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MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

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

Generalized vitiligo in Chinese patients is linked to other autoimmune diseases, especially in familial cases.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

More research is needed to understand sex and racial differences in long COVID.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Certain DNA regions in alpacas are linked to fiber diameter.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

The topical finasteride spray was safe and well-tolerated with stable effects.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

Olfactory receptors found outside the nose may offer new treatments for diseases like cancer and help in wound healing and hair growth.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Vitamin D receptor interacts with certain dietary components to help prevent diseases and regulate hair growth.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

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

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Certain gene variations might be linked to severe acne in women but not in men.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

Different hair protein amounts change the strength of keratin/chitosan gels, useful for making predictable tissue engineering materials.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.