<p>ALL cells recovered from the spleens of untreated mice were cultured with the indicated concentrations of FTY720 for 16 hours and viability assessed by flow cytometry using annexin V and propidium iodide staining. The viability of cells in control cultures was 42% for xenograft 1345, 90% for xenograft 1999, 93% for xenograft 0398, 51% for xenograft ALL-3, 63% for xenograft ALL-55 and 34% for ALL-56.</p
The object of investigation: the xenotransplantats of the man's tumours, the cellular lines of the s...
<p>(A) Cell death as assessed by DAPI fluorescence. Six hours after transfection of the HeLa cells w...
<p>(A) Spleens were collected at each time point (1, 3, 6, 11, 16, and 30 days) from xenotransplante...
<p>(<b>A</b>) MTT assays on the bone marrow cells. Mouse bone marrow cells were isolated and exposed...
<p>Established cell lines were comprehensively characterized and routinely cyropreserved together wi...
<p>Nude mice (7 or 8 mice per group) with Kasumi-1 tumor were injected intraperitoneally with vehicl...
<p>Fibroblasts were incubated with CFSE before initially seeding them together with tumour cells in ...
Splenocytes from C57BL/6 mice were stimulated 4 h with 50 ng/ml PMA and 1 μg/ml ionomycin in either ...
<p>(A) KYSE70 cells were treated with the indicated concentrations of CYT-Rx20, followed by evaluati...
<p>Flow cytometry analysis was employed to determine the cell death of macrophage cells (A–D). After...
(A) HuH6 cells (2.5 x 106 cells in 25% Matrigel) were injected subcutaneously into the right flank o...
<p>(a, b, c, d) Group 1: pieces were frozen immediately after operation, thawed and just after thawi...
<p>Mice with xenografts were treated for 11 days. Treatments: control (CTL) did not receive any trea...
<p><b>A</b> and <b>B</b>, Cells were treated with 0.1 μmol/L AUY922 for 24–72 hours. To analyze the ...
Abstract Objective Short-term viability assays of cultured cells in 96-well plates are routinely use...
The object of investigation: the xenotransplantats of the man's tumours, the cellular lines of the s...
<p>(A) Cell death as assessed by DAPI fluorescence. Six hours after transfection of the HeLa cells w...
<p>(A) Spleens were collected at each time point (1, 3, 6, 11, 16, and 30 days) from xenotransplante...
<p>(<b>A</b>) MTT assays on the bone marrow cells. Mouse bone marrow cells were isolated and exposed...
<p>Established cell lines were comprehensively characterized and routinely cyropreserved together wi...
<p>Nude mice (7 or 8 mice per group) with Kasumi-1 tumor were injected intraperitoneally with vehicl...
<p>Fibroblasts were incubated with CFSE before initially seeding them together with tumour cells in ...
Splenocytes from C57BL/6 mice were stimulated 4 h with 50 ng/ml PMA and 1 μg/ml ionomycin in either ...
<p>(A) KYSE70 cells were treated with the indicated concentrations of CYT-Rx20, followed by evaluati...
<p>Flow cytometry analysis was employed to determine the cell death of macrophage cells (A–D). After...
(A) HuH6 cells (2.5 x 106 cells in 25% Matrigel) were injected subcutaneously into the right flank o...
<p>(a, b, c, d) Group 1: pieces were frozen immediately after operation, thawed and just after thawi...
<p>Mice with xenografts were treated for 11 days. Treatments: control (CTL) did not receive any trea...
<p><b>A</b> and <b>B</b>, Cells were treated with 0.1 μmol/L AUY922 for 24–72 hours. To analyze the ...
Abstract Objective Short-term viability assays of cultured cells in 96-well plates are routinely use...
The object of investigation: the xenotransplantats of the man's tumours, the cellular lines of the s...
<p>(A) Cell death as assessed by DAPI fluorescence. Six hours after transfection of the HeLa cells w...
<p>(A) Spleens were collected at each time point (1, 3, 6, 11, 16, and 30 days) from xenotransplante...