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The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

DNMT3A is crucial for healthy skin and hair growth.

EGFR inhibitors cause skin issues and hair loss by weakening skin defenses, suggesting antibiotics and targeted treatments can help.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

ADM scaffolds help skin heal by promoting a healing-type immune response.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

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

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

A new mouse mutation causes skin and hair defects due to a gene change.

Finasteride can cause a unique skin reaction on the penile shaft.

Using minoxidil for hair growth may cause skin lesions in some people, and taking breaks from nitrate patches for angina might worsen symptoms.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

Androgen affects oil production and hair growth in the skin.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

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

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

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

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Filaggrin mutations are linked to atopic dermatitis and help explain how genetics and environment affect the disease.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

ODC transgenic mice can model human hair loss with skin lesions.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Patients with ichthyosis often experience symptoms similar to psoriasis and atopic dermatitis, suggesting that targeted therapies could improve their condition.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.