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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The gene HDC is important for the development of hair follicles in newborn mice.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The Hairless gene is crucial for healthy skin and hair growth.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Androgens can both promote and prevent hair growth due to differences in gene expression in hair follicles.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The conclusion is that we need more effective hair loss treatments than the current ones, and these could include new drugs, gene and stem cell therapy, hormones, and scalp cooling, but they all need thorough safety testing.

Beard and scalp hair cells have different gene expressions, which may affect beard growth characteristics.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Changing light exposure can affect hair growth timing in goats, possibly due to a key gene, CSDC2.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Advanced therapies like gene, cell, and tissue engineering show promise for hair regrowth in alopecia, but their safety and effectiveness need more verification.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Finasteride exposure affects gene expression and anogenital distance in male rat fetuses.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Certain gene variations increase the risk of alopecia areata in Koreans.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

The research found that the gene activity in mouse skin stem cells changes significantly as they age.