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Researchers aboard the ISS have announced the first successful use in space for a new technique for studying DNA repair in yeast. Astronauts aboard the space station have demonstrated a successful CRISPR/Cas9 genome editing method. An organism can suffer damaged DNA occurring during normal biological processes or as the result of environmental causes.

In both humans and animals, damaged DNA can lead to cancer. However, there are multiple natural strategies inside cells that allow damaged DNA to be repaired. NASA is working hard on studying DNA repair in space because astronauts traveling outside of the atmosphere have an increased risk of DNA damage due to ionizing radiation.

Until now, technological and safety obstacles have limited research into the issue. Now astronauts aboard the ISS have developed a new method for studying DNA repair in yeast cells that can be conducted completely in space. The process uses CRISPR/Cas9 genome editing technology to create precise damage in DNA strands to allow DNA repair mechanisms to be observed.

Businesses around the world rushed Saturday to contain a ransomware attack that has paralyzed their computer networks, a situation complicated in the U.S. by offices lightly staffed at the start of the Fourth of July holiday weekend.

It’s not yet known how many organizations have been hit by demands that they pay a ransom in order to get their systems working again. But some cybersecurity researchers predict the attack targeting customers of software supplier Kaseya could be one of the broadest ransomware attacks on record.

It follows a scourge of headline-grabbing attacks over recent months that have been a source of diplomatic tension between U.S. President Joe Biden and Russian President Vladimir Putin over whether Russia has become a safe haven for cybercriminal gangs.

A year after University at Buffalo scientists demonstrated that it was possible to produce millions of mature human cells in a mouse embryo, they have published a detailed description of the method so that other laboratories can do it, too.

The ability to produce millions of mature human in a living organism, called a chimera, which contains the cells of two species, is critical if the ultimate promise of to treat or cure is to be realized. But to produce those mature cells, human primed stem cells must be converted back into an earlier, less developed naive state so that the can co-develop with the inner cell mass in a blastocyst.

The protocol outlining how to do that has now been published in Nature Protocols by the UB scientists. They were invited to publish it because of the significant interest generated by the team’s initial publication describing their breakthrough last May.

Nuclear Pore Complexes and Genome Integrity — Dr. Veronica Rodriguez-Bravo Ph.D., Sidney Kimmel Cancer Center — Jefferson Health, Thomas Jefferson University.


Dr. Veronica Rodriguez-Bravo, PhD, is Assistant Professor, Department of Cancer Biology, at the Sidney Kimmel Cancer Center, Thomas Jefferson University, in Philadelphia, PA, USA. (https://sidneykimmelcancercenter.jeffersonhealth.org/)

Dr. Rodriguez-Bravo obtained her PhD in Pathology and Cell Biology (Summa Cum Laude) from the University of Barcelona in 2007, where she also received the Extraordinary Doctorate Award for her studies on the distinct DNA replication checkpoint mechanisms of tumor cells. During her postdoctoral training at the Experimental Oncology Department of the University Medical Center of Utrecht (UMC, The Netherlands) and at the Molecular and Cell Biology Programs of Memorial Sloan Kettering Cancer Center (MSKCC, New York), she specialized in the study of chromosome segregation during mitosis and the role of nuclear pores in genome integrity maintenance.

Dr. Rodriguez-Bravo’s post-doctoral work allowed her to apply genome-editing techniques crucial to dissect the function of mitotic and nuclear pore proteins in chromosomal stability and resulted in the recognition with the Memorial Sloan Kettering Cancer Center Postdoctoral Research Award.

Dr. Rodriguez-Bravo’s research focuses on the study of genome integrity maintenance mechanisms and the relationship of defects in cell division to cancer pathogenesis with special emphasis in the pathways contributing to cancer cells’ more aggressive phenotypes.

“Cannabis may contribute to increased risk for mental disorders, which has actually been shown in schizophrenia,” Penzes said. “Conversely, cannabis could be beneficial in some brain disorders, which prompted trials of medical marijuana in patients with autism.”


Summary: Findings reveal a role the endocannabinoid system plays in a range of psychiatric disorders, including schizophrenia, bipolar disorder, and ASD.

Source: Northwestern University

Northwestern Medicine scientists discovered an unexpected connection between a synapse protein that has been implicated in neuropsychiatric disorders and the endocannabinoid pathway, according to a study published in Biological Psychiatry.

These findings suggest a role for the endocannabinoid system in conditions including bipolar disorder, according to Peter Penzes, PhD, the Ruth and Evelyn Dunbar Professor of Psychiatry and Behavioral Sciences, professor of Physiology and Pharmacology, and senior author of the study.

Indiana University School of Medicine researchers are developing a new, noninvasive brain stimulation technique to treat neurological disorders, including pain, traumatic brain injury (TBI), epilepsy, Parkinson’s disease, Alzheimer’s disease and more.

“Given the increasing use of stimulation in human brain study and treatment of neurological diseases, this research can make a big impact on physicians and their patients,” said Xiaoming Jin, Ph.D., associate professor of anatomy, cell biology and physiology.

When someone experiences a , nerve injury, or neurodegeneration, such as in epilepsy and TBI, there is damage to the brain which can lead to loss and damage of nerve or neurons and development of hyperexcitability that underlies some neurological disorders such as neuropathic pain and epilepsy.

Researchers from Harvard University and the Massachusetts Institute of Technology, both based in Cambridge, Mass., have created small diagnostic biosensors that can be inserted into face masks and can diagnose COVID-19 within 90 minutes, The Mercury News reported June 29.

The insertable biosensors detect the virus from a wearer’s breath, producing easy to read results similar to those of an at-home pregnancy test. If the coronavirus is present, the system changes the pattern of lines in the readout strip.

To activate the test, the wearer pushes a button on the mask to release a small amount of water into the system, which activates the test.

Stem cells for teeth repair.


Teeth exhibit limited repair in response to damage, and dental pulp stem cells probably provide a source of cells to replace those damaged and to facilitate repair. Stem cells in other parts of the tooth, such as the periodontal ligament and growing roots, play more dynamic roles in tooth function and development. Dental stem cells can be obtained with ease, making them an attractive source of autologous stem cells for use in restoring vital pulp tissue removed because of infection, in regeneration of periodontal ligament lost in periodontal disease, and for generation of complete or partial tooth structures to form biological implants. As dental stem cells share properties with mesenchymal stem cells, there is also considerable interest in their wider potential to treat disorders involving mesenchymal (or indeed non-mesenchymal) cell derivatives, such as in Parkinson’s disease.

Teeth are complex organs containing two separate specialized hard tissues, dentine and enamel, which form an integrated attachment complex with bone via a specialized (periodontal) ligament. Embryologically, teeth are ectodermal organs that form from sequential reciprocal interactions between oral epithelial cells (ectoderm) and cranial neural crest derived mesenchymal cells. The epithelial cells give rise to enamel forming ameloblasts, and the mesenchymal cells form all other differentiated cells (e.g., dentine forming odontoblasts, pulp, periodontal ligament) (Box 1). Teeth continue developing postnatally; the outer covering of enamel gradually becomes harder, and root formation, which is essential for tooth function, only starts to occur as part of tooth eruption in children.

Tooth development is traditionally considered a series of stages that reflect key processes ( Figure I ). The first step is induction, in which signals from the epithelium to the mesenchyme initiate the developmental process. As localized proliferation of the dental epithelial cells takes place, the cells form a bud around which the mesenchymal cells condense. Differentiation and localized proliferation of the epithelial cells in the bud leads to the cap stage. It is at this stage that crown morphogenesis is initiated by the epithelial signalling centre, an enamel knot regulating the folding of the epithelium. By the bell stage, the precursors of the specialized tooth cells, ameloblasts, coordinate enamel deposition, and odontoblasts, which produce dentine, are formed. Tooth eruption involves the coordination of bone resorption and root development, and occurs postnatally.