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Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

Different cell types work together to repair skin, and targeting them may improve healing and reduce scarring.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Tumor suppressors help control inflammation in cancer and restoring their function could lead to new treatments.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

Cell therapy shows promise for treating severe psoriasis but needs more research to confirm safety and effectiveness.

The conclusion is that exogen is a unique hair cycle phase and the new sampling method specifically targets this stage, which may help in future hair loss research.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

A mouse gene mutation increases the risk of skin cancer.

Some supplements may help with hair loss, but there's not enough strong evidence to recommend them without doctor advice.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

All-trans retinoic acid causes hair loss by increasing TGF-β2 in hair follicle cells.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.