Family-centered empowerment process in individuals with spinal cord injury living in Iran: a grounded theory study.

Family-centered empowerment process in individuals with spinal cord injury living in Iran: a grounded theory study.

This study is a qualitative study using grounded theory to explain the process of empowerment method.To family-centered population of individuals with SCI living in Iran.Brain and SCI Research Center, Center for Social Welfare, and SCI Association of Tehran; Iran.Participants are 19 people with traumatic SCI, 13 caregivers of family members, and 11 health service providers selected through purposive sampling.

Data was collected using face-to-face, semi-structured interviews, which continued until saturation data. Interview data were methodically collected and analyzed using Strauss and (1998) recommended method Corbin’s grounded theory. constant comparative analysis performed simultaneously through a review report interviews, behavioral observation, field notes of the interviewer, and the interviewer memo.

This analysis is managed in software version MAXQDA 10.The process of family-centered empowerment SCI included the following five categories: (1) an interruption in the integrity of the individual existential; (2) build a life of recovery; (3) inhibitors of family-centered empowerment; (4) facilitators family-centered, and (5) back on track. recovery constructive life was chosen as the core variables using grounded theory method. The core variables identify the strategies most often used by participants to address the challenges of SCI-related disorders, disabilities, and overall life management.

Family empowerment process centered on individuals with SCI living in Iran emerged from the data. This model includes a disturbance early in the life of the bio-psycho-social and vocational individuals with SCI and their families, strategies for recovering from injury, inhibitors and facilitators family-centered, gradual return to work and daily activities, and expected social roles for individuals with SCI.

 Family-centered empowerment process in individuals with spinal cord injury living in Iran: a grounded theory study.
Family-centered empowerment process in individuals with spinal cord injury living in Iran: a grounded theory study.

 

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Description: The untransduced T cells are produced by mock lentiviral transduction of human primary CD4+CD8+ T cells. These cells are subjected to comparable manipulations as CAR-T cells: activation, spinoculation (without lentivirus), and expansion. These T cells are meant to be negative controls in experiments using lentivirus-transduced primary CAR-T cells.

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79753 10 million cells
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Description: Cryopreserved vial (10 x 10^6 cells) of CD8+ T cells that were negatively selected from freshly isolated primary human peripheral blood mononuclear cells (PBMCs). The PBMCs came from a healthy donor, and were isolated from whole blood or leukapheresis samples using a Ficoll gradient. Magnetic antibodies to monocytes, granulocytes, CD4+ T cells, gamma/delta T cells and other immune subsets present in PBMCs were then used to purify untouched CD8+ T cells via immunomagnetic separation. Before and after CD8+ T cell isolation, the cells were stained to evaluate purity and viability by flow cytometry. Cells were cryopreserved in CryoStor CS10 cryopreservation medium (Stemcell, #07930) at a controlled rate._x000D_Source
Normal human PBMC from Leukapheresis Sample

Anti-CD19 CAR-T Cells

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Description: The anti-CD19 CAR-T cells are produced by high-titer lentiviral transduction of human primary CD4+CD8+ T cells using the anti-CD19 CAR Lentivirus (CD19 ScFv-CD8-4-1BB-CD3ζ; SIN Vector). These ready-to use CAR-T cells express an anti-CD19 CAR consisting the ScFv of CD19 (clone FMC63) linked to a 2nd generation CAR (Chimeric Antigen Receptor) containing CD8 hinge and transmembrane domains, and the 4-1BB and CD3ζ signaling domains.These CAR-T cells have been validated using flow cytometry (to determine the CAR expression) and co-culture cytotoxicity assays.

Anti-BCMA CAR-T Cells

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Description: The anti-BCMA CAR-T cells are produced by high-titer lentiviral transduction of human primary CD4+CD8+ T cells using the anti-BCMA CAR Lentivirus (BPS Bioscience #78655). These ready-to-use CAR-T cells express an anti-BCMA CAR consisting of the ScFv of BCMA (clone C11D5.3) linked to a 2nd generation CAR (Chimeric Antigen Receptor) containing CD8 hinge and transmembrane domains, and the 4-1BB and CD3ζ signaling domains (Figure 1). These CAR-T cells have been validated using flow cytometry (to determine the CAR expression) and co-culture cytotoxicity assays.

Anti-BCMA CAR-T Cells

78660-2 5 vials
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Description: The anti-BCMA CAR-T cells are produced by high-titer lentiviral transduction of human primary CD4+CD8+ T cells using the anti-BCMA CAR Lentivirus (BPS Bioscience #78655). These ready-to-use CAR-T cells express an anti-BCMA CAR consisting of the ScFv of BCMA (clone C11D5.3) linked to a 2nd generation CAR (Chimeric Antigen Receptor) containing CD8 hinge and transmembrane domains, and the 4-1BB and CD3ζ signaling domains (Figure 1). These CAR-T cells have been validated using flow cytometry (to determine the CAR expression) and co-culture cytotoxicity assays.

Human Cord Blood CD3+ Pan T Cells

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Human Cord Blood CD3+ Pan T Cells

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Human Cord Blood CD3+ Pan T Cells

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Human Cord Blood CD3+ Pan T Cells

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T-47D Cells Complete Medium

CM-0228-125mL4 125 mL×4
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Description: Complete Growth Medium

Human Cord Blood CD8+ Cytotoxic T Cells

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Human Cord Blood CD8+ Cytotoxic T Cells

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Human Peripheral Blood CD3+ T Cells, Fresh

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Albumin Standard (2.0 mg/ml)

JB04-D001C 5*1ml/kit
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T24 [T-24] Cells Complete Medium

CM-0227-125mL4 125 mL×4
EUR 108
Description: Complete Growth Medium

Human Peripheral Blood CD3+ T Cells, Cryopreserved

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analysis of metabolites for cold-resistant yeast (Wickerhamomyces anomalus) strain antioxidant activity alone in the cold stored fish mince.

Effect of eight cold-resistant yeast strains (J3, J7, J8, J9, J12, J15, J18 and J25) of Wickerhamomyces anomalus on lipid oxidation of fish mince stored cold (4 ° C) was investigated. And yeast metabolites were determined by gas chromatography-mass spectrometry. This strain can effectively inhibit the increase in the value of hydroperoxide (p <0.05), and positively correlated with the level inhibits the contents isolongifolene, xylitol, turanose, thymol-glucoside, and uridine.

Especially, J3, J7, J8, J9, J12, and J18 can eliminate most of thiobarbituric acid reactive substances (TBARS) (p <0.05), the rate is proportional to eliminate aldehyde dehydrogenase activity. Some bacteriostatic metabolites were detected: thymol-glucoside, 2-phenylethanol, cedro, and 2,4-bis (1,1-dimethylethyl) phenol. In addition, W. anomalus produce many metabolites with fruit and floral notes. In conclusion, W. anomalus cold-resistant strain has potent antioxidant activity of the new bio-preservative in cold storage muscle products.

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Sheep Red Blood Cells Packed 10%

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Donkey Red Blood Cells Packed 10%

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Porcine Red Blood Cells Packed 10%

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Dog Red Blood Cells

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Pig Red Blood Cells

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Rat Red Blood Cells

88R-R002 5 x 2.0ml
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Rat Red Blood Cells

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Goat Red Blood Cells

88R-G003 20 ml
EUR 327.6
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Sheep Red Blood Cells

20R-RS001 10 ml
EUR 625.2
Description: Human IgG Senstitized Gluteraldehyde Stabilized Sheep Red Bllood Cells

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88R-H002 20 ml
EUR 327.6
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Mouse Red Blood Cells

88R-M001 10 ml
EUR 354
Description: Washed and freshly prepared 10% suspension of Mouse Red Blood Cells

Mouse Red Blood Cells

88R-M004 5 x 2 ml
EUR 327.6
Description: Glutaraldehyde-stabilized freshly prepared Mouse Red Blood Cells

Sheep Red Blood Cells

88R-S001 100 ml
EUR 614.4
Description: Washed and freshly prepared 10% suspension of Sheep Red Blood Cells

Sheep Red Blood Cells

88R-S003 20 ml
EUR 327.6
Description: Glutaraldehyde-stabilized freshly prepared Sheep Red Blood Cells

Sheep Red Blood Cells

88R-S004 10 ml
EUR 625.2
Description: Glutaraldehyde-stabilized freshly prepared albumin sensitised Sheep Red Blood Cells


Martini is (CG) coarse-grained force fields suitable for molecular dynamics (MD) simulations (bio) molecular systems. It is based on the mapping of two to four heavy atoms to a particle CG. Effective interaction between particles CG parametrized to reproduce partition free energy of small chemical compounds between the polar and apolar phases. In this chapter, a summary of the key elements of this CG magnetic field is presented, followed by an example of a practical application: a lipoplex-membrane fusion experiment

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