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Journal of the National Cancer Institute|March 22, 2001
Biomarker risk assessment and bladder cancer detection in a cohort exposed to benzidineG P Hemstreet, S Yin, Z Ma, et al.
Planta Medica|December 16, 2010
The extract of Rhodiolae Crenulatae Radix et Rhizoma induces the accumulation of HIF-1α via blocking the degradation pathway in cultured kidney fibroblastsKen Y Zheng, Ava J Guo, Cathy W Bi, et al.
Leukemia|October 17, 2003
Evaluation of candidate control genes for diagnosis and residual disease detection in leukemic patients using 'real-time' quantitative reverse-transcriptase polymerase chain reaction (RQ-PCR) - a Europe against cancer programE Beillard, N Pallisgaard, V H J van der Velden, et al.
Zhonghua Zhong Liu Za Zhi [Chinese Journal of Oncology]|October 28, 2020
[Cost-effectiveness of primary prophylaxis with PEG-rhG-CSF in early-stage breast cancer patients receiving chemotherapy in China]W Xia, S S Wang, H Hu, et al.
Human Genetics|April 26, 2007
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomaliesL E L M Vissers, P Stankiewicz, S A Yatsenko, et al.
Chemico-Biological Interactions|February 25, 2010
PRiMA directs a restricted localization of tetrameric AChE at synapsesHeidi Q Xie, K Wing Leung, Vicky P Chen, et al.
Orphanet Journal of Rare Diseases|June 14, 2015
De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformationsF J Probst, R A James, L C Burrage, et al.
Leukemia|October 17, 2003
Standardization and quality control studies of 'real-time' quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia - a Europe Against Cancer programJ Gabert, E Beillard, V H J van der Velden, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|December 8, 2022
[Endovascular abdominal aortic aneurysm repair with a new stent graft:early results from a multicenter study]H P Zhang, X W Zhang, X C Dai, et al.
Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
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