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

Hair proteins change location and structure as hair cells mature.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Reduced plakoglobin and steroid abuse increase the risk of heart rhythm issues.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

The gene Prss53 affects hair shape and bone development in rabbits.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Hair root sheaths can be used to accurately analyze genetic markers.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Vitamin C derivative helps hair grow longer by making cells produce a growth factor through a specific cellular pathway.

Hair loss gene linked to prostate issues.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

Artemis protein may help control hair growth and health by influencing cell processes.

Gab1 protein is crucial for hair growth and stem cell renewal, and Mapk signaling helps maintain these processes.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

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

MAP-2 is crucial for the structure of hair follicles and nails.

A new gene mutation causes insulin resistance in a girl and her mother.

The Agouti gene influences pigmentation and may have a developmental role in deer mice.

Cathepsin L is essential for normal hair growth and development.

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

Trichostatin A helps restore hair-growing ability in skin cells used for hair regeneration.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Weak cell junctions disrupt hair follicle stem cell rest.