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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  either a Casitone-based complex medium or a chemically defined medium.
5 re BCKAD enzyme activity than cells from the chemically defined medium.
6 or even survive--when plated in mitogen-free chemically defined medium.
7 beta1, TGFbeta2 or TGFbeta3 was added to the chemically defined medium.
8 y role to BrnQ1 during S. aureus growth in a chemically defined medium.
9 ophic for Arg, Gln/Glu, His, Leu, and Trp in chemically defined medium.
10 gated in serum (2-3 h) and differentiated in chemically defined medium (3-4 h).
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
15                                When grown in chemically defined medium at an alkaline pH, strain 86-0
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
19                                              Chemically defined medium (CDM) conditions for controlli
20 evelopment of competence was examined in the chemically defined medium (CDM) described by van de Rijn
21 ters were upregulated in vitro when grown in chemically defined medium (CDM) lacking BCAA.
22               The mtaR mutant grew poorly in chemically defined medium (CDM) prepared with methionine
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
25  murine soft tissue and in nutrient-limiting chemically defined medium (CDM).
26  40 to 70% less CAS reactivity in deferrated chemically defined medium (CDM).
27 ila was reduced approximately in half in the chemically defined medium compared with the same medium
28 , introducing two novel formulations: LM7, a chemically defined medium comprising seven essential com
29 ed cardiac differentiation strategy, using a chemically defined medium consisting of just three compo
30 s phenotypic abnormalities whereas growth in chemically defined medium containing 5 mM KCl more close
31 dc25A-rescued cells could not proliferate in chemically defined medium containing CSF-1 and continued
32 ts in decreased growth of H. influenzae in a chemically defined medium containing Neu5Ac, supporting
33  and the mesendoderm reporter MIXL1-GFP in a chemically defined medium containing the canonical WNT s
34  often observed when microbes are grown in a chemically defined medium containing two sugars (for exa
35                                         In a chemically defined medium, exogenous CSP does not induce
36 ious data showed that H. pylori grows in the chemically defined medium F-12, but not in other tissue
37        We also show that reprogramming using chemically defined medium favors formation of fully repr
38 ells were co-cultured in vitro in serum-free chemically defined medium, functional anchoring junction
39                                         In a chemically defined medium, growth of the wild-type strai
40 or alpha (TGFalpha) in the presence of a new chemically defined medium (HGM).
41 . pylori strains were cultured in Ham's F-12 chemically defined medium in the presence or absence of
42 opper, iron, and zinc to the DMSO-containing chemically defined medium induced DNA synthesis and cell
43  grown in continuous culture with a modified chemically defined medium is regulated by growth rate.
44               The fucose phenotype, shown in chemically defined medium, is strain specific and linked
45     Halobacterium synthesized cobalamin in a chemically defined medium lacking corrinoid precursors.
46 roduction was significantly decreased when a chemically defined medium lacking N-acetylneuraminic aci
47  give rise to cell lines that proliferate in chemically defined medium lacking serum.
48 e sequence TVKHRPDALHPQ or LTTAPKLPKVTR in a chemically defined medium (mTeSR), they expressed marker
49 ar matrix coating, and either conditioned or chemically defined medium (mTeSR).
50 nstrated that hemoglobin supplemented into a chemically defined medium significantly and specifically
51 n adipogenesis induction medium, but also in chemically defined medium specifically for osteogenesis,
52                            After growth in a chemically defined medium, stage I (lyophilized) culture
53 gue profiling after bacterial cultivation in chemically defined medium supplemented with [U-(13)C(6)]
54         We previously described the use of a chemically defined medium supplemented with epidermal gr
55  genes in an S. mutans PTS mutant grown in a chemically defined medium supplemented with glucose.
56 Pasteurella multocida was grown in iron-free chemically defined medium supplemented with hemoglobin,
57 on a rat-tail collagen coated dish and fed a chemically-defined medium supplemented with 2% dimethyls
58 nhancer/promoter, we found that a serum-free chemically defined medium supports formation of embryoid
59            Because RPMI is a more stable and chemically defined medium than M3, the determination at
60 biological role for these proteins, a simple chemically defined medium that supports growth of adult
61                                            A chemically defined medium that supports the growth of bo
62                   Also, we tested completely chemically defined medium that, when used together with
63             When control hESCs were grown in chemically defined medium, their expression of markers o
64  well in complex medium, but did not grow in chemically defined medium unless supplemented with the m
65  of H2O2 and failed to grow aerobically in a chemically defined medium, unless supplemented with acet
66                        Using iron-deficient, chemically defined medium, we determined that H. pylori
67                                      Using a chemically defined medium, we found that (p)ppGpp accumu
68 , and TGFbeta pathway activity in a minimal, chemically defined medium, we show parallel, robust, and
69 ains were assessed by monitoring growth in a chemically defined medium where the only source of the e
70 oderm and surface ectoderm, in a serum-free, chemically defined medium with 10-50 ng/ml of FGF-2 indu
71 tential by culturing them as aggregates in a chemically defined medium with TGFbeta1.
72 ically resected patient tumor tissue using a chemically defined medium without cell dissociation.
73 rs with a predominantly dorsal identity in a chemically defined medium without known morphogens.
74 cells are continuously grown in a completely chemically defined medium without serum supplementation,