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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.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Keloid scars are aggressive, excessive skin scars with unique features and complex diagnosis.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

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

A 64-year-old man had a rare skin cancer near his ear, unresponsive to antibiotics, with specific skin and hair follicle changes.

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.

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

Hedgehog signaling is crucial for hair development, cadherins affect cell adhesion, neutrophils play a role in skin lesions, and BP230 autoantibodies impact skin stability.

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.

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

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

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.

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.

Dr. Jorizzo questions the long-term benefits of minoxidil and tretinoin, while Dr. Olsen defends their effectiveness and stresses the need for public education on these treatments.

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

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

The September 2023 issue highlights the importance of safety in cosmetic procedures and updates on treatments for acne, rosacea, and hair restoration.

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.

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