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The HR protein's role as a repressor is essential for controlling hair growth.

Advanced human skin models improve drug development and could replace animal testing.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

DHT, a testosterone byproduct, causes male pattern baldness.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

Thermoresponsive nanogels show promise for delivering medicine through the skin but need more safety testing and regulatory approval before clinical use.

Finasteride doesn't affect erections much, but may decrease libido in men.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

The document concludes that hair loss is common and can be treated with medications like minoxidil or surgical options, and it significantly affects people's psychological well-being.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The conclusion is that treatments like finasteride and minoxidil can prevent baldness progression and improve hair density, but more research is needed on other therapies.

Corticosteroids are the most effective treatment for Satoyoshi syndrome.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Apoptosis may contribute to hair loss in androgenetic alopecia.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

A 28-year-old man with type 1 diabetes had skin and hair issues due to zinc deficiency.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

An infant with a zinc deficiency skin disorder improved with zinc treatment.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.