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Oncogene|February 23, 2011
Selective activation of Akt1 by mammalian target of rapamycin complex 2 regulates cancer cell migration, invasion, and metastasisE K Kim, S J Yun, J M Ha, et al.
Annals of Surgery|July 26, 2017
Oncologic Outcome and Morbidity in the Elderly Rectal Cancer Patients After Preoperative Chemoradiotherapy and Total Mesorectal Excision: A Multi-institutional and Case-matched Control StudySoo-Y Sung, Hong S Jang, Sung H Kim, et al.
Neuroscience|February 25, 2014
Brain sensorimotor system atrophy during the early stage of spinal cord injury in humansJ-M Hou, R-B Yan, Z-M Xiang, et al.
Transplantation Proceedings|June 23, 2011
The effect of human fetal liver-derived mesenchymal stem cells on CD34+ hematopoietic stem cell repopulation in NOD/Shi-scid/IL-2Rã(null) miceH-M Yang, M-R Cho, J-H Sung, et al.
Scientific Reports|May 16, 2014
USP8 modulates ubiquitination of LRIG1 for Met degradationYoung Mi Oh, Saet Byoul Lee, Jaehyun Choi, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|April 16, 2016
[Predictive and prognostic value of monitoring lymphocyte subsets in peripheral blood before and after chemotherapy in patients with metastatic breast cancer]B Shao, H P Li, L J DI, et al.
AJR. American Journal of Roentgenology|June 22, 2022
Incidental Adrenal Nodules in Patients Without Known Malignancy: Prevalence of Malignancy and Utility of Washout CT for Characterization-A Multiinstitutional StudyMichael T Corwin, Mohamed Badawy, Elaine M Caoili, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 3, 2008
Cardiovascular autonomic dysfunction predicts acute ischaemic stroke in patients with Type 2 diabetes mellitus: a 7-year follow-up studyS H Ko, K H Song, S A Park, et al.
Iscience|May 13, 2021
Multiple pathways coordinating reprogramming of endothelial cells into osteoblasts by BMP4Guoyu Yu, Pengfei Shen, Yu-Chen Lee, et al.
Clinical Genetics|September 7, 2013
Correlation between genotype and phenotype in patients with bi-allelic SLC26A4 mutationsH J Lee, J Jung, J W Shin, et al.
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