-
1
-
-
72749122051
-
Receptor mediated uptake of paclitaxel from a synthetic high density lipoprotein nanocarrier
-
COI: 1:CAS:528:DC%2BD1MXhsFChs77K
-
Mooberry, L. K., M. Nair, S. Paranjape, W. J. McConathy, and A. G. Lacko (2010) Receptor mediated uptake of paclitaxel from a synthetic high density lipoprotein nanocarrier. J. Drug Target. 18: 53–58.
-
(2010)
J. Drug Target
, vol.18
, pp. 53-58
-
-
Mooberry, L.K.1
Nair, M.2
Paranjape, S.3
McConathy, W.J.4
Lacko, A.G.5
-
2
-
-
36649031633
-
Prospects and challenges of the development of lipoproteinbased formulations for anti-cancer drugs
-
COI: 1:CAS:528:DC%2BD2sXht1elsrvP
-
Lacko, A. G., M. Nair, L. Prokai, and W. J. McConathy (2007) Prospects and challenges of the development of lipoproteinbased formulations for anti-cancer drugs. Expert. Opin. Drug. Deliv. 4: 665–675.
-
(2007)
Expert. Opin. Drug. Deliv
, vol.4
, pp. 665-675
-
-
Lacko, A.G.1
Nair, M.2
Prokai, L.3
McConathy, W.J.4
-
3
-
-
37849036853
-
Evaluation of synthetic/reconstituted high-density lipoproteins as delivery vehicles for paclitaxel
-
COI: 1:CAS:528:DC%2BD1cXitVShuw%3D%3D
-
McConathy, W. J., M. P. Nair, S. Paranjape, L. Mooberry, and A. G. Lacko (2008) Evaluation of synthetic/reconstituted high-density lipoproteins as delivery vehicles for paclitaxel. Anti-Cancer Drugs 19: 183–188.
-
(2008)
Anti-Cancer Drugs
, vol.19
, pp. 183-188
-
-
McConathy, W.J.1
Nair, M.P.2
Paranjape, S.3
Mooberry, L.4
Lacko, A.G.5
-
4
-
-
0036332185
-
High density lipoprotein complexes as delivery vehicles for anticancer drugs
-
COI: 1:CAS:528:DC%2BD38XmsF2lsbk%3D
-
Lacko, A. G., M. Nair, S. Paranjape, S. Johnso, and W. J. McConathy (2002) High density lipoprotein complexes as delivery vehicles for anticancer drugs. Anticancer Res. 22: 2045–2049.
-
(2002)
Anticancer Res
, vol.22
, pp. 2045-2049
-
-
Lacko, A.G.1
Nair, M.2
Paranjape, S.3
Johnso, S.4
McConathy, W.J.5
-
5
-
-
79953679621
-
Targeted delivery of small interfering RNA using reconstituted high-density lipoprotein nanoparticles
-
COI: 1:CAS:528:DC%2BC3MXkvFGqtbc%3D
-
Shahzad, M. M., L. S. Mangala, H. D. Han, C. Lu, J. Bpttsford-Miller, M. Nishimura, E. M. Mora, J. W. Lee, R. L. Stone, C. V. Pecot, D. Thanapprapasr, J. W. Roh, P. Gaur, M. P. Nair, Y. Y. Park, Sabnis N, M. T. Deavers, J. S. Lee, L. M. Ellis, G. Lopez-Berestein, W. J. McConathy, L. Prokai, A. G. Lacko, and A. K. Sood (2011) Targeted delivery of small interfering RNA using reconstituted high-density lipoprotein nanoparticles. Neoplasia. 13: 309–319.
-
(2011)
Neoplasia
, vol.13
, pp. 309-319
-
-
Shahzad, M.M.1
Mangala, L.S.2
Han, H.D.3
Lu, C.4
Bpttsford-Miller, J.5
Nishimura, M.6
Mora, E.M.7
Lee, J.W.8
Stone, R.L.9
Pecot, C.V.10
Thanapprapasr, D.11
Roh, J.W.12
Gaur, P.13
Nair, M.P.14
Park, Y.Y.15
N, S.16
Deavers, M.T.17
Lee, J.S.18
Ellis, L.M.19
Lopez-Berestein, G.20
McConathy, W.J.21
Prokai, L.22
Lacko, A.G.23
Sood, A.K.24
more..
-
6
-
-
80052705901
-
Manufacturing and shelf stability of reconstituted high-density lipoprotein for infusion therapy
-
COI: 1:CAS:528:DC%2BC3MXhtVyrurrN
-
Kim, J. S., Y. Kang, K. H. Son, S. M. Choi, and K. Y. Kim (2011) Manufacturing and shelf stability of reconstituted high-density lipoprotein for infusion therapy. Biotechnol. Bioproc. Eng. 16: 785–792.
-
(2011)
Biotechnol. Bioproc. Eng
, vol.16
, pp. 785-792
-
-
Kim, J.S.1
Kang, Y.2
Son, K.H.3
Choi, S.M.4
Kim, K.Y.5
-
7
-
-
80054771643
-
Lipoprotein-inspired nanoparticles for cancer theranostics
-
COI: 1:CAS:528:DC%2BC3MXlvFCls7o%3D
-
Ng, K. K., J. F. Lovell, and G. Zheng (2011) Lipoprotein-inspired nanoparticles for cancer theranostics. Acc. Chem. Res. 44: 1105–1113.
-
(2011)
Acc. Chem. Res
, vol.44
, pp. 1105-1113
-
-
Ng, K.K.1
Lovell, J.F.2
Zheng, G.3
-
8
-
-
78649512581
-
Nanobiotechnology applications of reconstituted high density lipoprotein
-
COI: 1:CAS:528:DC%2BC3cXhsFGjurjE
-
Ryan, R. O. (2010) Nanobiotechnology applications of reconstituted high density lipoprotein. J. Nanobiotechnol. 8: 28–37.
-
(2010)
J. Nanobiotechnol
, vol.8
, pp. 28-37
-
-
Ryan, R.O.1
-
9
-
-
0000497921
-
pH-sensitive liposomes: Acid-induced liposome fusion
-
COI: 1:CAS:528:DyaL2cXhvVOnt78%3D
-
Connor, J., M. B. Yatvin, and L. Huang (1984) pH-sensitive liposomes: Acid-induced liposome fusion. Proc. Natl. Acad. Sci. USA. 81: 1715–1718.
-
(1984)
Proc. Natl. Acad. Sci. USA
, vol.81
, pp. 1715-1718
-
-
Connor, J.1
Yatvin, M.B.2
Huang, L.3
-
10
-
-
12344269847
-
Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: Tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy
-
COI: 1:CAS:528:DC%2BD2cXhtFSlur3K
-
Bae, Y., N. Nishiyama, S. Fukushima, H. Koyama, M. Yasuhiro, and K. Kataoka (2005) Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: Tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy. Bioconjug. Chem. 16: 122–130.
-
(2005)
Bioconjug. Chem
, vol.16
, pp. 122-130
-
-
Bae, Y.1
Nishiyama, N.2
Fukushima, S.3
Koyama, H.4
Yasuhiro, M.5
Kataoka, K.6
-
11
-
-
67349269478
-
pH-sensitive properties of surface charge-switched multifunctional polymeric micelle
-
COI: 1:CAS:528:DC%2BD1MXntFyntr0%3D
-
Oh, K. T., D. Kim, H. H. You, Y. S. Ahn, and E. S. Lee (2009) pH-sensitive properties of surface charge-switched multifunctional polymeric micelle. Int. J. Pharm. 376: 134–140.
-
(2009)
Int. J. Pharm
, vol.376
, pp. 134-140
-
-
Oh, K.T.1
Kim, D.2
You, H.H.3
Ahn, Y.S.4
Lee, E.S.5
-
12
-
-
39649120532
-
A review of stimuli-responsive nanocarriers for drug and gene delivery
-
COI: 1:CAS:528:DC%2BD1cXis1ams7Y%3D
-
Ganta, S., H. Devalapally, A. Shahiwala, and M. Amiji (2008) A review of stimuli-responsive nanocarriers for drug and gene delivery. J. Control. Rel. 126: 187–204.
-
(2008)
J. Control. Rel
, vol.126
, pp. 187-204
-
-
Ganta, S.1
Devalapally, H.2
Shahiwala, A.3
Amiji, M.4
-
13
-
-
0142119372
-
Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: Polymeric micelles that are responsive to intracellular pH change
-
COI: 1:CAS:528:DC%2BD3sXot12ltb0%3D
-
Bae, Y., S. Fukushima, A. Harada, and K. Kataoka (2003) Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: Polymeric micelles that are responsive to intracellular pH change. Angew. Chem. Int. Ed. Engl. 42: 4640–4643.
-
(2003)
Angew. Chem. Int. Ed. Engl
, vol.42
, pp. 4640-4643
-
-
Bae, Y.1
Fukushima, S.2
Harada, A.3
Kataoka, K.4
-
14
-
-
42949109091
-
Fully aciddegradable biocompatible polyacetal microparticles for drug delivery
-
COI: 1:CAS:528:DC%2BD1cXjvFOlt70%3D
-
Paramonov, S. E., E. M. Bachelder, T. T. Beaudette, S. M. Standley, C. C. Lee, J. Dashe, and M. Fréchet (2008) Fully aciddegradable biocompatible polyacetal microparticles for drug delivery. Bioconjug. Chem. 19: 911–919.
-
(2008)
Bioconjug. Chem
, vol.19
, pp. 911-919
-
-
Paramonov, S.E.1
Bachelder, E.M.2
Beaudette, T.T.3
Standley, S.M.4
Lee, C.C.5
Dashe, J.6
Fréchet, M.7
-
15
-
-
84866537640
-
pH-responsive high-density lipoprotein-like nanoparticles to release paclitaxel at acidic pH in cancer chemotherapy
-
COI: 1:CAS:528:DC%2BC38XptVOju78%3D
-
Shin, J. Y., Y. Yang, P. Heo, J. C. Lee, B. Kong, J. Y. Cho, K. Yoon, C. S. Shin, J. H. Seo, S. G. Kim, and D. H. Kweon (2012) pH-responsive high-density lipoprotein-like nanoparticles to release paclitaxel at acidic pH in cancer chemotherapy. Int. J. Nanomed. 7: 2805–2816.
-
(2012)
Int. J. Nanomed
, vol.7
, pp. 2805-2816
-
-
Shin, J.Y.1
Yang, Y.2
Heo, P.3
Lee, J.C.4
Kong, B.5
Cho, J.Y.6
Yoon, K.7
Shin, C.S.8
Seo, J.H.9
Kim, S.G.10
Kweon, D.H.11
-
16
-
-
0034895987
-
BMS-247550: A novel epothilone analog with a mode of action similar to paclitaxel but possessing superior antitumor efficacy
-
COI: 1:CAS:528:DC%2BD3MXktlels7Y%3D
-
Lee, F. Y., R. Borzilleri, C. R. Fairchild, S. H. Kim, B. H. Long, C. Reventos-Suarez, G. D. Vite, W. C. Rose, and R. A. Kramer (2001) BMS-247550: A novel epothilone analog with a mode of action similar to paclitaxel but possessing superior antitumor efficacy. Clin. Cancer Res. 7: 1429–1437.
-
(2001)
Clin. Cancer Res
, vol.7
, pp. 1429-1437
-
-
Lee, F.Y.1
Borzilleri, R.2
Fairchild, C.R.3
Kim, S.H.4
Long, B.H.5
Reventos-Suarez, C.6
Vite, G.D.7
Rose, W.C.8
Kramer, R.A.9
-
17
-
-
77956651097
-
Higher sensitivity to patupilone versus paclitaxel chemotherapy in primary uterine serous papillary carcinoma cell lines with high versus low HER-2/neu expression in vitro
-
COI: 1:CAS:528:DC%2BC3cXhtFClsbjM
-
Paik, D., E. Cocco, S. Bellone, F. Casagrande, M. Bellone, E. E. Siegel, C. E. Richter, P. E. Schwartz, T. J. Rutherford, and A. D. Santin (2010) Higher sensitivity to patupilone versus paclitaxel chemotherapy in primary uterine serous papillary carcinoma cell lines with high versus low HER-2/neu expression in vitro. Gynecol. Oncol. 119: 140–145.
-
(2010)
Gynecol. Oncol
, vol.119
, pp. 140-145
-
-
Paik, D.1
Cocco, E.2
Bellone, S.3
Casagrande, F.4
Bellone, M.5
Siegel, E.E.6
Richter, C.E.7
Schwartz, P.E.8
Rutherford, T.J.9
Santin, A.D.10
-
18
-
-
0031027531
-
Activities of the microtubule-stabilizing agents epothilones A and B with purified tubulin and in cells resistant to paclitaxel (Taxol®)
-
COI: 1:CAS:528:DyaK2sXotFCitw%3D%3D
-
Kowalski, R. J., P. Giannakakou, and E. Hamel (1997) Activities of the microtubule-stabilizing agents epothilones A and B with purified tubulin and in cells resistant to paclitaxel (Taxol®). J. Biol. Chem. 272: 2534–2541.
-
(1997)
J. Biol. Chem
, vol.272
, pp. 2534-2541
-
-
Kowalski, R.J.1
Giannakakou, P.2
Hamel, E.3
-
19
-
-
12944277104
-
A common pharmacophore for epothilone and taxanes: molecular basis for drug resistance conferred by tubulin mutations in human cancer cells
-
Giannakakou, P., R. Gussio, E. Nogales, K. H. Downing, D. Zaharevitz, B. Bollbuck, G. Poy, D. Sackett, K. C. Nicolaou, and T. Fojo (1999) A common pharmacophore for epothilone and taxanes: molecular basis for drug resistance conferred by tubulin mutations in human cancer cells. Proc. Natl. Acad. Sci. USA. 97: 2904–2909.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 2904-2909
-
-
Giannakakou, P.1
Gussio, R.2
Nogales, E.3
Downing, K.H.4
Zaharevitz, D.5
Bollbuck, B.6
Poy, G.7
Sackett, D.8
Nicolaou, K.C.9
Fojo, T.10
-
20
-
-
74849137129
-
Evaluation of novel epothilone analogues by means of a common pharmacophore and a QSAR pseudoreceptor model for taxanes and epothilone
-
COI: 1:CAS:528:DC%2BD1MXhs1Sqsb%2FP
-
Forli, S., F. Manetti, K. Altmann, and M. Botta (2010) Evaluation of novel epothilone analogues by means of a common pharmacophore and a QSAR pseudoreceptor model for taxanes and epothilone. Chem. Med. Chem. 5: 35–40.
-
(2010)
Chem. Med. Chem
, vol.5
, pp. 35-40
-
-
Forli, S.1
Manetti, F.2
Altmann, K.3
Botta, M.4
-
21
-
-
0033007667
-
The microtubule-stabilizing agents epothilones A and B and their desoxyderivatives induce mitotic arrest and apoptosis in human prostate cancer cells
-
COI: 1:CAS:528:DyaK1MXhsVGju7o%3D
-
Sepp-Lorenzino, L., A. Balog, D. S. Su, D. Meng, N. Timaul, H. I. Scher, S. J. Danichegsky, and N. Rosen (1999) The microtubule-stabilizing agents epothilones A and B and their desoxyderivatives induce mitotic arrest and apoptosis in human prostate cancer cells. Prostate Cancer Prostatic Dis. 2: 41–52.
-
(1999)
Prostate Cancer Prostatic Dis
, vol.2
, pp. 41-52
-
-
Sepp-Lorenzino, L.1
Balog, A.2
Su, D.S.3
Meng, D.4
Timaul, N.5
Scher, H.I.6
Danichegsky, S.J.7
Rosen, N.8
-
22
-
-
38449120471
-
Novel tubulin-targeting agents: Anticancer activity and pharmacologic profile of epothilones and related analogues
-
Fumoleau, P., B. Coudert, N. Isambert, and E. Ferrant (2007) Novel tubulin-targeting agents: Anticancer activity and pharmacologic profile of epothilones and related analogues. Ann. Oncol. 18: v9–v15.
-
(2007)
Ann. Oncol
, vol.18
, pp. 9-15
-
-
Fumoleau, P.1
Coudert, B.2
Isambert, N.3
Ferrant, E.4
-
23
-
-
84905497676
-
Dictyopteris undulata extract induces apoptosis in human colon cancer cells
-
COI: 1:CAS:528:DC%2BC2cXhtFynu7bN
-
Kim, A. D., K. A. Kang, M. J. Piao, K. C. Kim, J. Zheng, C. W. Yao, J. W. Cha, C. L. Hyun, S. J. Boo, N. H. Lee, S. Y. Na, and J. W. Hyu (2014) Dictyopteris undulata extract induces apoptosis in human colon cancer cells. Biotechnol. Bioproc. Eng. 19: 419–425.
-
(2014)
Biotechnol. Bioproc. Eng
, vol.19
, pp. 419-425
-
-
Kim, A.D.1
Kang, K.A.2
Piao, M.J.3
Kim, K.C.4
Zheng, J.5
Yao, C.W.6
Cha, J.W.7
Hyun, C.L.8
Boo, S.J.9
Lee, N.H.10
Na, S.Y.11
Hyu, J.W.12
-
24
-
-
79953800922
-
Apolipoprotein AI structural organization in high-density lipoproteins isolated from human plasma
-
COI: 1:CAS:528:DC%2BC3MXjtVGmtLo%3D
-
Huang, R., R. A. Silva, W. G. Jerome, A. Kontush, M. J. Chapman, L. K. Curtiss, T. J. Hodges, and W. S. Davidson (2011) Apolipoprotein AI structural organization in high-density lipoproteins isolated from human plasma. Nat. Struct. Mol. Biol. 18: 416–422.
-
(2011)
Nat. Struct. Mol. Biol
, vol.18
, pp. 416-422
-
-
Huang, R.1
Silva, R.A.2
Jerome, W.G.3
Kontush, A.4
Chapman, M.J.5
Curtiss, L.K.6
Hodges, T.J.7
Davidson, W.S.8
-
25
-
-
78649934086
-
pH-responsive nanoparticles for drug delivery
-
COI: 1:CAS:528:DC%2BC3cXhtleqtbvN
-
Gao, W., J. M. Chan, and O. C. Farokhzad (2010) pH-responsive nanoparticles for drug delivery. Mol. Pharma. 7: 1913–1920.
-
(2010)
Mol. Pharma
, vol.7
, pp. 1913-1920
-
-
Gao, W.1
Chan, J.M.2
Farokhzad, O.C.3
-
26
-
-
84934436662
-
pH-responsive nanoparticles for cancer drug delivery
-
COI: 1:CAS:528:DC%2BD1cXkslOhtbo%3D
-
Shen, Y., H. Tang, M. Radosz, E. Van Kirk, and W. J. Murdoch (2008) pH-responsive nanoparticles for cancer drug delivery. Methods Mol. Biol. 437: 183–216.
-
(2008)
Methods Mol. Biol
, vol.437
, pp. 183-216
-
-
Shen, Y.1
Tang, H.2
Radosz, M.3
Van Kirk, E.4
Murdoch, W.J.5
-
27
-
-
0027076642
-
The charge and structural stability of apolipoprotein A-I in discoidal and spherical recombinant high density lipoprotein particles
-
COI: 1:CAS:528:DyaK38Xmt1yksrk%3D
-
Sparks, D. L., S. Lund-Katz, and M. C. Phillips (1992) The charge and structural stability of apolipoprotein A-I in discoidal and spherical recombinant high density lipoprotein particles. J. Biol. Chem. 267: 25839–25847.
-
(1992)
J. Biol. Chem
, vol.267
, pp. 25839-25847
-
-
Sparks, D.L.1
Lund-Katz, S.2
Phillips, M.C.3
-
28
-
-
0026354712
-
Phase II trial of taxol, an active drug in the treatment of metastatic breast cancer
-
COI: 1:STN:280:DyaK38%2FnvFaqtw%3D%3D
-
Holmes, F. A., R. S. Walters, R. L. Theriault, A. D. Forman, L. K. Newton, M. N. Raber, A. U. Buzdar, D. K. Frye, and G. N. Hortobagyi (1991) Phase II trial of taxol, an active drug in the treatment of metastatic breast cancer. J. Natl. Cancer Inst. 83: 1797–1805.
-
(1991)
J. Natl. Cancer Inst
, vol.83
, pp. 1797-1805
-
-
Holmes, F.A.1
Walters, R.S.2
Theriault, R.L.3
Forman, A.D.4
Newton, L.K.5
Raber, M.N.6
Buzdar, A.U.7
Frye, D.K.8
Hortobagyi, G.N.9
-
29
-
-
0030026934
-
Loss of normal p53 function confers sensitization to Taxol by increasing G2/M arrest and apoptosis
-
COI: 1:CAS:528:DyaK28XivVSmsA%3D%3D
-
Wahl, A. F., K. L. Donaldson, C. Fairchild, F. Y. Lee, S. A. Foster, G. W. Demers, and D. A. Galloway (1996) Loss of normal p53 function confers sensitization to Taxol by increasing G2/M arrest and apoptosis. Nat. Med. 2: 72–79.
-
(1996)
Nat. Med
, vol.2
, pp. 72-79
-
-
Wahl, A.F.1
Donaldson, K.L.2
Fairchild, C.3
Lee, F.Y.4
Foster, S.A.5
Demers, G.W.6
Galloway, D.A.7
-
30
-
-
0032214980
-
Overexpression of ErbB2 blocks taxol-induced apoptosis by upregulation of p21Cip1, which inhibits p34Cdc2 kinase
-
COI: 1:CAS:528:DyaK1MXhtV2lsw%3D%3D
-
Yu, D., T. Jing, B. Liu, J. Yao, M. Tan, T. J. McDonnell, and M. C. Hung (1998) Overexpression of ErbB2 blocks taxol-induced apoptosis by upregulation of p21Cip1, which inhibits p34Cdc2 kinase. Mol. Cell. 2: 581–591.
-
(1998)
Mol. Cell
, vol.2
, pp. 581-591
-
-
Yu, D.1
Jing, T.2
Liu, B.3
Yao, J.4
Tan, M.5
McDonnell, T.J.6
Hung, M.C.7
-
31
-
-
84873053339
-
Antibody-drug conjugates in cancer therapy
-
COI: 1:CAS:528:DC%2BC3sXjsFKls7w%3D
-
Sievers, E. L. and P. D. Senter (2013) Antibody-drug conjugates in cancer therapy. Annu Rev. Med. 64: 15–29.
-
(2013)
Annu Rev. Med
, vol.64
, pp. 15-29
-
-
Sievers, E.L.1
Senter, P.D.2
-
32
-
-
67649886201
-
Potent antibody drug conjugates for cancer therapy
-
COI: 1:CAS:528:DC%2BD1MXosVWltbg%3D
-
Senter, P. D. (2009) Potent antibody drug conjugates for cancer therapy. Curr. Opin. Chem. Biol. 13: 235–244.
-
(2009)
Curr. Opin. Chem. Biol
, vol.13
, pp. 235-244
-
-
Senter, P.D.1
|