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DDR-II hair follicle cells don't respond to 1, 25-dihydroxyvitamin D3, aiding diagnosis.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Vitamin D receptor is crucial for normal hair growth and preventing hair loss.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

Removing Mediator 1 from certain mouse cells causes teeth to grow hair instead of enamel.

Increasing EGR1 levels makes hair root cells grow faster.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

A special receptor in sensory nerve endings helps control how they respond to stretching.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

The RHC complex with nicotinamide promotes hair growth and health.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

Noncoding dsRNA helps produce exosomes that aid in skin regeneration.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

Retinoic acid production and signaling in hair follicles are regulated by location and timing, affecting hair growth and cycling.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

A new gene mutation is linked to monilethrix in the studied family.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

A soluble factor in developing mouse whisker pads boosts nerve growth factor mRNA production.

17β-estradiol can reduce inflammation in the skin.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.