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A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Blocking mTORC1 reduces skin tumor growth in mice.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

RNase L suppresses regeneration in mammals.

miR-199a-3p controls hair growth and is linked to alopecia areata.

A specific gene mutation causes long hair in Angora rabbits.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

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

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

A new mouse model helps study melanocyte cells using GFP expression.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Pu-erh tea reduces hair loss risk in offspring.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

Blocking prolactin increases the activity of secondary hair follicles in cashmere goats.

The 4C32 gene may help in mouse skin development and differentiation.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Four circRNAs were found to be significantly different in cashmere goat skin, affecting cashmere fineness.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

AR polyglycine repeat doesn't cause baldness.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

FGFR2 signaling controls Merkel cell formation in different skin regions.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

p63 is essential for skin cell growth and differentiation by controlling specific gene networks.

Overexpressing PKCα in mice skin increases inflammation but doesn't affect tumor growth.