-
1
-
-
77950063625
-
Homoisoflavonoid derivatives from the roots of Ophiopogon japonicus and their in vitro anti-inflammation activity
-
10.1016/j.bmcl.2010.03.043 20346658
-
Homoisoflavonoid derivatives from the roots of Ophiopogon japonicus and their in vitro anti-inflammation activity. Hung TM, Thu CV, Dat NT, Ryoo SW, Lee JH, Kim JC, Na M, Jung HJ, Bae K, Min BS, Bioorg Med Chem Lett 2010 20 2412 2416 10.1016/j.bmcl.2010.03.043 20346658
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 2412-2416
-
-
Hung, T.M.1
Thu, C.V.2
Dat, N.T.3
Ryoo, S.W.4
Lee, J.H.5
Kim, J.C.6
Na, M.7
Jung, H.J.8
Bae, K.9
Min, B.S.10
-
2
-
-
33846913943
-
Synthesis, structural revision, and antioxidant activities of antimutagenic homoisoflavonoids from Hoffmanosseggia intricata
-
DOI 10.1016/j.bmcl.2006.12.008, PII S0960894X06013904
-
Synthesis, structural revision, and antioxidant activities of antimutagenic homoisoflavonoids from Hoffmanosseggiaintricata. Siddaiah V, Maheswara M, Rao CV, Venkateswarlu S, Subbaraju GV, Bioorg Med Chem Lett 2007 17 1288 1290 10.1016/j.bmcl.2006.12.008 17196384 (Pubitemid 46240845)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.5
, pp. 1288-1290
-
-
Siddaiah, V.1
Maheswara, M.2
Venkata Rao, C.3
Venkateswarlu, S.4
Subbaraju, G.V.5
-
3
-
-
41249096543
-
Design, synthesis and antiproliferative activity of some 3-benzylidene-2,3-dihydro-1-benzopyran-4-ones which display selective toxicity for malignant cells
-
DOI 10.1016/j.ejmech.2007.06.017, PII S0223523407002590
-
Design, synthesis and antiproliferative activity of some 3-benzylidene-2,3-dihydro-1-benzopyran-4-ones which display selective toxicity for malignant cells. Perjési P, Das U, De Clercq E, Balzarini J, Kawase M, Sakagami H, Stables JP, Lorand T, Rozmer Z, Dimmock JR, Eur J Med Chem 2008 43 839 845 10.1016/j.ejmech.2007.06.017 17692998 (Pubitemid 351446154)
-
(2008)
European Journal of Medicinal Chemistry
, vol.43
, Issue.4
, pp. 839-845
-
-
Perjesi, P.1
Das, U.2
De Clercq, E.3
Balzarini, J.4
Kawase, M.5
Sakagami, H.6
Stables, J.P.7
Lorand, T.8
Rozmer, Z.9
Dimmock, J.R.10
-
4
-
-
0025347587
-
SYNTHESE ET ACTIVITE FONGICIDE DE QUELQUES 3-BENZYLIDENE-CHROMAN-4-ONES, 3-BENZYLIDENE-THIOCHROMAN-4-ONES, ET 2-BENZYLIDENE-1-TETRALONES
-
DOI 10.1016/0223-5234(90)90010-Z
-
Synthesis and antifungal activity of some 3-benzylidenechroman-4-ones, 3-benzylidenethiochroman-4-ones and 2-benzylidene-1-tetralones. Al Nakib T, Bezjak V, Meegan MJ, Chandy R, Eur J Med Chem 1990 25 455 462 10.1016/0223-5234(90)90010-Z (Pubitemid 20204932)
-
(1990)
European Journal of Medicinal Chemistry
, vol.25
, Issue.5
, pp. 455-462
-
-
Al Nakib, T.1
Bezjak, V.2
Meegan, M.J.3
Chandy, R.4
-
5
-
-
33750690473
-
Antiviral activity of substituted homoisoflavonoids on enteroviruses
-
DOI 10.1016/j.antiviral.2006.07.003, PII S0166354206002038
-
Antiviral activity of substituted homoisoflavonoids on enteroviruses. Tait S, Salvati AL, Desideri N, Fiore L, Antiviral Res 2006 72 252 255 10.1016/j.antiviral.2006.07.003 16934879 (Pubitemid 44708308)
-
(2006)
Antiviral Research
, vol.72
, Issue.3
, pp. 252-255
-
-
Tait, S.1
Salvati, A.L.2
Desideri, N.3
Fiore, L.4
-
6
-
-
0035996875
-
Antimutagenic potential of homoisoflavonoids from Muscari racemosum
-
DOI 10.1016/S0378-8741(02)00135-6, PII S0378874102001356
-
Antimutagenic potential of homoisoflavonoids from Muscari racemosum. Miadokova E, Masterova I, Vlckova V, Duhova V, Toth J, J Ethnopharmacol 2002 81 381 386 10.1016/S0378-8741(02)00135-6 12127240 (Pubitemid 34786323)
-
(2002)
Journal of Ethnopharmacology
, vol.81
, Issue.3
, pp. 381-386
-
-
Miadokova, E.1
Masterova, I.2
Vlckova, V.3
Duhova, V.4
Toth, J.5
-
7
-
-
84863987076
-
Anti-inflammatory homoisoflavonoids from the tuberous roots of Ophiopogon japonicus
-
10.1016/j.fitote.2012.05.011 22626747
-
Anti-inflammatory homoisoflavonoids from the tuberous roots of Ophiopogon japonicus. Li N, Zhang JY, Zeng KW, Zhang L, Che YY, Tu PF, Fitoterapia 2012 83 1042 10455 10.1016/j.fitote.2012.05.011 22626747
-
(2012)
Fitoterapia
, vol.83
, pp. 1042-10455
-
-
Li, N.1
Zhang, J.Y.2
Zeng, K.W.3
Zhang, L.4
Che, Y.Y.5
Tu, P.F.6
-
8
-
-
84877578749
-
A dihydrochalcone and several homoisoflavonoids from Polygonatum odoratum are activators of adenosine monophosphate-activated protein kinase
-
10.1016/j.bmcl.2013.04.027 23639538
-
A dihydrochalcone and several homoisoflavonoids from Polygonatum odoratum are activators of adenosine monophosphate-activated protein kinase. Guo H, Zhao H, Kanno Y, Li W, Mu Y, Kuang X, Inouye Y, Koike K, Jiang H, Bai H, Bioorg Med Chem Lett 2013 23 3137 3139 10.1016/j.bmcl.2013.04.027 23639538
-
(2013)
Bioorg Med Chem Lett
, vol.23
, pp. 3137-3139
-
-
Guo, H.1
Zhao, H.2
Kanno, Y.3
Li, W.4
Mu, Y.5
Kuang, X.6
Inouye, Y.7
Koike, K.8
Jiang, H.9
Bai, H.10
-
9
-
-
73449097871
-
HPLC analysis and NMR identification of homoisoflavonoids and stilbenoids from the inter-bulb surfaces of Scilla nervosa
-
19911573
-
HPLC analysis and NMR identification of homoisoflavonoids and stilbenoids from the inter-bulb surfaces of Scilla nervosa. Bezabih M, Famuyiwa SO, Abegaz BM, Nat Prod Commun 2009 4 1367 1370 19911573
-
(2009)
Nat Prod Commun
, vol.4
, pp. 1367-1370
-
-
Bezabih, M.1
Famuyiwa, S.O.2
Abegaz, B.M.3
-
10
-
-
33646909937
-
Homoisoflavanones and spirocyclic nortriterpenoids from three Eucomis species: E. Comosa, E. Schijffii and E. Pallidiflora subsp. Pole-evansii (Hyacinthaceae)
-
DOI 10.1016/j.sajb.2005.12.006, PII S0254629906000329
-
Homoisoflavanones and spirocyclic nortriterpenoids from three Eucomis species: E. comosa, E. schijffii and E. pallidiflora subsp. pole-evansii (Hyacinthaceae). Koorbanally C, Crouch NR, Langlois A, Du Toit K, Mulholland DA, Drewes SE, S Afr J Bot 2006 72 428 433 10.1016/j.sajb.2005.12.006 (Pubitemid 43794981)
-
(2006)
South African Journal of Botany
, vol.72
, Issue.3
, pp. 428-433
-
-
Koorbanally, C.1
Crouch, N.R.2
Langlois, A.3
Du Toit, K.4
Mulholland, D.A.5
Drewes, S.E.6
-
11
-
-
1842858408
-
Estrogenic/antiestrogenic activity of homoisoflavonoids from bulbs of Muscari racemosum (L.) Miller
-
DOI 10.1016/S0367-326X(02)00241-1, PII S0367326X02002411
-
Estrogenic/antiestrogenic activity of homoisoflavonoids from bulbs of Muscari racemosum (L.) Miller. Urbancíková M, Masterová I, Tóth J, Fitoterapia 2002 73 724 726 10.1016/S0367-326X(02)00241-1 12490242 (Pubitemid 35477779)
-
(2002)
Fitoterapia
, vol.73
, Issue.7-8
, pp. 724-726
-
-
Urbancikova, M.1
Masterova, I.2
Toth, J.3
-
12
-
-
0037369350
-
Homoisoflavonoids and xanthones from the tubers of wild and in vitro regenerated Ledebouria graminifolia and cytotoxic activities of some of the homoisoflavonoids
-
DOI 10.1016/S0031-9422(02)00622-2, PII S0031942202006222
-
Homoisoflavonoids and xanthones from the tubers of wild and in vitro regenerated Ledebouria graminifolia and cytotoxic activities of some of the homoisoflavonoids. Mutanyatta J, Matapa BG, Shushu DD, Abegaz BM, Phytochemistry 2003 62 797 804 10.1016/S0031-9422(02)00622-2 12620333 (Pubitemid 36227776)
-
(2003)
Phytochemistry
, vol.62
, Issue.5
, pp. 797-804
-
-
Mutanyatta, J.1
Matapa, B.G.2
Shushu, D.D.3
Abegaz, B.M.4
-
13
-
-
77955123233
-
New features on the fragmentation patterns of homoisoflavonoids in Ophiopogon japonicus by high-performance liquid chromatography/diode-array detection/electrospray ionization with multi-stage tandem mass spectrometry
-
10.1002/rcm.4608
-
New features on the fragmentation patterns of homoisoflavonoids in Ophiopogon japonicus by high-performance liquid chromatography/diode-array detection/electrospray ionization with multi-stage tandem mass spectrometry. Qi J, Xu D, Zhou YF, Qin MJ, Yu BY, Rapid Commun Mass Spectrum 2010 24 2193 2206 10.1002/rcm.4608
-
(2010)
Rapid Commun Mass Spectrum
, vol.24
, pp. 2193-2206
-
-
Qi, J.1
Xu, D.2
Zhou, Y.F.3
Qin, M.J.4
Yu, B.Y.5
-
14
-
-
0034005615
-
Synthesis and anti-inflammatory effect of chalcones
-
10.1211/0022357001773814 10714946
-
Synthesis and anti-inflammatory effect of chalcones. Hsieh HK, Tsao LT, Wang JP, Lin CN, J Pharm Pharmacol 2000 52 163 171 10.1211/0022357001773814 10714946
-
(2000)
J Pharm Pharmacol
, vol.52
, pp. 163-171
-
-
Hsieh, H.K.1
Tsao, L.T.2
Wang, J.P.3
Lin, C.N.4
-
15
-
-
18644361984
-
Synthesis and evaluation of new antimalarial phenylurenyl chalcone derivatives
-
DOI 10.1021/jm058208o
-
Synthesis and evaluation of new antimalarial phenylurenylchalcone derivatives. Domínguez JN, León C, Rodrigues J, de Domínguez NG, Gut J, Rosenthal PJ, J Med Chem 2005 48 3654 3658 10.1021/jm058208o 15887974 (Pubitemid 40664115)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.10
, pp. 3654-3658
-
-
Dominguez, J.N.1
Leon, C.2
Rodrigues, J.3
De Dominguez, N.G.4
Gut, J.5
Rosenthal, P.J.6
-
16
-
-
17144427687
-
Cationic chalcone antibiotics. Design, synthesis, and mechanism of action
-
DOI 10.1021/jm049424k
-
Cationic chalcone antibiotics. design, synthesis, and mechanism of action. Nielsen SF, Larsen M, Boesen T, Schønning K, Kromann H, J Med Chem 2005 48 2667 2677 10.1021/jm049424k 15801857 (Pubitemid 40516456)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.7
, pp. 2667-2677
-
-
Nielsen, S.F.1
Larsen, M.2
Boesen, T.3
Schonning, K.4
Kromann, H.5
-
17
-
-
84859792163
-
Chalcone-Benzoxaborole hybrid molecules as potent antitrypanosomal agents
-
10.1021/jm2012408 22360533
-
Chalcone-Benzoxaborole hybrid molecules as potent antitrypanosomal agents. Qiao Z, Wang Q, Zhang F, Wang Z, Bowling T, Nare B, Jacobs RT, Zhang J, Ding D, Liu Y, Zhou H, J Med Chem 2012 55 3553 3557 10.1021/jm2012408 22360533
-
(2012)
J Med Chem
, vol.55
, pp. 3553-3557
-
-
Qiao, Z.1
Wang, Q.2
Zhang, F.3
Wang, Z.4
Bowling, T.5
Nare, B.6
Jacobs, R.T.7
Zhang, J.8
Ding, D.9
Liu, Y.10
Zhou, H.11
-
18
-
-
51849097711
-
Inhibition of IκB kinase-β and anticancer activities of novel chalcone adamantyl arotinoids
-
Inhibition of IκB kinase-β and anticancer activities of novel chalcone adamantyl arotinoids. Lorenzo P, Alvarez R, Ortiz MA, Alvarez S, Piedrafita FJ, de Lera AR, J MedChem 2008 51 5431 5440
-
(2008)
J MedChem
, vol.51
, pp. 5431-5440
-
-
Lorenzo, P.1
Alvarez, R.2
Ortiz, M.A.3
Alvarez, S.4
Piedrafita, F.J.5
De Lera, A.R.6
-
19
-
-
79953769169
-
Homoisoflavonoids: Natural scaffolds with potent and selective monoamine oxidase-B inhibition properties
-
10.1021/jm1013709 21405131
-
Homoisoflavonoids: natural scaffolds with potent and selective monoamine oxidase-B inhibition properties. Desideri N, Bolasco A, Fioravanti R, Monaco LP, Orallo F, Yáñez M, Ortuso F, Alcaro S, J Med Chem 2011 54 2155 2164 10.1021/jm1013709 21405131
-
(2011)
J Med Chem
, vol.54
, pp. 2155-2164
-
-
Desideri, N.1
Bolasco, A.2
Fioravanti, R.3
Monaco, L.P.4
Orallo, F.5
Yáñez, M.6
Ortuso, F.7
Alcaro, S.8
-
20
-
-
35848965019
-
Synthesis and antioxidant properties of substituted 3-benzylidene-7- alkoxychroman-4-ones
-
DOI 10.1016/j.bmcl.2007.10.034, PII S0960894X07012036
-
Synthesis and antioxidant properties of substituted 3-benzylidene-7- alkoxychroman-4-ones. Foroumadi A, Samzadeh-Kermani A, Emami S, Dehghan G, Sorkhi M, Arabsorkhi F, Heidari MR, Abdollahi M, Shafiee A, Bioorg Med Chem Lett 2007 17 6764 6769 10.1016/j.bmcl.2007.10.034 17967537 (Pubitemid 350061310)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.24
, pp. 6764-6769
-
-
Foroumadi, A.1
Samzadeh-Kermani, A.2
Emami, S.3
Dehghan, G.4
Sorkhi, M.5
Arabsorkhi, F.6
Heidari, M.R.7
Abdollahi, M.8
Shafiee, A.9
-
21
-
-
84878545543
-
Synthesis and cytotoxic properties of novel (E)-3-benzylidene-7- methoxychroman-4-one derivatives
-
10.1186/2008-2231-21-31
-
Synthesis and cytotoxic properties of novel (E)-3-benzylidene-7- methoxychroman-4-one derivatives. Noushini S, Alipour E, Emami S, Safavi M, Ardestani SK, Gohari AR, Shafiee A, Foroumadi A, DARU J Pharm Sci 2013 21 31 10.1186/2008-2231-21-31
-
(2013)
DARU J Pharm Sci
, vol.21
, pp. 31
-
-
Noushini, S.1
Alipour, E.2
Emami, S.3
Safavi, M.4
Ardestani, S.K.5
Gohari, A.R.6
Shafiee, A.7
Foroumadi, A.8
-
22
-
-
84865173217
-
Anti-inflammatory activities of selected synthetic homoisoflavanones
-
10.1080/14786419.2011.565004 21950651
-
Anti-inflammatory activities of selected synthetic homoisoflavanones. Shaikh MM, Kruger HG, Bodenstein J, Smith P, du Toit K, Nat Prod Res 2012 26 1473 1482 10.1080/14786419.2011.565004 21950651
-
(2012)
Nat Prod Res
, vol.26
, pp. 1473-1482
-
-
Shaikh, M.M.1
Kruger, H.G.2
Bodenstein, J.3
Smith, P.4
Du Toit, K.5
-
23
-
-
0032544154
-
In vitro anti-human immunodeficiency virus (HIV) activity of the chromanone derivative, 12-oxocalanolide A, a novel NNRTI
-
DOI 10.1016/S0960-894X(98)00380-1, PII S0960894X98003801
-
In vitro anti-human immunodeficiency virus (HIV) activity of the chromanone derivative, 12-oxocalanolide A, a novel NNRTI. Xu ZQ, Bucheit RW, Stup TL, Flavin MT, Khilevich A, Rezzo JD, Lin L, Zembower DE, Bioorg Med Chem Lett 1998 8 2179 2184 10.1016/S0960-894X(98)00380-1 9873509 (Pubitemid 28561602)
-
(1998)
Bioorganic and Medicinal Chemistry Letters
, vol.8
, Issue.16
, pp. 2179-2184
-
-
Xu, Z.-Q.1
Buckheit Jr., R.W.2
Stup, T.L.3
Flavin, M.T.4
Khilevich, A.5
Rizzo, J.D.6
Lin, L.7
Zembower, D.E.8
-
25
-
-
0017318090
-
Homoisoflavonone IV. Neue inhaltsstoffe der eucomin-reihe von Eucomis bicolor
-
10.1002/hlca.19760590618 1017955
-
Homoisoflavonone IV. Neue inhaltsstoffe der eucomin-reihe von Eucomis bicolor. Heller W, Andermatt P, Schaad WA, Tamm E, HelV Chim Acta 1976 59 2048 2058 10.1002/hlca.19760590618 1017955
-
(1976)
HelV Chim Acta
, vol.59
, pp. 2048-2058
-
-
Heller, W.1
Andermatt, P.2
Schaad, W.A.3
Tamm, E.4
-
26
-
-
84870246519
-
Molecular hybridization of bioactives: Synthesis and antitubercular evaluation of novel dibenzofuran embodied homoisoflavonoids via Baylis-Hillman reaction
-
10.1016/j.bmcl.2012.10.056
-
Molecular hybridization of bioactives: synthesis and antitubercular evaluation of novel dibenzofuran embodied homoisoflavonoids via Baylis-Hillman reaction. Yempala T, Sriram D, Yogeeswari P, Kantevari S, Bioorg Med ChemLett 2012 22 7426 7430 10.1016/j.bmcl.2012.10.056
-
(2012)
Bioorg Med ChemLett
, vol.22
, pp. 7426-7430
-
-
Yempala, T.1
Sriram, D.2
Yogeeswari, P.3
Kantevari, S.4
-
27
-
-
49449108208
-
Naturally occurring homoisoflavonoids function as potent protein tyrosine kinase inhibitors by c-Src-based high-throughput screening
-
10.1021/jm701501x 18610999
-
Naturally occurring homoisoflavonoids function as potent protein tyrosine kinase inhibitors by c-Src-based high-throughput screening. Lin LG, Xie H, Li HL, Tong LJ, Tang CP, Ke CQ, Liu QF, Lin LP, Geng MY, Jiang H, Zhao WM, Ding J, Ye Y, J Med Chem 2008 51 4419 4429 10.1021/jm701501x 18610999
-
(2008)
J Med Chem
, vol.51
, pp. 4419-4429
-
-
Lin, L.G.1
Xie, H.2
Li, H.L.3
Tong, L.J.4
Tang, C.P.5
Ke, C.Q.6
Liu, Q.F.7
Lin, L.P.8
Geng, M.Y.9
Jiang, H.10
Zhao, W.M.11
Ding, J.12
Ye, Y.13
-
28
-
-
84858452064
-
Asymmetrical 2,6-bis(benzylidene)cyclohexanones: Synthesis, cytotoxic activity and QSAR study
-
22341788
-
Asymmetrical 2,6-bis(benzylidene)cyclohexanones: synthesis, cytotoxic activity and QSAR study. Nakhjiri M, Safavi M, Alipour E, Emami S, Atash AF, Jafari-Zavareh M, Ardestani SK, Khoshneviszadeh M, Foroumadi A, Shafiee A, Eur J Med Chem 2012 50 113 123 22341788
-
(2012)
Eur J Med Chem
, vol.50
, pp. 113-123
-
-
Nakhjiri, M.1
Safavi, M.2
Alipour, E.3
Emami, S.4
Atash, A.F.5
Jafari-Zavareh, M.6
Ardestani, S.K.7
Khoshneviszadeh, M.8
Foroumadi, A.9
Shafiee, A.10
-
29
-
-
84878660165
-
Synthesis and in vitro cytotoxic activity evaluation of (E)-16-(substituted benzylidene) derivatives of dehydroepiandrosterone
-
10.1186/2008-2231-21-34
-
Synthesis and In vitro cytotoxic activity evaluation of (E)-16-(substituted benzylidene) derivatives of dehydroepiandrosterone. Vosooghi M, Yahyavi H, Divsalar K, Shamsa H, Kheirollahi A, Safavi M, Ardestani SK, Sadeghi-Neshat S, Mohammadhosseini N, Edraki N, Khoshneviszadeh M, Shafiee A, Foroumadi A, DARU J Pharm Sci 2013 21 34 10.1186/2008-2231-21-34
-
(2013)
DARU J Pharm Sci
, vol.21
, pp. 34
-
-
Vosooghi, M.1
Yahyavi, H.2
Divsalar, K.3
Shamsa, H.4
Kheirollahi, A.5
Safavi, M.6
Ardestani, S.K.7
Sadeghi-Neshat, S.8
Mohammadhosseini, N.9
Edraki, N.10
Khoshneviszadeh, M.11
Shafiee, A.12
Foroumadi, A.13
-
30
-
-
33751001333
-
1 receptor full agonist
-
DOI 10.1021/jm0604979
-
Trans-2,3-Dihydroxy-6a,7,8,12b-tetrahydro-6H-chromeno[3,4-c]isoquinoline: synthesis, resolution, and preliminary pharmacological characterization of a new dopamine D1 receptor full agonist. Cueva JP, Giorgioni G, Grubbs RA, Chemel RB, Watts VJ, Nichols DE, J Med Chem 2006 49 6848 6857 10.1021/jm0604979 17154515 (Pubitemid 44749752)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.23
, pp. 6848-6857
-
-
Cueva, J.P.1
Giorgioni, G.2
Grubbs, R.A.3
Chemel, B.R.4
Watts, V.J.5
Nichols, D.E.6
-
31
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. Mosmann T, J Immunol Methods 1983 65 55 63 10.1016/0022-1759(83)90303-4 6606682 (Pubitemid 14203433)
-
(1983)
Journal of Immunological Methods
, vol.65
, Issue.1-2
, pp. 55-63
-
-
Mosmann, T.1
-
32
-
-
33750354408
-
Analysis of cycloheximide-induced apoptosis in human leukocytes: Fluorescence microscopy using annexin V/propidium iodide versus acridin orange/ethidium bromide
-
DOI 10.1016/j.cellbi.2006.06.016, PII S106569950600148X
-
Analysis of cycloheximide-induced apoptosis in human leukocytes: fluorescence microscopy using annexin V/propidium iodide versus acridin orange/ethidium bromide. Baskic D, Popovic S, Ristic P, Arsenijevic NN, Cell BiolInt 2006 30 924 932 (Pubitemid 44635308)
-
(2006)
Cell Biology International
, vol.30
, Issue.11
, pp. 924-932
-
-
Baskic, D.1
Popovic, S.2
Ristic, P.3
Arsenijevic, N.N.4
|