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Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

Endothelial TLR2 is crucial for timely wound healing, but HFSC TLR2 is not needed.

Behavioral interventions, especially habit reversal training, are most effective for treating trichotillomania in children.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Isoproterenol helps hair follicle stem cells turn into beating heart muscle cells.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

Hsc70 protein may influence hair growth by responding to androgens.

Trichorhinophalangeal syndrome causes hair, facial, and bone issues, with no specific treatment beyond gentle care.

17β-estradiol may help hair growth by increasing cannabinoid receptor type 1.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Serotonin helps hair grow by activating certain cells.

Specific keratin gene mutations can cause monilethrix.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.