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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.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.

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

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Researchers found a gene mutation responsible for a rare hair loss condition.

A new mutation in the HR gene causes hair loss in a specific family.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

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

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

The CORIN gene variant causes the golden color in Siberian cats.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

Chicken feather gene mutation helps understand human hair disorders.