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An American Bully with a genetic skin condition improved significantly with specific topical treatments.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The conclusions are: fecal short-chain fatty acids may help prevent cancer, fiber intake can reduce obesity, weight loss is hard for obese people, low BMI cancer patients are more prone to chemotherapy side effects, intermittent fasting benefits gut health, cherry laurel has health benefits in rats, certain gene variations can increase stress in hair loss patients, fecal acids can affect blood sugar levels, cold agglutinin can affect blood test results in autoimmune patients, and people with Crohn's disease have higher levels of a certain chemical in their blood.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A group has developed therapies that show promise for treating cancer and various other conditions.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Experts agree that PCOS affects women's health in complex ways, but more research is needed to understand and treat it effectively.

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

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

RTA 408 cream protects mice from radiation skin damage.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

Engineered skin substitutes can grow hair but have limitations like missing sebaceous glands and hair not breaking through the skin naturally.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

The study found that a specific signaling pathway helps skin wounds heal faster but may lead to larger scars.

The Itpr3 gene causes a specific hair pattern in mice.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

A woman with alopecia totalis regrew dark hair in bands after using a corticosteroid ointment.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

A mouse gene mutation increases the risk of skin cancer.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Light therapy may improve eye conditions by stimulating cell activity and increasing oxygen availability.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.