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ALRN-6924 may prevent hair loss caused by chemotherapy.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

Lichen spinulosus, usually seen in young people, can rarely occur in adults, as shown by a 52-year-old woman with a rough, bumpy rash.

The mineralocorticoid receptor temporarily affects mouse skin development, but the glucocorticoid receptor has a more lasting impact.

Mesenchymal stem cells and their secretome may offer a safe and effective treatment for systemic lupus erythematosus.

The treatment with valproate, acetylcarnitine, folic acid, and vitamin B12 may improve muscle strength in children with SMA without significant side effects.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

The prototype for analyzing skin aging works technically and clinically.

MC-1R in skin cells may influence inflammation and collagen production.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

Sox9 is present in most canine skin tumors and may help understand stem cells' role in these cancers.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Sox13 is a new marker for early hair follicle development and differentiation.

The cooling system effectively and safely treats benign pigmented lesions in Asians.

Hedgehog pathway inhibitors could be effective in treating melanoma.

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The hexosamine pathway helps protect skin cells from stress and may improve skin and hair health.

Mice with CBS deficiency are healthier on a low-methionine diet.

The dog improved significantly after treatment for skin mites and fungi.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The enzyme pyruvate kinase M2 helps hair regrowth and could be a potential treatment for hair loss.

New compounds were developed that promote hair growth in mice.

Microneedles offer a painless, effective, and easy-to-use hair loss treatment.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.