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HPLC may detect prediabetes and diabetes earlier than Immunoturbidimetry because it shows higher A1c levels.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

HAT-L4 is crucial for preventing body fluid loss by maintaining skin barrier integrity.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

HAP-cell-sheets improved wound healing in diabetic mice.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A diabetic cat with another gland issue got better after treatment with cabergoline, no longer needing insulin.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

The ALADIN score can predict how well patients with alopecia areata will respond to JAK inhibitor treatments.

Enhancing Tregs can protect against alopecia areata.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

Hidradenitis suppurativa has had many names, but its naming is still not agreed upon.

Targeting the MC-5-HT-HTR2A axis may help treat chronic itching.

A woman developed lupus after taking hydroxyurea for two years.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A reliable method was created to measure dutasteride and related molecules in capsules.

A woman had unusual hair growth on one side of her chin without a known cause.

A woman recovered from hair loss and skin eruptions after stopping a tuberculosis drug and using steroids.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

A protein called HIF-1a helps control hair growth genes and could be targeted to treat hair loss.

hHbl gene is active in hair shaft cells and some pilomatricomas.

Vitamin D receptor mutations can cause alopecia by affecting hair growth genes.

Mutations in the HOXC13 gene cause hair and nail development issues.

Key proteins and potential drugs for treating alopecia areata were identified.

Injecting non-cross-linked hyaluronic acid into the face improved skin hydration, texture, pores, and reduced wrinkles.

Upadacitinib significantly improved alopecia universalis and psoriatic arthritis in a patient.

High-frequency ultrasound effectively evaluates and diagnoses frontal fibrosing alopecia.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.