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First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

Adapted classification better assesses male pattern hair loss and its link to heart disease.

Early diagnosis and treatment of congenital adrenal hyperplasia are crucial to manage symptoms and prevent complications.

Odontogenic keratocysts are caused by abnormal Hedgehog signaling and can lead to tooth and bone issues.

Elongating cilia boosts SKP stem cell renewal, especially with PDGF.

The journal covers diverse plant science research and is now published online quarterly.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

The KDM1 gene helps Venus flytraps close by managing potassium ions.

PCOS in Karnataka is influenced by genetics, lifestyle, obesity, and diabetes.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

Sebaceous glands are often preserved and PPARy expression is constant in some cases of Central Centrifugal Cicatricial Alopecia.

Kenikir leaf extract nanosuspension may help inhibit breast cancer cell growth.

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

Keratinocytes in hair follicles differentiate similarly to skin cells, with specific patterns in different regions.

Ritlecitinib is effective and safe for long-term use in treating severe alopecia areata in people aged 12 and older.

Keratosis pilaris is common in young females, and dermoscopy helps diagnose it accurately.

Baricitinib effectively treats certain skin conditions but may have serious side effects.

The May issue discussed publishing agreements and four studies on cholesterol in hair, cancer cell changes, hormones in the uterus, and skin protein effects.

Phosphatidylinositol 4-kinases are crucial for root growth, defense, and immunity in Arabidopsis thaliana.

Kerion, a scalp fungal infection, requires lab confirmation and is treated with antifungal medication and medicated shampoo.

The study developed a mouse model for Alopecia Areata that responds to treatment, useful for future research.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Brepocitinib improves cicatricial alopecia and reduces key immune markers.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Patients and doctors often agree on the severity of eyebrow and eyelash hair loss in severe alopecia areata.