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Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Joint replacement surgery normalized high alkaline phosphatase levels in a patient with severe osteoarthritis.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Upadacitinib may effectively treat twenty-nail dystrophy without causing pain.

A gene mutation in Lama3 is linked to a common type of hair loss.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

A new treatment using dissolvable microneedles with nickel-copper and minoxidil improves hair growth and health in androgenic alopecia.

N-WASP is essential for healthy skin and preventing inflammation.

Zinc supplements effectively treat acrodermatitis enteropathica.

Two genetic disorders affect biotin metabolism, causing severe skin, hair, and metabolic issues.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Certain genetic variations are linked to hair loss in Mexican men.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.

A peptide from hair follicle stem cells can boost hair growth.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

15-lipoxygenase helps keep skin healthy by reducing inflammation.

Monitor for early signs of azathioprine toxicity and check blood counts regularly.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

The S9 fraction with GC-IDMS is effective for measuring 5α-reductase activity.

NIPP1 is important for healthy skin and could help treat skin inflammation.

Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

VCAM1 appears early in kidney injury and signals future nephron loss.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.