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1 available at http://www.canevolve.org/dChip-GemiNi.
2 o side chains emanating at C-20 are known as gemini.
3 rticularly sensitive to the structure of the gemini.
4 ce in properties between the two families of geminis.
12 s 21-(3-methyl-3-hydroxy-butyl)-19-nor D(3) (Gemini-19-nor), which has 2 side chains and removal of t
14 double-blind, multicentre, randomised trial (GEMINI-ACS-1) done at 371 clinical centres in 21 countri
15 f variant filters or prioritization methods, GEMINI allows researchers to compose complex queries bas
17 novel bis(alkyl-1,3-diene)-based phosphonium gemini amphiphiles exhibit "normal" hexagonal (H(I)), Ty
24 er nuclear domains, including coiled bodies, gemini bodies, PML bodies and the perinucleolar compartm
29 (Type I) lyotropic gyroid phase formed by a gemini dicarboxylate surfactant self-assembly using a co
31 cA-beta-(1,4)-GlcNAc] and related dimerized (gemini) disaccharides (4a and 4b) via n-pentenyl glycosi
34 ing intron downstream of exon 5 (tae) of the gemini gene switches parthenogenesis from arrhenotoky to
38 resent contribution, two related families of geminis have been synthesized, both with trehalose, a di
40 monomolecular films, constructed from these geminis, have interfacial areas that are dominated by th
51 2-2-12 2Br gemini (the only one of the three geminis known to form threadlike micelles) shows a marke
53 ane functional group, was synthesized from a gemini monomer through photoreaction in the solid state.
54 d materials, the Q(I) phases formed by these gemini monomers are consistent with four possible bicont
58 mid-latitude clouds from the W. M. Keck and Gemini Observatories show that they cluster near 350 deg
59 on of survival motor neuron (SMN)-associated Gemini of coiled bodies (GEMs) in motor neurons, its abs
63 4), Philips Allegro PET (n = 5), and Philips Gemini PET/CT (n = 11)-were 0.99, 1.01, 1.00, 0.98, and
71 karyokinesis and cytokinesis suggesting that GEMINI POLLEN1 may be required for the localization of p
77 ations, we selected as lead compound a 20(R) gemini, related to calcitriol in terms of it is A-ring,
78 e compared activities of 125D, 20E-125D, and Gemini, respectively, in several assays: binding to wild
80 nergy minimization calculations indicate the Gemini side chain possesses significantly more energy mi
82 ursor and a high concentration of a designed Gemini surfactant (Gem(16-3-16)) that has a large g valu
84 stitute the first example of a polymerizable gemini surfactant, and the first example of a cross-link
86 ydrogen bonding between electrically neutral gemini surfactants of the type CnH2n+1NH(CH2)2NH2 and si
88 ions of three didodecyl dicationic dibromide gemini surfactants with different methylene spacer lengt
90 The Hubble Space Telescope (HST) and the Gemini Telescope imaged this galaxy 6 to 9 months before
92 Metabolism Integrated for Network Inference (GEMINI) that links a compendium of candidate regulatory
93 ces, we have developed a fast search engine, GEMINI, that uses a genomic profile as a query to search
97 re from 2054 five-year-old children from the Gemini twin birth cohort, including parental ratings of
99 s from 1939 children aged 21 months from the Gemini twin cohort, we assessed prospective associations
100 characterization, and self-assembly of a new gemini-type amphiphilic hexathienocoronene (HTCGemini),
101 three individual components of the systems (geminis, vesicles, and gels) have widespread practical a
102 tigated for the inhibitory effect of a novel Gemini vitamin D analog, 1alpha,25-dihydroxy-20R-21(3-hy
104 t tumors, suggesting an inhibitory role of a Gemini vitamin D derivative on breast cancer stem cells.
105 We have previously shown that the novel Gemini vitamin D(3) analogue, Ro-438-3582 [Ro3582; 1 alp
110 al diastereotopic distortion, we synthesized gemini with equal side chains but introduced deuterium d
111 an effort to analyze the deuterium effect on gemini with minimal diastereotopic distortion, we synthe
112 xy-21-(3-hydroxy-3-methylbutyl)vitamin D(3) (Gemini) with two six-carbon side chains (both 20N and 20
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