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Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Certain gene variations increase the risk of alopecia areata in Koreans.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

The CORIN gene variant causes the golden color in Siberian cats.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

GLI1 RNA CISH effectively identifies basal cell carcinoma but is less specific for benign follicular tumors.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

FGF13 gene changes cause excessive hair growth in a rare condition.

Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.

Ginkgo biloba has high genetic diversity, useful for future breeding.

GLI and EGF signalling affect Basal Cell Carcinoma development and could be therapeutic targets.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Enzymatic synthesis improved the water solubility of the flavonoid baicalin, which may help treat hair loss conditions.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Certain gene variants are linked to severe acne, especially in males.

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 new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

A person with Werner syndrome was initially thought to just have female pattern hair loss.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

BCG injection helps reduce long COVID symptoms and affects hair loss differently in men and women.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.