Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sheila M. Knepper"'
Publikováno v:
BioTechniques, Vol 25, Iss 5, Pp 886-890 (1998)
Here, we present a low-cost method to produce compact arrays using microporous materials and reagent jetting. Oligonucleotides are immobilized on membrane sheets as a series of lines. The membrane sheet is then rolled and bound, and the spiral struct
Externí odkaz:
https://doaj.org/article/3602991ede0e462eb26c872907ce94c1
More than 10,000 kg of pallasites, micrometeorites (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e47fe26f12d2a243c963392dd2fecfa
https://doi.org/10.21203/rs.3.rs-2443755/v1
https://doi.org/10.21203/rs.3.rs-2443755/v1
Autor:
Russ Chess-Williams, Lynne M. Ireland, Steven A. Buckner, Christopher R. Chapple, Michael Williams, Ivan Milicic, Sheila M. Knepper, Amanda J. Noble, Sweta P. Katwala, Arthur A. Hancock, Patricia A. Morse, Michael E. Brune, James F. Kerwin, Michael Meyer
Publikováno v:
Drug Development Research. 44:140-162
New compounds selective for α 1A -adrenoceptors in the prostate may offer enhanced efficacy for benign prostatic hyperplasia (BPH), with fewer side effects than current treatment. A-131701 (3-[2-((3aR,9bR)-cis-6-methoxy-2,3,3a,4,5,9b,hexanydro-[1H]-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13a75d7ba78a25c3b653ca0c8b98ebc9
https://doi.org/10.1002/(sici)1098-2299(199808)44:4<140::aid-ddr2>3.0.co
https://doi.org/10.1002/(sici)1098-2299(199808)44:4<140::aid-ddr2>3.0.co
Publikováno v:
European Journal of Pharmacology. 297:241-248
Adrenoceptor agonists were used to characterize the alpha 1-adrenoceptor subtype responsible for mediating tension (phasic and tonic combined) in the denuded rat aorta and compared with radioligand binding at alpha 1-adrenoceptor subtypes. The rank o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::191ecdbf9c3fa6ae8a81c5fd1885c30c
https://doi.org/10.1016/0014-2999(95)00755-5
https://doi.org/10.1016/0014-2999(95)00755-5
Publikováno v:
Journal of Receptors and Signal Transduction. 15:863-885
Terazosin and its enantiomers, antagonists of α1-adrenoceptors, were studied in radioligand binding and functional assays to determine relative potencies at subtypes of α1- and α2-adrenoceptors in vitro. The racemic compound and its enantiomers sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05e4eacce3a9eb7564c0a0746413f33c
https://doi.org/10.3109/10799899509049862
https://doi.org/10.3109/10799899509049862
Publikováno v:
Biotechnology and bioengineering. 87(1)
Bio-Strand, Inc., has developed a novel DNA microarray platform utilizing a three-dimensional (3D) DNA format. DNA probes or polymerase chain reaction (PCR) products are spotted onto a thread-like scaffold, which is then wound onto a cylindrical core
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcb8de4dcd30808313cf193572ab9929
https://pubmed.ncbi.nlm.nih.gov/15211493
https://pubmed.ncbi.nlm.nih.gov/15211493
Publikováno v:
Journal of Neurochemistry. 43:1758-1761
Norepinephrine (NE) and the selective alpha1-adrenoceptor agonist phenylephrine (PE) both markedly stimulate the formation of [3H]inositol phosphates in a concentration-dependent manner upon incubation with [3H]myo-inositol. The selective alpha2 agon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47af2220440a6ed1dafe74c7fec33053
https://doi.org/10.1111/j.1471-4159.1984.tb06106.x
https://doi.org/10.1111/j.1471-4159.1984.tb06106.x
Publikováno v:
Journal of Cancer Research and Clinical Oncology. 109:5-8
Weekly intragastric administration of 20, 40, and 80 mg/kg body weight diallylnitrosamine to BD IX rats selectively induced nasal and paranasal cavity tumors with incidences of 30%, 85%, and 65% in females and of 0%, 75%, and 80% in males, respective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13865b15c4a37109b419cd42ce41e812
https://doi.org/10.1007/bf01884247
https://doi.org/10.1007/bf01884247
Autor:
Charles O. Rutledge, Sheila M. Knepper
Publikováno v:
Biochemical pharmacology. 36(18)
The role of calcium in the stimulation of phosphoinositide (PIn) hydrolysis by norepinephrine and the calcium ionophore A23187 was investigated in chopped cerebral cortex in which the PIns had been labeled previously with ([3H]myo-inositol. The accum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35cbb9db3ae1c3722d305acde9cef599
https://pubmed.ncbi.nlm.nih.gov/2820430
https://pubmed.ncbi.nlm.nih.gov/2820430