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Experimental cancer therapy shows success in more than 70% of patients in global clinical trials

Researchers from The Mount Sinai Hospital found that talquetamab, a bispecific antibody, was successful in killing multiple myeloma cells in over 70% of patients. This therapy directs the immune system to target cancer cells and has shown promise even for those who have resisted all other treatments.

SourceThe Mount Sinai Hospital / Mount Sinai School of Medicine·JournalNew England Journal of Medicine·DateDec 10, 2022

Patient’s own immune cells effective as living medicine for melanoma

The TIL trial has demonstrated that cell therapy using patient's own immune cells is an extremely powerful immunotherapy for metastatic melanoma, with significant shrinkage of metastases in half of patients. Progression-free survival after six months was 53%, significantly better than standard immunotherapy with ipilimumab.

SourceNetherlands Cancer Institute·JournalNew England Journal of Medicine·TypeRandomized controlled/clinical trial·DateDec 7, 2022

Researchers identify a new entryway into cells for virus causing COVID-19

A University of Ottawa-led team identified a new entry route for SARS-CoV-2 using metalloproteinases, which may lead to more widespread cell infection and severe illness. The study suggests that variants like the Delta strain may prefer this entry method, while others like Omicron do not.

SourceUniversity of Ottawa·JournaliScience·TypeRandomized controlled/clinical trial·DateDec 6, 2022
Apple iPhone 17 Pro

Apple iPhone 17 Pro delivers top performance and advanced cameras for field documentation, data collection, and secure research communications.

HIV ‘drug factory’ implant promises once-a-year therapy

Rice University researchers are developing implants that can produce and deliver monoclonal anti-HIV antibody therapeutics for at least a year. The project aims to reduce the cost and improve the logistics of HIV treatment, making it more accessible and beneficial for patients worldwide.

SourceRice University·DateDec 5, 2022

Engineered proteins: A future treatment option for COVID-19

Researchers at Texas A&M University engineered DARPins to block the interaction between the COVID-19 virus and host cells, significantly reducing disease progression. The nasal sprays showed effectiveness against various variants, including omicron, and could provide a lower-cost therapeutic option for those at high risk.

SourceTexas A&M University·JournalNature Chemical Biology·DateNov 29, 2022
Rigol DP832 Triple-Output Bench Power Supply

Rigol DP832 Triple-Output Bench Power Supply powers sensors, microcontrollers, and test circuits with programmable rails and stable outputs.

Overcoming challenges in the delivery of nucleic acid therapeutics

Nucleic acid therapies aim to treat genetic disorders and diseases, but delivering therapeutics is a significant challenge. Researchers are investigating nanoparticle delivery systems to target specific cells and sub-cellular compartments for effective delivery.

SourceWiley·JournalWiley Interdisciplinary Reviews Nanomedicine and Nanobiotechnology·DateNov 23, 2022

Gene-delivering viruses reach the brain in step toward gene therapy for neurological diseases

Researchers have engineered a family of adeno-associated viral vectors that can deliver cargo to the primate brain, offering a safer and more efficient way to treat genetic diseases. The PAL family of AAVs has been shown to be three times better at delivering their cargo into the brain than current leading AAV delivery vehicle AAV9.

SourceBroad Institute of MIT and Harvard·JournalMed·TypeExperimental study·DateNov 22, 2022

Rice bioengineer seeks better signals from cells

A Rice University bioengineer has developed a noninvasive technology to measure gene expression in deep tissues, particularly in the brain. This innovation could improve the monitoring of gene therapy treating neurodegenerative disorders such as epilepsy, ALS, and Huntington's disease.

SourceRice University·DateNov 10, 2022

“CAR pooling” screens identify most effective cancer immunotherapy cells

USCF researchers have developed a new approach called CAR Pooling to compare different re-engineered T cells with varying molecular features. The screen revealed new and surprising receptors that make these therapeutic cells more powerful, promising a better treatment for blood cancers.

SourceUniversity of California - San Francisco·JournalScience Translational Medicine·DateNov 10, 2022
SAMSUNG T9 Portable SSD 2TB

SAMSUNG T9 Portable SSD 2TB transfers large imagery and model outputs quickly between field laptops, lab workstations, and secure archives.

Immune system reboot in MS patients

Researchers from the University of Zurich have discovered why a stem cell transplant is effective in treating multiple sclerosis. The study found that memory T cells reappear immediately after the transplant and do not trigger an autoimmune reaction due to pre-damage caused by chemotherapy. This knowledge enables the body to gradually ...

SourceUniversity of Zurich·JournalScience Translational Medicine·TypeExperimental study·DateNov 10, 2022

Researchers find treatment options for patients whose blood cancer relapses after CAR-T

Researchers have found therapies that can help patients with relapsed multiple myeloma who tried CAR-T therapy, including bispecific antibodies and other types of CAR-T cell therapy. The study analyzed 79 patients and found that stem cell transplants and other drug combinations showed some efficacy in these patients.

SourceThe Mount Sinai Hospital / Mount Sinai School of Medicine·JournalBlood·DateNov 4, 2022
Davis Instruments Vantage Pro2 Weather Station

Davis Instruments Vantage Pro2 Weather Station offers research-grade local weather data for networked stations, campuses, and community observatories.

Hormone therapy could lower risk of immunotherapy-associated myocarditis in women

A new preclinical study discovered the underlying cause of gender differences in immunotherapy-associated myocarditis and identified potential treatment strategies. Hormone therapies targeting the endocrine-cardiac-immune pathway may reduce this risk without affecting treatment efficacy.

SourceUniversity of Texas M. D. Anderson Cancer Center·JournalScience Translational Medicine·DateNov 2, 2022

The origin-of-life molecule, a key to cancer research

Researchers at the University of Seville have discovered a method to attack cancer cells using an origin-of-life molecule. The study found that inhibiting RNA production boosts the utility of radiation therapy in cancer cells, offering a promising approach to treating various types of cancer.

SourceUniversity of Seville·JournalNature Communications·TypeNews article·DateOct 28, 2022

New cancer drug candidate targets immune system “brakes”

Researchers have designed a potential therapeutic that dampens the activity of regulatory T cells, which can prevent the immune system from unleashing its full potential against tumor cells. The molecule, known as FOX3P, acts as a transcription factor for many Treg genes but isn't vital for other types of T cells.

SourceUniversity of Chicago·JournalProceedings of the National Academy of Sciences·DateOct 18, 2022
Aranet4 Home CO2 Monitor

Aranet4 Home CO2 Monitor tracks ventilation quality in labs, classrooms, and conference rooms with long battery life and clear e-ink readouts.

Peering into single cells reveals key processes in acute kidney injury

Researchers have used single-cell sequencing to uncover novel gene expression patterns in injured kidney cells, providing new avenues for biomarker discovery and treatment. The studies reveal that epithelial cells of all tubule segments are involved in the injury processes, with distinct molecular patterns across patients.

SourceCharité - Universitätsmedizin Berlin·JournalGenome Medicine·DateOct 5, 2022

Scientists identify a biomarker that predicts CAR T therapy efficacy

Researchers at Universidad de Navarra identified a biomarker that predicts CAR T cell therapeutic capacity, which could improve treatment outcomes for patients. The study found that high CAR density in CAR T cells is associated with a worse clinical response in hematological tumors.

SourceUniversidad de Navarra·JournalScience Advances·DateSep 30, 2022

Combi-seq: a leap forward for personalized cancer therapy

Researchers have developed a new approach to test the efficacy of multiple anticancer drug combinations simultaneously, rapidly, and accurately. Combi-seq overcomes limitations of conventional technologies by using microfluidics to carry out large-scale experiments with small sample volumes.

SourceEuropean Molecular Biology Laboratory·JournalNature Communications·DateSep 29, 2022
Apple MacBook Pro 14-inch (M4 Pro)

Apple MacBook Pro 14-inch (M4 Pro) powers local ML workloads, large datasets, and multi-display analysis for field and lab teams.

Dual-targeting CAR NK cells can prevent cell dysfunction and tumor escape

A new CAR NK cell engineering approach requires two signals to eliminate target cells, improving tumor specificity and enhancing anti-tumor activity. This strategy mitigates NK cell exhaustion and fratricide, leading to better focus on and attack of only the tumor cells.

SourceUniversity of Texas M. D. Anderson Cancer Center·JournalNature Medicine·DateSep 29, 2022

Awakening «dormant» cells to fight cancer

A team from UNIGE and HUG identified a protein regulation mechanism that reduces melanoma cells' capacity to adapt and resist treatment. They found that targeting this mechanism with an enzyme inhibitor reduces therapeutic resistance in all melanoma cells.

SourceUniversité de Genève·JournalBiochemical and Biophysical Research Communications·DateSep 22, 2022

Keeping aggressive cancer cells in check

A team of researchers has identified TSG101 as a crucial regulator of the PARP1 enzyme, which is responsible for repairing DNA damage. In cancer cells with BRCA mutations, TSG101 is essential for PARP1 activation, making it a promising target for cancer treatment.

SourceMax Delbrück Center for Molecular Medicine in the Helmholtz Association·JournalThe EMBO Journal·DateSep 20, 2022
Kestrel 3000 Pocket Weather Meter

Kestrel 3000 Pocket Weather Meter measures wind, temperature, and humidity in real time for site assessments, aviation checks, and safety briefings.

Pushing the reset button on autoimmune diease

Researchers have made a breakthrough in treating autoimmune diseases by using genetically modified CAR T cells to target and destroy harmful B cells. This innovative therapy has shown promising results in six young patients with severe forms of systemic lupus erythematosus, curing them completely without returning.

SourceFriedrich-Alexander-Universität Erlangen-Nürnberg·JournalNature Medicine·DateSep 20, 2022

Scientists identify unique breast cancer cells that control their ability to proliferate and colonize the lungs

Researchers discovered a type of triple-negative breast cancer cell that can trigger dormancy, evading therapies and allowing for efficient survival in distant organs. This finding highlights the need for more selective therapeutic strategies targeting both dividing and invasive dormant cells.

SourceThe Mount Sinai Hospital / Mount Sinai School of Medicine·JournalCell Reports·DateSep 20, 2022

Bird’s enzyme points toward novel therapies

Researchers create mammalian cells that synthesize a noncanonical amino acid, which can be used to make therapeutic proteins. The discovery could lead to the development of new treatments for various diseases.

SourceRice University·JournalNature Communications·TypeExperimental study·DateSep 19, 2022

Japanese regulations on regenerative medicine are failing patients

A study by Kyoto University Professor Misao Fujita found that Japan's Act on the Safety of Regenerative Medicine lacks key provisions to prevent unproven treatments from being administered to patients. The lack of scientific verification and clear definitions for medical innovations and interventions are major concerns.

SourceKyoto University·JournalCell Stem Cell·TypeMeta-analysis·DateSep 13, 2022

Researchers identify immune cell that helps kill bladder cancer tumors

Bladder cancer researchers discovered a subset of CD8 T cells that adapts to tumor evasion strategies, offering a strategy to reduce tumor cells' ability to fight them off. The study also identified potential ways to make immunotherapy more effective against this deadly cancer by targeting the HLA-E/NKG2A axis.

SourceThe Mount Sinai Hospital / Mount Sinai School of Medicine·JournalCancer Cell·DateSep 12, 2022
CalDigit TS4 Thunderbolt 4 Dock

CalDigit TS4 Thunderbolt 4 Dock simplifies serious desks with 18 ports for high-speed storage, monitors, and instruments across Mac and PC setups.

How slow muscle fibers convince their neighbors to join them

Researchers at Tokyo Metropolitan University discovered that a protein excreted by type I muscle fibers can differentiate surrounding myoblasts into type I fibers, upending the notion that fiber ratios are fixed at birth. This finding has significant implications for treating conditions such as type 2 diabetes and aging populations.

SourceTokyo Metropolitan University·JournalScientific Reports·DateSep 10, 2022

Study uncovers possible path for improving T cell therapies

A study led by researchers at the University of Arizona Health Sciences has uncovered a possible path for improving T cell therapies. The study found that the CD4 molecule plays a more active role in regulating T cell receptor signaling, allowing for even more powerful versions of T cell therapy.

SourceUniversity of Arizona Health Sciences·JournaleLife·DateSep 6, 2022

Simple blood test predicts neurotoxic complications of CAR-T cell therapy

A new study from Washington University School of Medicine suggests that levels of neurofilament light chain (NfL) in the blood can predict neurotoxic side effects in patients undergoing CAR-T cell therapy. High NfL levels are present even before treatment begins and remain elevated throughout treatment.

SourceWashU Medicine·JournalJAMA Oncology·DateSep 1, 2022
Apple AirPods Pro (2nd Generation, USB-C)

Apple AirPods Pro (2nd Generation, USB-C) provide clear calls and strong noise reduction for interviews, conferences, and noisy field environments.

Brain’s support cells may hold key to new Huntington’s treatments

A new study identifies how the suppression of a specific transcription gene triggers changes that impair oligodendrocyte function in Huntington's disease. The researchers believe replacing or fixing defective glia cells may prove a far easier proposition than replenishing neurons lost in the disease.

SourceUniversity of Rochester Medical Center·JournalCell Reports·DateAug 30, 2022

Specific components of the tumor immune microenvironment may affect the durability of responses to BCMA CAR T-cell therapy

Researchers found that patients with longer progression-free survival after BCMA-targeted CAR T-cell therapy had more diverse baseline T-cell repertoires, fewer markers of immune exhaustion, and distinct changes to immune cell populations. These factors were associated with improved responses to the treatment.

SourceAmerican Association for Cancer Research·JournalBlood Cancer Discovery·DateAug 30, 2022
Sky-Watcher EQ6-R Pro Equatorial Mount

Sky-Watcher EQ6-R Pro Equatorial Mount provides precise tracking capacity for deep-sky imaging rigs during long astrophotography sessions.

Light-based therapy weakens antibiotic-resistant bacteria

Researchers developed a light-based therapy, photodynamic therapy (aPDT), to combat antibiotic-resistant bacteria. The treatment showed promise in weakening bacteria, allowing lower doses of current antibiotics to effectively eliminate them.

SourceTexas A&M University·JournalProceedings of the National Academy of Sciences·DateAug 29, 2022

Therapeutic viruses help turbocharge the immune system against cancer

A combination of immunotherapy and virotherapy using myxoma virus provides new hope for patients with treatment resistant cancers. The approach boosts the immune capacity to effectively target and destroy cancer cells, inducing a form of cell death called autosis.

SourceArizona State University·JournalCancer Cell·TypeExperimental study·DateAug 26, 2022

A cellular engineering breakthrough: High-yield CRISPR without viral vectors

Researchers at Gladstone Institutes and UCSF have developed a new approach to introduce long DNA sequences into cells with remarkable efficiency. The technology, which uses single-stranded DNA templates, overcomes the limitations of traditional viral vectors and has the potential to make cell therapies faster, better, and less expensive.

SourceGladstone Institutes·JournalNature Biotechnology·DateAug 25, 2022
Sony Alpha a7 IV (Body Only)

Sony Alpha a7 IV (Body Only) delivers reliable low-light performance and rugged build for astrophotography, lab documentation, and field expeditions.

Technology developed at UH could advance treatment of lymphoma

A University of Houston engineer has developed technology to determine which patients are likely to respond to CAR T-cell therapy for lymphoma, saving time and increasing success rates. The TIMING method analyzes interactions between T cells and tumor cells, identifying a key ligand molecule that predicts patient response.

SourceUniversity of Houston·JournalJournal of Clinical Investigation·DateAug 24, 2022
Creality K1 Max 3D Printer

Creality K1 Max 3D Printer rapidly prototypes brackets, adapters, and fixtures for instruments and classroom demonstrations at large build volume.

Old drug, new trick: Researchers find combining antiviral drugs and antibody therapy could treat seasonal flu and help prevent next flu pandemic

Researchers at McMaster University have discovered a combination of antiviral drugs and antibody therapies that is more effective than either approach alone. The combination boosts the virus-fighting properties of antibodies, which work by binding to infected cells and triggering the immune system to kill them.

SourceMcMaster University·JournalCell Reports Medicine·DateAug 16, 2022
Nikon Monarch 5 8x42 Binoculars

Nikon Monarch 5 8x42 Binoculars deliver bright, sharp views for wildlife surveys, eclipse chases, and quick star-field scans at dark sites.

Study identifies potential targets for treating venous ulcers

A study published in eLife identified three microRNAs that may impair healing in venous ulcers, a common type of chronic wound. The findings suggest that drugs targeting these microRNAs could help facilitate healing in patients, offering new approaches for treating this painful and slow-to-heal condition.

SourceeLife·JournaleLife·DateAug 9, 2022

Fast-acting immune cells provide powerful protection against stroke

A novel subset of CD8+ regulatory-like T cells (CD8+TRLs) has been identified as 'first responders' to stroke, providing fast-acting and lasting protection. These cells reach the brain within 24 hours after stroke onset, releasing molecules that provide direct neuroprotective effects.

SourceUniversity of Pittsburgh·JournalJournal of Clinical Investigation·DateAug 1, 2022

Mode-of-action of T-cell immunotherapies in focus

Researchers used a new 3D imaging technique to analyze the interaction between T-cell therapies and solid mini-tumors, revealing a wide variety of behaviors in engineered T cells. The study identified specific gene signatures of highly potent T cells that can target multiple tumor cells.

SourcePrincess Máxima Center for Pediatric Oncology·JournalNature Biotechnology·TypeObservational study·DateJul 25, 2022

Engineers develop new tool that will allow for more personalized cell therapies

Researchers have developed a new quantitative approach to predict and customize site-specific recombination, enabling more efficient genetic and cell therapies. The tool combines high-throughput experiments with machine learning models to control the rate of DNA editing, paving the way for personalized treatment.

SourceUniversity of Minnesota·JournalNature Communications·TypeExperimental study·DateJul 20, 2022
Anker Laptop Power Bank 25,000mAh (Triple 100W USB-C)

Anker Laptop Power Bank 25,000mAh (Triple 100W USB-C) keeps Macs, tablets, and meters powered during extended observing runs and remote surveys.

Wireless activation of targeted brain circuits in less than one second

Researchers from Rice University, Duke University, Brown University and Baylor College of Medicine developed a magnetic technology to wirelessly control neural circuits in fruit flies. They used genetic engineering to express heat-sensitive ion channels in neurons that control the behavior, and iron nanoparticles to activate the channels.

SourceRice University·JournalNature Materials·TypeExperimental study·DateJul 14, 2022

Killing resistant prostate cancer with iron

Researchers have found that high levels of iron can generate toxic free radicals, which damage lipids and ultimately lead to cell death. The team is exploring the use of compounds like JKE-1674 to induce ferroptosis in prostate cancer cells, making them more vulnerable to treatment.

SourceMedical College of Georgia at Augusta University·DateJul 7, 2022