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Folliculotropic mycosis fungoides can affect the central nervous system in advanced stages.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Non-coding RNAs help control hair growth in cashmere goats.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Key genes can rewire networks, changing skin appendage types.

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

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

A specific gene mutation causes long hair in Angora rabbits.

c-Kit is important for heart regeneration and cancer development.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

S100A3 protein is crucial for hair shaft formation in mice.

Activated LEF/TCF complexes are crucial for hair development and cycling.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

Hair follicle stem cells can become different cell types and may help treat neurodegenerative disorders.

Slug (Snai2) helps regulate hair growth timing in mice.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

Nrf-2-modified stem cells from hair follicles significantly improve ulcerative colitis in rats.

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.