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Radiofrequency microneedling is an effective and safe treatment for various skin conditions and works well with other treatments and on darker skin.

Vitamin D receptor helps control hair growth and could be used to treat certain skin tumors.

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

Researchers developed a cost-effective, ethical skin model using hairless guinea pig cells for toxicology studies.

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.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

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.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell development.

UVF-dermoscopy is a useful tool for accurately diagnosing types of alopecia, especially in people with lighter skin.

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

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

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

The fuzzy gene is crucial for controlling hair growth cycles.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

A specific gene mutation causes Olmsted syndrome.

Alopecia frontal fibrosante affects facial vellus hair and can be diagnosed with dermatoscopy.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Wounds heal without scarring in early development but later result in scars, and studying Wnt signaling could help control scarring.

Early surgery and quitting smoking can help manage hidradenitis suppurativa.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

Overexpressing the epigen gene in mice leads to enlarged sebaceous glands and greasy fur.

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.

Transplanted hair follicles can improve and remodel mature scars.

MPA increases cancer spread by boosting Eph A2 activity.

Small white dots on the scalp seen with a dermoscope correspond to sweat ducts and vary with different hair disorders.

The HCR gene contributes to psoriasis risk.

New treatments like biologics and JAK inhibitors show promise for severe scalp inflammation when traditional methods fail.

Topical treatments like AHAs, BHAs, and urea may help keratosis pilaris, but evidence is limited.