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The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

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.

S100A3 protein is crucial for hair shaft formation in mice.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

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

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

EDA2R gene linked to hair loss.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

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.

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

Finasteride may help reduce symptoms in male Tourette syndrome patients.

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

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

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

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

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

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

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

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

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

A new gene variant causes glucocorticoid resistance in a mother and son.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Finasteride effectively treats mild to moderate hair loss in men aged 18-41, with some side effects.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.