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18 eredmény a kulcsszóra: 'mda mb breast cancer cells'

ARTICLE IN PRESS

mAb, Monoclonal antibody; MCF-7, Michigan Cancer Foundation-7 breast-cancer cell line; MDA-MB-231, Breast-cancer cell line; NSCLC, Non-small cell lung cancer; OEC- M1, Human

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Contents JournalofInorganicBiochemistry

Effect of aluminium on migration of oestrogen unresponsive MDA-MB-231 human breast cancer cells in culture. Long-term exposure to aluminium increases migration, invasion and

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Contents JournalofInorganicBiochemistry

The synthesis, characterization and the cytotoxicity of Pd(II) complexes of N,N- disubstituted-N ′ -acyl thioureas against DU-145 (human prostate cancer cells), MDA-MB-231 (human

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        Stereocontrolled Synthesis of the Four Possible 3-Methoxy and 3-Benzyloxy-

The antiproliferative activities were determined in vitro by means of MTT assays against human adherent cervical (SiHa, HeLa) and breast cancer (MCF-7 and

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Protoflavone-Chalcone Hybrids Exhibit Enhanced Antitumor Action through Modulating Redox Balance, Depolarizing the Mitochondrial Membrane, and Inhibiting ATR-Dependent Signaling

The MCF-7 cell line was used as a representative model for estrogen receptor (ER)-positive breast cancer, while the MDA-MB-231 cell line was used as a model of triple-negative

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important for HDR efficiency and is a powerful predictor of sensitivity to breast cancer chemotherapy and an important target for therapy.

Also, both overexpression of RAD51 in MDA-MB-231-BR3 cells with DNM2 knockdown and chemical stimulation of RAD51 in MDA-MB-231-BR3 cells treated with dynasore failed to

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Metabolomics and in vitro cytotoxicity of extracts obtained from a desert plant and its soil SL-2

This study comparatively evaluates the metabolomics and in vitro cytotoxicity (MDA-MB231 breast cancer cells) of aqueous extracts obtained from an arid desert shrub

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A humán H1975 tüdő- és MDA-MB-231 emlőadenokarcinóma-sejtes modellek egysejt-tömegcitometriás összehasonlító elemzése

Our aim was to study female-derived human H1975 lung and MDA-MB-231 triple-negative breast cancer ade- nocarcinoma cell line models using single cell mass cytom- etry.. Nine

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Sesquiterpene Lactones and Flavonoids from Psephellus pyrrhoblepharus with Antiproliferative Activity on Human Gynecological Cancer Cell Lines

Compounds 1–6, the isolated flavonoids and scopoletin were evaluated for their antiproliferative activities on human gynecological cancer cell lines (SiHa, HeLa, and MDA-MB-231

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MedChemComm Broadening the field of opportunity for medicinal chemists

Compounds 1–5 were tested for their antiproliferative activ- ities on a diverse set of tumor cell lines including a panel of human breast cancer cell lines (MCF-7, T47D, MDA-MB-231

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foranticancerdrugsenablingtheselectivedeliveryofaneffectivecytotoxicagentorradionuclides likethelackofselectivity,toxicitytohealthytissueandthedevelopmentofmultidrugresistanceforcedbyhighdosetreatments.Ingeneral,ligandswithhighbindingaffinitiestotumor-spec

Western blot performed on whole cell lysates of MDA-MB-231, HT-29 and MCF-7 cancer cells, Figure S19: Stability of the bioconjugates K2 and 10 in human plasma, Figure S20: Mean

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INTRODUCTION CocrystalFormationofBetulinicAcidandAscorbicAcid:Synthesis,Physico-ChemicalAssessment,Antioxidant,andAntiproliferativeActivity

To investigate the biological effect, BA + VitC cocrystals were tested on HaCat (immortalized human keratinocytes), B164A5 and B16F0 (murine melanoma), MCF7 and MDA-MB-231 (human

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TÖREKVÉSEK AZ EMLİRÁK INDIVIDUÁLIS ÉS SZELEKTÍV KEZELÉSÉRE

Antagonists of growth hormone-releasing hormone arrest the growth of MDA-MB-468 estrogen-independent human breast cancers in nude mice.. Kahán Z, Sun B, Schally AV,

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Progesteronereceptormembranecomponent1regulateslipidhomeostasisanddrivesoncogenicsignalingresultinginbreastcancerprogression RESEARCHARTICLEOpenAccess

Since lipid rafts play a role in breast cancer progression and due to the fact that (a) PGRMC1 overexpressing hormone receptor-positive breast cancer cells have higher amounts

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Synthesis and evaluation of anticancer activities of2- or 4-substituted 3-(N-benzyltriazolylmethyl)-13α-oestrone derivatives

The antiproliferative activities of the newly synthesised brominated and phosphonated compounds against a panel of human cancer cell lines (A2780, MCF-7, MDA-MB 231) were

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DEVELOPMENT OF BIOCONJUGATES AND THEIR MODUL CONSTRUCTS FOR TARGETED THERAPY OF CANCERS WITH HIGH MORTALITY

Cellular localization was detected by confocal microscopy, as expected, peptides could be detected at the membrane of MDA-MB-453 cells suggesting their binding to the

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Bevesszük a kanyart?
[Csath Magdolna: Bevesszük a kanyart? – Tudás-Érték-Jövő. Kairosz Kiadó, 2019, 231 oldal]

Ezeket (az alkalmazhatóság statisztikai módszerekkel történő vizsgálata után) használhatjuk a gazdasági szerkezet átalakulásának nyomon követésére, ugyanakkor ebben az

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Solid Polymeric Nanoparticles of Albendazole: Synthesis, Physico-Chemical Characterization and Biological Activity

The in vitro anticancer properties of albendazole encapsulated in polyurethane structures versus the un-encapsulated compound were tested on two breast cancer cell lines, MCF-7

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