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Certain immune markers may predict chemotherapy response in mesothelioma, and nivolumab is a tolerable and effective treatment for advanced non-small cell lung cancer.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

CUX1 boosts sheep hair cell growth and affects curl patterns.

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.

SOX4 is crucial for the development of melanoma.

Measuring minimal residual disease on day 15 helps identify high-risk leukemia patients.

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

Two new gene mutations cause a rare hair disorder.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Increasing EGR1 levels makes hair root cells grow faster.

Deleting NIPP1 in mouse skin cells causes early aging and chronic skin issues.

Piezo1 helps skin grow by managing metabolism and inflammation.

lncRNAs may regulate hair follicle development in Hu sheep.

ERK activation spreads between cells in mouse skin, linked to cell division and influenced by TPA and EGF receptors.

MicroRNA-181a slows sheep hair growth by targeting GNAI2 and affecting a key growth pathway.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

EGFR is crucial for preventing hair follicle inflammation and hair loss.

MEF2C is crucial for normal hair cycle progression.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Multiphoton microscopy effectively images mouse skin layers and structures.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Antizyme slows skin tumor growth by reducing cell growth in mice.

A new method helps grow skin stem cells better, which could improve skin grafts for burn victims.