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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

The modified Crawford technique resulted in less lagophthalmos and better cosmetic outcomes for patients with lateral droop.

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

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Age-related hair curvature increases due to internal structural changes from grooming.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

A specific gene mutation causes congenital hair loss.

Adult esophageal cells can start to become like skin cells, with a key pathway influencing this change.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

A new mutation in the HR gene causes hair loss in a specific family.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

A new gene mutation causes a rare type of hair loss.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

The study found that baicalin has different stable shapes in gas and water, with two shapes better for interacting with positive charges in water.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Using minoxidil for hair growth may cause skin lesions in some people, and taking breaks from nitrate patches for angina might worsen symptoms.

The conclusion is that supportive environments are crucial for the mental health and well-being of transgender individuals during gender transition or de-transition.

Efficient enzyme function relies on specific residue interactions and structural coordination.

Changing the direction of cuts can make it easier to put in implants.

Lhx2 helps retinal cells respond to signals for eye development.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.