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A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

Found different long non-coding RNAs in balding Chinese men, which may help create new treatments.

Different forms of FGF5 either promote or inhibit hair growth.

ILC1-like cells can cause alopecia areata by themselves.

A KRT32 gene variant causes loose anagen hair syndrome.

Overexpression of COX-2 in mice skin causes abnormal skin and hair development.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

Type XVII collagen may help prevent skin aging.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Men with low testosterone or breast growth should be checked for Cushing syndrome.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

Low-dose glucocorticoid treatment improves pregnancy and birth rates in women with nonclassical 21-hydroxylase deficiency.

Forearm hair has more cortisol than lower leg hair.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Hair sample weight is a better measure for cortisol levels in hair than hair protein concentration.

Key genes can rewire networks, changing skin appendage types.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Sex and stress steroids quickly change brain cell structures in the hippocampus.

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