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

KLHL24-mutant stem cells help understand skin and heart disease.

AKR1C enzymes in scalp glands decrease with age, possibly affecting hair loss.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Ganoderma lucidum extract can potentially reduce stress-induced hair loss by slowing down premature hair aging and removing harmful substances.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

The study created a new method to test drugs that affect hormone processing in skin.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Researchers developed a precise method to detect illegal hair-growth drugs in dietary supplements.

Two specific genes are more active during hair growth in mice.

KY19382 speeds up wound healing by activating a specific cell signaling pathway.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.

A gene mutation in mice causes permanent hair loss and skin issues.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Keratinocyte growth factor significantly alters skin and tissue development.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.