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Type VII collagen absence helps skin development by allowing tissue remodeling.

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

Biomimetic dermal papilla spheres can help regenerate hair to some extent.

Sonidegib and vismodegib have different side effects and reporting patterns.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

The assay effectively detects hormonal activity of certain chemicals.

Researchers developed a method to grow hair follicle cells for transplantation using a special chip.

Two cows had a rare hair disorder causing hair loss but were otherwise healthy.

The study concluded that the developed models are effective for studying hair growth mechanisms and testing new treatments.

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The study concluded that changing the culture conditions can cause sika deer skin cells to switch from a flat to a 3D pattern, which is important for creating hair follicles.

The patient's hair has unique structural differences with alternating bright and dark bands.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

The study successfully gathered a diverse group of 438 women to understand the prevalence of polycystic ovary syndrome, with most participants recruited online and at community fairs.

MESTSV is a rare tumor that is mostly benign but needs long-term monitoring due to potential recurrence.

Chemistry42 effectively creates and optimizes new molecules for drug discovery.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

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The symptoms described align more with Haberland syndrome, not Delleman-Oorthuys syndrome.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

Certain gene variations are found in people with polycystic ovary syndrome.

Hair diameter diversity could improve androgenetic alopecia assessment and treatment planning.

Neuromyotonia and morphoea can occur together in the same body areas.

Restoring EDA and WNT pathways early may help improve skin, hair, and teeth issues in hypohidrotic ectodermal dysplasia.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.