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Elastic Net DNA methylation clocks are inaccurate for predicting age and health status; a "noise barometer" may better indicate aging and disease.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Specific keratin gene mutations can cause monilethrix.

Ancestry affects skin healing, with non-Hispanic Black patients showing more healing-related fibroblasts than White patients.

Higher levels of certain DNAs in blood may indicate hair follicle damage in alopecia areata patients.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The vitamin D receptor has many roles in the body beyond managing calcium, affecting the immune system, hair growth, muscles, fat, bone marrow, and cancer cells.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Snakes and worm lizards lost claw proteins due to similar evolutionary changes.

SLICK cattle have better heat tolerance due to specific gene expression and pathway differences.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

The research found specific genes that are more active in balding cells, which could be causing hair loss.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

Dorper sheep's wool shedding is linked to specific genes and pathways, which may help understand human hair growth.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

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

A truncated protein linked to breast cancer may change cell adhesion.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Vitamin D receptor may help protect against UV-induced skin cancer.

Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.