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se169900489p
https://labs.utsouthwestern.edu/sites/default/files/2022-11/22_Niklason_Science.pdf
10 to 70% methanol in 50 mM KH2PO4 over 25 min, 10 ml/min, monitor at 380 nm). Next, the HPLC- purified mixture was desalted on the same column (methanol was removed on a rotary evaporator, and the sample loaded in H2O and eluted with 90% methanol) and lyophilized, yielding the purified Nvoc-aa-S-CoA (40 to 80% yield) as a yellow solid. For preparation of the deprotected aa-S-CoAs, the solution of Nvoc-aa-S-CoA collected from the HPLC purification was directly photolysed (4°C, 350 nm, 1 hour
Benign Prostatic Hyperplasia | Strand Lab | UT Southwestern, Dallas, Texas
https://labs.utsouthwestern.edu/strand-lab/research/benign-prostatic-hyperplasia
The goal of the Strand Laboratory is to understand the cellular and molecular biology of lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH) or bladder dysfunction. BPH/LUTS is present in the vast majority of men over 70 years old resulting in medical treatment or surgical
Membrane-encased polymer millirods for sustained release of 5-fluorouracil
https://labs.utsouthwestern.edu/sites/default/files/2022-11/25_Qian_JBMR_Membrane.pdf
Membrane-encased polymer millirods for sustained release of 5-fluorouracil Feng Qian, Norased Nasongkla, Jinming Gao Cancer-Targeted Drug Delivery Laboratory, Department of Biomedical Engineering, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, Ohio 44106 Received 10 November 2001; revised 26 November 2001; accepted 26 November 2001 Abstract: This article describes the design and develop- ment of a novel membrane-encased polymer millirod for the sustained release of an
Research | Strand Lab | UT Southwestern, Dallas, Texas
https://labs.utsouthwestern.edu/strand-lab/research
The main goals of the Strand Lab are to create accurate cellular atlases of the human and mouse lower urinary tract, characterize the molecular and cellular alterations in human lower urinary tract disease, and build appropriate models of the human disease in novel mouse models.
2010 Photos | Conrad Lab | UT Southwestern, Dallas, Texas
https://labs.utsouthwestern.edu/conrad-lab/2010-photos
See 2010 photos
Awards for 2022 | Mirpuri Lab | UT Southwestern, Dallas, Texas
https://labs.utsouthwestern.edu/mirpuri-lab/news/awards-2022
Awards for 2022 - Mirpuri Lab
PII: S0168-3659(02)00217-1
https://labs.utsouthwestern.edu/sites/default/files/2022-11/28_Qian_JCR_Modelling.pdf
Journal of Controlled Release 83 (2002) 427–435 www.elsevier.com/ locate/ jconrel C ombined modeling and experimental approach for the development of dual-release polymer millirods *Feng Qian, Gerald M. Saidel, Damon M. Sutton, Agata Exner, Jinming Gao Cancer-Targeted Drug Delivery Laboratory, Department of Biomedical Engineering, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, OH 44106,USA Received 3 July 2002; accepted 7 August 2002 Abstract This paper describes a
Donors | Meng Lab | UT Southwestern, Dallas, Texas
https://labs.utsouthwestern.edu/meng-lab/donors
Donors contribute to research by the Meng Lab at UT Southwestern.
X-ray computed tomography methods for in vivo evaluation of local drug release systems - Medical Imaging, IEEE Transactions on
https://labs.utsouthwestern.edu/sites/default/files/2022-11/29_Salem_IEEE.pdf
1310 IEEE TRANSACTIONS ON MEDICAL IMAGING, VOL. 21, NO. 10, OCTOBER 2002 X-Ray Computed Tomography Methods forIn Vivo Evaluation of Local Drug Release Systems Kyle A. Salem, Student Member, IEEE, Agata Szymanski-Exner, Roee S. Lazebnik, Michael S. Breen, Jinming Gao, and David L. Wilson�, Member, IEEE Abstract—Recent advances in drug delivery techniques have necessitated the development of tools forin vivomonitoring of drug distributions. Gamma emission imaging and magnetic resonance imaging
News | Mirpuri Lab | UT Southwestern, Dallas, Texas
https://labs.utsouthwestern.edu/mirpuri-lab/news
Mirpuri Lab news.