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Patients with long COVID after Omicron had fewer hospitalizations and milder symptoms but more fatigue, insomnia, and cough compared to those with Delta.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

MC1R gene variations affect skin, hair color, UV sensitivity, and melanoma risk.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

A specific genetic variation affects wool quality in sheep.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

LIPH mutations cause woolly hair in some Chinese people.

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

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Mutations in the SNRPE gene cause hereditary hair loss.

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

HPV type 56 can hide in hair follicles even without visible warts.