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The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Combining hair transplantation with PRP is more effective for treating hair loss than hair transplantation alone.

RK81 can help promote hair growth.

Family members have similar hair protein patterns, which could be useful for genetic studies.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

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

K39 and K40 are the last keratins expressed in hair development, completing the hair keratin catalog.

A new keratin gene was found in mice, explaining hair growth.

ADF8 and ADF11 help root hairs grow by responding to hormones and environmental signals.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

Two specific genetic markers increase the risk of hair loss in Asian populations.

WNT10A and EBF1 interaction affects hair growth in male-pattern baldness.

PP2Acα is essential for proper hair and skin development.

Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

A rare gene variant causes hair and nail issues in a family.

Hair proteins have weak spots in their α-helical segments.