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Report of consensus panel 5 from the 11th international workshop on Waldenstrom's macroglobulinemia on COVID-19 prophylaxis and management

Seminars in hematology, 2023-03, Vol.60 (2), p.107-112

2023

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Down-modulation of cancer targets using locked nucleic acid (LNA)-based antisense oligonucleotides without transfection

Gene therapy, 2011-04, Vol.18 (4), p.326-333

2011

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Endogenous knockdown of survivin improves chemotherapeutic response in ALL models

Leukemia, 2012-02, Vol.26 (2), p.271-279

2012

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Fumitremorgin C reverses multidrug resistance in cells transfected with the breast cancer resistance protein

Cancer research (Chicago, Ill.), 2000, Vol.60 (1), p.47-50

2000

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6-Substituted-4-(3-bromophenylamino)quinazolines as Putative Irreversible Inhibitors of the Epidermal Growth Factor Receptor (EGFR) and Human Epidermal Growth Factor Receptor (HER-2) Tyrosine Kinases with Enhanced Antitumor Activity

Journal of medicinal chemistry, 2001-08, Vol.44 (17), p.2719-2734

2001

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Reversal of a novel multidrug resistance mechanism in human colon carcinoma cells by fumitremorgin C

Cancer research (Chicago, Ill.), 1998-12, Vol.58 (24), p.5850-5858

1998

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Atypical multidrug resistance: breast cancer resistance protein messenger RNA expression in mitoxantrone-selected cell lines

JNCI : Journal of the National Cancer Institute, 1999-03, Vol.91 (5), p.429-433

1999

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4-Anilino-6,7-dialkoxyquinoline-3-carbonitrile Inhibitors of Epidermal Growth Factor Receptor Kinase and Their Bioisosteric Relationship to the 4-Anilino-6,7-dialkoxyquinazoline Inhibitors

Journal of medicinal chemistry, 2000-08, Vol.43 (17), p.3244-3256

2000

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Design, Synthesis, and Preclinical Characterization of Novel, Highly Selective Indole Estrogens

Journal of medicinal chemistry, 2001-05, Vol.44 (11), p.1654-1657

2001

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Major photoaffinity drug labeling sites for iodoaryl azidoprazosin in P-glycoprotein are within, or immediately C-terminal to, transmembrane domains 6 and 12

The Journal of biological chemistry, 1993-05, Vol.268 (15), p.11417-11425

Greenberger, L.M.

1993

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Combination therapy for treating breast cancer using antiestrogen, ERA-923, and the mammalian target of rapamycin inhibitor, temsirolimus

Endocrine-related cancer, 2006-09, Vol.13 (3), p.863-873

2006

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Multiple mechanisms confer drug resistance to mitoxantrone in the human 8226 myeloma cell line

Cancer research (Chicago, Ill.), 1999-03, Vol.59 (5), p.1021-1028

1999

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Marked therapeutic efficacy of a novel polyethylene glycol-SN38 conjugate, EZN-2208, in xenograft models of B-cell non-Hodgkin's lymphoma

Haematologica (Roma), 2009-10, Vol.94 (10), p.1456-1459

2009

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Targeting Vascular and Avascular Compartments of Tumors with C. novyi-NT and Anti-microtubule Agents

Cancer biology & therapy, 2004-03, Vol.3 (3), p.326-337

2004

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An Anti-MUC1 Antibody−Calicheamicin Conjugate for Treatment of Solid Tumors. Choice of Linker and Overcoming Drug Resistance

Bioconjugate chemistry, 2005-03, Vol.16 (2), p.346-353

2005

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Irreversible inhibition of epidermal growth factor receptor tyrosine kinase with In Vivo activity by N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-2-butynamide (CL-387,785)

Biochemical pharmacology, 1999-04, Vol.57 (8), p.917-925

1999

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Experimentally induced changes in the endocytic traffic of P-glycoprotein alter drug resistance of cancer cells

American Journal of Physiology: Cell Physiology, 1997-08, Vol.273 (2), p.C687-C702

1997

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Progesterone Interacts with P-Glycoprotein in Multidrug-resistant Cells and in the Endometrium of Gravid Uterus

The Journal of biological chemistry, 1989-01, Vol.264 (2), p.782-788

1989

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Domain mapping of the photoaffinity drug-binding sites in P-glycoprotein encoded by mouse mdr1b

The Journal of biological chemistry, 1991-11, Vol.266 (31), p.20744-20751

1991

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PENILE STUMP ADVANCEMENT AS AN ALTERNATIVE TO PERINEAL URETHROSTOMY AFTER PENILE AMPUTATION

The Journal of urology, 1999-03, Vol.161 (3), p.893-894

1999

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Toward Increased Notice of FMLA and ADA Protections

New York University law review (1950), 2005-12, Vol.80 (6), p.1797

Greenberger, Debra L

2005

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A New Antiestrogen, 2-(4-Hydroxy-phenyl)-3-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-benzyl]-1H-indol-5-ol hydrochloride (ERA-923), Inhibits the Growth of Tamoxifen-sensitive and -resistant Tumors and Is Devoid of Uterotropic Effects in Mice and Rats

Clinical cancer research, 2001-10, Vol.7 (10), p.3166-3177

2001

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Localization of the forskolin labeling sites to both halves of P-glycoprotein: similarity of the sites labeled by forskolin and prazosin

Molecular pharmacology, 1994-08, Vol.46 (2), p.329-337

1994

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Molecular cloning of cDNAs which are highly overexpressed in mitoxantrone-resistant cells : Demonstration of homology to ABC transport genes

Cancer research (Chicago, Ill.), 1999, Vol.59 (1), p.8-13

1999

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Alternative technique for laparoscopic port-site closure

Journal of endourology, 2012-04, Vol.26 (4), p.311-312

2012

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Report of consensus panel 5 from the 11th international workshop on Waldenstrom's macroglobulinemia on COVID-19 prophylaxis and management

Down-modulation of cancer targets using locked nucleic acid (LNA)-based antisense oligonucleotides without transfection

Endogenous knockdown of survivin improves chemotherapeutic response in ALL models

Fumitremorgin C reverses multidrug resistance in cells transfected with the breast cancer resistance protein

6-Substituted-4-(3-bromophenylamino)quinazolines as Putative Irreversible Inhibitors of the Epidermal Growth Factor Receptor (EGFR) and Human Epidermal Growth Factor Receptor (HER-2) Tyrosine Kinases with Enhanced Antitumor Activity

Reversal of a novel multidrug resistance mechanism in human colon carcinoma cells by fumitremorgin C

Atypical multidrug resistance: breast cancer resistance protein messenger RNA expression in mitoxantrone-selected cell lines

4-Anilino-6,7-dialkoxyquinoline-3-carbonitrile Inhibitors of Epidermal Growth Factor Receptor Kinase and Their Bioisosteric Relationship to the 4-Anilino-6,7-dialkoxyquinazoline Inhibitors

Design, Synthesis, and Preclinical Characterization of Novel, Highly Selective Indole Estrogens

Major photoaffinity drug labeling sites for iodoaryl azidoprazosin in P-glycoprotein are within, or immediately C-terminal to, transmembrane domains 6 and 12

Combination therapy for treating breast cancer using antiestrogen, ERA-923, and the mammalian target of rapamycin inhibitor, temsirolimus

Multiple mechanisms confer drug resistance to mitoxantrone in the human 8226 myeloma cell line

Marked therapeutic efficacy of a novel polyethylene glycol-SN38 conjugate, EZN-2208, in xenograft models of B-cell non-Hodgkin's lymphoma

Targeting Vascular and Avascular Compartments of Tumors with C. novyi-NT and Anti-microtubule Agents

An Anti-MUC1 Antibody−Calicheamicin Conjugate for Treatment of Solid Tumors. Choice of Linker and Overcoming Drug Resistance

Irreversible inhibition of epidermal growth factor receptor tyrosine kinase with In Vivo activity by N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-2-butynamide (CL-387,785)

Experimentally induced changes in the endocytic traffic of P-glycoprotein alter drug resistance of cancer cells

Progesterone Interacts with P-Glycoprotein in Multidrug-resistant Cells and in the Endometrium of Gravid Uterus

Domain mapping of the photoaffinity drug-binding sites in P-glycoprotein encoded by mouse mdr1b

PENILE STUMP ADVANCEMENT AS AN ALTERNATIVE TO PERINEAL URETHROSTOMY AFTER PENILE AMPUTATION

Toward Increased Notice of FMLA and ADA Protections

A New Antiestrogen, 2-(4-Hydroxy-phenyl)-3-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-benzyl]-1H-indol-5-ol hydrochloride (ERA-923), Inhibits the Growth of Tamoxifen-sensitive and -resistant Tumors and Is Devoid of Uterotropic Effects in Mice and Rats

Localization of the forskolin labeling sites to both halves of P-glycoprotein: similarity of the sites labeled by forskolin and prazosin

Molecular cloning of cDNAs which are highly overexpressed in mitoxantrone-resistant cells : Demonstration of homology to ABC transport genes

Alternative technique for laparoscopic port-site closure

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