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VJRegenMed @UC0iwviIBH-FtBkMznwtdjTA@youtube.com

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The Video Journal of Regenerative Medicine (VJRegenMed) is a


03:48
Preliminary results from Phase I study of CD123 CAR-T therapy in pediatric R/R AML
02:47
KarMMa-3 results: ide-cel vs standard regimens in triple-class exposed multiple myeloma
03:02
Phase I study of rapcabtagene autoleucel in patients with R/R DLBCL
03:19
Safety and efficacy of LV20.19 CAR-T therapy in Richter's transformation and R/R MCL
03:52
Outcomes of children and young adults with B-ALL following tisa-cel reinfusion
05:15
CD33 CRISPR/Cas9 gene-edited donor allograft in patients with AML at risk of relapse post-HSCT
01:13
An insight into novel third-generation TLR2 co-stimulatory CAR-T cells
02:15
Challenges with CAR-T therapy in AML & insights into IF-BETTER-gated CAR-T cells
01:26
Rapid CAR-T manufacturing and challenges in this space
02:17
The importance of managing hematologic toxicity associated with CAR-T therapy
02:21
Exploring the potential role of CD7-targeting CAR-T cells in T-ALL
00:55
Multivalent gamma-delta T-cells: promising agents for the treatment of cancers
08:25
CAR-T therapy in acute and chronic leukemias: current applications and future outlooks
01:05
Novel CAR-T constructs emerging for patients with multiple myeloma who experience loss of BCMA
05:36
Investigating real-world outcomes of patients with R/R LBCL after CD19 CAR-T cell therapy
01:00
Trials evaluating the efficacy of CD20 CAR-T cell therapy in WM and CNS lymphoma
02:45
Phase I study of CC-98633 in R/R multiple myeloma
03:59
Results from the first-in-human trial of huCART19-IL18 in patients with R/R NHL and CLL
02:08
Results from a Phase I trial of rapidly manufactured Prgn-3006 Ultracar-T in R/R AML
02:52
The safety and efficacy of UCART123v1.2 in R/R AML: results from AMELI-01
01:23
CARBON trial: investigating CTX110 allogeneic CRISPR-Cas9–engineered CAR-Ts in R/R LBCL
01:59
Developing gene therapies for GJB2 gene related hearing loss
02:05
Novel gene therapy solutions for Usher syndrome type I
02:51
Treating otoferlin deficiency with gene therapy
02:41
Developing a therapeutic cancer vaccine for patients with NSCLC
01:34
Assessing PDC*mel, dendritic cell-based vaccine in melanoma
01:43
Plasmacytoid dendritic cell-based cancer vaccines
02:56
SCUlpTOR: CYP-004 in osteoarthritis
03:00
CYP-001 in adults with steroid-resistant GvHD
03:10
Utilizing flow cytometry in CAR T-cell research
01:28
Implementing automation technology in the CGT space
02:08
Streamlining cell therapy manufacturing with CliniMACS Prodigy
01:04
Applications of stem cell gene therapy beyond genetic diseases
02:24
CAR T-cell therapy for neuroblastoma
01:13
PiggyBac Transposon-generated CAR T-cells in solid tumors
02:34
Generating iSPC-derived MSCs with the Cymerus™ Platform
03:00
Addressing challenges in using MSCs in cell therapies
01:01
The future of omentum-based autologous tissue engineering
01:36
Meeting the growing demand for gene therapy manufacturing
02:12
Innovations in treating rare diseases with gene therapies
01:38
Overcoming manufacturing issues in gene therapies for rare diseases
01:35
Restoring cardiac tissue with omentum-based hydrogel implants
02:36
Autologous tissue-engineered solutions for spinal cord injuries
01:27
Direct detection and isolation of CAR cells from patient samples
04:06
Optimizing the upscaling and outscaling of CAR T-cell therapies
01:22
Engineering NK cell-based cancer treatments
02:30
Moving CAR T-cell therapies to earlier lines of therapy in multiple myeloma
05:56
Targeting neoantigens in multiple myeloma with CAR T-cell
02:59
Photoporation with polydopamine nanosensitizers for mRNA delivery to T cells
02:37
The benefits of PiggyBac transposon-mediated CAR-T cell technology
01:23
Enhancing the long-term functionality of CAR-T cells in solid tumors
05:33
Improving immune-imaging tools to assess cancer immunotherapies
04:27
Developing individualized cancer therapies with neoantigen-specific TCRs
02:20
Overcoming barriers in treating liquid tumors with T-cell therapies
03:22
Assessing immunotherapies with a novel tumor model using humanized mice
03:25
An overview of mouse models to study cell therapies for cancer
05:36
Harnessing lipid-specific TCRs to target CD1c-expressing leukemia
03:05
The anti-leukemic potential of CD1c-restricted T cells
01:33
Improving the efficiency of cancer vaccines with adoptive T cell therapy approaches
03:52
Addressing immunogenic barriers facing CRISPR-Cas9-based therapies