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Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Adults should not consume more than 255 micrograms of selenium per day to avoid risk of hair loss and other side effects.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

Pegvaliase effectively reduces blood phenylalanine levels in most PKU patients, but requires personalized plans and good communication to manage side effects.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Sex hormones' effects on COVID-19 are unclear and more research is needed to understand their potential as treatment.

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

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Actin filaments help root hairs grow faster and longer under low potassium stress.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Meis2 is essential for touch sensation and nerve function in mice.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Nutrease powder, a high-protein, low-carb supplement, can help manage Polycystic Ovary Syndrome symptoms, regulate periods, improve ovulation, and restore fertility.

People with autoimmune skin diseases often have hearing problems and should get their hearing checked early.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

A man lost all his hair as a rare side effect after hepatitis C treatment.

Polycystic ovary syndrome is a complex condition that affects women's mental, reproductive, and metabolic health throughout their lives.