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Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Nelfb is crucial for forming skin fat tissue by regulating genes needed for fat cell development.

Dermoscopy helps diagnose rare GLPLS in males.

Lhx2 helps retinal cells respond to signals for eye development.

IVL-DrugFluidic® can mass-produce high-quality, long-acting injectable drug microspheres, improving patient compliance and reducing side effects.

PLD is an effective and safer alternative for treating breast cancer.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

A child's rare skin disease was triggered by chickenpox.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Cord blood platelet-rich plasma may safely improve vulvar lichen sclerosus symptoms.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

Defects in certain proteins cause major heart abnormalities during early development.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

GLPLS and LPP are variants of lichen planus.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Lymphatic vessels are essential for hair follicle regeneration and growth.

Vepdegestrant may become the first FDA-approved PROTAC degrader, marking a new era in drug development.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

New LPP subtype affects vellus hairs, mimics AGA, and needs biopsy for diagnosis.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Lower lipin 1β in belly fat is linked to insulin resistance in people with polycystic ovary syndrome.