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A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

A rare skin condition called linear lichen planopilaris caused itchy red bumps and hair loss on a man's face.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

lncRNAs influence cashmere fiber traits like diameter and color in goats.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

The LTF gene may help predict and manage nonspecific orbital inflammation.

rPanglaoDB helps study rare cell types by merging RNA data, showing fibrocytes aid in healing.

The Itpr3 gene causes a specific hair pattern in mice.

The protein's size was reduced, but more work is needed to confirm its function.

IPM enhances skin penetration of hydrophilic drugs.

Mutations in the SNRPE gene cause hereditary hair loss.

ILC1-like cells can cause alopecia areata by themselves.

Facial lichen planopilaris may be triggered by shaving and mustard oil, and early detection is crucial for better treatment outcomes.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

New LSS gene variants help understand congenital hypotrichosis 14 better.

Erosive palmoplantar lichen planus in North-East India mainly affects the feet and often involves nails, with unique inflammatory skin changes.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Low-dose naltrexone helps improve symptoms and stabilize frontal fibrosing alopecia and lichen planopilaris.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

Liarozole may be more effective than cyproterone acetate for treating advanced prostate cancer, with better PSA response and survival rates, while maintaining quality of life.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Auxin helps root hairs grow in high phosphate by affecting ROS and involving RSL2 and RSL4.

lncRNAs significantly influence koi carp skin color.