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논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas
Yonsei Medical Journal
2018 .01
한국인에서의 SLC26A4 돌연변이
대한이비인후-두경부외과학회지
2014 .01
Aberrant Hypomethylation of Solute Carrier Family 6 Member 12 Promoter Induces Metastasis of Ovarian Cancer
Yonsei Medical Journal
2017 .01
Solute Carrier SLC41A1 "A MINI REVIEW"
한국환경성돌연변이·발암원학회지
2005 .06
Replicated Association between SLC4A4 Gene and Blood Pressure Traits in the Korean Population
대한의생명과학회지
2012 .12
No Association Study of SLC6A4 Polymorphisms with Korean Autism Spectrum Disorder
생물정신의학
2009 .01
Carrier frequency of SLC26A4 mutations causing inherited deafness in the Korean population
Journal of genetic medicine
2014 .01
주의력결핍 과잉행동장애와 노르에피네프린 수송체 유전자 다형성의 연관성
소아청소년정신의학
2010 .03
SLC4A1 유전자 변이에 의한 한국인 유전구형적혈구증 2예
Laboratory Medicine Online
2018 .01
SLC35B2 Expression is Associated with a Poor Prognosis of Invasive Ductal Breast Carcinoma
Asian Pacific journal of cancer prevention : APJCP
2014 .01
[Free Paper] High-Frequency Minisatellite Instability of the Mitochondrial Genome in Colorectal Cancer
대한외과학회 학술대회 초록집
2011 .11
Auditory Outcome of Cochlear Implantation in Adolescent and Adult Patients with Enlarged Vestibular Aqueduct and Biallelic SLC26A4 Mutations
대한이비인후-두경부외과학회지
2017 .01
A Family of H723R Mutation for SLC26A4 Associated with Enlarged Vestibular Aqueduct Syndrome
Clinical and Experimental Otorhinolaryngology
2009 .01
Novel SLC37A4 Mutations in Korean Patients With Glycogen Storage Disease Ib
Annals of Laboratory Medicine
2017 .01
Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome
Clinical and Experimental Otorhinolaryngology
2013 .01
Genetic Variants of SLC22A2 (Organic Cation Transporter 2, OCT2) Significantly Influence on the Disposition of Metformin
대한임상약리학회 학술대회
2007 .01
Identification of SLC26A3 Mutations in a Korean Patient with Congenital Chloride Diarrhea
Annals of Laboratory Medicine
2012 .01
주의력결핍 과잉행동장애에서 노르에피네프린 수송체 유전자와 오로스 메칠페니데이트 부작용의 연관성
소아청소년정신의학
2014 .06
A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct
Clinical and Experimental Otorhinolaryngology
2017 .01
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