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1 The observed effects were more striking in a chemically defined medium.
2 ne stifle joints were cultured in serum-free chemically defined medium.
3 nts and cultured as monolayers in serum-free chemically defined medium.
4 y role to BrnQ1 during S. aureus growth in a chemically defined medium.
5 either a Casitone-based complex medium or a chemically defined medium.
6 re BCKAD enzyme activity than cells from the chemically defined medium.
7 or even survive--when plated in mitogen-free chemically defined medium.
8 beta1, TGFbeta2 or TGFbeta3 was added to the chemically defined medium.
9 ophic for Arg, Gln/Glu, His, Leu, and Trp in chemically defined medium.
11 nd expansion of the initial SC population in chemically defined medium; (3) a magnetic-activated cell
12 -Hewitt supplemented with excess glucose and chemically defined medium allowed survival for less than
13 ed in dimethyl sulfoxide (DMSO)-supplemented chemically defined medium are an excellent model system
14 term dimethylsulfoxide (DMSO) culture, fed a chemically defined medium, are highly differentiated and
16 ively) were grown in continuous culture in a chemically defined medium at fast mass doubling time (t(
17 Oral viridans group streptococci, growing in chemically defined medium at pH 6.8, released HlpA into
18 tococcal proteases were recovered from spent chemically defined medium (CDM) and fractionated by ammo
20 evelopment of competence was examined in the chemically defined medium (CDM) described by van de Rijn
23 cally, when aerobically grown in a low-iron, chemically defined medium (CDM), L. pneumophila secretes
24 was used to develop in silico and in vitro a chemically defined medium (CDM), which was validated exp
26 ila was reduced approximately in half in the chemically defined medium compared with the same medium
27 ed cardiac differentiation strategy, using a chemically defined medium consisting of just three compo
28 s phenotypic abnormalities whereas growth in chemically defined medium containing 5 mM KCl more close
29 dc25A-rescued cells could not proliferate in chemically defined medium containing CSF-1 and continued
30 ts in decreased growth of H. influenzae in a chemically defined medium containing Neu5Ac, supporting
31 and the mesendoderm reporter MIXL1-GFP in a chemically defined medium containing the canonical WNT s
32 often observed when microbes are grown in a chemically defined medium containing two sugars (for exa
34 ious data showed that H. pylori grows in the chemically defined medium F-12, but not in other tissue
36 ells were co-cultured in vitro in serum-free chemically defined medium, functional anchoring junction
39 . pylori strains were cultured in Ham's F-12 chemically defined medium in the presence or absence of
40 opper, iron, and zinc to the DMSO-containing chemically defined medium induced DNA synthesis and cell
41 grown in continuous culture with a modified chemically defined medium is regulated by growth rate.
44 roduction was significantly decreased when a chemically defined medium lacking N-acetylneuraminic aci
46 e sequence TVKHRPDALHPQ or LTTAPKLPKVTR in a chemically defined medium (mTeSR), they expressed marker
48 nstrated that hemoglobin supplemented into a chemically defined medium significantly and specifically
49 n adipogenesis induction medium, but also in chemically defined medium specifically for osteogenesis,
51 gue profiling after bacterial cultivation in chemically defined medium supplemented with [U-(13)C(6)]
54 Pasteurella multocida was grown in iron-free chemically defined medium supplemented with hemoglobin,
55 on a rat-tail collagen coated dish and fed a chemically-defined medium supplemented with 2% dimethyls
56 nhancer/promoter, we found that a serum-free chemically defined medium supports formation of embryoid
58 biological role for these proteins, a simple chemically defined medium that supports growth of adult
61 well in complex medium, but did not grow in chemically defined medium unless supplemented with the m
62 of H2O2 and failed to grow aerobically in a chemically defined medium, unless supplemented with acet
65 , and TGFbeta pathway activity in a minimal, chemically defined medium, we show parallel, robust, and
66 ains were assessed by monitoring growth in a chemically defined medium where the only source of the e
67 oderm and surface ectoderm, in a serum-free, chemically defined medium with 10-50 ng/ml of FGF-2 indu
70 cells are continuously grown in a completely chemically defined medium without serum supplementation,
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