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A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Seven new genetic risk areas for prostate cancer were found.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A specific gene mutation causes long hair in Angora rabbits.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Some women with PCOS have rare genetic variants linked to the condition.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

PCOS shares similar genetic traits across different diagnosis criteria and is linked to other health conditions.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A mutation in the KRTHB5 gene causes hair and nail issues.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

A new gene variant causes glucocorticoid resistance in a mother and son.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.