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DHA-NLC may improve drug delivery and reduce side effects for cancer treatment.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Haplogroup X found in Altaian population supports Amerindian origin.

CT60 polymorphism might increase the risk of Alopecia Areata.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Unmarried individuals and those with diabetes have a poorer quality of life with alopecia areata.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Vitamin D receptor FokI gene variation is not linked to alopecia areata.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

CD28 is a promising target for treating alopecia areata with belatacept.

CD28 is a promising target for treating alopecia areata with belatacept.

DALL-E 2 is only accurate for acne in pediatric dermatology and needs better data for other conditions.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

2-deoxy D-glucose does not help with hair regrowth in alopecia areata.

Certain NK cell changes in blood may indicate alopecia areata progression.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

Higher levels of IL-1R1 and hsa-miR-19b-3p may help diagnose and predict alopecia areata severity.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Laser hair removal improves quality of life but emotional benefits decrease over time, suggesting more treatments are needed for lasting effects.

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

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

The Brazilian version of the Alopecia Areata Quality of Life Index is reliable for assessing patients' quality of life.