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A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Hair transplant surgery successfully restored a boy's moustache hair on a cleft lip scar, with natural-looking results and patient satisfaction.

Hair transplant surgery successfully restored a boy's moustache hair on a cleft lip scar, with natural-looking results and patient satisfaction.

Alopecia areata and lichen planus can occur together in children, which is important for diagnosis and treatment.

Langerhans' cells are not involved in hair depigmentation in these mice.

ILC1-like cells can cause alopecia areata by attacking hair follicles.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Disrupting Bcl-xL in mice reduces skin cancer risk.

A 12-year-old boy's rare skin condition improved with topical treatments and may resolve by puberty.

Lymphotoxin-β is crucial for proper skin development in embryos.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

15-lipoxygenase helps keep skin healthy by reducing inflammation.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

Up to 10% of hair loss patients might have early signs of a condition called Lichen Planopilaris.

Sunlight exposure improved a patient's skin condition, and there may be a link between a certain disease and skin growths; a leukemia treatment caused changes in hair color and growth.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

Women are more likely to have Lichen planopilaris, and treatments with cyclosporine and methotrexate are most effective but less safe than mycophenolate mofetil.

Activated LEF/TCF complexes are crucial for hair development and cycling.

Lysophosphatidic acid affects sensory neurons and may cause neuropathic pain and itch.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Accurate diagnosis of NLS with dilated hair follicles is crucial to distinguish it from other conditions.

Finasteride and luteolin may help promote hair growth.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.