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Alopecia areata can be transferred through stem cell transplants from affected siblings.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

Researchers found two new genetic variants linked to Alzheimer's disease.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Vitamin D receptor gene variations are not linked to alopecia areata.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

The authors maintain that shorter androgen receptor alleles may lead to milder COVID-19 by positively affecting the immune response, not due to changes in testosterone levels or activity.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Vitamin D and its receptor regulate skin functions like cell growth, immunity, hair cycle, and tumor prevention.

The vitamin D receptor is essential for skin stem cells to grow, move, and become different cell types needed for skin healing.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

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

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Vitamin D and estrogen may help protect heart and kidney health, and maintaining sufficient vitamin D levels could be especially beneficial for African Americans, postmenopausal women, and people with chronic kidney disease.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

Using special RNA to target a mutant gene fixed hair problems in mice.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

A patient with sickle cell trait and low vitamin D might have lupus, a rare combination that needs more attention.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

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.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.