A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population

C3435T Polymorphism of the ABCB1/MDR1 gene encoding P-glycoprotein in patients with inflammatory bowel disease in a Polish population

(2014) Michał Dudarewicz et al.   Pharmacological Reports

CYP3A5 Polymorphism in Mexican Renal Transplant Recipients and its Association with Tacrolimus Dosing

(2012) Pilar García-Roca et al.   ARCHIVES OF MEDICAL RESEARCH

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

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

Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities

(2012) Xi Lin et al.   HEARING RESEARCH

Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

(2012) Tomas Kirchhoff et al.   PLoS One

Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation

(2012) Jae Woong Bae et al.   PLoS One

Molecular and Functional Characterization of Human Pendrin and its Allelic Variants

(2011) Silvia Dossena et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Estimation of carrier frequencies of six autosomal-recessive Mendelian disorders in the Korean population

(2011) Min-Jung Song et al.   JOURNAL OF HUMAN GENETICS

Application of the SNaPshot minisequencing assay to species identification in the Lactobacillus casei group

(2011) Chien-Hsun Huang et al.   MOLECULAR AND CELLULAR PROBES

Easy, Rapid, and Cost-Effective Methods for Identifying Carriers of Recurrent GJB2 Mutations Causing Nonsyndromic Hearing Impairment in the Greek Population

(2010) Haris Kokotas et al.   Genetic Testing and Molecular Biomarkers

Salicylate restores transport function and anion exchanger activity of missense pendrin mutations

(2010) Kenji Ishihara et al.   HEARING RESEARCH

Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss

(2010) Tomofumi Kato et al.   JOURNAL OF HUMAN GENETICS

A single multiplex PCR and SNaPshot minisequencing reaction of 42 SNPs to classify admixture populations into mitochondrial DNA haplogroups

(2010) Greiciane G. Paneto et al.   MITOCHONDRION

Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity

(2010) Min-Xin Guan   MITOCHONDRION

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

(2009) Soraya Bardien et al.   BMC Medical Genetics

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

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

Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population

(2008) Sung-Hee Han et al.   JOURNAL OF HUMAN GENETICS

Authentication of meat from game and domestic species by SNaPshot minisequencing analysis

(2008) Fabio La Neve et al.   MEAT SCIENCE