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Showing results 6155 to 6174 of 13448

Publication YearTitleAJOU
Author
-I-131 therapy with retinoic acid in patients with radioiodine- refractory papillary thyroid carcinoma-
2009IATROGENIC CHEMICAL BURN ON FACIAL SKIN BY 37% PHOSPHORIC ACID ETCHANT신혜진
2014Iatrogenic pancreatitis in patients with IPMN after ERCP: incidence and predictive signs.이다근
1998ICE-like protease (caspase) is involved in transforming growth factor beta1-mediated apoptosis in FaO rat hepatoma cell line.최경숙임인경
2010Id proteins facilitate self-renewal and proliferation of neural stem cells.김소연김성수이영돈서해영
2009Ideal Internal Carotid Artery Trapping Technique without Bypass in a Patient with Insufficient Collateral Flow.임용철
2011idenification of nursing activities at medical and surgical nursing units in VietnamNguyen Thi Hong Minh
2007Identification and Analysis of Peanut and Soybean Cross Reacting Allergens in Korean Children Sensitive to Peanut전계리
2017Identification and Functional Characterization of ST3GAL5 and ST8SIA1 Variants in Patients with Thyroid-Associated Ophthalmopathy국경훈
2015Identification and in vivo functional characterization of novel compound heterozygous BMP1 variants in osteogenesis imperfecta.손영배
2005Identification and purification of a soluble region of BubR1: a critical component of the mitotic checkpoint complex.강엽
2010Identification of 15 loci influencing height in a Korean population.조남한
2010Identification of a cholangiocarcinoma-like gene expression trait in hepatocellular carcinoma.우현구
2016Identification of a Circadian Clock in the Inferior Colliculus and Its Dysregulation by Noise Exposure박정섭
2013Identification of a GDF5 mutation in a Korean patient with brachydactyly type C without foot involvement.김옥화
2015Identification of a mitochondrial defect gene signature reveals NUPR1 as a key regulator of liver cancer progression.이영경왕희정우현구윤계순
2004Identification of a novel HLA-B*55 variant (B*5513) from a Korean family.박해심
2003Identification of a novel insertion sequence in vanB2-containing Enterococcus faecium.이위교
2017Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies김정현
2011Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach.정선용김현주

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