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Green tea component EGCG may help prevent hair loss by changing microRNA levels in certain scalp cells.

Rat dermal papilla cells have unique genes crucial for hair growth.

Found 32 genes linked to male baldness, affecting hair growth and stress-related pathways.

The model can effectively test gene functions and drug responses in human skin.

DHT affects hair follicle cells by changing microRNA levels, leading to less cell growth and more cell death.

A herbal extract may help treat certain types of hair loss by reducing a specific gene's activity.

Ficus carica leaf extract may help treat skin disorders by reducing inflammation and androgen effects in skin cells.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Researchers found a gene mutation responsible for a rare hair loss condition.

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

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Chicken feather gene mutation helps understand human hair disorders.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Alopecia areata involves immune response and gene changes affecting hair loss.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.