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Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Scientists identified a group of human skin cells with high growth and regeneration potential.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

Removing STAT5 from 3D-cultured human skin cells reduces their ability to grow hair.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

DPP may help hair regrowth by improving blood vessel function under stress.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

Human hair follicles can be used to create heart muscle cells.

Adalimumab significantly improved symptoms and quality of life in two patients with Hidradenitis Suppurativa.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

Two siblings have a rare hair condition caused by a new genetic variant.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

CD98hc's role in skin health decreases with age.

Immortalized human dermal papilla cells were created that grow better and can still help form hair.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

Hair cortisol may help identify adrenal insufficiency in sickle cell disease patients.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.