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Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

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

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

The study concluded that androstendione and DHEA are important for diagnosing high male hormone levels in women with excessive hair growth.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

High levels of the protein Flightless I worsen ulcerative colitis symptoms in mice.

Proper diet management is crucial for phenylketonuria patients to avoid severe health issues.

Targeting the actin cytoskeleton could improve skin healing and reduce scarring.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

Lack of certain vitamins causes fur loss and greying in silver foxes.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

Activating TRPV3 channels stops hair growth by killing hair follicle cells.

Researchers developed a way to study human body clocks using hair tissue, which works similarly in both healthy and dementia patients.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Some skin diseases and their treatments can negatively affect male fertility.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

The document explains that hirsutism, often caused by hormonal issues, can be managed with treatment to improve both physical appearance and mental health.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

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

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

The study suggests that a new protease inhibitor can make hair harder to pull out, potentially reducing hair loss.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Ptprq has multiple forms that change during inner ear development.

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