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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

An 84-year-old man developed a rare scalp condition from a cancer drug but continued treatment as it was otherwise well tolerated.

The drug IPI-926 is safe at 160 mg daily and may help treat certain tumors, especially basal cell carcinoma.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

The treatment was effective and tolerable for advanced gastric cancer.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A new carrier improves skin delivery of tofacitinib for treating inflammatory skin diseases.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Markers CRABP1, Nestin, and Ephrin B2 are present in skin cancer environments and may influence their development.

Finasteride helps female-pattern hair loss.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

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.

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

The assay quickly identifies substances that increase or decrease blood vessel growth.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

WNT10A is important for tissue development and linked to various human disorders.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Peptide nanoparticles can effectively deliver CRISPR-Cas9 to target KRAS mutations in cancer.

Rac1 is crucial for normal hair structure and pigmentation.

PDGF signaling is crucial for maintaining and renewing hair follicle stem cells, which could help treat hair loss.

Stat3 influences keratinocyte stem cell behavior, affecting differentiation and migration.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.