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Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

FGF5 gene mutations cause long hair in domestic cats.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Mice with human gene experienced hair loss when treated with DHT.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

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

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

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

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

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

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

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

The SOSTDC1 gene is crucial for determining sheep wool type.

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

The KRTAP36-2 gene in sheep affects wool yield.

The study suggests that analyzing DNA can help treat hair loss, but more research is needed.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Scientists found a gene in mice that causes early hearing loss.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.