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Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Human hair loss may have evolved to help increase brain size.

Different combinations of human hair keratins affect how hair fibers form.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

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.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms 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.

Finasteride negatively affects fish reproduction and gonadal development.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Researchers found four key proteins that affect the development of a specific hair type in Yangtze River Delta white goats.

Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

Light-based treatment, Photobiomodulation, shows promise for non-invasive skin therapy with few side effects.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

Improving artificial vascular grafts requires better materials and surface designs to reduce blood clotting and support blood vessel cell growth.