Zobrazeno 1 - 10
of 36
pro vyhledávání: '"J. S. Patton"'
Publikováno v:
Journal of Lipid Research, Vol 26, Iss 4, Pp 428-434 (1985)
Benzo(a)pyrene (BP) was dissolved in dietary fat and fed in a single dose to killifish (Fundulus heteroclitus). Fluorescence microscopic examinations of small intestinal content and frozen sections of whole small intestine revealed that during fat di
Externí odkaz:
https://doaj.org/article/f73fbbbbac154fbdae2c7ea17720024a
Publikováno v:
Journal of Lipid Research, Vol 25, Iss 12, Pp 1337-1342 (1984)
This study assessed the effect of concomitant lipid absorption on the bioavailability and lymphatic transport of benzo(a)pyrene (BP), a carcinogenic polycyclic aromatic hydrocarbon (PAH). Conscious, male Sprague-Dawley rats, equipped with biliary and
Externí odkaz:
https://doaj.org/article/03a6255ac44147dfafac4236f0f77e0c
Publikováno v:
Journal of Lipid Research, Vol 25, Iss 2, Pp 189-197 (1984)
The fat solubilities of some long chain fatty acids, alcohols, alkanes, and triacyglycerols, and of some aromatic, chlorinated aromatic, and chlorinated aliphatic hydrocarbons were measured in trioleoylglycerol. Above their melting temperature, all t
Externí odkaz:
https://doaj.org/article/5111ab3e621c49bea541b6fb997ab15e
Publikováno v:
Journal of Lipid Research, Vol 28, Iss 7, Pp 810-817 (1987)
Following the intestinal absorption of dietary benzo[a]pyrene (BP) by the killifish, this compound becomes incorporated along with dietary triglycerides into membrane-bound fat vacuoles within the intestinal epithelial cell (1985. J. Lipid Res. 26: 4
Externí odkaz:
https://doaj.org/article/beaa75f379974df5946b571dd3705e82
Publikováno v:
Journal of Lipid Research, Vol 27, Iss 8, Pp 836-857 (1988)
The technique of freeze fracture was used to visualize triglyceride (TG) hydrolysis and the production of lipolytic products (LPs) in vitro and in vivo in the presence of bile salts (BS). Three systems were investigated: pure lipolytic products (olei
Externí odkaz:
https://doaj.org/article/1b5cdc1d900444658cbdaf11944c76d1
Publikováno v:
Scopus-Elsevier
Severe alleles of the ovarian tumor (otu) and ovo genes result in female sterility in Drosophila melanogaster, producing adult ovaries that completely lack egg chambers. We examined the developmental stage in which the agametic phenotype first become
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d2734ecf543c76a947480c1cbd83326
https://doi.org/10.1093/genetics/141.1.191
https://doi.org/10.1093/genetics/141.1.191
Publikováno v:
Development. 121:579-587
Gametogenesis in Drosophila requires sex-specific interactions between the soma and germline to control germ cell viability, proliferation, and differentiation. To determine what genetic components are involved in this interaction, we examined whethe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723c45bcee36acb3b642f3badc968f20
https://doi.org/10.1242/dev.121.2.579
https://doi.org/10.1242/dev.121.2.579
Publikováno v:
Genetics. 133:265-278
The mutations in the ovarian tumor (otu) gene arrest oogenesis at several stages in development. A series of deletion mutations in the otu region were characterized, each of which causes the absence or reduction of the otu transcript. These alleles r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::897c4c34019ba8eddcf45f8447e8a44b
https://doi.org/10.1093/genetics/133.2.265
https://doi.org/10.1093/genetics/133.2.265
Publikováno v:
Genetics. 148(1)
The suppressor of Hairy-wing [SU(HW)] binding region disrupts communication between a large number of enhancers and promoters and protects transgenes from chromosomal position effects. These properties classify the SU(HW) binding region as an insulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29703736a72a0d5a61a2213eb9a99618
https://pubmed.ncbi.nlm.nih.gov/9475743
https://pubmed.ncbi.nlm.nih.gov/9475743
Publikováno v:
Journal of Clinical Oncology. 29:e13019-e13019
e13019 Background: MPC-3100 is an oral synthetic inhibitor of HSP90, in a phase I safety study in cancer patients. Major cytochrome P450 (CYP450) and UDP-glucuronosyltransferase (UGT) isozymes were...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::526d7dc62417c45b1b8769dffd1c1c81
https://doi.org/10.1200/jco.2011.29.15_suppl.e13019
https://doi.org/10.1200/jco.2011.29.15_suppl.e13019