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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Four specific genes are linked to keloid formation and could be potential treatment targets.

Non-coding RNAs are important for hair growth and could lead to new hair loss treatments, but more research is needed.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

DNA methylation changes in women with PCOS could be used as disease markers and suggest new treatment targets.

Taking triterpenoids from Ganoderma lucidum over a long time can help slow down brain aging and improve overall health in mice.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

SIM01 significantly reduced post-COVID symptoms and is safe.

Oxidative stress worsens PCOS by damaging cells and disrupting metabolism, suggesting antioxidant treatments might help.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Lung and liver macrophages protect our tissues and their dysfunction can cause various diseases.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

5-alpha reductase inhibitors, like finasteride and dutasteride, may cause depression, but more research is needed to understand why.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Urologists should monitor mental health in patients taking finasteride due to potential links to suicidal thoughts, adjusting dosage or stopping use if necessary. More research is needed to confirm if finasteride causes these thoughts.

A specific pathway involving AR, miR-221, and IGF-1 plays a key role in causing common hair loss.

Moxibustion may help improve ovarian function by changing androgen levels.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

Researchers found genes linked to hair loss in male giant pandas.

The summit concluded that new treatments like Jak inhibitors show promise for Alopecia Areata and personalized approaches are needed.