Zobrazeno 1 - 10
of 111
pro vyhledávání: '"E. Piscopo"'
Autor:
Rhalena A. Thomas, Julien Sirois, Shuming Li, Alexandre Gestin, Valerio E. Piscopo, Paula Lépine, Meghna Mathur, Carol X.Q. Chen, Vincent Soubannier, Taylor M. Goldsmith, Lama Fawaz, Thomas M. Durcan, Edward A. Fon
Motivated by the growing number of single cell RNA sequencing datasets (scRNAseq) revealing the cellular heterogeneity in complex tissues, particularly in brain and in induced pluripotent stem cell (iPSC)-derived brain models, we have developed a hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5847c5d521ffe378723a66eba43622a8
https://doi.org/10.1101/2022.11.11.516066
https://doi.org/10.1101/2022.11.11.516066
4-hydroxy-isophthalaldehyde acid (1), its alkyl esters (methyl, ethyl, propyl and butyl) and alkyl ethers (propyl, butyl, pentyl and esyl), as well as 6-hydroxy-isophthalaldehyde acid (2) ita alkyl esters (methyl and ethyl), 4-hydroxy-5-iodo-isophtha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::500605f0e70d74e45508b340147c493a
http://hdl.handle.net/11588/465644
http://hdl.handle.net/11588/465644
Autor:
S E, Piscopo, I W, Smoak
Publikováno v:
American journal of veterinary research. 58(9)
To evaluate and compare effects of albendazole sulfoxide (ABZSO) on rat embryos and bovine embryos produced in vitro.In vitro produced bovine embryos. Rat embryos recovered from naturally bred Sprague-Dawley rats.4- and 8-cell bovine embryos were ran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::88c17bd482c2feba1258388d57300a4e
https://pubmed.ncbi.nlm.nih.gov/9285012
https://pubmed.ncbi.nlm.nih.gov/9285012
Publikováno v:
American journal of veterinary research. 58(1)
To determine time and concentration of peak plasma and uterine fluid concentrations of albendazole (ABZ) sulfoxide (ABZSO) in heifers after oral administration of ABZ.25 young Angus and Simmental heifers maintained on pasture with ad libitum access t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b4d3ccf474c97c1171fcadc9b204894
https://pubmed.ncbi.nlm.nih.gov/8989498
https://pubmed.ncbi.nlm.nih.gov/8989498
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 50(2)
A series of 1-(p-substituted)phenyl-3-(p-alkoxy)phenyl-4-phenyl-azetidin-2-one s 1a-20a, was synthesized and characterized. Their antimicrobial activity, against Gram+ and Gram- bacteria and Fungi, was tested. The compounds 8a, 13a, 14a, 18a and 6a,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::317d180177e3c7cddb3790c647a90fe9
https://pubmed.ncbi.nlm.nih.gov/7766278
https://pubmed.ncbi.nlm.nih.gov/7766278
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 48(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c155462c739079e2b149e039b4bc1f18
https://pubmed.ncbi.nlm.nih.gov/8323674
https://pubmed.ncbi.nlm.nih.gov/8323674
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 47(9)
The N-(2-hydroxy-5-carboxy-benzyliden)-4-substituted anilines (1-6) and the corresponding 5-carbomethoxy derivatives (7-12) were synthesized and characterized. Antimicrobial and antifungal activity was tested against Gram+ and Gram- bacteria and Fung
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c1de46305257cc0d1b8371c534d1d3b
https://pubmed.ncbi.nlm.nih.gov/1300124
https://pubmed.ncbi.nlm.nih.gov/1300124
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 47(2)
A set of substituted 1,3,4-triaryl-2-azetidinones were synthesized and characterized. Their antimicrobial activity, against Gram+ and Gram- bacteria and Fungi, was tested. The compounds 23 and 30 showed remarkable activity against Pseudomonas aerugin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c6410d529c39e455eb38e70533deff9
https://pubmed.ncbi.nlm.nih.gov/1510796
https://pubmed.ncbi.nlm.nih.gov/1510796
Publikováno v:
Bollettino della Societa italiana di biologia sperimentale. 67(12)
The following 2-substituted phenyl-3-(N,N-dimethylaminopropyl)-1,3-thiazolidin-4-one of general formula (A): [formula: see text] where: X = H (I), 3-F (II), 3-Cl (III), 3-Br (IV), 3-CH3 (V), 3-OCH3 (VI), 3-NO2 (VII), 4-F (VIII), 4-Cl (IX), 4-Br (X),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9da985bd15b578c6367bbf390f1aecd
https://pubmed.ncbi.nlm.nih.gov/1840799
https://pubmed.ncbi.nlm.nih.gov/1840799
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 46(5)
4-hydroxy-isophthalaldehyde acid (1), its alkyl esters (methyl, ethyl, propyl and butyl) and alkyl ethers (propyl, butyl, pentyl and esyl), as well as 6-hydroxy-isophthalaldehyde acid (2) ita alkyl esters (methyl and ethyl), 4-hydroxy-5-iodo-isophtha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b766e6622aa233d947cf2a5932cc08a0
https://pubmed.ncbi.nlm.nih.gov/1953927
https://pubmed.ncbi.nlm.nih.gov/1953927