$B9V1i(B $B;~9o(B | $B9V1i(B $BHV9f(B | $B9V1iBjL\!?H/I=| $B%-!<%o!<%I(B | $BJ,N`(B $BHV9f(B | $B$BHV9f(B | |
| $B%P%$%*(B |
| (9:00$B!A(B10:00)$B!!(B($B:BD9(B $BKv867{0lO:(B) |
| 9:00$B!A(B 9:20 | I301 | $B?)IJN.DL8!::$X8~$1$?0dEA;RB?7?4J0WH=JLK!$N3+H/(B ($B6eBg1!9)(B) $B!{(B($B3X(B)$BKL2,(B $BEm;R(B$B!&(B($B85(BJST) $B2,B<(B $BD*;R(B$B!&(B($B6eBg1!G@(B) $B0l@%(B $BGnJ8(B$B!&(B($B6eBg1!9)(B) ($B@5(B)$B?@C+(B $BE5Jf(B$B!&(B($B@5(B)$B8eF#(B $B2m9((B | fluorogenic ribonuclease protection assay fluorescence resonance energy transfer single nucleotide polymorphism
| 7-d | 344 |
| 9:20$B!A(B 9:40 | I302 | ANALYSIS OF THE SPECIFIC CHROMOSOMAL REGION ADJACENT TO THE DHFR GENE AMPLIFIED IN CHO CELL LINE ($B:eBg1!9)@8L?@hC<9)(B) $B!{(B($B3X(B)$BKQ(B $B=S1G(B$B!&(B$B9bLZ(B $B9/90(B$B!&(B$BLpLn(B $B=(K!(B$B!&(B$BAb(B $B0n2Z(B$B!&(B$B6b(B $By(El(B$B!&(B($B@5(B)$BBg@/(B $B7r;K(B$B!&(B($B7DXfBg0e3X(B) $B@u@n(B $B=$0l(B$B!&(B($B7DXfBg@hF32J(BGSP$B%;%s%?!<(B) $B@6?e(B $B?.5A(B$B!&(B($B:eBg1!9)@8L?@hC<9)(B) ($B@5(B)$BBgC](B $B5WIW(B | Chinese Hamster Ovary cell Bacterial Artificial Chromosome library amplification
| 7-d | 587 |
| 9:40$B!A(B 10:00 | I303 | $B%;%k%=!<%?!<$GJ,N%$7$?%K%o%H%j;O86@8?#:YK&$N2r@O(B ($BL>Bg9)(B) $B85Ln(B $B@?(B$B!&(B$B!{(B($B@5(B)$B@>Eg(B $B8,0l(B$B!&(B($B@5(B)$BHSEg(B $B?.;J(B | chicken primordial germ cell
| 7-d | 573 |
| (10:00$B!A(B11:00)$B!!(B($B:BD9(B $B@>Eg8,0l(B) |
| 10:00$B!A(B 10:20 | I304 | $BAjF1AH49$(K!$K$h$k%O%$%V%j%I!<%^:YK&$G$N93BN9ZAGM;9g%?%s%Q%/@8;:(B ($BElBg1!9)!&2=@8(B) $B!{(B($B3X(B)$BEDJU(B $BL@?M(B$B!&(B($BElBg1!9)!&%P%$%*(B) $B0K86(B $B@54n(B$B!&(B($BElBg1!9)!&2=@8(B) ($B@5(B)$B>eED(B $B9((B | antibody fusion protein hybridoma
| 7-d | 604 |
| 10:20$B!A(B 10:40 | I305 | $BBgD26]:YK&2AK!$N3+H/$H!$3h@-8~>e$X$N1~MQ(B ($BElBg1!9)!&2=@8(B) $B!{(B($B3X(B)$B0KF#(B $B7=;J(B$B!&(B$B4dK\(B $B>O42(B$B!&(B($BElBg1!9)!&%P%$%*(B) $B0K86(B $B@54n(B$B!&(B($BElBg1!9)!&2=@8(B) ($B@5(B)$B>eED(B $B9((B | antibody fluorescein flow cytometry
| 7-d | 570 |
| 10:40$B!A(B 11:00 | I306 | Cre$BAH49$(9ZAG$K$h$k%U%!!<%8Ds<(93BN$N%*!<%W%s%5%s%I%$%C%A(BELISA$B7O$X$N8zN(E*JQ49(B ($BElBg1!9)!&2=@8(B) $B!{(B($B3X(B)$B>.Eh(B $BH~$B!&(B($BElBg1!9)!&%P%$%*(B) $B0K86(B $B@54n(B$B!&(B($BIY;N%U%#%k%`(B) $B@n>e(B $B2mG7(B$B!&(B(Aarhus U.) Kristensen Peter$B!&(B($BElBg1!9)!&2=@8(B) ($B@5(B)$B>eED(B $B9((B | Antibody Phage display Open sandwich
| 7-d | 760 |
| (11:00$B!A(B12:00)$B!!(B($B:BD9(B $B>eJ?@5F;(B) |
| 11:00$B!A(B 11:20 | I307 | $BD69%G.6](BPyrococcus horikoshii$BM3MhBQG.@-%"%_%N%"%7%i!<%<$N3h@-$*$h$S0BDj@-$K5Z$\$96bB0%$%*%s$N1F6A(B ($B:eBg1!4p9)(B) $B!{(B($B@5(B)$B@>2,(B $B5a(B$B!&(B($B3X(B)$BC+85(B $B9@0l(B$B!&(B$BEl(B $B5*;R(B$B!&(B($B;:Am8&(B) $B@P@n(B $B0lI'(B$B!&(B($B:eBg1!4p9)(B) ($B@5(B)$BEDC+(B $B@5?N(B | thermostable enzyme aminoacylase metal ion
| 7-d | 352 |
| 11:20$B!A(B 11:40 | I308 | Cellvibrio sp.$B$+$iF@$i$l$?(B2$B ($B9bCN9)Bg9)(B) $B!{(B($B3X(B)$B0f>e(B $B5.M3(B$B!&(B($BIt(B)$BM-2l(B $B=$(B | agarase neoagarooligosaccharide nucleotide sequence
| 7-a | 609 |
| 11:40$B!A(B 12:00 | I309 | $BO":?5e6](BStreptococcus anginosus$B$NTsKlB?E|@89g@.0dEA;R72$N2r@O(B ($BL>Bg1!9)!&2=@89)(B) $B!{(B($B@5(B)$B;0Bp(B $B9n1Q(B$B!&(B$B9KEg(B $BM5G7(B$B!&(B($B@5(B)$BHSEg(B $B?.;J(B | Streptococcus anginosus Capsular polysaccharide glycosyltransferases
| 7-d | 646 |
| (13:00$B!A(B14:00)$B!!(B($B:BD9(B $B;0Bp9n1Q(B) |
| 13:00$B!A(B 13:20 | I313 | $BKlLL1UBNG]M\K!$rMQ$$$?9m6]$NG]M\FC@-5Z$S0dEA;RH/8=(B ($B2,;3Bg9)(B) $B!{(B($B3X(B)$BEDCf(B $BAO5H(B$B!&(B($B@5(B)$B:#Cf(B $BMN9T(B$B!&(B($B@5(B)$B:#B<(B $B0]9n(B$B!&(B($B@5(B)$BCf@>(B $B0l90(B | #Aspergillus oryzae# membrane-surface liquid culture DNA chip
| 7-d | 641 |
| 13:20$B!A(B 13:40 | I314 | $B%(%s%Y%m!<%W$N2~JQ$K$h$k93BN0MB8E*%&%$%k%9%Y%/%?!<$rMQ$$$?0dEA;RF3F~(B ($B6eBg1!9)!&2=9)(B) $B!{(B($B3X(B)$B55;3(B $BM:FsO:(B$B!&(B($B@5(B)$B2On5(B $B2BE5(B$B!&(B($B@5(B)$B0fF#(B $B>4(B$B!&(B($B@5(B)$B>eJ?(B $B@5F;(B | retroviral vector envelop target infection
| 7-d | 44 |
| 13:40$B!A(B 14:00 | I315 | $BJ|@~6]$G$N%?%s%Q%/ ($B6bBtBg1!<+(B) $B!{(B($B3X(B)$B5HLn(B $BOB7D(B$B!&(B($B3X(B)$B0KF#(B $B5H4p(B$B!&(B($B3X(B)$B5\2<(B $BE0(B$B!&(B($B3X(B)$B0KF#(B $BM5;R(B$B!&(B($B@5(B)$B@6?e(B $B@kL@(B$B!&(B($B?@8MBg1!9)(B) ($B@5(B)$B2.Ln(B $B@i=)(B | Streptomyces secretion protein production
| 7-d | 618 |
| (14:00$B!A(B15:00)$B!!(B($B:BD9(B $BJ?Bt(B $B7I(B) |
| 14:00$B!A(B 14:20 | I316 | $BJ|@~6]$rMQ$$$?%j%s;i ($B6bBtBg1!<+(B) $B!{(B($B3X(B)$B0KF#(B $B5H4p(B$B!&(B($B3X(B)$B0KF#(B $BM5;R(B$B!&(B($B3X(B)$B5\2<(B $BE0(B$B!&(B($B3X(B)$B5HLn(B $BOB7D(B$B!&(B($B@5(B)$B@6?e(B $B@kL@(B$B!&(B($B?@8MBg1!9)(B) ($B@5(B)$B2.Ln(B $B@i=)(B | Streptomyces Mutation analysis
| 7-d | 588 |
| 14:20$B!A(B 14:40 | I317 | $BJ,;R?J2=9)3XE* ($B:eI\Bg1!9)(B) $B!{(B($B3X(B)$B2OED(B $BBsLi(B$B!&(B($B@5(B)$B2.Ln(B $BGn9/(B | lipase directed evolution stability
| 7-d | 688 |
| 14:40$B!A(B 15:00 | I318 | $BAH49$(9ZAG$rMQ$$$?G[NsFC0[E*0dEA;RA}I}5;=Q$N3+H/(B ($B6eBg1!9)!&2=9)(B) $BEOn5(B $BNC;R(B$B!&(B$BC]G7Fb(B $BM:B@(B$B!&(B($B3X(B)$B55;3(B $BM:FsO:(B$B!&(B$B!{(B($B@5(B)$B2On5(B $B2BE5(B$B!&(B($B@5(B)$B0fF#(B $B>4(B$B!&(B($B@5(B)$B>eJ?(B $B@5F;(B | gene amplification site-specific recombination gene delivery
| 7-d | 43 |
| (15:00$B!A(B16:20)$B!!(B($B:BD9(B $BEDC+@5?N(B) |
| 15:00$B!A(B 15:20 | I319 | $B<'NO$rMQ$$$?4J0W%P%$%*%;%s%5!<$N3+H/(B ($B>.;39b@lJ*$B!&(B$BBg@P(B $B86Li(B$B!&(B$B=UED(B $B9aJfN$(B | biosensor bioluminescence immobilization
| 7-f | 48 |
| 15:20$B!A(B 15:40 | I320 | $B4D6-0x;R$K$h$kAXJL2= ($BL>Bg1!9)(B) $B!{(B($B3X(B)$B5mED(B $BBYFA(B$B!&(B($B3X(B)$BIZED(B $B9/G7(B$B!&(B($B3X(B)$BCf[=(B $B>;90(B$B!&(B($B@5(B)$B2CF#(B $BN5;J(B$B!&(B($B0&CN3X1!;u(B) $B2#ED(B $B=<90(B$B!&(B($BL>Bg1!9)(B) ($B@5(B)$BK\B?(B $BM5G7(B | myocardial infarction stratification analysis single nucleotide polymorphism
| 7-f | 275 |
| 15:40$B!A(B 16:00 | I321 | $B%9%H%l%94D6-2<$K$*$1$k9ZJl0l0dEA;RGK2u3t$N%U%'%N!<%`2r@O(B ($B:eBg1!>pJs!&%P%$%*(B) ($B3X(B)$B5H@n(B $B>!FA(B$B!&(B($B3X(B)$BEDCf(B $BCi>;(B$B!&(B($B@5(B)$B1J5W(B $B7=2p(B$B!&(B($B@5(B)$BJ?Bt(B $B7I(B$B!&(B($B@5(B)$B8E_7(B $BNO(B$B!&(B$B!{(B($B@5(B)$B@6?e(B $B9@(B | phenomics yeast stress tolerance
| 7-f | 203 |
| 16:00$B!A(B 16:20 | I322 | Membrane Chip$B$K$h$k0[>o@8BNKl$NI>2A(B ($B:eBg1!4p9)(B) ($B3X(B)$B@P0f(B $B<#G7(B$B!&(B$B!{(B($B3X(B)$BBg;3(B $B7CF`(B$B!&(B($B@5(B)$BEgFb(B $B$B!&(B($B@5(B)$BGO1[(B $BBg(B$B!&(B($B@5(B)$B5WJ]0f(B $BN<0l(B | Membrane Stress Biotechnology membrane chip membrane oxidation
| 7-f | 752 |