transistor

(2019) Reza Hajian et al.   Nature Biomedical Engineering

Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China

(2019) Yan-bao Xiang et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

HOLMESv2: A CRISPR-Cas12b-Assisted Platform for Nucleic Acid Detection and DNA Methylation Quantitation

(2019) Linxian Li et al.   ACS Synthetic Biology

Association of SLC26A4 mutations, morphology, and hearing in pendred syndrome and NSEVA

(2019) Kristianna Mey et al.   LARYNGOSCOPE

Recombinase polymerase amplification applied to plant virus detection and potential implications

(2018) Binoy Babu et al.   ANALYTICAL BIOCHEMISTRY

A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing

(2018) Samira Asgharzade et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Field-deployable viral diagnostics using CRISPR-Cas13

(2018) Cameron Myhrvold et al.   SCIENCE

CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity

(2018) Janice S. Chen et al.   SCIENCE

Multiplexed and portable nucleic acid detection platform with Cas13, Cas12a, and Csm6

(2018) Jonathan S. Gootenberg et al.   SCIENCE

CRISPR-Cas12a-assisted nucleic acid detection

(2018) Shi-Yuan Li et al.   Cell Discovery

CRISPR Methods for Nucleic Acid Detection Herald the Future of Molecular Diagnostics

(2018) Asma Hatoum-Aslan   CLINICAL CHEMISTRY

A Mutational Analysis of GJB2, SLC26A4, MT-RNA1, and GJB3 in Children with Nonsyndromic Hearing Loss in the Henan Province of China

(2018) Liang Ming et al.   Genetic Testing and Molecular Biomarkers

A CRISPR–Cas9-triggered strand displacement amplification method for ultrasensitive DNA detection

(2018) Wenhua Zhou et al.   Nature Communications

Nucleic acid detection with CRISPR-Cas13a/C2c2

(2017) Jonathan S. Gootenberg et al.   SCIENCE

Developing regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum

(2014) Kaitian Chen et al.   Journal of Translational Medicine

Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

(2013) Feng Xin et al.   Journal of Translational Medicine

Genetic Screening ofGJB2andSLC26A4in Korean Cochlear Implantees: Experience of Soree Ear Clinic

(2012) Joong-Wook Shin et al.   Clinical and Experimental Otorhinolaryngology

Taperin (c9orf75), a mutated gene in nonsyndromic deafness, encodes a vertebrate specific, nuclear localized protein phosphatase one alpha (PP1 ) docking protein

(2011) T. Ferrar et al.   Biology Open

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness

(2009) Soraya Bardien et al.   BMC Medical Genetics

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

(2009) Saima Anwar et al.   JOURNAL OF HUMAN GENETICS

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

(2008) Pu Dai et al.   GENETICS IN MEDICINE

Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients

(2008) K.Y. Lee et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening

(2007) Cai-Xia Li et al.   HUMAN MUTATION