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A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Inhibiting SFRP1 may help treat hair loss.

Certain gene variants are linked to severe acne, especially in males.

Key genes and RNAs related to hair growth in sheep were identified, aiding future breeding improvements.

The LTF gene may help predict and manage nonspecific orbital inflammation.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

N6-methyladenosine affects hair follicle development differently in Rex and Hycole rabbits.

Delta-opioid receptors affect skin cell circadian rhythms, possibly impacting wound healing and cancer.

Human hair follicles have a scent receptor that can influence hair growth.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

A low dose of rapamycin increases inner ear hair cell creation by boosting SOX2+ cell numbers.

Basonuclin helps keratinocytes multiply and prevents them from fully maturing.

ERG increases SOX9, promoting prostate cancer growth and invasion.

The vector successfully directed specific gene expression in hair follicles.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

A protein called sFRP4 can slow down hair regrowth.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

RORs may influence cashmere growth cycles.